Physical Exercise for Prevention of Falls and Fractures

Fractures
Fractures

Fisioterapia

31/03/2013

1. Introduction
Osteoporosis is a metabolic bone disease that specially affects postmenopausal women resulting in devastating effects associated to the high social-economic impact in the population in general. The World Health Organization defines osteoporosis as a skeletal disorder characterized by a reduction in bone mass with alterations in the microarchitecture of the bone tissue leading to a decrease in bone resistance and increased susceptibility to fractures (World Health Organization, 1994; Bennell et al., 2000; Gali, 2001;Szejnfeld et al., 2007).

Bone is a highly metabolic active tissue that maintains its remodeling throughout life (Hunter & Sambrook, 2000). On the other side, bone mineral density is a result of a dynamic process of bone formation and resorption called remodeling. Resorption causes the tissue deterioration, while its deposition is responsible for the reconstruction and strengthening of the deteriorated tissue. This process occurs through life in cycles of four to six months (Bemben et al., 2000).

The bone wear out in daily life demands a process of permanent remodeling. This remodeling process renews in a year about 10% of the skeleton, that is, all bone tissue is remade every 10 years (Manolagas, 2000). The global rate of bone resorption is regulated by the osteoclastic differentiation through the regulation of fundamental functional proteins, which specific role is to control its migration and resorption (Bruzzaniti & Baron, 2006). Osteoblasts are the cells responsible for the bone formation through the synthesis and mineralization of the skeleton and formation of osteoids (Bodine & Komm, 2006). Because the osteoids are not able to reproduce when they are damaged they go through a process of apoptosis, releasing osteoclast-forming inductors which will phagocyte them. This is the first stage for its replacement that will be performed by the osteoblasts (Manolagas, 2000).

In a regular remodeling process, there is a balance between the enzymatic production of osteoclasts and the production of a primary matrix of collagen and fixation of calcium promoted by the osteoblasts (Position Statement, 2002).

*Joelma Magalhães, Stella Peccin, Rebeca Teixeira, Kelson Silva,
Tiago Teixeira, Jander Souza and Virgínia Trevisani
Universidade Federal de São Paulo, Brasil
Universidade Federal do Amazonas, Brasil

Human beings reach their bone mass peak around age 30 years being strongly affected by genetic, representing 60-80% of the bone mass peak showed by an individual (Ramalho &Castro, 1999). In the adult, 90% of bone mass is resting, while 10% is in constant activity to revitalize the bone tissue. Neoformation occurs only after the resorption of a damaged bone. In a year, 25% of the trabecular bone and 1% of cortical bone are remodeled by a still unknown mechanism. During growth, the balance of this renewal is positive. In the adulthood, it is even and after age 40 it starts being negative. During the age where this balance is negative, the portion destroyed is not completely remodeled and around 1% of the bone mass is lost annually (Carvalho, 2006).

The decrease in bone mineral density (BMD) with age is considered as a physiological osteopeny, being a universal phenomenon that affects all races and cultures; nonpathological by itself in most of the individuals, but it is the background to development of osteoporosis and consequently, a higher risk of fractures (Ramalho & Castro, 1999). The sequence of this negative renewal throughout the years is responsible for the primary osteoporosis (Carvalho, 2006).

During the age-related bone loss, there is an unbalance in bone remodeling, with an increase of bone resorption compared to formation. In the stage of accelerated postmenopausal bone loss, there is a high rate of bone remodeling, with an increase in the number of osteoclasts that forms a very deep resorption cavity leading to a trabecular perforation. In the slow process of bone loss, osteoclasts build a bone resorption cavity with a normal depth, however the osteoclasts fail in replacing the new bone in a proper way (Yoshinari & Bonfá, 2000).

The incidence of osteoporotic fractures (Figure 1) is strictly related to the individual bone mass that depends on the speed of loss throughout life as well as the amount of bone tissue in the end of puberty and beginning of adulthood. The great variation in bone mass peak is explained not only by hereditary factors but also by gender, race, eating habits, several hormone influence, body composition of lean mass and body fat, intercurrent diseases, chronic use of medications and physical activity (Brandão & Vieira, 1999).

Like any other chronic disease, the ethiology of osteoporosis is multifactorial. Genetic factors contribute approximately with 46% to 62% of bone mineral density (BMD) whereas other causes include lifestyle, diet and physical exercise (Neto et al., 2002).

Osteoporosis is considered a “silent disease” until a fracture occurs. Approximately 1.5 million fractures per year are attributable to this disease. Only in the USA, these fractures result in 500.000 hospitalizations, 800.000 emergency room visits, 2.6 million physician visits. The treatment cost is high. In 2002, 12 billion dollars to 18 billion dollars were spent (Gass & Huges, 2006). In 1998, cost management of osteoporosis fractures in the UK recorded 942 million pounds per year (Szejnfeld et al., 2007). Because it is considered a “silent” disease, it may progress for decades before being diagnosed.

Osteoporosis has become one of the major public health problems. Nowadays, the impact of osteoporosis is compared to the impact caused by most important health problems, such as cardiovascular diseases and cancer (Froes et al., 2002).

It exposes the fallers to a high risk of fractures (Johnell et al., 2005; Siris et al., 2006). The first hip fracture is associated to 2.5-fold increased risk of subsequent fracture (Cólon-Emeric et al., 2003) with a high level of morbidity and mortality (Cathleen et al., 2006).

A femoral neck fracture of the hip. It is believed that about 25% of menopausal women in the USA will exhibit some kind of fracture as a consequence of osteoporosis. The most severe fractures are the fractures of femur and they are associated with higher medical expenses than all other osteoporotic fractures together (Moreira & Xaxier, 2001). The incidence of these fractures has doubled in the last 25 years and it is estimated that six million people in the world will suffer fracture of the proximal femur in 2050. Fractures resulted from the decrease of bone mineral loss are considered an orthopedic epidemic leading to an increase in costs for several countries an consequently representing a big social and economic problem (Ramalho et al., 2001).

There have been a significant number of evidences showing that the decrease in bone quality, from generation to generation, is caused by a change in life style, having as a main determinant the lack of physical activity. This evidence varies with the biology of the basic bone. However, epidemiological studies indicate that physical activity is the most important factor to maintain bone mass and prevent fractures (Mosekilde, 1995).

Almost all hip fractures (more than 90%) occur as a result of a fall and these fractures are related not only to the decreased bone mass, but also to other factors such as reduction of balance, muscle strength and power in the lower extremities (American College of Sports Medicine [ACSM], 1995; Parkkari et al. 1999). Therefore, aging and alterations in balance and muscle strength, as well as sensorial changes, predispose patients with osteoporosis to a higher risk of having fractures due to falls.

2. Physiology of aging and falls
The aaging process is associated to several anatomic and physiological changes which are directly related to musculoskeletal frailty and falls (Walsh et al., 2006). The visual system with aging tends to decrease the visual acuity and visual field, also decreasing the speed in adjusting to dark and increase in the threshold for luminosity (Sloane et al., 1989).

When the somatosensorial system gets old, it show a loss of proprioceptive fibers related to kinesthetic sensitivity. Histological studies have shown the decrease in the number of Pacini, Merkel and Meissner corpuscles in the (Sloane et al., 1989). The main structural and electrophysiological changes in the vestibular system due to aging are: after the age of 40 years, microscopic synaptic changes in the vestibular nerve, increase in the degeneration of the vestibular receptors mainly in the ampullary crest of semicircular canals and saccule at the age of 50 years, preceding the decrease in the proportion of cells in the Scarpa ganglion. After the age of 60, there is an increase in friction among the fibers of the vestibular nerve, selective loss of density in the myelin fibers leading to a decrease in conduction velocity of the electrical stimuli in the vestibular nerve, decrease of the nystagmic response to caloric and rotational tests in elderly people, decrease in the ptokinetic nystagmus amplitude and pursue eye movements, mainly for the visual stimulus with high speed (Vicini et al., 1989).

