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

IF 5.3 2区 医学 Q1 GERIATRICS & GERONTOLOGY
Yalan Liu, Li Zhang, Zhaofeng Jin, Lin Zhang, Yan Song, Li He
{"title":"Association of longitudinal body mass index trajectories with phenotypic age acceleration: a cross-sectional study based on growth mixture modeling","authors":"Yalan Liu, Li Zhang, Zhaofeng Jin, Lin Zhang, Yan Song, Li He","doi":"10.1007/s11357-025-01681-y","DOIUrl":null,"url":null,"abstract":"<p>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 (<i>β</i> = 4.34, 95% confidence interval 3.67–5.02). Early BMI changes of less than 6% were associated with being phenotypically younger (<i>β</i> = − 5.06, <i>P</i> = 0.029), whereas increases exceeding 6% were linked to being phenotypically older (<i>β</i> = 2.83, <i>P</i> &lt; 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 (<i>P</i> &lt; 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.</p>","PeriodicalId":12730,"journal":{"name":"GeroScience","volume":"275 1","pages":""},"PeriodicalIF":5.3000,"publicationDate":"2025-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"GeroScience","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s11357-025-01681-y","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"GERIATRICS & GERONTOLOGY","Score":null,"Total":0}
引用次数: 0

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.

纵向体重指数轨迹与表型年龄加速的关联:基于生长混合模型的横断面研究
研究体重指数(BMI)轨迹、早期和近期BMI变化与表型年龄加速(PhenoAgeAccel)之间的关系,解决先前关于体重变化和衰老的研究中不一致的发现。研究使用了2005年至2018年全国健康与营养调查的数据,选择了50岁及以上的参与者。采用生长混合模型来确定BMI轨迹。使用线性和多项逻辑回归模型评估不同BMI轨迹与PhenoAgeAccel之间的关系。通过阈值效应分析确定BMI变化的非线性效应。在5404名参与者中,确定的四种BMI轨迹如下:稳定体重(29.07%),中年体重增加(24.31%),晚年体重增加(32.22%)和慢性肥胖(14.41%)。慢性肥胖组的PhenoAgeAccel水平升高最为显著,表明他们的表型比其他组更老(β = 4.34, 95%可信区间3.67-5.02)。早期BMI变化小于6%与表型年轻相关(β = - 5.06, P = 0.029),而增加超过6%与表型衰老相关(β = 2.83, P < 0.001)。最近BMI变化的关键阈值为2%;低于这个水平的变化与表型上更年轻有关,而超过这个阈值的变化与表型上更老有关(P < 0.001)。这项横断面研究表明,长期慢性肥胖的个体在表型上往往更老,而体重稳定的个体在表型上更可能更年轻。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
GeroScience
GeroScience Medicine-Complementary and Alternative Medicine
CiteScore
10.50
自引率
5.40%
发文量
182
期刊介绍: GeroScience is a bi-monthly, international, peer-reviewed journal that publishes articles related to research in the biology of aging and research on biomedical applications that impact aging. The scope of articles to be considered include evolutionary biology, biophysics, genetics, genomics, proteomics, molecular biology, cell biology, biochemistry, endocrinology, immunology, physiology, pharmacology, neuroscience, and psychology.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信