Long-Term Cardiometabolic Outcomes in Children With Metabolically Healthy and Unhealthy Obesity.

IF 18 1区 医学 Q1 PEDIATRICS
Resthie R Putri,Pernilla Danielsson,Emilia Hagman,Claude Marcus
{"title":"Long-Term Cardiometabolic Outcomes in Children With Metabolically Healthy and Unhealthy Obesity.","authors":"Resthie R Putri,Pernilla Danielsson,Emilia Hagman,Claude Marcus","doi":"10.1001/jamapediatrics.2026.0343","DOIUrl":null,"url":null,"abstract":"Importance\r\nMetabolically healthy obesity (MHO) in children has been considered a low-risk phenotype, potentially not requiring treatment. However, their long-term cardiometabolic outcomes remain unclear.\r\n\r\nObjective\r\nTo compare the occurrence of type 2 diabetes, hypertension, dyslipidemia, and mortality up to young adulthood in children with metabolically healthy obesity (MHO), metabolically unhealthy obesity (MUO), and general population peers, and to investigate the association between obesity treatment response and disease risk.\r\n\r\nDesign, Setting, and Participants\r\nThis was a prospective cohort study including children undergoing obesity treatment recorded in the Swedish Childhood Obesity Treatment Register (BORIS) between 1997 and 2020 and their general population comparators, linked with national registers. Children in the cohort with obesity were aged 7 to 17 years at obesity treatment initiation and had complete cardiometabolic data. General population comparators were matched (ratio 1:5) based on sex, birth year, and residential area. Study data were analyzed from February to March 2025.\r\n\r\nExposures\r\nExposures included metabolically healthy obesity (MHO), defined as the absence of high blood pressure, impaired fasting glycemia, elevated transaminases, elevated triglycerides, and low high-density lipoprotein cholesterol; otherwise, children were categorized as having metabolically unhealthy obesity (MUO).\r\n\r\nMain Outcomes and Measures\r\nType 2 diabetes, hypertension, dyslipidemia, and mortality up to age 30 years.\r\n\r\nResults\r\nA total of 7275 children (median [first quartile {Q1}-third quartile {Q3}] age, 11.1 [9.1-13.5] years; 4004 male [55.0%]) were included, along with 35 636 general population comparators (median [Q1-Q3] age, 11.1 [9.1-13.5] years; 19 596 male [55.0%]). MHO at baseline was present in 3626 children (49.8%; median [Q1-Q3] age, 10.6 [8.8-12.8] years; 1981 male [54.6%]), and MUO was present in 3649 children (50.2%; median [Q1-Q3] age, 11.6 [9.4-14.0] years; 2023 male [55.4%]). By age 30 years, cumulative incidences were as follows: type 2 diabetes (MHO, 9.1%; MUO, 16.8%; general population, 0.5%), hypertension (MHO, 10.8%; MUO, 18.3%; general population, 3.7%), and dyslipidemia (MHO, 5.3%; MUO, 12.7%; general population, 0.9%). A reduction of at least 0.25 body mass index (BMI) z score was associated with reduced incidence rate ratio (IRR) of type 2 diabetes (IRR, 0.22; 95% CI, 0.14-0.35), hypertension (IRR, 0.56; 95% CI, 0.34-0.93), and dyslipidemia (IRR, 0.28; 95% CI, 0.14-0.57), with similar risk reduction for MHO and MUO.\r\n\r\nConclusions and Relevance\r\nResults of this cohort study reveal that a reduction in BMI z score of at least 0.25 was associated with similar risk reductions for both MHO and MUO. Children with MHO face a substantially increased cardiometabolic disease risk already as young adults compared with the general population. Hence, obesity treatment should be recommended for all children with obesity, regardless of initial metabolic status.","PeriodicalId":14683,"journal":{"name":"JAMA Pediatrics","volume":"92 1","pages":""},"PeriodicalIF":18.0000,"publicationDate":"2026-03-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"JAMA Pediatrics","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1001/jamapediatrics.2026.0343","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PEDIATRICS","Score":null,"Total":0}
引用次数: 0

