Sarcopenic obesity in rheumatoid arthritis: prevalence and impact on physical functioning
- PMID: 34559201
- PMCID: PMC9157125
- DOI: 10.1093/rheumatology/keab710
Sarcopenic obesity in rheumatoid arthritis: prevalence and impact on physical functioning
Abstract
Objective: We determined the prevalence of sarcopenic obesity in patients with RA using multiple methods and assessed associations with physical functioning.
Methods: This study evaluated data from three RA cohorts. Whole-body dual-energy absorptiometry (DXA) measures of appendicular lean mass index (ALMI, kg/m2) and fat mass index (FMI) were converted to age, sex and race-specific Z-Scores and categorized using a recently validated method and compared it to a widely-used existing method. The prevalence of body composition abnormalities in RA was compared with two reference populations. In the RA cohorts, associations between body composition and change in the HAQ and the Short Physical Performance Battery (SPPB) in follow-up were assessed using linear and logistic regression, adjusting for age, sex, race and study.
Results: The prevalence of low lean mass and sarcopenic obesity was higher in patients with RA (14.2; 12.6%, respectively) compared with the reference population cohorts (7-10%; 4-4.5%, respectively, all P <0.05). There was only moderate agreement among methods of sarcopenic obesity categorization (Kappa 0.45). The recently validated method categorized fewer subjects as obese, and many of these were categorized as low lean mass only. Low lean mass, obesity and sarcopenic obesity were each associated with higher HAQ and lower SPPB at baseline and numerically greater worsening.
Conclusion: RA patients had higher rates of low lean mass and sarcopenic obesity than the general population. The recently validated methods characterized body composition changes differently from traditional methods and were more strongly associated with physical function.
Keywords: disability; fat mass; lean mass; physical function; rheumatoid arthritis.
Published by Oxford University Press on behalf of the British Society for Rheumatology 2021. This work is written by a US Government employee and is in the public domain in the US.
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- P60 AR053308/AR/NIAMS NIH HHS/United States
- M01 RR002719/RR/NCRR NIH HHS/United States
- P60-AR053308/AR/NIAMS NIH HHS/United States
- K12 HD068373/HD/NICHD NIH HHS/United States
- I01 CX001703/CX/CSRD VA/United States
- M01RR02719/Johns Hopkins Bayview Medical Center General Clinical Research Center
- R55 AR050026/AR/NIAMS NIH HHS/United States
- K24 DK076808/GF/NIH HHS/United States
- AR050026-01/ESCAPE RA Study was funded by NIH NIAMS
- IK2 CX000955/CX/CSRD VA/United States
- UL1 RR024134/RR/NCRR NIH HHS/United States
- UL1 RR024131/RR/NCRR NIH HHS/United States
- UL1-RR024131/National Center for Research Resources through a University of California San Francisco Clinical and Translational Sciences Institute grant
- R01 AR050026/AR/NIAMS NIH HHS/United States
- K24 DK076808/DK/NIDDK NIH HHS/United States
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