Qualitative and quantitative changes in the ciliated cells are observed as well cystic degenerations, fusion of cilia and lipofuscin inclusion in the cell (Isuji et al., 2000). The loss of ciliated cells is relevant and in general occurs in five sensorial structures of the vestibular system (three semicircular canals, saccule and utricle) in elderly patients, being greater in the crista of semicircular canals than at the saccular and utricular maculae (Isuji et al., 2000).

In the elderly, the vestibulo-ocular reflex (VOR) shows a bigger capacity of compensation than the vestibular-spinal reflex (VSR) aggravating the difficult in maintaining the stability in posture stability (Enrietto et al., 1999; Norré et al., 1987). Another factor that has an influence on the postural instability in the elderly is the alteration in the neuromuscular system.
Studies have shown that the muscle strength reaches its peak around the age of 30 years and it is satisfactory preserved up to the age of 50 years (Deschenes, 2004). However, a decrease in strength is observed around the age of 50 and 60 years, with a faster decrease after the age of 60 years (Krueger et al., 2001). The muscle mass decrease around 50% between 20 and 90 years of age and the number of fibers in the elderly is approximately 20% smaller than in the adults (Rossi & Sadler, 2002).

When measured after the 50s, the progression rate related to a reduction in strength is around 8 to 15% by decade and men, as well as women, show the same pattern of strength decrease during aging (Deschenes, 2004; Krueger et al., 2001). However, longitudinal investigations have shown a greater increase in the strength reduction in seniors than the

results found in transversal studies (Deschenes, 2004). Additional complications in muscle function associated to severe or chronic diseases, hospitalizations after trauma or surgery and lack of activity might accelerate the muscular strength decrease (Krueger et al., 2001). Age-associated decrease of muscle strength mainly results in a substantial reduction in muscle mass that follows the aging process, generating a great loss of muscle mass and an increase in the subcutaneous and intramuscular fat, denominated “sarcopenia” (Wilmore & Costill, 1999; Deschenes, 2004; Hunter et al., 2004; Krueger et al., 2001).

According to Deschenes, 2004, the decrease in the number of muscle fibers is the main cause of sarcopenia, although fiber atrophy is also involved.

A decline in strength of around 30% is observed in people with ages ranging from 50 to 70 years. These changes in the muscle structure are more common in women than in men, in the lower limbs than in the upper limbs and most of this decrease is caused by a selective atrophy in type IIB muscle fibers (American College of Sports Medicine, 1998). However, it is believed that the aging process is responsible for the loss of α motoneurons; therefore, elderly individuals would show smaller amounts of motor units. This is explained by the degeneration of neural elements, re-organization of the other components, variation in the ratio of different types of motor units and alterations in the propriety of each motor unit.

Physical Exercise for Prevention of Falls and Fractures 471 Other physiological factors also contribute for the development of sarcopenia in advanced age, such as the decreased production of anabolic hormones, which jeopardizes the musculoskeletal capacity to incorporate aminoacids and to perform the protein synthesis. An increase in the release of catabolic agents also increases the muscle wear in seniors causing a decreased supply of glycolytic enzymes and smaller supply of ATP (Deschenes et al., 2004). Studies have shown that the muscle mass starts to decrease in approximately 1% a year after the fourth decade of life. Most of the times, sarcopenia is marked by the stability of weight, due to the changes related to age in the body composition. However, several groups have reported the prevalence of sarcopenia, but these findings need to be further researched since they use different techniques to measure the lean mass and also use populations of different references. The prevalence of osteopenia and osteoporosis were estimated as 42% and 17%, respectively in women over 50 years old, where caucasian women showed the greatest number of cases of low bone density. Since the proportion of elderly older than 65 years in the population might increase, the incidence of sarcopenia and osteopenia might also increase. In women, menopause has been associated to a reduction in lean mass (LM) and bone mineral density (BMD). Several researches have demonstrated a positive relationship between LM and BMD and females with osteoporosis have been shown to have a significantly lower appendicular skeletal muscle mass compared to control groups. Based on the theory that the muscle mass is an indicator of BMD, one might speculate that sarcopenia is a risk factor for the development of oestopenia and that it is more prevalent in osteopenic individuals (Walsh et al., 2006).

Studies conducted by Walsh et al., 2006, revealed that 12.5% of postmenopausal women were osteopenic and that 25% of those postmenopausal osteopenic women and 50% of postmenopausal women with osteoporosis have sarcopenia. Therefore, they might present a higher risk of fractures compared to osteopenic women and osteoporotic women with a relatively normal skeletal muscle index.

Possible neural mechanisms that evidence this decrease in power associated to aging include the undefined changes in the CNS, a delay in the conduction velocity of motor nerve fibers and a delayed transmission in the neuromuscular junction or all three (Krueger et al., 2001). Similarly, a decrease in the number or the relative cross-sectional area of type II fibers, alterations in the sarcoplasmic reticulum and metabolism of calcium within the fibers, changes in the composition of isoforms of myosin in different fibers, functional and enzymatic properties of the myosin, an increase in the non contractile tissue, generating a greater resistance or combination of factors, might be responsible for the decreased power in the elderly (Hunter et al., 2004; Krueger et al., 2001).
The reduced capillary density and blood flow, impairment of glucose transport and lower mitochondrial density, decreased activity of oxidative enzymes and reduced rate of phosphocreatinine repletion contribute to the decrease in muscle endurance verified in people with advanced age (Krueger et al., 2001) The loss of power might cause more damage to the elderly than the loss of maximum muscle strength since the development of explosive force is an important mechanism to prevent falls and to perform heavy duties such as velocity in rising from a chair and walking (Krueger et al., 2001; Hunter et al., 2004).

A fall can be defined as a sudden, unintentional change in position causing an individual to land at a lower level in relation to his initial position (Feder et al., 2000). Almost all hip fractures occur as a result of a fall. These fractures are related not only to a decreased bone mass but also to factors such as a reduction in balance, strength and muscle

472 Osteoporosis power in the lower extremities (American College of Sports Medicine, 1995; Nyberg et al.,1996). The pathogenesis of fall is multifactorial (Nevitt et al., 1989; Tinetti et al., 1989). According to the Brazilian Society of Geriatric and Gerontology, 2008, the causes for falling might be divided in intrinsic and extrinsic and they are the following:

2.1 Intrinsic risk factors
? Previous history of falls – One or more falls in the previous year increase the risk of new falls in the subsequent year;
? Age – The prevalence of falls increases with age, however a review has shown that from 11 studies, only four found a positive association between aging and future falls;
? Females – In older women, the rate of women who fall is greater than in men and shows a greatest risk of fractures;
? Medications – Medications such as psychotropic drugs, cardiac medications like diuretics, antiarrhythmic, vasodilators and cardiac glycoside and polipharmacy (simultaneous use of four or more medications) are predisposing factors;
? Clinical condition – Diseases such as systemic arterial hypertension, diabetes mellitus and neurological or osteoarticular diseases affecting muscle strength, balance and gait are common risk factors. Orthostatic hypotension might be systematically researched due to its high prevalence. Severe diseases or unbalanced chronic conditions that affect the brain perfusion might also trigger a fall;
? Gait and balance disorders – They might be caused by aging itself, predisposing to falls when there is a decrease in force and endurance below the minimum threshold to perform independent daily life activities;
? Lack of physical exercise – The lack of physical exercise might cause an important musculoskeletal disorder;
? Psychological state – The fear of falling again after a fall is correlated to the worse performance of gait and new episodes of fall, which might restrict physical and social activities. Depression is also correlated to falls;
? Nutritional deficiency – It is related to the gait disorder, loss of muscle strength and osteoporosis;
? Cognitive impairment – Even a small deficit might increase the risk of fall;
? Visual impairment – Changes in acuity and visual field, as well as cataracts, glaucoma and macular degeneration are correlated to the increased risk of fall;
? Orthopedic disease – Diseases such as cervical spondilosis that might provoke dizziness, unbalance and feet problems, such as callus, deformities, ulcers and pain when walking also contribute to the genesis of fall;
? Functional state – the risk of falling is progressively increased according to the individual degree of dependence;

2.2 Extrinsic risk factors
The participation of environmental risk factors might reach, according to studies, up to 50% of the falls in elderly that live in the community. These factors include poor lighting, slippery surfaces, loose or folded rugs, high or narrow stairs, obstacles in the way (lowwww.intechopen.com Physical Exercise for Prevention of Falls and Fractures 473 furniture, small objects, wires), lack of rails in halls and bathrooms, extremely low or high shelves, inadequate shoes and clothes, poorly maintained streets with holes or irregularities and inappropriate orthosis.

