Acessibilidade / Reportar erro

Association between sarcopenia, sarcopenic obesity, muscle strength and quality of life variables in elderly women

Abstracts

OBJECTIVE: To investigate the association between sarcopenia, sarcopenic obesity and muscle strength and variables related to quality of life in elderly women. METHOD: The sample consisted of 56 female volunteers who underwent body composition analysis (BMI and x-ray absorptiometry dual-energy DXA). Handgrip strength was measured using a Jamar dynamometer. We used the SF-36 health questionnaire to analyze quality of life. The data were analyzed with descriptive statistics and the Pearson correlation coefficient; SPSS 15.0 was used to perform the statistical analysis. RESULTS: The mean age of the subjects was 64.92±5.74 years; of the 56 volunteers evaluated, 19.64% (n=11) were classified as sarcopenic obese and 45 (80.36%) were not. Thirteen volunteers (23.21%) were classified as sarcopenic while 43 (76.78%) were not. Although there were no statistically significant differences between the studied parameters and quality of life among those with sarcopenia or sarcopenic obesity, the values were lower in affected individuals. Interestingly, handgrip strength correlated positively and significantly with all of the SF-36 dimensions except VIT (p=0.08) and SM (p=0.25). Conclusions: Seeing that handgrip strength is a determining factor in quality of life aspects in this population, the screening and identification of small functional changes using simple clinical measures may facilitate early intervention and help prevent disability. In contrast, neither sarcopenia nor sarcopenic obesity were found to be associated with quality of life.

sarcopenic obesity; aging; muscle strength; rehabilitation; quality of life


OBJETIVO: Verificar a associação entre sarcopenia, obesidade sarcopênica e força muscular com variáveis relacionadas à qualidade de vida em idosas. MÉTODO: A amostra foi composta por 56 voluntárias do sexo feminino que se submeteram à análise de composição corporal (IMC e absortometria de raios-x de dupla energia DXA). A força de preensão palmar (FPP) foi mensurada pelo dinamômetro Jamar. Para análise de qualidade de vida, usou-se o questionário SF-36; para análise estatística, os dados foram apresentados por meio da estatística descritiva e Coeficiente de Correlação de Pearson. O software SPSS, versão 15,0, foi utilizado para realização de todas as análises. RESULTADOS: As idosas apresentaram média de idade de 64,92±5,74 anos. Das 56 voluntárias avaliadas, 19,64% (n=11) foram classificadas com obesidade sarcopênica. Treze voluntárias (23,21%) foram classificadas como sarcopênicas. Os principais achados do presente estudo demonstraram que, embora não fosse encontrada significância estatística entre os parâmetros estudados em idosas classificadas com sarcopenia e obesidade sarcopênica e as dimensões de qualidade de vida, os valores médios foram inferiores nas acometidas. De forma interessante, a variável FPP correlacionou-se positiva e significativamente com todos os domínios do SF-36, com exceção de VIT (p=0,08) e SM (p=0,25). CONCLUSÕES: A FPP é um fator determinante nos aspectos relacionados à qualidade de vida na população estudada. O rastreamento e a identificação de pequenas alterações funcionais por meio de medidas clínicas simples, como a FPP, podem favorecer a intervenção precoce e prevenir incapacidades. Em contraste, sarcopenia e obesidade sarcopênica não foram associadas à qualidade de vida.

sarcopenia; obesidade sarcopênica; força muscular; envelhecimento; reabilitação; qualidade de vida


IMaturity University Project, Universidade Federal do Tocantins (UFT), Palmas, TO, Brazil

IIPostgraduate Programin Science and Technology in Health, Universidade de Brasília (UnB), Brasília, DF, Brazil

IIIMaster in Gerontology, Universidade Católica de Brasília (UCB), Brasília, DF, Brazil

IVFaculty of Physical Education, UnB, Brasília, DF, Brazil

Correspondence to

ABSTRACT

OBJECTIVE: To investigate the association between sarcopenia, sarcopenic obesity and muscle strength and variables related to quality of life in elderly women.

