Different Metabolic Phenotypes of Obesity and 2 Decades Risk of Cardio-Renal-Metabolic Multimorbidity: Tehran Lipid and Glucose Study.

IF 5.3 1区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
Journal of the American Heart Association Pub Date : 2025-09-16 Epub Date: 2025-09-01 DOI:10.1161/JAHA.124.040930
Danial Molavizadeh, Soroush Masrouri, Farzad Esmaeili, Fereidoun Azizi, Farzad Hadaegh
{"title":"Different Metabolic Phenotypes of Obesity and 2 Decades Risk of Cardio-Renal-Metabolic Multimorbidity: Tehran Lipid and Glucose Study.","authors":"Danial Molavizadeh, Soroush Masrouri, Farzad Esmaeili, Fereidoun Azizi, Farzad Hadaegh","doi":"10.1161/JAHA.124.040930","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Less is known regarding the association between metabolic phenotypes of general and abdominal obesity and incident cardio-renal-metabolic (CRM) multimorbidity, defined as coexistence of at least 2 of the following: diabetes, chronic kidney disease, and cardiovascular diseases (hypertension or stroke or coronary heart disease).</p><p><strong>Methods: </strong>Among 6343 participants (3555 women), with a mean age of 37.06 years, metabolically healthy status was defined as absence of any metabolic syndrome components. Participants were classified as metabolically healthy/unhealthy normal weight, overweight, and obese on the basis of body mass index; and metabolically healthy/unhealthy nonabdominal obese and abdominal obese according to waist circumference. Multivariable Cox hazards regression models were used to estimate hazard ratios (HRs) and 95% CIs, adjusted for age, sex, smoking status, education level, marital status, pulse rate, estimated glomerular filtration rate, family history of premature cardiovascular disease, and family history of diabetes.</p><p><strong>Results: </strong>During a median follow-up of 14.3 years, CRM multimorbidity occurred in 4.8, 13.4, 15.0, 10.8, 17.4, and 29.9% of participants with metabolically healthy normal weight, metabolically healthy overweight, metabolically healthy obese, metabolically unhealthy normal weight, metabolically unhealthy overweight, and metabolically unhealthy obese phenotypes, respectively. In multivariable analyses, compared with the metabolically healthy normal weight, participants with metabolically healthy overweight (HR, 2.08 [95% CI, 1.35-3.20]), metabolically healthy obese (HR, 2.04 [95% CI, 1.11-3.75]), metabolically unhealthy normal weight (HR, 2.29 [95% CI, 1.61-3.27]), metabolically unhealthy overweight (HR, 2.83 [95% CI, 2.01-3.99]), and metabolically unhealthy obese (HR, 5.16 [95% CI, 3.64-7.32]) phenotypes had higher risk of developing CRM multimorbidity. Compared with the metabolically healthy abdominal obese phenotype, participants with metabolically healthy nonabdominal obese (HR, 1.77 [95% CI, 1.19-2.64)], metabolically unhealthy nonabdominal obese (HR, 1.95 [95% CI, 1.48-2.57]), and metabolically unhealthy abdominal obese (HR, 3.26 [95% CI, 2.49-4.28]) exhibited elevated risk. Generally, we found no statistically significant effect modification by sex and age; however, these associations were more pronounced among women and younger individuals.</p><p><strong>Conclusions: </strong>Our results indicate that there is no benign phenotype of obesity beyond metabolically healthy normal weight regarding the incidence of CRM multimorbidity.</p>","PeriodicalId":54370,"journal":{"name":"Journal of the American Heart Association","volume":" ","pages":"e040930"},"PeriodicalIF":5.3000,"publicationDate":"2025-09-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of the American Heart Association","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1161/JAHA.124.040930","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/9/1 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"CARDIAC & CARDIOVASCULAR SYSTEMS","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Less is known regarding the association between metabolic phenotypes of general and abdominal obesity and incident cardio-renal-metabolic (CRM) multimorbidity, defined as coexistence of at least 2 of the following: diabetes, chronic kidney disease, and cardiovascular diseases (hypertension or stroke or coronary heart disease).

Methods: Among 6343 participants (3555 women), with a mean age of 37.06 years, metabolically healthy status was defined as absence of any metabolic syndrome components. Participants were classified as metabolically healthy/unhealthy normal weight, overweight, and obese on the basis of body mass index; and metabolically healthy/unhealthy nonabdominal obese and abdominal obese according to waist circumference. Multivariable Cox hazards regression models were used to estimate hazard ratios (HRs) and 95% CIs, adjusted for age, sex, smoking status, education level, marital status, pulse rate, estimated glomerular filtration rate, family history of premature cardiovascular disease, and family history of diabetes.