3. Exercise prescription
Intensity, duration, frequency and progression of the training are arguable, therefore future
studies with better designs are required to evaluate these variables. Below are the exercise
prescriptions for the elderly based on some consensus found in the literature:
3.1 Pre-participation
In general, the counter-indications are similar to the ones for a young adult. However, the need of a stress ECG is contradictory and it should be considered for patients with cardiac risk factors.
3.2 How to start
The exercises might have as a purpose to improve the functional limitations that seniors might have (pain, reduced movement range or muscle weakness). As soon as the limitations are improved, a program of general conditioning should be implemented to improve health and functional capacity of the elderly. Training sessions should include three stages: warm-up, which involves low impact exercises to gain joint range of motion, training period (the effort itself), that involves muscle strengthening and/or aerobic exercises and the final stage that consists of stretching (cool down).

3.3 Stretching
Stretching should be performed during the warm up and in the last phase. A great joint range of motion (ROM) increases the muscle, reduces the risk of lesion and increases the cartilage nutrition. Painful joints should not be stretched excessively to a point that will result in more pain; all movements should be made in order to get the maximum pain-free ROM. The use of heat before stretching reduces pain and increases the range. At least three sessions of stretching might be performed a week. In the beginning, three to five repetitions and a gradual increase up to 10 repetitions is the ideal. The muscle should be stretched during 10 to 30 seconds.

3.4 Muscle strengthening
Muscle strengthening should be acquired with weights or elastic bands which will give endurance to the movement. The training protocols should include the following principles:
- muscle contraction exercises should be made in a moderate speed;
- exercises should be chosen according to joint stability and degree of pain and edema;
- muscles should not be exercised to fatigue;
- exercise endurance should be submaximal;
- inflamed articular joints should be strengthen with isometric exercises and at first it should include few repetitions;
- pain or edema in a joint after an hour of exercise indicates excessive activity.
- Isometric exercises are indicated for unstable or swollen joints. On the other hand, isometric contractions result in a low articular pressure and are well tolerated by older patients. It should start with contractions with an intensity of approximately 30% of maximal strength, slowly increasing to 80%. The contraction should not be kept for more than 6-10 seconds and the repetitions should be increased from 8 to 10, if tolerated by the patient. It should be performed twice a day during the inflammatory period and after the inflammation is over, it should be increased from 5 to 10 times a day.
- Isotonic exercises should include from 8 to 10 exercises involving the major muscle groups (four exercises for the upper limbs and from four to six for the lower limbs). At first, patients should use weights with 40% of the individual’s maximal load, increasing up to 80%. Generally, a series of four to six repetitions should be made, avoiding the muscle fatigue. At first, the frequency should be at most twice a week but in case of individuals with advanced age or significant fragility the exercises should be made only once a week. Between the sessions, there might be at least one full day of rest.

4. Physical exercise to prevent falls
Prevention in individuals older than 60 years has an important role in avoiding adverse consequences resulting from falls (Weatherall, 2004). The work to prevent fractures related to osteoporosis should focus the prevention or increase of material and structural properties of the bone, the prevention of falls and improvement of total mass of lean tissue (American College of Sports Medicine, 1995).The American College of Sports Medicine recommends that:

1. physical activity of transporting weight is essential to the normal development and maintenance of a health skeleton. Activities that focus the increase of muscle strength might also be beneficial, particularly for bones that do not support weight;
2. a sedentary woman might progressively increase her bone mass by becoming active, but the primary benefit of increasing the activity is to prevent a future bone reduction that resulting from the lack of activity;
3. exercise should not be recommended as a replacement to medications treatment; 4. the optimal program for an older woman might include activities that improve the strength, flexibility and coordination which might indirectly, but effectively decrease the incidence of osteoporotic fractures by reducing the probability of falls. Therefore, the treatment of osteoporosis should aim the prevention of falls and fractures and preservation or improvement of bone mineral density.

4.1 Exercises for postural control
Postural control is a result of the combination of several types of sensorial information, such as visual, vestibular and somatosensorial information, and passive and active properties of the nervous system and skeletomuscle system that composes the human postural control system (Figure 2), (Shumway-Cook et al., 2000). The postural control system use three functions that are required to maintain balance: support, stabilization and balance. The body should contract the adequate muscles to sustain the body against gravity; the articular segments should be stabilized and the body should be stabilized in the body’s support base (Rothwell, 1994).
Currently, proprioception is defined as a set of afferent information provided by joints, muscles, tendons and other tissues that reaches the Central Nervous System (CNS) where it Physical Exercise for Prevention of Falls and Fractures 475 is processed, having an influence on reflex responses and voluntary motor control. Proprioception contributes to postural control, joint stability and several conscious sensations (Lephart & Fu, 2000).

It is extremely important to understand that proprioception is only limited to the acquisition of the mechanical stimulus and its transduction in neural stimuli, not having any influence on the CNS processing and its motor response (Lephart & Fu, 2000). Proprioception is part of a system denominated somatosensorial system. This includes all mechanical information provided by the mechanoreceptors. The feeling of pain is provided by the nociceptors and the thermal information provided by thermoreceptors (Guyton & Hall, 2006).

All propriocetive information are originated at the muscular and tendon receptors called muscular fusion and Golgi tendon organ and receptors located in ligaments, articular capsule, meniscus and cutaneous tissues (Guyton & Hall, 2006). Four elements should be focused to reestablish the sensorimotor deficits: proprioception, stabilization, reactive neuromuscular control and functional motor patterns (Lephart & Henry, 1995).

The proprioceptive mechanism comprises both conscious and unconscious pathways. Therefore, the prescribed exercises need to include conscious exercises to stimulate the cognition as well as sudden and unexpected alterations of joint position that initiate reflex muscle contraction. These exercises should involve balance in an unstable surface while the individual perform functional activities. The purpose of the dynamic stabilization training is to improve the co-activation between the antagonist muscles (Hurd et al., 2006)

Exercises to stimulate proprioception and dynamic stabilization should be performed in closed-chain activities and with small movements, since the compression stimulates the articular receptors and the changes in the curve length-tension stimulate the muscle receptors. Limbs repositioning exercises should also be performed to stimulate the sense of joint position and neuromuscular control (Lephart & Henry, 1995).

The improvement of dynamic stiffness is another important aspect. It is suggested that muscle receptors increase its sensitivity through the increase of dynamic stiffness (Adler et al., 2008). Fig. 2. Balance control: Sensory and motor system. Credit: http://resourcesonbalance.com

Exercises that involve eccentric training, like going down the stairs and landing after jumps, are the most efficient to increase anticipatory and reactive muscular stiffness (Bastian et al.,2006). The reactive neuromuscular control is reached through exercises that create unexpected situations, such as perturbations in unstable surfaces in unipodal support and during gait. Apparently, this kind of training improves the preparatory and reactive muscle activation (Swanik et al., 2002).

The training protocol might include:
1. 5 – 10 minutes of warm-up, with stretching movements for upper and lower limbs, 03 repetitions for each movement being kept for 30 seconds, with 30-second intervals among the series. After stretching, movements of fast gait as previous warm-up were performed and in the end of the session, slow gait movements and stretching.

2. Proprioceptive exercises followed an evolution sequence based on the use of stable surfaces to unstable, walking straight forward progressing to changes in direction, from gait with no obstacles to gait with obstacles, alteration in the support base (from open to closed), exercises with eyes open to closed eyes, always respecting the functional capacity of each patient and progressively increasing the difficulty of each exercise. To aid the training, cones, balance boards, sticks, mats and trampolines were used. According to the patient’s evolution, the exercises were combined creating the circuits

Evidences have shown that specific exercises might reduce the risk factors for falls and number of falls in older people (Lord & Clark, 1996; Robertson et al., 2001-1, 2001-2; Hartard et al., 1996).