METHOD: The sample consisted of 56 female volunteers who underwent body composition analysis (BMI and x-ray absorptiometry dual-energy DXA). Handgrip strength was measured using a Jamar dynamometer. We used the SF-36 health questionnaire to analyze quality of life. The data were analyzed with descriptive statistics and the Pearson correlation coefficient; SPSS 15.0 was used to perform the statistical analysis.

RESULTS: The mean age of the subjects was 64.92±5.74 years; of the 56 volunteers evaluated, 19.64% (n=11) were classified as sarcopenic obese and 45 (80.36%) were not. Thirteen volunteers (23.21%) were classified as sarcopenic while 43 (76.78%) were not. Although there were no statistically significant differences between the studied parameters and quality of life among those with sarcopenia or sarcopenic obesity, the values were lower in affected individuals. Interestingly, handgrip strength correlated positively and significantly with all of the SF-36 dimensions except VIT (P=0.08) and SM (P=0.25).

Conclusions: Seeing that handgrip strength is a determining factor in quality of life aspects in this population, the screening and identification of small functional changes using simple clinical measures may facilitate early intervention and help prevent disability. In contrast, neither sarcopenia nor sarcopenic obesity were found to be associated with quality of life.

Keywords: sarcopenia; sarcopenic obesity; aging; muscle strength; rehabilitation; quality of life.

Introduction

Aging is a continuous process involving changes in several physiological systems and a decrease in functional capacity, which impacts quality of life1,2. The musculoskeletal system is among the systems affected by aging and involves basic body functions such as muscle contraction, movement and locomotion. An important change recognized among the elderly is the loss of lean body mass, particularly muscle mass and a concomitant decrease in strength2,3. This phenomenon was termed sarcopenia in a pioneering study conducted by Rosenberg4, based on the Greek root sarx (flesh) and the suffix -penia (disability, poverty). Another known alteration of body composition associated with aging is increased fat mass, which elevates the risk of developing obesity. The World Health Organization5 defines obesity as an excess of adipose tissue in the body and considers it a chronic disease which is directly or indirectly related with other pathological situations that contribute to morbidity and mortality, such as cardiovascular diseases, osteomuscular disorders and cancer6.

Currently, the term sarcopenia does not refer exclusively to reduction of fat-free mass (FFM) but also to a concomitant loss of strength and muscle function. This phenomenon is observed in both men and women7 and is associated with loss of autonomy8, increased risk of falls9, reduced bone mineral density10 and a decline in functional capacity11,12. Moreover, it is important to mention that a recent study observed that reduced appendicular FFM (AFFM) was a significant predictor of mortality in elderly13. Since evidence has been reported that sarcopenia affects healthcare costs14, this phenomenon should be better understood, particularly its effects on quality of life.

The difficulty in classifying individuals as sarcopenic represents an obstacle in clinical practice and research. A pioneering study on sarcopenia8 proposed the cutoff point of FFM two standard deviations below the mean of a population of adults between 18 and 40 years old, similar to the way osteoporosis is classified. The cutoff values presented by the authors were AFFM (i.e., upper and lower limbs divided by height squared) below 7.26 kg/m² and 5.45 kg/m² for men and women, respectively. However, this approach has been little studied in elderly Brazilians. Lima et al.10 observed an association between muscle strength and bone mineral density, while Oliveira et al.11 demonstrated that the elderly individuals classified as sarcopenic had significantly lower functional capacity. It is important, however, to investigate this approach in relation to the quality of life of this population.

More recently, Newman et al.15 highlighted the importance of considering fat mass (FM) when examining sarcopenia. These authors demonstrated that when FM is not included, individuals with high body weight are not classified as sarcopenic, although their FFM is insufficient in relation to total body size. This low FFM and high FM condition has been termed sarcopenic obesity. A study reported that sarcopenic obesity was associated with worse physical function than obesity or sarcopenia alone16, and thus it has been identified as an important cause of frailty among the elderly17-19. Thus, it may influence quality of life, although further study is required.