Results: During a median follow-up of 14.3 years, CRM multimorbidity occurred in 4.8, 13.4, 15.0, 10.8, 17.4, and 29.9% of participants with metabolically healthy normal weight, metabolically healthy overweight, metabolically healthy obese, metabolically unhealthy normal weight, metabolically unhealthy overweight, and metabolically unhealthy obese phenotypes, respectively. In multivariable analyses, compared with the metabolically healthy normal weight, participants with metabolically healthy overweight (HR, 2.08 [95% CI, 1.35-3.20]), metabolically healthy obese (HR, 2.04 [95% CI, 1.11-3.75]), metabolically unhealthy normal weight (HR, 2.29 [95% CI, 1.61-3.27]), metabolically unhealthy overweight (HR, 2.83 [95% CI, 2.01-3.99]), and metabolically unhealthy obese (HR, 5.16 [95% CI, 3.64-7.32]) phenotypes had higher risk of developing CRM multimorbidity. Compared with the metabolically healthy abdominal obese phenotype, participants with metabolically healthy nonabdominal obese (HR, 1.77 [95% CI, 1.19-2.64)], metabolically unhealthy nonabdominal obese (HR, 1.95 [95% CI, 1.48-2.57]), and metabolically unhealthy abdominal obese (HR, 3.26 [95% CI, 2.49-4.28]) exhibited elevated risk. Generally, we found no statistically significant effect modification by sex and age; however, these associations were more pronounced among women and younger individuals.

Conclusions: Our results indicate that there is no benign phenotype of obesity beyond metabolically healthy normal weight regarding the incidence of CRM multimorbidity.

不同代谢表型的肥胖和20年的心肾代谢多病风险:德黑兰脂质和葡萄糖研究。
背景:一般肥胖和腹部肥胖的代谢表型与心肾代谢(CRM)多病之间的关系尚不清楚,多病定义为至少同时存在以下2种:糖尿病、慢性肾病和心血管疾病(高血压、中风或冠心病)。方法:在6343名参与者(3555名女性)中,平均年龄为37.06岁,代谢健康状态被定义为没有任何代谢综合征成分。根据体重指数将参与者分为代谢健康/不健康的正常体重、超重和肥胖;代谢健康/不健康的非腹部肥胖和腹部肥胖根据腰围。多变量Cox风险回归模型用于估计风险比(hr)和95% ci,校正了年龄、性别、吸烟状况、教育程度、婚姻状况、脉搏率、肾小球滤过率、早发性心血管疾病家族史和糖尿病家族史。结果:在14.3年的中位随访期间,在代谢健康正常体重、代谢健康超重、代谢健康肥胖、代谢不健康正常体重、代谢不健康超重和代谢不健康肥胖表型的参与者中,分别有4.8%、13.4%、15.0%、10.8%、17.4%和29.9%的人出现了CRM多病。在多变量分析中,与代谢健康的正常体重相比,代谢健康的超重(HR, 2.08 [95% CI, 1.35-3.20])、代谢健康的肥胖(HR, 2.04 [95% CI, 1.11-3.75])、代谢不健康的正常体重(HR, 2.29 [95% CI, 1.61-3.27])、代谢不健康的超重(HR, 2.83 [95% CI, 2.01-3.99])和代谢不健康的肥胖(HR, 5.16 [95% CI, 3.64-7.32])表型的参与者发生CRM多病的风险更高。与代谢健康型腹部肥胖表型相比,代谢健康型非腹部肥胖(风险比,1.77 [95% CI, 1.19-2.64)]、代谢不健康型非腹部肥胖(风险比,1.95 [95% CI, 1.48-2.57])和代谢不健康型腹部肥胖(风险比,3.26 [95% CI, 2.49-4.28])的参与者表现出更高的风险。总的来说,我们发现性别和年龄没有统计学上的显著影响;然而,这些关联在女性和年轻人中更为明显。结论:我们的研究结果表明,除了代谢健康的正常体重外,没有良性肥胖表型与CRM多病的发病率有关。
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
Journal of the American Heart Association
Journal of the American Heart Association CARDIAC & CARDIOVASCULAR SYSTEMS-
CiteScore
9.40
自引率
1.90%
发文量
1749
审稿时长
12 weeks
期刊介绍: As an Open Access journal, JAHA - Journal of the American Heart Association is rapidly and freely available, accelerating the translation of strong science into effective practice. JAHA is an authoritative, peer-reviewed Open Access journal focusing on cardiovascular and cerebrovascular disease. JAHA provides a global forum for basic and clinical research and timely reviews on cardiovascular disease and stroke. As an Open Access journal, its content is free on publication to read, download, and share, accelerating the translation of strong science into effective practice.
×
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:604180095
Book学术官方微信