In 2006, Carvalho stated that the main goal of the osteoporosis treatment is to prevent fractures and as 90% of the fractures resulted from falls, the fundamental part of fracture treatment is to prevent them. This prevention represents a great area of interest in researches on older people’s health (Weatherall, 2004).

Because of the strong interaction between osteoporosis and falls, the selection of participants in protocols for the prevention of fractures should be based on factors related to bones and falls (Pfeifer et al., 2004).
The German Society of Sport Medicine and the American College of Sport Medicine also recommend that the ideal program for women with osteoporosis should include activities that improve strength, flexibility and coordination that might indirectly and more effectively decrease the incidence of osteoporotic fractures by the reduction in the probability of falls(Lange et al., 2005).

Data combined from three studies conducted by Gillespie et al., 2006, with a total of 556 women aged 80 years or older, who underwent to the same progressive muscular strengthening program, balance training and gait training indicate that this intervention decreased the number of individuals that fell during a year, having also reduced the number of injurious falls. Although the studies had methodological limitations, there is a determined consistency as for the decrease of falls in multiple interventions exercises (Gillespie et al.,2009). As for the physical exercise, we only know that it improves balance without a direct association with the decrease in the number of falls (Howe Tracey et al., 2009) and that although the decline in muscle strength is a risk factor for falls, the muscle strength training could not be associated to the reduced number of falls (Sherrington et al., 2008; Gillespie, et al., 2009).

Few studies take into consideration the importance of the proprioceptive training as a fundamental and unseparable part of a muscular strengthening program. Mechanoreceptors located in the joints, tendons, muscles and neighbor tissue provide information to the Nervous System about the position and articular movements and about the forces generated in the muscles (Hurley, 2003; Van der Esch et al., 2007).

The knee proprioception is essential for the modulation and accurate activation of the muscle contraction, once the functional skill and muscular balance are strongly affected by the proprioceptive inaccuracy and muscle weakness (Van der Esch et al., 2007). Studies including patients with knee ligament lesions show that the proprioceptive training promotes additional sensorial information that contributes to the improvement in postural control (Bonfin et al., 2008). This relationship becomes even more important when the muscle strengthening program aims to improve the functional balance and prevention of falls.

The significant results found in the present research might be explained by the concern in following the ACSM recommendations when prescribing exercises, respecting the basic concepts of prescription exercises.

Additionally, one should take into consideration that the skill to develop muscle strength decreases with aging (Hakkinen et al., 1998) explaining the importance of the gradual progression (Adams et al., 1999). With sedentary elderly people, a period of adaptation and low working load for two weeks should be applied for further implementation of a loading progression protocol (American College of Sports Medicine, 2002).

Teixeira et al., 2010, after eighteen weeks of training, observed an average increase of 87.5% in the maximal dynamic muscle strength in the quadriceps (1-RM) in volunteers in the intervention group, which is similar to the results found by Humphries et al., 2000, showing an increase from 20 to 200% in the dynamic muscle strength of the quadriceps depending on the figures in baseline and time of training. This increased knee extension strength is significantly important since the knee extension strength is an independent risk factor for falls and fractures caused by osteoporosis (Nguyen et al., 1993). The increase in strength results from neural alterations and muscle adaptations (Resende et al., 2008).

The combination of muscle strength and proprioceptive training was fundamental for a research that included postmenopausal women with osteoporosis conducted by Teixeira et al., 2010. The authors found an increase in mobility and functional capacity that might be related to a 36% decrease in time for performing the timed up & go test. We could observe that the shorter the time spent to perform the test, the better the balance (Resende et al.,2008). In this research, Teixeira et al., 2010, observed an improvement in balance evaluated by the Berg Balance Scale, where although there were small numerical changes, it was consistent, agreeing with the outcomes found by Madureira et al., 2006.

Bemben et al., 2000, compared the effects of high and low-intensity training in 25 postmenopausal women (41 to 60 years old) using a high repetition (40% 1-RM, 16 repetitions) and high load (80 % 1-RM, 8 repetitions) protocols for six months showing increases from 30 to 40%, respectively in the dynamic strength in quadriceps.

In a randomized controlled trial of 10 weeks of strength, balance and stretching training in 53 postmenopausal women with osteoporosis, Malmros et al., 1998, showed that strength and muscle mass and also the static balance improved significantly.

In another randomized clinical trial, physiotherapy-directed exercise in 30 patients with osteoporosis significantly improved static balance measured by functional reach and increased quadriceps dynamic strength (Mitchell et al., 1998).

These two studies indicate that the exercises programs improved the profile of fall risk but showed limitations because of the small number of samples and short time of the interventions.

Hartard et al., 1996, studied the effects of muscle strength training in 16 postmenopausal women with osteopenia, where fifteen belonged to the control group. Although they used a small group, a proper load protocol for 6 months, twice a week at 70% 1RM was applied demonstrating a considerable increase in muscle strength ranging from 44 to 76%, with results similar to the ones found in the present investigation.
Kemmler et ak., 2002, evaluated the dynamic force (1RM tests) in 137 postmenopausal women with osteopenia divided in two groups and observed a significant increase of 43% in the leg press in the intervention group training at 70% of 1-RM for fourteen months. Carter et al., 2001, in a program that trains instructors to work with the community selected 93 postmenopausal women with osteoporosis who were randomized and underwent physical exercises of balance and muscle strength for twenty weeks. No improvement in the quality of life was found, which might be explained by the high quality of life at baseline. Researchers observed an improvement of 6.3% in the dynamic balance and an increase of 12.8% in the muscular strength.

On the other hand, Teixeira et al., 2010, showed a significant improvement in the quality of life evaluated by SF-36, where the values (regarding the physical aspects as well as mental aspects) were considerably superior than the controls and values at baseline. These results might be related to the systemic physiologic benefits provided by training, resulting in a better skill to perform daily life activities. We also related these results to the psychological effects of training, socialization with other patients and low initial levels of quality of life.

Madureira et al., 2006, conducted a randomized clinical trial that included 66 postmenopausal women with osteoporosis assigned to two groups. One of the groups underwent a 12-month of balance training once a week combined with oriented training at home showing significant results concerning balance, mobility and decrease in the number of falls.

Swanenburg et al., 2007, studied 24 women (65 years old or older) with osteoporosis or osteopeny who underwent three months of strength, balance and coordination training. After twelve months, they observed a reduction in the risk of fall (Berg Scale) and increase in the muscle strength of lower limbs. They also found a decrease in the number of falls in the intervention group (89%), showing a significant number although it was a pilot study.

As for the reduction of the risk of fall, although it shows an average of 40% (Barnett et al., 2003; Teixeira et al., 2010) it still is not well evidenced, which might be explained by the use of different populations and mainly the interventions used. Several studies have shown to be effective in increasing the strength, improving the balance and functional capacity and decreasing the risk of falls (Table 2). Only the researches carried out by Madureira et al., 2006, Swanenburg et al., 2007 and Teixeira et al., 2010, directly associate these results and the number of falls demonstrating how effective these interventions were.

5. Muscle strength training and the use of vibration platform Although factors as genetic, hormonal homeostasis and nutrition may be affect the bone
mineral density, the level of physical activity seems to have an important influence on this variable. The physiological mechanism that explains the osteogenic action of physical activity is not clearly understood. The moment the bone is compressed; negative charges in the place compressed are generated and positive charges in other areas (Figure 4).

Fig. 4. a) The application of force to a slightly bent bone produces a greater compressive force on the inside curvatures. Compressive force producers weak electrical currents which stimulate osteoblast; b) Over time, bone is deposited in the inside curvature and removed from outside curvature; c) The final results is a bone matched to the compressive force to which it is exposed. Credit: Copyright, Person Education, Benjamin Cumings. Minimal amounts of electric current stimulate the osteoblasts (bone-forming cells) in the negative extremity that is being compressed, increasing the bone formation in this area (Bankoff et al., 1998).