Newman et al.15 proposed an approach for determining low FFM adjusted for height and FM in relation to functional limitations and inflammatory markers20 in the elderly. However, they stressed the importance of determining such an association in conjunction with other health-related variables such as strength, muscle function and quality of life indexes. Moreover, they did not establish a cutoff value for classifying sarcopenic obesity. Subsequently, Oliveira et al.21 applied Newman et al.15's approach in elderly Brazilian women, and the results showed an association between muscle strength and indexes of cardiorespiratory fitness. However, such initial data call for more detailed studies, especially studies investigating the effects of these diseases on health-related quality of life of this population. Although quality of life is a broad and subjective construct, health-related quality of life focuses on functional aspects and the health-disease process, as well as the effects of various treatments22.

Thus, the objective of the present study was to examine the association between sarcopenia, sarcopenic obesity and muscle strength and quality of life variables in elderly women.

Method

Sample

The sample of this cross-sectional study included 56 women with a mean age of 64.92±5.74 (range: 60 to 79) who were recruited from among participants of the Outreach Program of the University of Maturity of the Universidade Federal de Tocantins (UFT), Palmas, TO, Brazil. All participants answered a questionnaire on medical history, hormone replacement therapy, city of birth and comorbidities. The physical activity level of the participants was measured with the IPAQ-short version, from the International Physical Activity Questionnaire validated and adapted for Brazil. The questionnaire was administered in individual interviews, as recommended for developing countries, allowing classification as very active, active, insufficiently active and sedentary23.

Women unable to walk without assistance, or who had a metal prosthesis, a metabolic or endocrine disorder known to affect the muscular system or a cardiac conduction abnormality that prevented participation in the evaluations were excluded. All volunteers signed an informed consent form that contained information on the procedures, risks and benefits of the research. Prior to data collection, the project was evaluated and approved by the Human Research Ethics Committee of the UFT, under protocol 076/2010.

Evaluation of body composition

A Filizolla digital scale with an accuracy of 0.1 kg was used to measure the body mass of the volunteers, who were shoeless and wearing light clothes. Height was measured to the nearest 0.1 cm with a stadiometer (CARDIOMED, Brazil) that was attached to a wall. The body mass index (BMI) was calculated by dividing the body weight by the height squared (kg/m2).

Dual-energy X-ray absorptiometry (DXA) with a Lunar DPX absorptiometer and Encore 2005 software were used to measure body composition. For this procedure, the volunteers were positioned in dorsal decubitus on the DXA table and then carefully positioned so that they were completely centered on the equipment. All evaluations were carried out by the same technician. After analyzing the entire body area, DXA allowed the bone mineral density and the tissue density to be determined. The tissues were also divided into FM and FFM. The upper and lower limbs, trunk and head were initially distinguished with program-generated lines that were later adjusted more accurately by hand. Thus, FFM values were determined for both the whole body and for the upper limbs, lower limbs and trunk.

Identification of sarcopenic obesity and sarcopenia

Using the body composition values obtained with DXA, sarcopenic obesity was determined according to the cutoff point established by Oliveira et al.21, which was a residual value less than or equal to two standard deviations from the mean of a reference group of young women (18 to 40 years of age). The prediction equation for AFFM in the above-mentioned study was: AFFM = -14.529 + (17.989 x height in meters) + 0.1307 x total kg of FM. The cutoff point corresponded to a residual value <-3.4 (i.e., the measured AFFM minus the AFFM predicted by the equation). Thus, the volunteers who showed a residual value <-3.4 were classified as having inadequate FFM for their body area, which indicates sarcopenic obesity. To determine sarcopenia, the cutoff point for women proposed by Baumgartner et al.8 was adopted, i.e., <5.45 kg/m2 (AFFM divided by height squared).

Evaluation of handgrip strength

Handgrip strength was measured with a Jamar dynamometer in the following manner: the volunteers were seated in a standardized position used by the American Society of Hand Therapists in which the hips and knees are flexed at 90º, the shoulder adducted in neutral position, the elbow flexed at 90º and the forearm in semi-pronation without radial or ulnar deviation. The grip dynamometer was adjusted individually according to each volunteer's hand size, so that the bar closest to the body of the dynamometer was positioned on the second phalanges of the index, middle and ring fingers24. The tests were performed three times, with the dominant hand first and then the non-dominant hand, with an interval of 1 minute between each attempt in order to avoid fatigue during the test. Force was applied for 5 seconds in each attempt, and the highest value was considered25. The results were recorded in kg/f.

