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. 2025 May 1.
doi: 10.1007/s11357-025-01681-y. Online ahead of print.

Association of longitudinal body mass index trajectories with phenotypic age acceleration: a cross-sectional study based on growth mixture modeling

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Association of longitudinal body mass index trajectories with phenotypic age acceleration: a cross-sectional study based on growth mixture modeling

Yalan Liu et al. Geroscience. .

Abstract

To examine the association between body mass index (BMI) trajectories, early and recent BMI changes, and phenotypic age acceleration (PhenoAgeAccel), addressing inconsistent findings in previous studies on weight change and aging. Data from the National Health and Nutrition Examination Survey from 2005 to 2018 were used, selecting participants aged 50 years and older. A growth mixture model was employed to identify BMI trajectories. The association between different BMI trajectories and PhenoAgeAccel was assessed using linear and multinomial logistic regression models. The nonlinear effects of BMI changes were identified through threshold effect analysis. Among 5404 participants, the four BMI trajectories identified were as follows: stable weight (29.07%), midlife weight gain (24.31%), late-life weight gain (32.22%), and chronic obesity (14.41%). The chronic obesity group exhibited the most significant elevations in PhenoAgeAccel, indicating they were phenotypically older compared to other groups (β = 4.34, 95% confidence interval 3.67-5.02). Early BMI changes of less than 6% were associated with being phenotypically younger (β = - 5.06, P = 0.029), whereas increases exceeding 6% were linked to being phenotypically older (β = 2.83, P < 0.001). The key threshold for recent BMI changes was 2%; changes below this level were associated with being phenotypically younger, while those exceeding this threshold were linked to being phenotypically older (P < 0.001). This cross-sectional study suggests that individuals with long-term chronic obesity tend to be phenotypically older, whereas those with stable body weight are more likely to be phenotypically younger.

Keywords: BMI; Growth mixture model; Phenotypic age acceleration; Threshold effect; Trajectory.

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Conflict of interest statement

Declarations. Ethics approval: This study followed the guidelines set by the National Center for Health Statistics (NCHS) Ethics Review Board, adhering to the principles of the 1964 Helsinki Declaration and its subsequent revisions or equivalent ethical standards. Informed consent: All participants provided informed consent prior to their inclusion in the study. Conflict of interest: The authors declare no competing interests.

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References

    1. Chang L, Fan W, Pan X, Zhu X. Stem cells to reverse aging. Chin Med J. 2022;135:901–10. - DOI - PubMed - PMC
    1. Ghisletta P. On some challenges of psychological research in late adulthood and aging. Curr Opin Psychol. 2024;55: 101745. - DOI - PubMed
    1. Li H, Miao S, Zhang M, et al. U-shaped association between serum Klotho and accelerated aging among the middle-aged and elderly US population: a cross-sectional study. BMC Geriatr. 2023;23:780. - DOI - PubMed - PMC
    1. Feng Y, Lin H, Tan H, Liu X. Heterogeneity of aging and mortality risk among individuals with hypertension: insights from phenotypic age and phenotypic age acceleration. J Nutr Health Aging. 2024;28:100203. - DOI - PubMed
    1. Chen L, Tan KM, Xu J, et al. Exploring multi-omics and clinical characteristics linked to accelerated biological aging in Asian women of reproductive age: insights from the S-PRESTO study. Genome Med. 2024;16:128. - DOI - PubMed - PMC

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