Abstract
Background
Various methods have been used to assess adiposity and its associations with morbidity and mortality. In this study, we aimed to examine the association of four adiposity markers with all‑cause and cause‑specific mortality, while evaluating the potential influence of reverse causation bias.
Methods
This prospective cohort study included 158,699 participants from the Mexico City Prospective Study. Cox regression models were performed to estimate the associations of body mass index, waist circumference, waist-to-height ratio, and waist-to-hip ratio with mortality risk. To minimize the influence of reverse causation, we excluded participants with prevalent diseases at baseline and conducted additional analyses excluding deaths occurring within the first 2, 5, and 10 years of follow-up.
Results
Over a median of 15.5 years, 28,296 death were recorded. Waist circumference values above the recommended cutoff considered high were associated with higher all-cause mortality after the exclusion of the first 2, 5, and 10 years of follow-up (HR: 1.83; 95% CI: 1.26–2.55, HR: 1.83; 95% CI: 1.23–2.62, and HR: 1.85; 95% CI: 1.14–2.70, respectively). Elevated waist-to-hip ratio was associated with increased all-cause mortality across the same exclusion periods (HR: 1.71; 95% CI: 1.07–2.30, HR: 1.70; 95% CI: 1.05–2.49, and HR: 1.71; 95% CI: 1.01-2.52). High waist circumference was strongly associated with CVD mortality after exclusion of the first 2, 5, and 10 years (HR: 4.76; 95% CI: 1.70–11.82, HR: 4.75; 95% CI: 1.56–11.88, and HR: 4.73; 95% CI: 1.42–12.90, respectively). Elevated waist-to-hip ratio similarly showed associations with CVD mortality (HR: 2.69; 95% CI: 1.10–5.60, HR: 2.66; 95% CI: 1.12–5.75, and HR: 2.64; 95% CI: 1.03–7.32). Body mass index, waist circumference, waist-to-height ratio, and waist-hip ratio were not associated with respiratory and cancer mortality.
Conclusions
Waist circumference was the adiposity marker most strongly associated with all-cause and CVD mortality, even after excluding the first 10 years of follow-up.
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Data availability
Data from the Mexico City Prospective Study are available to bona fide researchers for collaborative and/or open-access research purposes. The study’s Data and Sample Sharing policy can be downloaded (in English or Spanish: https://www.ctsu.ox.ac.uk/research/mcps). Available study data can be examined in the study Data Showcase (https://datashare.ndph.ox.ac.uk/mexico).
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Acknowledgements
This research has been conducted using Mexico City Prospective Study (MCPS) Data under Application Number 2022-020. MCPS (https://www.ctsu.ox.ac.uk/research/mcps) has received funding from the Mexican Health Ministry, the National Council of Science and Technology for Mexico, Wellcome, and core grants from the UK Medical Research Council to the MRC Population Health Research Unit at the University of Oxford. We would like to thank the participants from the Mexico City Prospective Study. We thank everyone who took part in the Mexico City Prospective Study.
Funding
The present research received financial support from Vicerrectoría de Investigación y Doctorados, Universidad Autónoma de Chile. National Council for Scientific and Technological Development - CNPq (311109-2023-3; LFMR). This study was financed in part by the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - Brasil (CAPES) - Finance Code 001 (WAdS). GF was funded by the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - Brasil (CAPES) – Code: 88887.979411/2024-00.
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WAdS, and GF, contributed to the conception and design of the study. WAdS, and GF advised on all statistical aspects. LFMR, AM, MdMN, EN, DC, and RFdC performed the literature search, the analyses and interpreted the data. All authors critically reviewed this and previous drafts. All authors approved the final draft for submission.
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da Silva, W.A., Rezende, L.F.M., Marques, A. et al. Which adiposity marker is most strongly associated with all‑cause and cause‑specific mortality? a prospective study of 158,699 Mexican adults. Int J Obes 49, 1792–1799 (2025). https://doi.org/10.1038/s41366-025-01827-0
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DOI: https://doi.org/10.1038/s41366-025-01827-0