Evaluation of quality of life

Quality of life level was measured using the Medical Outcomes Survey Short-form General Health Survey (SF-36) translated and validated for Brazil by Ciconelli et al.26. The scale consists of 36 items about limitations in daily life due to health problems and provides a subjective estimate of the individual's functional state. The SF-36 results in a classification of eight dimensions: physical functioning, social functioning, role limitations (physical problems), role limitation (emotional problems), mental health, vitality, pain, and general health. The answers for each dimension are coded, summed and transformed into scores from 0 to 100, where zero corresponds to "worst health" and 100 to "best health".

Data analysis

The Kolmogorov-Smirnov test was used to verify the normality of data distribution. The data were analyzed using descriptive statistics, including mean and standard deviation. A t test for independent samples was used to compare the dependent variables (quality of life and handgrip strength) between volunteers with and without sarcopenic obesity. The same procedure was followed to compare those with and without sarcopenia. The chi-square test was used to verify whether there were differences between groups with respect to hormone replacement. The Pearson correlation coefficient was used to verify the relationship between AFFM variables and dependent variables. The significance level adopted was p<0.05. SPSS 15.0 was used to perform all analyses.

Results

The results for all variables are presented as means and standard deviations. Table 1 shows the volunteers' characteristics, including age, handgrip strength and body composition according to DXA. Table 2 presents the quality of life variables from the SF-36 questionnaire.

Table 3 shows the quality of life and muscle strength variables according to the proposed classification for sarcopenic obesity21. Again we point out that the model cutoff point, adapted from Oliveira et al.21, was based on that of Newman et al.15, which was derived from the residues of a regression that predicts AFFM from FM and height. Of the 56 evaluated volunteers, 19.64% (n=11) were classified as sarcopenic obese and 80.36% (n=45) were not. Comparing the results of sarcopenic obese women with those were not, significant differences were observed in the variables AFFM and body fat percentage. The chi-square test revealed that the number of participants who underwent hormone replacement did not differ significantly between groups. Interestingly, FFM and variables related to quality of life showed, in general, lower (although not significantly so) mean values in the volunteers classified as having sarcopenic obesity.

Table 4 shows the quality of life and the strength variables according to Baumgartner et al.8 approach. Of the 56 participants of this study, 13 (23.21%) were classified as sarcopenic, while 43 (76.78%) were not. Significant differences were observed for the variables body weight, BMI, AFFM, body fat percentage and handgrip strength. As was observed for sarcopenic obesity, the SF-36's quality of life variables generally showed lower mean values in the elderly classified as sarcopenic. Additionally, the test chi-square test revealed that the number of participants who underwent hormone replacement did not differ significantly between groups.

Table 5 shows the correlations of residual values, AFFM and handgrip strength with the SF-36 quality of life dimensions. There were positive and significant correlations between residual values (Newman et al.15) and AFFM, as well as between AFFM and handgrip strength. Additionally, both the AFFM and the residual values tended toward a significant correlation with the SF-36's pain dimension (p=0.06 and 0.08), respectively. Interestingly, the variable handgrip strength was positively and significantly correlated with all SF-36 dimensions except VIT (p=0.08) and MH (p=0.25). Finally, it was observed that age was negatively and significantly correlated with handgrip strength (r=-0.30; p=0.02).

Discussion

Although statistically significant differences were not observed between the studied variables and quality of life parameters in elderly women with sarcopenia or sarcopenic obesity, the mean values were lower in the affected women. Such results deserve attention, since sarcopenia and sarcopenic obesity have been identified as harmful to geriatric health27 in that they entail increased risk of disease and mortality13 and reduced functional capacity and quality of life28-33. Additionally, the reduced AFFM values observed in both sarcopenia and sarcopenic obesity were associated with lower values of handgrip strength. Importantly, this variable was positively and significantly correlated with the quality of life dimensions, which therefore suggests a relevant phenotype of the studied population. Jointly, the observed results suggest that handgrip strength, a relatively low cost and easy measurement, is a predictor of quality of life in the elderly. In fact, the importance of handgrip strength for individuals with advanced age is consistent with the literature34-38.