Another aspect that should be taken into consideration when ideally prescribing the strengthening training in order to stimulate the bone formation is the type of muscle contraction used. In studies comparing the eccentric and concentric strength training with the same relative load, the first showed to be more effective increasing the BMD (Hawkins et al., 1999; Hortobágvi et al., 1996; Aagaard et al., 2000).

The mechanism to increase the bone mineral density (BMD) through the strength training depends on the magnitude of bone deformation caused during this activity. In fact, higherintensity training related to maximum load is generally associated to greater stimuli for the increase of BMD compared to low-intensity training (Kerr et al., 2001; Vincent & Braith, 2002). Besides that, the use of higher-intensity training implies in more immediate responses in the BMD.

Therefore, it can be concluded that in order to have a strength training providing beneficial effects over bone density, it is important to follow and respect some basic principles of physical training, such as proper overload, volume and intensity. On the other side, this training modality is the one that allows the greatest control of these variables.

5.1 Vibration platform
Vibration platform is a new type of exercise involving the application of a vibratory stimulus to the entire body as opposed to local stimulation of specific muscle groups (Merriman & Jackson, 2009) and has been increasingly tested for the ability to prevent bone fractures and osteoporosis in frail people (Gusi et al., 2006). It has become increasingly popular over the last several year as a form of physical training (Merriman & Jackson, 2009),since it is a non-pharmacological treatment alternative for osteoporosis (Cardinale & Wakeling, 2005). The platform can increase bone strength and bone mass (Sehmisch et al.,2009) since the vibration provides a low level of mechanical load stimulating, therefore the bone remodeling (Hannan et al., 2004). This can be explained by the combined effect on the neuromuscular and neuroendocrine systems (Cardinale & Wakeling, 2005). Vibrational physical exercise causes reflecting muscle contractions like tonic vibration reflex. This type of intervention leads to a high intensi e stimulation of proprioceptors called muscle spindles which result in alteration in parameters of activity and development of human physiological functions (Piatin et al., 2009).

The vibrating devices currently marketed show two types of vibrating plates: a) the whole plate oscillates up and down; b) vertical displacements on the left and right side of a fulcrum, increasing the lateral accelerations (Gusi et al., 2006), (Figure 5). The units provide a vibration by using either a rotational or vertical stimulus, that is, the platform rotates about an anterior-posterior axis so that the positioning of feet further apart results in increased amplitude of movement and applies force asynchronously to the left and right foot, similar to standing near the middle of a ‘teeter-totter. Vibration units that provide a vertical stimulus have a platform that translates vertically and symmetrically causing simultaneous movement of the lower extremities in the same direction. In addition to the duration of the vibration stimulus, there are several treatment parameters that are important to consider. These include frequency (Hz), amplitude (mm), duration and vibration magnitude (g), which is a gravitational acceleration imposed on the body.
However, some studies have used frequencies ranging from 25-50 Hz, amplitudes from 2-10 mm, and total durations of 30 sec — 10 minutes. Currently, there is no consensus regarding the correct parameters needed to achieve a specific physiological response (Merriman & Jackson, 2009). However, some researchers have used frequencies ranging from 15-35 Hz to obtain a maximum transmissibility of the mechanical stimulus produced by the vibratory plate. Some recent studies have included in their protocols 15/10-Hz frequencies to allow a smooth adjustment in individuals considered frail, like the elderly (Gusi et al., 2006).

The effects of this vibration have been studied extensively in occupational medicine, mainly in industrial settings. It has been shown that when the body undergoes chronically to whole body vibrations spinal degeneration is likely to be one of the deleterious outcomes. Symptom of low back pain has been shown to be the leading major cause of industrial disability in the population under the age of 45 years (Cardinale & Pope, 2003).

In a research conducted by Rubin et al., 2001, in adult rats, they found out that a combination of low magnitude and high frequency vibration significantly increased the anabolic activity of bone, bone density and specifically bone formation. Studies (Torniven et al., 2003) in animals have shown that the vibrations might be an effective and safe way to improve mass competence and bone mechanic, providing a great potential to prevent osteoporosis.

High frequency (28Hz), very-low-magnitude vibration exercise has recently been reported to increase bone mass in experimental animals and in humans (Russo et al., 2003). Therefore, in order to obtain bone reinforcement, the frequency and amplitude of vibration should not exceed specified levels for the treatment. Furthermore, low-frequency vibration does not stimulate the bone sufficiently to cause significant remodeling (Aleyaasin & Harrigan, 2008).

Fractures are among the commonest and most expensive health problems in the elderly population, therefore the physical exercise is considered an effective and frequently recommended strategy. However, hard bone stress induced by the vigorous activity of weight bearing might increase the risk of lesions (Gusi et al., 2006; Gilsanz et al., 2006).

Although evidence is overwhelming that physical exercise positively affects muscle strength at all ages, compliance of older persons with traditional exercise programs is low, and only a small percentage of older persons exercise regularly (Russo et al., 2003). According to Liu et al., 2011, osteoporosis and its associated fractures are common complications of aging and that the purpose of most therapeutical strategies is to prevent and/or treat bone loss focused on nonpharmacological approaches. Therefore, aerobic exercise and/or whole-body vibration (WBV) might have beneficial effect on bone mass and provide an alternative approach to increase or maintain bone mineral density and reduce the risk of fracture (Table 3).

However, the mechanism through which the vibrations influence the bone tissue is still obscure. There is a lack of understanding the physiological mechanisms involved in the adaptive responses or the most appropriate vibration parameters to be used in order to maximize gains (Santin-Medeiros & Garatachea, 2010; Cardinale & Rittweger, 2006). The high-frequency postural displacements induced by the alternating movements of the platform produce reflex muscle contractions aimed at stabilizing posture. Thus, vibration can be viewed as a special form of muscle training that may particularly affect muscle power. It has been proposed that the force applied to bone during muscle contraction has a pivotal role in the homeostatic and adaptive regulation of bone strength (Russo et al., 2003).

However, researchers (Torniven et al., 2003) carried out a study with the vibration platform and concluded there was no effect on the bones of young and healthy adults.

Physical Exercise for Prevention of Falls and Fractures 485
In a systematic review (Merriman & Jackson, 2009) conducted about the vibration platform to understand the effects on bone density, muscle performance, balance, and functional mobility in older adults concluded that most of the studies is methodologically weak and should be interpreted with caution. The study protocols use widely variable parameters which make the study interpretation difficult. The effects of this long term vibration ( >1 year) still need to be studied. Some but not all of the studies in this review reported that individuals exposed to those vibrations showed similar improvements in muscle performance, balance, and functional mobility as compared to traditional exercise programs and that the vibration platform does not provide any additional benefit. Bone studies consistently showed that WBV improved bone density in the hip and tibia but not in the lumbar spine. Additional studies are needed to determine safe and effective parameters for WBV training in older adults.

However, the treatment has to follow specific safety guidelines to prevent vibration exercise-related injuries, such as limiting the exposure to vibration to a maximum of 10 minutes and maintaining a good posture of the participant.

Due to a great controversy in studies on its effects and parameters, more studies in humans with specific clinical recommendations and protocols are necessary for the vibration training (Gusi et al, 2006; Torniven et al., 2003).

6. Conclusion
Physical activity is an essential factor in bone health. The benefits of exercise have been demonstrated throughout the life cycle. Exercise can positively affect peak bone mass in children and adolescents; has been shown to help maintain or even modestly increase bone density in adulthood and; can assist in minimizing age related bone mass peak loss in older adults. Physical exercises that cause mechanical stress are the most recommended to increase or keep bone mass. However, the prevention of falls seems to be the most important factor in decreasing the risk of fractures in women with osteoporosis and in elderly people, since more than 90% of hip fractures results from falls.

