Sarcopenic Obesity Phenotype Index (SOPi): A Population-Based Study
- PMID: 41097857
- PMCID: PMC12528550
- DOI: 10.1002/jcsm.70099
Sarcopenic Obesity Phenotype Index (SOPi): A Population-Based Study
Abstract
Background: Sarcopenic obesity (SO) is a clinical condition defined by the coexistence of high body fat mass and low muscle function and mass, which increases the risk of adverse health outcomes, including disability and mortality. Early detection and frequent monitoring of SO are essential for preventive interventions and management strategies. The current binary approach for SO diagnosis is limited in capturing the spectrum of SO or its progression over time. The main objective of this study was to develop a continuous SOPi that integrates diagnostic criteria such as muscle function and body composition. We aimed to evaluate the association between SOPi and all-cause mortality, to identify baseline-related factors with SOPi and to assess changes in the SOPi over time.
Methods: Participants from the Rotterdam Study with baseline and follow-up measures of handgrip strength (HGS), dual-energy X-ray absorptiometry-measured appendicular lean mass index (ALM/kg) and body fat percentage (BF%) were included. SOPi was calculated as a sex-specific equation integrating z-scores (Z) of (BF%)-(HGS)-(ALM/kg). Cox regression and multivariable linear regression models were fitted to evaluate mortality risk and associated factors with SOPi, respectively. Subgroup analysis of SOPi changes was performed by linear mixed-effects models.
Results: In the total population (n = 5888, age 69.5 ± 9.1 years, BMI 27.5 ± 4.3 kg/m2, 56.8% females) and over the 9.9-year median follow-up period, 1538 (26.1%) participants died. Each standard deviation (SD) increase in sex-specific SOPi was associated with a 10% higher risk of premature death (HR = 1.10 [95%CI: 1.07; 1.13]). Thirteen factors were associated with high SOPi, such as reduced physical activity, higher triglyceride-glucose index, HOMA-IR, systemic inflammation, osteopenia, hypertension, liver steatosis, asthma, coronary heart disease, oral corticosteroid use, lower protein intake, lower quality of life and lower educational status. In participants with obesity, lower physical activity and/or insulin resistance (n = 1682), a significantly higher and faster increase in SOPi was observed compared to participants without these factors (males: β = 2.63 [95%CI: 2.22; 3.03]; females: β = 2.90 [95%CI: 2.58; 3.23]).
Conclusion: SOPi is a significant predictor of premature death and can identify associated factors, particularly useful among persons at risk of SO. SOPi is higher and increases faster in individuals with specific phenotypes. SOPi integrates prognosis information, which could be used as a risk indicator and for prevention of SO.
Keywords: phenotype; population‐based study; sarcopenia; sarcopenic obesity; survival.
© 2025 The Author(s). Journal of Cachexia, Sarcopenia and Muscle published by Wiley Periodicals LLC.
Conflict of interest statement
Elizabeth Benz, Alfonso J. Cruz‐Jentoft, Doris Eglseer, Eva Topinkova and Josje Schoufour reported receiving grants from the SO‐NUTS project, which is funded by JPI HDHL under the ERA‐NET cofund action No. 727565, outside the submitted work. Rocco Barazzoni disclosed his membership on advisory board panels for Novo Nordisk, Pfizer, Boehringer, Nutricia Research, as well as personal fees from Eli‐Lilly, unrelated to the submitted work. Yves Boirie disclosed receiving a grant from the Agence Nationale de la Recherche (ANR) during the conduct of the study and personal fees from Fresenius Kabi, Sanofi France, Novo Nordisk and Lilly outside the submitted work. Alexandre Pinel, Christelle Gillet, Frederick Capel, Bruno Pereira, Dimitris Rizopoulos, Lorenzo M. Donini, Fernando Rivadeneira, Marinka Steur, Trudy Voortman and Peter J.M. Weijs declared that they have no conflicts of interest.
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References
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- JPI HDHL PREPHOBES
- the Netherlands Organization for Health Research and Development
- French National Research Agency
- Federal Ministry of Education, Science and Research represented by the Austrian Research Promotion Agency
- PCI2020-120683-2/Spanish State Research Agency
- Ministry of Education, Youth and Sports Department of Research and Development Czech Republic
- European Union's Horizon 2020 research and innovation programme
- 727565/ERA-NET HDHL INTIMIC, Cofund action
- Erasmus Medical Center and Erasmus University, Rotterdam, Netherlands Organization for the Health Research and Development
- Research Institute for Diseases in the Elderly
- Ministry of Education, Culture and Science
- Ministry for Health, Welfare and Sports
- European Commission
- Municipality of Rotterdam
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