Sarcopenic obesity, reduced FFM and increased body fat percentage19, although only a recently identified condition, has been identified as an important cause of frailty among the elderly19,28,39. Thus, new insight into sarcopenic obesity becomes even more important, since the elderly population is increasing worldwide16. In the present study, using the classification proposed by Oliveira et al.21 to compare the mean quality of life values between the sarcopenic obese and non-sarcopenic individuals, it was observed that the affected individuals had lower, though not statistically significant, values. Such findings may be related to the subjective nature of the questionnaire40. Thus, it is important to mention that a recent study21 has demonstrated that sarcopenic obesity is related to decreased muscle strength and functional capacity in the elderly. Moreover, Bouchard and Janssen41, in a cross-sectional study involving 2,039 men and women over 55 years of age, observed that sarcopenic obesity was associated with poorer functioning when compared separately to either obesity or sarcopenia.

Using Baumgartner et al.8 approach for sarcopenia classification (i.e., AFFM divided by the height squared less than 5.45 kg/m2), a prevalence of 23.21% was observed, which is similar to other studies involving elderly Brazilian women8,9. Similar to what was observed for sarcopenic obesity, the SF-36 quality of life dimensions did not differ significantly in the affected women, although the mean values were lower. However, it was observed that handgrip strength was lower in the sarcopenic seniors, and this variable was significantly associated with quality of life42,43. It is worth repeating that the general concept of quality of life is broad and subjective, involving the individual's perception of life as well as his expectations and concerns44. Nevertheless, in the 1990s, the term "health-related quality of life" emerged, which is focused on the health-disease process, functional aspects and their impact on an individual's daily life. This outcome, specifically, was the object of the present study, although "quality of life" was used generically throughout.

Consistent with previous findings38,42,43,45,46, the observed results highlight the importance of handgrip strength as a predictor in the elderly. Its usefulness is enhanced by its broad applicability, low cost, quick implementation and non-invasiveness. In particular, our results suggest an association between handgrip strength and health-related quality of life in the studied population, since there was a correlation with most of the dimensions, specifically physical functioning, social functioning, role limitations (physical problems), role limitation (emotional problems), as well as reference to pain and general health. Dixon et al.47, in a study involving men and women over 50 years of age, demonstrated that handgrip strength in women was associated with low bone mineral density of the spine and hip as well as an increased risk of fractures, regardless of lifestyle or differences in body size. Importantly, handgrip strength has even been associated with mortality in individuals with advanced age. In a 25-year longitudinal study conducted by Metter et al.48, it was demonstrated that handgrip strength has an impact on mortality from all causes and that although low lean body mass is important, it did not totally explain the effects of strength. Moreover, Galley et al.49, in a 24-year longitudinal study, observed that handgrip strength is a long-term predictor of mortality from all causes, including cardiovascular diseases, as well as from cancer in men. Finally, the negative correlation observed between age and handgrip strength in the present study indicates that after 60 years of age this variable declines.

The results of this study have important clinical implications. Regarding the functional evaluation of the elderly, muscle strength, especially handgrip strength, stands out as a non-invasive and low cost measurement that is easy to implement. Additionally, regarding the adoption of preventive or therapeutic measures for the elderly, interventions that minimize sarcopenia-related phenotypes, especially muscle strength, warrant attention. Thus, the adoption of a physically active lifestyle has been consistently associated with the preservation of body mass and muscle strength, with resistance training and appropriate nutrition being of particular relevance2,50.

The present study has some limitations. Since the volunteers were Brazilian women, the results cannot be extrapolated to other populations or to men. Moreover, the cross-sectional design does not allow the establishment of a cause-effect relationship, although it provides evidence that the dependent variables are associated with handgrip strength. Finally, cutoff points for classifying sarcopenia and sarcopenic obesity should be better defined in the literature. Nevertheless, the selected cutoff points had been previously used with elderly Brazilian women and were significantly associated with muscle strength, bone mineral density and functional capacity10,11,21.