7. Acknowledgments
The authors would like to thank Universidade Federal de São Paulo and Universidade Federal do Amazonas for all the support given when developing this project and also translator Cybeles Lehner for her great contribution to this chapter.
8. References
Aagaard, P.; Simonsen, EB.; Andersen, JL.; Magnusson, SP; Halkjaer-kristensen, J. & Dyhrepoulsen, P. (2000). Neural inhibition during maximal eccentric and concentric quadriceps contraction: effects of resistance training. J Appl Physiol. 89:2249-57.
Adams, KL.; Barnard, KL.; Swank, AM.; Mann, E. & Kushnick, MR. (1999). Denny M. Combined high-intensity strength and aerobic training in diverse phase 11 cardiac rehabilitation patient. J Cardiopulm Rehabil. 19:209-215.
Adler, SS.; Beckers, D. & Buck M. (2008). PNF in practice: an illustrated guide. 3rd ed. Berlin: Springer.
Aleyaasin, M & Harrigan, JJ. (2008). Vibration exercise for treatment of osteoporosis: a theoretical model. Proc Inst Mech Eng H. Oct;222(7):1161-6. American College of Sports Medicine. (1995). Guidelines for Exercise Testing and Prescription. 5th Ed. Baltimore: Williams and Wilkins, pp. 1–373.
American College of Sports Medicine. (1998). Position Exercise and physical activity for older adults. Med Sci Sports Exerc. 30: 992-1008.
American College of Sports Medicine. (2002). Position Stand on Progression Models in Resistance Training for Healthy Adults. Med Sci Sports Exerc. 34 (2): 364-380.
Bankoff, ADP.; Zylberberg, TP. & Schiavon, LMA. (1998). A osteoporose nas mulheres pósmenopausa e a influência da atividade física: “uma análise de literatura”. Revista da Educação Física/UEM. 9(1), 93-101.
Barnett, A.; Smith, B.; Lord, SR.; Williams, M. & Baumand, A. (2003). Community-based group exercise improves balance and reduces falls in at-risk older people: a randomized controlled trial. Age Ageing. 32: 407-414.
Bastian, AJ. (2006). Learning to predict the future: the cerebellum adapts feedforward movement control. Curr Opin Neurobiol. 16 (6): 645-9.
Bemben, DA.; Fetters, NI.; Bemben, MG.; Nabavi, N. & Koh, ET. (2000). Musculoskeletal responses to high- and low-intensity resistance training in early postmenopausal women. Med Sci Sports Exerc. 32: 1949-1957.
Bennell, K.; Khathan, K. & Mckay, H. (2000). The role of physiotherapy in the prevention and treatment of osteoporosis. Man Ther. 5(4): 198-213.
Bodine, P N. & Komm, BS. (2006). Wnt signaling and osteoblastogenesis. Rev Endocr Metab Disord. 7: 33-39
Bonfim, TR.; Grossi, B.; Paccola, AJ. & Barela, JA. (2008). Additional sensory information reduces body sway of individuals with anterior cruciate ligament injury. Neuroscience Letters. 441: 257-260.
Brandão, CMA. & Vieira, JGH. (1999). Fatores envolvidos no pico de massa óssea. Arq Bras Endocrinol Metabol. 43(6):401-408.
Bruzzaniti, A. & Baron, R. (2006). Molecular regulation of osteoclast activity. Rev Endocr Metab Disord. 7: 123-139.
Buksman, S.; Vilela, ALS.; Pereira, SEM.; Lino, VS. & Santos, VH. (2008). Quedas em idosos: Prevenção. Guidelines: Brazilian Society of Geriatric and Gerontology. p. 1-10.
Burke TN.; França FJ.; Ferreira de Meneses SR.; Cardoso VI. & Marques AP. (2010). Postural control in elderly persons with osteoporosis: Efficacy of an intervention program to improve balance and muscle strength: a randomized controlled trial. Am J Phys Med Rehabil. Jul; 89(7):549-56.
Cardinale, M. & Pope, MH. (2003). The effects of whole body vibration on humans: dangerous or advantageous?. Acta Physiol Hung. 90(3):195-206.
Cardinale, M. & Rittweger, J. (2006). Vibration exercise makes your muscles and bones stronger: fact or fiction?. Jounal of the British Menopause Society. Mar;12(1):12-17. ]
Cardinale, M. & Wakeling, J. (2005). Whole body vibration exercise: are vibrations good for you?. Br J Sports Med. Sep;39(9):585-9.
Carter, ND.; Kannus. P. & Khan, KM. (2001). Exercise in the prevention of falls in older people. Sports Med. 31(6): 427-438. Physical Exercise for Prevention of Falls and Fractures 487
Carvalho, MI. (2006). Osteoporose: Visão do Ortopedista. Rev Bras Ortop. 41(4): 91-97.
Cathleen, S.; Colón-Emeric, C. & Saag, KG. (2006). Osteoporotic fractures in older adults. Best Pract Res Clin Rheumatol. August; 20(4): 695–706.
Cólon-Emeric, C.; Kuchibhatla, M.; Pieper, C.; Hawkes, W.; Fredman, L.; Magaziner, J.; Zimmerman, S. & Lyles, KW. (2003). The contribution of hip fracture to risk of subsequent fractures: data from two longitudinal studies. Osteoporos Int. 14 (11): 879–883.
Deschenes, M. R. (2004). Effects of aging on muscle fibre type and size. Sports Medicine, v. 34, n. 12, p. 809-824.
Enrietto, JA.; Jacobson, KM. & Baloh RW. (1999). Aging effects on auditory and vestibular response: a longitudinal study. Am J Otolaryngol. 20(6):371-8.
Feder, G.; Cryer, C.; Donovan, S. & Carter, Y. (2000). Guidelines for the prevention of falls in people over 65. BMJ. 321: 1007-1011.
Froes, NDTC.; Pereira, ES. & Negrelli, WF. (2002). Fatores de risco da osteoporose: prevenção e detecção através do monitoramento clínico e genético. Acta Ortop Bras. 10 (1): 52-57.
Gali, JC. (2001). Osteoporose. Acta Ortop Bras. 9: 3-12.Gass, M. & Huges, BD. (2006). Preventing osteoporosis – related fractures: An overview. Am J Med. 119(4A): 3-11.
Gillespie, LD.; Gillespie, WJ.; Robertson, MC.; Lamb, SE.; Cumming, RG. & Rowe, BH.2006) Interventions for preventing falls in older people living in the community (Cochrane Review). In: Cochrane Database Syst Rer. Issue 1. Oxford: Update Software.
Gillespie, LD.; Gillespie, WJ.; Robertson, MC.; Lamb, SE.; Cumming, RG. & Rowe, BH. (2009). Interventions for preventing falls in older people living in the community(Cochrane Review). In: Cochrane Database Syst Rer. Issue 1. Oxford: Update Software.
Gilsanz, V.; Wren, TA.; Sanchez, M.; Dorey, F.; Judex, S. & Rubin, C. (2006). Low-level, highfrequency mechanical signals enhance musculoskeletal development of young women with low BMD. J Bone Miner Res. Sep;21(9):1464-74.
Gusi, N.; Raimundo, A. & Leal A. (2006). Low-frequency vibratory exercise reduces the risk of bone fracture more than walking: a randomized controlled trial. BMC Musculoskeletal Disorder. 7:92.
Guyton, AC. & Hall, JE. (2006). Textbook of medical physiology. 11 ed. Philadelphia: WB Saunders.
Häkkinen, K.; Kallinen, M.; Izquierdo, M.; Jokelainen, K.; Lassila, H.; Mälkiä, E.; Kraemer, WJ.; Newton, RU. & Alen, M. (1998). Changes in agonist-antagonist EMG. muscle CSA. and force during strength training in middle-aged and older people. J Appl Physiol. 84 (4): 1341-1349.
