Coexistence of osteoporosis, sarcopenia and obesity in community-dwelling adults - The Yishun Study

​Objectives

To 1) report prevalence of 'osteosarcopenia' (OS) and osteosarcopenic obesity (OSO) entities using evidence-based diagnostic techniques and definitions, 2) examine if OSO offers additional predictive value of functional decline over its components, and 3) identify associated factors in a multi-racial Southeast Asian population.

Methods
We performed a cross-sectional study of a representative sample of 542 community-dwelling adults (21-90 years old), and assessed anthropometry, cognition, functional performance, and self-report sociodemographic, health and lifestyle questionnaires. Low muscle mass, and the Asian Working Group for Sarcopenia (AWGS) 2019 criteria, were used to assess sarcopenia. Obesity was defined using percentage body fat and fat mass index. Osteopenia/osteoporosis was determined using lumbar spinal bone mineral density. Associated factors were examined using logistic regression, and OSO's value investigated using linear regressions with functional performance.

Results
OS and OSO prevalence were 1.8% and 0% (21-59 years), 12.9% and 2.8% (≥60 years), 17.3% and 4.1% (≥65 years) and 25.5% and7.0% (≥75 years), respectively. OSO entity as defined was not a significant predictor (P > 0.05) and did not improve explanations for functional decline over sarcopenia or sarcopenic obesity. Age, sex, race and body mass index (BMI) were associated with OS, while age, sex, race and alcoholism were associated with OSO.

Conclusions
Our results do not support OSO as a distinct entity in relation to functional decline. Aside from biological age, sex, and race, amenable lifestyle factors such as BMI and alcohol intake are important variables that can influence the co-existence of osteopenia/osteoporosis, sarcopenia and obesity.

SOURCE:
Osteoporosis and Sarcopenia

DOI:
https://doi.org/10.1016/j.afos.2020.12.002

AUTHOR(S):
Pang BWJ, Wee SL, Chen KK, Lau LK, Jabbar KA, Seah JWT, Ng DHM, Tan QLL, Jagadish MU, Ng TP