Conclusions

Based on the observed results, although there were no significant associations between sarcopenia and sarcopenic obesity with the quality of life dimensions, they were associated with reduced handgrip strength values. On the other hand, handgrip strength was positively and significantly correlated with various dimensions from the SF-36 test, suggesting its importance as a predictor of quality of life in elderly women. Consistent with previous findings, this study demonstrates that handgrip strength is a low cost, easy to implement measurement that can be incorporated into the clinical routine of health professionals, aiding in prevention and intervention procedures.

Acknowledgment

The authors would like to thank the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES), Brasília, DF, Brazil, the Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq), Brasília, DF, Brazil, the University of Maturity of UFT, the Universidade Católica de Brasília and the Plows, Kaminish & Costa Laboratory.

References

  • 1. Matsudo SM, Matsudo VKR, Barros Neto TL. Efeitos benéficos da atividade física na aptidão física e saúde mental durante o processo de envelhecimento. Rev Bras Ativ Fis Saúde. 2000;5(2):60-76.
  • 2. Goodpaster BH, Chomentowski P, Ward BK, Rossi A, Glynn NW, Delmonico MJ, et al. Effects of physical activity on strength and skeletal muscle fat infiltration in older adults: a randomized controlled trial. J Appl Physiol. 2008;105(5):1498-503.
  • 3. Frontera WR, Hughes VA, Fielding RA, Fiatarone MA, Evans WJ, Roubernoff R. Aging of skeletal muscle: a 12-yr longitudinal study. J Appl Physiol. 2000;88(4):1321-6.
  • 4. Rosenberg IH. Summary comments. Am J Clin Nutr. 1989;50(5):1231-3.
  • 5
    WHO Consultation on Obesity. Obesity: Prevention and Managing: The Global Epidemic. Report of a WHO Consultation on Obesity. Geneva, 3-5 June1997.
  • 6. Cabrera MAS, Jacob Filho W. Obesidade em idosos: prevalência, distribuição e associação com hábitos e co-morbidades. Arq Bras Endocrinol Metab. 2001;45(5):494-501.
  • 7. Baumgartner RN, Waters DL, Gallagher D, Morley JE, Garry PJ. Predictors of skeletal muscle mass in elderly men and women. Mech Ageing Dev. 1999;107(2):123-36.
  • 8. Baumgartner RN, Koehler KM, Gallagher D, Romero L, Heymsfield SB, Ross RR, et al. Epidemiology of sarcopenia among the elderly in New Mexico. Am J Epidemiol. 1998;147(8):755-63.
  • 9. Whipple RH, Wolfson LI, Amerman PM. The relationship of knee and ankle weakness to falls in nursing home residents: an isokinetic study. J Am Geriatr Soc. 1987;35(1):13-20.
  • 10. Lima RM, Bezerra LMA, Rabelo HT, Silva MAF, Silva AJR, Bottaro M, et al. Fat-free mass, strength, and sarcopenia are related to bone mineral density in older women. J Clin Densitom. 2009;12(1):35-41.
  • 11. Oliveira RJ, Bottaro M, Mota AM, Pitanga F, Guido M, Leite TKM, et al. Association between sarcopenia-related phenotypes with aerobic capacity indexes of older women. J Sci Med Sport. 2009;8:337-43.
  • 12. Carmeli E, Imam B, Merrick J. The relationship of pre-sarcopenia (low muscle mass) and sarcopenia (loss of muscle strength) with functional decline in individuals with intellectual disability (ID). Arch Gerontol Geriatr. 2012;55(1):181-5.
  • 13. Bunout D, de la Maza MP, Barrera G, Leiva L, Hirsch S. Association between sarcopenia and mortality in healthy older people. Australas J Ageing. 2011;30(2):89-92.