Hannan, MT.; Cheng, DM.; Green, E.; Swift. C.; Rubin. CT. & Kiel, DP. (2004). Establishing the compliance in elderly women for use of a low level mechanical stress device in a clinical osteoporosis study. Osteoporos Int. Nov;15(11):918-26.
Hartard, M.; Haber, P.; Ilieva, D.; Preisinge, E.; Seidl, G. & Huber, J. (1996). Strength training as a model of therapeutic intervention: A Controlled Trial in Postmenopausal Women with Osteopenia. Am J Phys Med Rehabil. 75(1):21-28.
Hawkins, SA.; Schroeder, T.; Wiswel, RA.; Jaque, SV.; Marcell, TJ. & Costa, K. (1999). Eccentric muscle action increases site specific osteogenic response. Med Sci Sports Exerc. 31: 1287-92.
Hortobágyi, T.; Hill, J.; Houmard, JÁ.; Fraser, DD.; Lambert, NJ. & Israel, RG. (1996). Adaptative responses to muscle lengthening and shortening in humans. J Appl Physiol. 80:765-72.
Hourigan SR.; Nitz JC.; Brauer SG.; O'Neill S.; Wong J. & Richardson CA. (2008). Positive effects of exercise on falls and fracture risk in osteopenic women. Osteoporos Int. 200 Jul;19(7):1077-86. Epub 2008 Jan 11.
Howe, TE.; Rochester, L.; Jackson, A.; Banks, PMH. & Blair, VA. (2009). Exercise for improving balance in older people (Cochrane Review). In: The Cochrane Library, Issue 1. Oxford: Update Software.
Humphries, B.; Newton, RU.; Bronks, R.; Marshall, S.; McBride, J.; Triplett-McBride, T.;
Hakkinen, K.; Kraemer, WJ. & Humprhies, N. (2000). Effect of exercise intensity on bone density, strength, and calcium tumover in older women. Med Sci Sports Exerc. 32: 1043-50.
Hunter, DJ. & Sambrook, PN. (2000). Bone loss: Epidemiology of bone loss. Arthritis Res. 2(6): 441-445.
Hunter, GR.; McCarthy, JP. & Bam-Man, MM. (2004). Effects of resistance training on older adults. Sports Medicine. v.34, p. 330-348.
Hurd, WJ.; Chmielewski, TL. & Snyder-Mackler L. (2006). Perturbation-enhanced neuromuscular training alters muscle activity in female athletes. Knee Surg Sports Traumatol Arthrosc. 14(1): 60-69. Hurley, MV. (2003). Muscle dysfunction and effective rehabilitation of knee osteoarthritis: what we know and what we need to find out. Arthritis Rheum. 49: 444–52.
John, R. (1994). Control of Human Voluntary Movement. 2.ed. London: Chapman & Hall.
Johnell, O.; Kanis, JA.; Oden, A.; Johansson, H.; De Laet, C.; Delmas, P.; Eisman, JA.;
Fujiwara, S.; Kroger, H.; Mellstrom, D.; Meunier, PJ. Melton, LJ 3rd.; O'Neill, T.; Pols, H.; Reeve, J.; Silman, A. & Tenenhouse, A. (2005). Predictive value of BMD for hip and other fractures. J Bone Miner Res. 20 (7):1185–1194.
Kemmler, W.; Engelke, K.; Lauber, D.; Weineck, J.; Hensen, J. & Kalendertitle, WA. (2002). Exercise effects on fitness and bone mineral density in early postmenopausal women: 1-year EFOPS: Med Sci Sports Exerc. 34 (12) 2115-23.
Kerr, D.; Ackland, T.; Maslen, B.; Morton, A. & Prince, R. (2001). Resistance training over 2 years increase bone mass in calcium-replete in postmenopausal women. J Bone Miner Res.16:170-81.
Krueger, DBS.; Chegovich, MM.; Binkley, NMD. (2001). Osteoporose. In: Kauffman, T. L. Manual de reabilitação geriátrica. Guanabara Koogan: Rio de Janeiro.
Lange, U.; Teichmann, J. & Uhlemann, C. (2005). Current knowledge physiotherapeutic strategies in osteoporosis prevention and treatment. Rheumatol Int. 26: 99-106.
Lephart SM, Fu FH, Borsa JP, Warner JP. (1994). Proprioceptive of the shoulder joint in healthy, unstable, and surgically repaired shoulders. J Shoulder Elbow Surg. 3: 371–380.
Lephart, SM. & Henry TJ. (1995). Functional rehabilitation for the upper and lower extremity. Orthop Clin North Am. 26(3): 579-92.
Liu, PY.; Brummel-Smith, K. & Ilich, JZ. (2011). Aerobic exercise and whole-body vibration in offsetting bone loss in older adults. J Aging Res. Jan 3;2011:379674.
Lord, SR. & Clark RD. (1996). Simple physiological and clinical tests for accurate prediction of falling in older people. Gerontology. 42:199-203.
Madureira, MM.; Takayama, L.; Gallinaro, AL.; Caparbo, VF.; Costa, RA. & Pereira, RM. (2006). Balance training program is highly efective in improving funtional status and reducing the risk of falls in elderly women with osteoporosis: a randomized controlled trial. Osteoporos Int. 252-5.
Malmros, B.; Mortenson, L.; Jensen, MB. & Charles, P. (1998). Positive effects of physiotherapy on chronic pain and performance in osteoporosis. Osteoporos Int. 8:215-21.
Manolagas, SC. (2000). Birth and death of bone cells: basic regulatory mechanisms and implications for the pathogenesis and treatment of osteoporosis. Endocr Rev. 21(2):115-37
Merrimam, H. & Jackson, K. (2009). The Effects of Whole-Body Vibration Training in Aging Adults: A Systematic Review. Journal of Geriatric Physical Therapy. 32(3):134-145.
Mitchell, SL.; Grant, S. & Atchison, T. (1988). Physiological effects of exercise on postmenopausal osteoporotic women. Physiotherapy. 84:157-63.
Moreira, C. & Xavier, JD. (2001). Doenças Ósteo-metabólicas. In: Reumatologia, diagnóstico e tratamento. Guanabara Koogan, 2ª ed, pp. 327-350. Mosekilde L. (1995). Osteoporosis and Exercise. Bone. 17(3): 193-195.
Neto, AMP.; Soares, A.; Urbanetz, AA.; Souza, ACA.; Ferrari, AEM. & Amaral, B et al. (2002). Consenso Brasileiro de Osteoporose. Rev Bras Reumatol. 42(6):343-354.
Nevitt, MC.; Cummings, SR.; Kidd, S. & Black D. (1989). Risk factors for recurrent nonsyncopal falls. A prospective study. JAMA. 261:2663–2668.
Nguyen, T.; Sambrook, P.; Kelly, P.; Jones, G.; Lord, S.; Freund, J. & Eisman, J. (1993). Prediction of osteoporotic fractures by postural instability and bone density. BMJ. 307(6912):1111-5.
Nyberg, L.; Gustafson, Y.; Berggren, D.; Brännström, B. & Bucht, G. (1996). Falls leading to femoral neck fractures in lucid older people. J Am Geriatr Soc. 44 (2):156–160.
Parkkari, J.; Kannus. P.; Palvanen, M.; Natri, A.; Vainio, J.; Aho, H.; Vuori, I. & Järvienen, M. (1999). Majority of Hip Fractures Occur as a Results of a Fall and Impact on the Greater Trochanter of the Femur: A Prospective Controlled Hip Fracture Study with 206 Consecutive Patients. Calcif Tissue Int. 65:1983-187.
Pfeifer, M.; Sinaki, M.; Geusens, P.; Boonen, S.; Preisinger, E. & Minne, HW. (2004). Musculoskeletal rehabilitation in osteoporosis: A review. J Back Musculoskeletal Rehabil. 19(8):1208-1213.
Piatin, VF.; Shirolapov, IV. & Nikitin, OL. (2009). Vibrational physical exercises as the rehabilitation in gerontology. Adv Gerontol. 22(2):337-42.
Position Statement. Management of postmenopausal osteoporosis: position of The North American Menopause Society. (2002). Menopause. 9(2):84-100.
Ramalho, AC.; Castro, ML.; Hauache, O.; Vieira, JG.; Takala, E.; Calalli, F. & Tavares, F. (2001). Osteoporotic fractures of proximal femur: clinical and epidemiological features in a population of the city of São Paulo. Sao Paulo Med J. 119(2): 48-53.
