TY - JOUR
T1 - Screening for frailty phenotype with objectively-measured physical activity in a west Japanese suburban community
T2 - Evidence from the Sasaguri Genkimon Study
AU - Chen, Sanmei
AU - Honda, Takanori
AU - Chen, Tao
AU - Narazaki, Kenji
AU - Haeuchi, Yuka
AU - Supartini, Atin
AU - Kumagai, Shuzo
N1 - Funding Information:
We would like to thank Dr. Nofuji Yu and Ms. Matsuo Eri’s contributions to the data collection. We also would like give our thanks to the municipal staffs in primary care-giving division of Sasaguri town, especially Ms. Gunjima Kumiko who provided us with official data about the inhabitants without placement in long-term care insurance and helped us coordinate the survey in the community. None of them had role in the study design, data analysis, data interpretation, writing of the manuscript, nor in the decision to submit the manuscript. This study was supported in part by Health and Labour Sciences Research Grant of the Japan Ministry of Health, Labour and Welfare (H25-Ninchisho-Ippan-004) and a research grant from Sasaguri town, Fukuoka, Japan. As a financial sponsor, they had no role in the study design, data analysis, data interpretation, writing of the manuscript, or in the decision to submit the manuscript. CSM is supported by China Scholarship Council (CSC).
Publisher Copyright:
© 2015 Chen et al.; licensee BioMed Central.
PY - 2015/4/2
Y1 - 2015/4/2
N2 - Background: The low physical activity domain of the frailty phenotype has been assessed with various self-reported questionnaires, which are prone to possible recall bias and a lack of diagnostic accuracy. The primary purpose of this study was to define the low physical activity domain of the frailty phenotype using accelerometer-based measurement and to evaluate the internal construct validity among older community-dwellers. Secondly, we examined potential correlates of frailty in this population. Methods: We conducted a cross-sectional study of 1,527 community-dwelling older men and women aged 65 and over. Data were drawn from the baseline survey of the Sasaguri Genkimon Study, a cohort study carried out in a west Japanese suburban community. Frailty phenotypes were defined by the following five components: unintentional weight loss, low grip strength, exhaustion, slow gait speed, and low physical activity. Of these criteria, physical activity was objectively measured with a tri-axial accelerometer. To confirm our measure's internal validity, we performed a latent class analysis (LCA) to assess whether the five components could aggregate statistically into a syndrome. We examined the correlates of frailty using multiple stepwise logistic regression models. Results: The estimated prevalence of frailty was 9.3% (95% confidence intervals, CI, 8.4-11.2); 43.9% were pre-frail (95% CI, 41.5-46.4). The percentage of low physical activity was 19.5%. Objectively-assessed physical activity and other components aggregated statistically into a syndrome. Overall, increased age, poorer self-perceived health, depressive and anxiety symptoms, not consuming alcohol, no engagement in social activities, and cognitive impairment were associated with increased odds of frailty status, independent of co-morbidities. Conclusions: This study confirmed the internal construct validity of the frailty phenotype that defined the low energy expenditure domain with the objective measurement of physical activity. Accelerometry may potentially standardize the measurement of low physical activity and improve the diagnostic accuracy of the frailty phenotype criteria in primary care setting. The potential role of factors associated with frailty merits further studies to explore their clinical application.
AB - Background: The low physical activity domain of the frailty phenotype has been assessed with various self-reported questionnaires, which are prone to possible recall bias and a lack of diagnostic accuracy. The primary purpose of this study was to define the low physical activity domain of the frailty phenotype using accelerometer-based measurement and to evaluate the internal construct validity among older community-dwellers. Secondly, we examined potential correlates of frailty in this population. Methods: We conducted a cross-sectional study of 1,527 community-dwelling older men and women aged 65 and over. Data were drawn from the baseline survey of the Sasaguri Genkimon Study, a cohort study carried out in a west Japanese suburban community. Frailty phenotypes were defined by the following five components: unintentional weight loss, low grip strength, exhaustion, slow gait speed, and low physical activity. Of these criteria, physical activity was objectively measured with a tri-axial accelerometer. To confirm our measure's internal validity, we performed a latent class analysis (LCA) to assess whether the five components could aggregate statistically into a syndrome. We examined the correlates of frailty using multiple stepwise logistic regression models. Results: The estimated prevalence of frailty was 9.3% (95% confidence intervals, CI, 8.4-11.2); 43.9% were pre-frail (95% CI, 41.5-46.4). The percentage of low physical activity was 19.5%. Objectively-assessed physical activity and other components aggregated statistically into a syndrome. Overall, increased age, poorer self-perceived health, depressive and anxiety symptoms, not consuming alcohol, no engagement in social activities, and cognitive impairment were associated with increased odds of frailty status, independent of co-morbidities. Conclusions: This study confirmed the internal construct validity of the frailty phenotype that defined the low energy expenditure domain with the objective measurement of physical activity. Accelerometry may potentially standardize the measurement of low physical activity and improve the diagnostic accuracy of the frailty phenotype criteria in primary care setting. The potential role of factors associated with frailty merits further studies to explore their clinical application.
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U2 - 10.1186/s12877-015-0037-9
DO - 10.1186/s12877-015-0037-9
M3 - Article
C2 - 25887474
AN - SCOPUS:84926628773
SN - 1471-2318
VL - 15
JO - BMC Geriatrics
JF - BMC Geriatrics
IS - 1
M1 - 36
ER -