  • 14. Janssen I, Baumgartner RN, Ross R, Rosenberg IH, Roubenoff R. Skeletal muscle cutpoints associated with elevated physical disability risk in older men and women. Am J Epidemiol. 2004;159(4):413-21.
  • 15. Newman AB, Kupelian V, Visser M, Simonsick E, Goodpaster B, Nevitt M, et al. Sarcopenia:alternative definitions and associations with lower extremity function. J Am Geriatr Soc. 2003;51(11):1602-9.
  • 16. Baumgartner RN. Body composition in healthy aging. Ann N Y Acad Sci. 2000;904:437-48.
  • 17. Taaffe DR, Henwood TR, Nalls MA, Walker DG, Lang TF, Harris TB. Alterations in muscle attenuation following detraining and retraining in resistance-trained older adults. Gerontology. 2009;55(2):217-23.
  • 18. Narici MV, Maffulli N. Sarcopenia: characteristics, mechanisms and functional significance. Br Med Bull. 2010;95(1):139-59.
  • 19. Roubenoff R. Sarcopenic obesity: the confluence of two epidemics. Obes Res. 2004;12(6):887-8.
  • 20. Cesari M, Kritchevsky SB, Baumgartner RN, Atkinson HH, Penninx B, Lenchik L, et al. Sarcopenia, obesity, and inflammation-results from the Trial of Angiotensin Converting Enzyme Inhibition and Novel Cardiovascular Risk Factors study. Am J Clin Nutr. 2005;82(2):428-34.
  • 21. Oliveira RJ, Bottaro M, Júnior JT, Farinatti PTV, Bezerra LA, Lima RM. Identification of sarcopenic obesity in postmenopausal women: a cutoff proposal. Braz J Med Biol Res. 2011;44(11):1171-6.
  • 22. Centers for Disease Control and Prevention. Measuring Health Days. Atlanta, Georgia: CDC; 2000.
  • 23. Matsudo S, Araujo T, Matsudo V, Andrade D, Andrade E, Oliveira LC, et al. Questionário Internacional de Atividade Física (IPAQ): estudo de validade e reprodutibilidade no Brasil. Rev Bras Ativ Fis Saúde. 2001;6(2):5-18.
  • 24. Desrosiers J, Bravo G, Hébert R, Dutil E. Normative data for grip strength of elderly men and women. Am J OccupTher. 1995;49(7):637-44.
  • 25. Moreira D, Godoy JRP, Silva Júnior W. Estudo sobre a realização da preensão palmar com a utilização do dinamômetro: considerações anatômicas e cinésiológicas. Fisioter Bras. 2001;2(5):295-300.
  • 26. Ciconelli RM, Ferraz MB, Santos W, Meinão I, Quaresma MR. Tradução para a língua portuguesa e validação do questionário genérico de avaliação de qualidade de vida SF-36 (Brasil SF-36). Rev Bras Reumatol. 1999;39(3):143-50.
  • 27. Thornell LE. Sarcopenic obesity: satellite cells in the aging muscle. Curr Opin Clin Nutr Metab Care. 2011;14(1):22-7.
  • 28. Schrager MA, Metter EJ, Simonsick E, Ble A, Bandinelli S, Lauretani F, et al. Sarcopenic obesity and inflammation in the InCHIANTI study. J Appl Physiol. 2007;102(3):919-25.
  • 29. Baumgartner RN, Wayne SJ, Waters DL, Janssen I, Gallagher D, Morley JE. Sarcopenic obesity predicts instrumental activities of daily living disability in the elderly. Obes Res. 2004;12(12):1995-2004.
  • 30. Zamboni M, Mazzali G, Zoico E, Harris TB, Meigs JB, Di Francesco V, et al. Health consequences of obesity in the elderly: a review of four unresolved questions. Int J Obes. 2005;29(9):1011-29.
  • 31. Booth FW, Zwetsloot KA. Basic concepts about genes, inactivity and aging. Scand J Med Sci Sports. 2010;20(1):1-4.
  • 32. Stephen WC, Janssen I. Sarcopenic-obesity and cardiovascular disease risk in the elderly. J Nutr Health Aging. 2009;13(5):460-6.
  • 33. Cheung CL, Tan KC, Bow CH, Soong CS, Loong CH, Kung AW. Low handgrip strength is a predictor of osteoporotic fractures: cross-sectional and prospective evidence from the Hong Kong Osteoporosis Study.Age (Dordr). 2011;