Resende, SM.; Rassi, CM. & Viana, FP. (2008). Effects of hydrotherapy in balance and prevention of falls among elderly. Rev Bras Fisioter. 12 (1):57-63.
Robertson, MC.; Devlin, N.; Gardner, MM. & Campbell, AJ. (2001). Effectiveness and economic evaluation of a nurse delivered home exercise programme to prevent falls. 1: Randomised controlled trial. BMJ. 322(7288):697-701.
Robertson, MC.; Gardner, MM.; Devlin, N.; McGee, R. & Campbell, AJ. (2001). Effectiveness and economic evaluation of a nurse delivered home exercise programme to prevent falls. 2: Controlled trial in multiple centres. BMJ. 322(7288): 701-4.
Rossi, E. & Sader, C. (2002). Envelhecimento do sistema osteoarticular. In: Freitas, EV et al. Tratado de geriatria e gerontologia. Rio de Janeiro: Guanabara Koogan, 2002. p. 508-514.
Rubin, C.; Turner, AS.; Bain. S; Mallinckrodt, C. & McLeod, K. (2001). Anabolism. Low mechanical signals strengthen long bones. Nature. 412:603-604.
Russo, CR.; Lauretani, F.; Bandinelli S, Bartali, B.; Cavazzini, C.; Guralnik, JM. & Ferrucci, L. (2003). High-frequency vibration training increases muscle power in postmenopausalwomen. Arch Phys Med Rehabil. 84:1854-7.
Santin-Medeiros, F. & Garatachea, VN. (2010). Musculoskeletal effects of vibration training in the elderly. Rev Esp Geriatr Gerontol. Sep-Oct;45(5):281-4.
Sehmisch, SR.; Galal, L.; Kolios, MT.; Dullin, CS.; Zimmer, KM.; Stuermer. & Stuermer, E. K. (2009). Effects of low-magnitude, high-frequency mechanical stimulation in the rat osteopenia model. Osteoporos Int. December; 20(12): 1999–2008.
Sherrington, C.; Whitney, JC.; Lord, SR.; Herbert, RD.; Cumming, RG. & Close, JCT. (2008). Effective Exercise for the Prevention of Falls: A Systematic Review and Meta- Analysis JAGS. 56:2234–2243.
Shumway-Cook, A. & Woollacott, M. (1995). Motor Control Theory and Applications. Williams and Wilkins: Baltimore.
Shumway-Cook, A.; Brauer, S. & Woollacott, M. (2000). Predicting the probability for falls in community-dwelling older adults using the Timed Up & Go Test. Phys Ther. 80: 896 –903.
Siris, ES.; Brenneman, SK.; Barrett-Connor, E.; Miller, PD.; Sajjan, S.; Berger, ML. & Chen, YT. (2006). The effect of age and bone mineral density on the absolute, excess, and relative risk of fracture in postmenopausal women aged 50–99: results from the National Osteoporosis Risk Assessment (NORA). Osteoporos Int . 17 (4): 565–574.
Slatkovska L.; Alibhai SM.; Beyene J. & Cheung AM. (2010). Effect of whole-body vibration on BMD: a systematic review and meta-analysis. Osteoporos Int. Dec;21(12):1969- 80. Epub 2010 Apr 21.
Sloane, PD.; Baloh, RW. & Honrubia V. (1989). The vestibular system in the elderly: clinical implications. Am J Otolaryngol. 10(6):422-9.
Swanenburg, J.; de Bruin, ED.; Stauffacher, M.; Mulder, T. & Uebelhart, D. (2007). Effects of exercise and nutrition on postural balance and risk of falling in elderly people with decreased bone mineral density: randomized controlled trial pilot study. Clin Rehabil. 21(6): 523-34.
Swanik, KA.; Lephart, SM.; Swanik, CB.; Lephart, SP.; Stone, DA. & Fu FH. (2002). The effects of shoulder plyometric training on proprioception and selected muscle performance characteristics. J Shoulder Elbow Surg. 11(6):579-86.
Szejnfeld, VL.; Jennings, F.; Castro, CHM.; Pinheiro, MM. & Lopes, AC. (2007). Conhecimento dos Médicos Clínicos do Brasil sobre as Estratégias de Prevenção e Tratamento da Osteoporose. Rev Bras Reumatol. 47(4):251-257.
Teixeira, LE.; Silva, KN.; Imoto, AM.; Teixeira, TJ.; Kayo, AH.; Montenegro-Rodrigues, R. &
Trevisani, VFM. (2010). Progressive load training for the quadriceps muscle associated with proprioception exercises for the prevention of falls in postmenopausal women with osteoporosis: a randomized controlled trial. Osteoporosis International; 21: 589-96.
Tinetti, ME. & Speechley, M. (1989). Prevention of falls among the elderly. N Engl J Med. 320:1055–1059.
Torvinen, S.; Kannus, P.; Sievänen, H.; Järvinen, TA.; Pasanen, M.; Kontulainen, S.; Nenonen, A.; Järvinen, TL.; Paakkala, T.; Järvinen, M. & Vuori, I. (2003). Effect of 8- month vertical whole body vibration on bone, muscle performance, and body balance: a randomized controlled study. J Bone Miner Res. May;18(5):876-84.
Tsuji, K.; Velázquez-Villaseñor, L.; Rauch, SD.; Glynn, RJ.; Wall, C 3rd. & Merchant SN. (2000). Temporal bone studies of the human peripheral vestibular system. Ann Otol Rhinol Laryngol. Suppl 181:20-5.
Van der Esch, M.; Steultjens, M.; Harlaar, J.; Knol, D.; Lems, W. & Dekker, J. (2007). Joint Proprioception, Muscle Strength, and Functional Ability in Patients With Osteoarthritis of the Knee. Arthritis & Rheum. 57(5):787-793.
Verschueren SM.; Roelants M.; Delecluse C.; Swinnen S.; Vanderschueren D. & Boonen S. (2004). Effect of 6-month whole body vibration training on hip density, muscle strength, and postural control in postmenopausal women: a randomized controlled pilot study. J Bone Miner Res. Mar;19(3):352-9. Epub 2003 Dec 22.Vicini, C.; Alpini, D. & Caruso E. (1989). Manuale pratico di reabilitazione vestibolare. Firenze: F & F Parretti; 1989.
Vincent, KR. & Braith, RW. (2002). Resistance training and bone turnover in elderly men and women. Med Sci Sports Exerc. 34:17-23.
Walsh, MC.; Hunter, GR. & Livingstone, MB. (2006). Sarcopenia in premenopausal and ostmenopausal women with osteopenia, osteoporosis and normal bone mineral density. Osteoporos Int. 17:61-67.
Weatherall, M. (2004). Prevention of falls and falls-related fractures in community-dwelling older adults: a meta-analysis of estimates of effectivenessbased on recent guidelines. Intern Med J. 34:102-108.
Wilmore, JH. & Costill, DL. (1999). Physiology of sport and exercise. 2. ed. United States: uman Kinetics.
World Health Organization (WHO) Working Group. (1994). Assessment of fracture risk and its application to screening for postmenopausal osteoporosis. World Health Organ Tech Rep Ser. 843, Geneva: WHO.
Yoshinari, NH. & Bonfá, ESD. (2000). Reumatologia para o clínico. Roca, 1ª Ed.149-1.

Author:
Lucas Teixeira
Joelma Magalhães da Costa

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Joelma Magalhães da Costa

por Joelma Magalhães da Costa

Graduada em Fisioterapia; Especialização em Acupuntura; Especialização em Fisiologia Humana; Titulo de Especialista em Traumato-Ortopedia; Mestre em Ciências da Reabilitação, Na Linha de Pesquisa em Avaliação e Reabilitação das Disfunções do Sistema Estomatognático - ATM; Participa e atua em cursos, congressos, pesquisas e projetos referentes ao Sistema Musculoesquelético, ATM e Dor Orofacial.

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