  • 34. Castro RNS. Correlação entre força de preensão manual e a força da musculatura respiratória em mulheres asmáticas e não asmáticas.
  • 35. Bohannon RW. Hand-grip dynamometry predicts future outcomes in aging adults. J Geriatr Phys Ther. 2008;31(1):3-10.
  • 36. Geraldes AAR, Oliveira ARM, Albuquerque RB, Carvalho JM, Farinatti PTV. A forca de preensão manual éboapreditora do desempenho funcional de idosos frágeis: um estudo correlacionalmúltiplo. Rev Bras Med Esporte. 2008;14(1):12-6.
  • 37. Lauretani F, Russo CR, Bandinelli S, Bartali B, Cavazzini C, Di Iorio A, et al. Age-associated changes in skeletal muscles and their effect on mobility: an operational diagnosis of sarcopenia. J Appl Physiol. 2003;95(5):1851-60.
  • 38. Garcia PA, Dias JMD, Dias RC, Santos P, Zampa CC. Estudo da relação entre função muscular, mobilidade funcional e nível de atividade física em idosos comunitários. Rev Bras Fisioter. 2011;15(1):15-22
  • 39. Jarosz PA, Bellar A. Sarcopenic obesity: an emerging cause of frailty in older adults. Geriatr Nurs. 2009;30(1):64-70.
  • 40. Vecchia RD, Ruiz T, Bocchi SCM, Corrente JE. Qualidade de vida na terceira idade: um conceito subjetivo. Rev Bras Epidemiol. 2005;8(3):246-52.
  • 41. Bouchard DR, Janssen I. Dynapenic-obesity and physical function in older adults. J Gerontol A Biol Sci Med Sci. 2010;65(1):71-7.
  • 42. Norman K, Schütz T, Kemps M, Josef Lübke HJ, Lochs H, Pirlich M. The subjective global assessment reliably identifies malnutrition-related muscle disfunction. Clin Nutr. 2005;24(1):43-50.
  • 43. Mathiowetz V, Kashman N, Volland G, Weber K, Dowe M, Rogers S. Grip and pinch strength: normative data for adults. Arch Phys Med Rehabil. 1985;66(2):69-72.
  • 44. The world health organization quality of life assessment (WHOQOL): position paper from the World Health Organization. Soc Sci Med. 1995;41(10):1403-9.
  • 45. Mathiowetz V, Rennells C, Donahoe L. Effect of elbow position on grip and key pinch strength. J Hand Surg. 1985;10(5):694-7.
  • 46. Günther CM, Bürger A, Rickert M, Crispin A, Schulz CU. Grip strength in healthy caucasian adults: reference values. J Hand Surg. 2008;33(4):558-65.
  • 47. Dixon WG, Lunt M, Pye SR, Reeve J, Felsenberg D, Silman AJ, et al. Low grip strength is associated with bone mineral density and vertebral fracture in women. Rheumatology (Oxford). 2005;44(5):642-6.
  • 48. Metter EJ, Talbot LA, Schrager M, Conwit R. Skeletal muscle strength as a predictor of all-cause mortality in healthy men. J Gerontol A Biol Sci Med Sci. 2002;57(10):B359-65.
  • 49. Gale CR, Martyn CN, Cooper C, Sayer AA. Grip strength, body composition,and mortality. Int J Epidemiol. 2007;36(1):228-35.
  • 50. Iannuzzi-Sucich M, Prestwood KM, Kenny AM. Prevalence of sarcopenia and predictors of skeletal muscle mass in healthy, older men and women. J Gerontol A Biol Sci Med Sci. 2002;57(12):M772-7.
  • Association between sarcopenia, sarcopenic obesity, muscle strength and quality of life variables in elderly women

    Luiz S. Silva NetoI; Margô G. O. KarnikowiskiII; Adriano B. TavaresIII; Ricardo M. LimaIV
  • Publication Dates

    • Publication in this collection
      13 Sept 2012
    • Date of issue
      Oct 2012

    History

    • Received
      20 Sept 2011
    • Accepted
      24 Apr 2012
    • Reviewed
      08 Feb 2012
    Associação Brasileira de Pesquisa e Pós-Graduação em Fisioterapia Rod. Washington Luís, Km 235, Caixa Postal 676, CEP 13565-905 - São Carlos, SP - Brasil, Tel./Fax: 55 16 3351 8755 - São Carlos - SP - Brazil
    E-mail: contato@rbf-bjpt.org.br