Abstract

Importance Metabolically healthy obesity (MHO) in children has been considered a low-risk phenotype, potentially not requiring treatment. However, their long-term cardiometabolic outcomes remain unclear. Objective To compare the occurrence of type 2 diabetes, hypertension, dyslipidemia, and mortality up to young adulthood in children with metabolically healthy obesity (MHO), metabolically unhealthy obesity (MUO), and general population peers, and to investigate the association between obesity treatment response and disease risk. Design, Setting, and Participants This was a prospective cohort study including children undergoing obesity treatment recorded in the Swedish Childhood Obesity Treatment Register (BORIS) between 1997 and 2020 and their general population comparators, linked with national registers. Children in the cohort with obesity were aged 7 to 17 years at obesity treatment initiation and had complete cardiometabolic data. General population comparators were matched (ratio 1:5) based on sex, birth year, and residential area. Study data were analyzed from February to March 2025. Exposures Exposures included metabolically healthy obesity (MHO), defined as the absence of high blood pressure, impaired fasting glycemia, elevated transaminases, elevated triglycerides, and low high-density lipoprotein cholesterol; otherwise, children were categorized as having metabolically unhealthy obesity (MUO). Main Outcomes and Measures Type 2 diabetes, hypertension, dyslipidemia, and mortality up to age 30 years. Results A total of 7275 children (median [first quartile {Q1}-third quartile {Q3}] age, 11.1 [9.1-13.5] years; 4004 male [55.0%]) were included, along with 35 636 general population comparators (median [Q1-Q3] age, 11.1 [9.1-13.5] years; 19 596 male [55.0%]). MHO at baseline was present in 3626 children (49.8%; median [Q1-Q3] age, 10.6 [8.8-12.8] years; 1981 male [54.6%]), and MUO was present in 3649 children (50.2%; median [Q1-Q3] age, 11.6 [9.4-14.0] years; 2023 male [55.4%]). By age 30 years, cumulative incidences were as follows: type 2 diabetes (MHO, 9.1%; MUO, 16.8%; general population, 0.5%), hypertension (MHO, 10.8%; MUO, 18.3%; general population, 3.7%), and dyslipidemia (MHO, 5.3%; MUO, 12.7%; general population, 0.9%). A reduction of at least 0.25 body mass index (BMI) z score was associated with reduced incidence rate ratio (IRR) of type 2 diabetes (IRR, 0.22; 95% CI, 0.14-0.35), hypertension (IRR, 0.56; 95% CI, 0.34-0.93), and dyslipidemia (IRR, 0.28; 95% CI, 0.14-0.57), with similar risk reduction for MHO and MUO. Conclusions and Relevance Results of this cohort study reveal that a reduction in BMI z score of at least 0.25 was associated with similar risk reductions for both MHO and MUO. Children with MHO face a substantially increased cardiometabolic disease risk already as young adults compared with the general population. Hence, obesity treatment should be recommended for all children with obesity, regardless of initial metabolic status.
代谢健康和不健康肥胖儿童的长期心脏代谢结局
儿童代谢健康型肥胖(MHO)一直被认为是一种低风险表型,可能不需要治疗。然而,他们的长期心脏代谢结果仍不清楚。目的比较代谢性健康型肥胖(MHO)、代谢性不健康型肥胖(MUO)儿童在成年前2型糖尿病、高血压、血脂异常和死亡率的发生率,并探讨代谢性健康型肥胖治疗反应与疾病风险之间的关系。设计、环境和参与者:这是一项前瞻性队列研究,包括在1997年至2020年期间在瑞典儿童肥胖治疗登记册(BORIS)中记录的接受肥胖治疗的儿童及其与国家登记册相关联的一般人群比较者。肥胖队列中的儿童在肥胖治疗开始时年龄为7至17岁,并具有完整的心脏代谢数据。一般人口比较者按性别、出生年份和居住区域进行匹配(比例1:5)。研究数据分析时间为2025年2月至3月。暴露包括代谢健康型肥胖(MHO),定义为没有高血压、空腹血糖受损、转氨酶升高、甘油三酯升高和低高密度脂蛋白胆固醇;否则,儿童被归类为代谢不健康肥胖(MUO)。主要结局和测量:2型糖尿病、高血压、血脂异常和30岁前的死亡率。结果共纳入7275例儿童(年龄中位数[第一四分位数{Q1}-第三四分位数{Q3}], 11.1[9.1 ~ 13.5]岁;男性4004例[55.0%]),以及35 一般人群比较者(年龄中位数[Q1 ~ Q3], 11.1[9.1 ~ 13.5]岁;男性19 596例[55.0%])。3626名儿童出现MHO (49.8%; [Q1-Q3]中位年龄10.6[8.8-12.8]岁;1981名男性[54.6%]),3649名儿童出现MUO (50.2%; [Q1-Q3]中位年龄11.6[9.4-14.0]岁;2023名男性[55.4%])。到30岁时,累积发病率如下:2型糖尿病(MHO, 9.1%; MUO, 16.8%;一般人群,0.5%),高血压(MHO, 10.8%; MUO, 18.3%;一般人群,3.7%),血脂异常(MHO, 5.3%; MUO, 12.7%;一般人群,0.9%)。体重指数(BMI) z评分降低至少0.25与2型糖尿病(IRR, 0.22; 95% CI, 0.14-0.35)、高血压(IRR, 0.56; 95% CI, 0.34-0.93)和血脂异常(IRR, 0.28; 95% CI, 0.14-0.57)的发病率比(IRR, 0.28; 95% CI, 0.14-0.57)相关,MHO和MUO的风险降低相似。结论和相关性本队列研究的结果显示,BMI z评分降低至少0.25与MHO和MUO的风险降低相似。与一般人群相比,患有MHO的儿童作为年轻人已经面临着显著增加的心脏代谢疾病风险。因此,应建议所有肥胖儿童接受肥胖治疗,无论其初始代谢状态如何。
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
JAMA Pediatrics
JAMA Pediatrics PEDIATRICS-
CiteScore
31.60
自引率
1.90%
发文量
357
期刊介绍: JAMA Pediatrics, the oldest continuously published pediatric journal in the US since 1911, is an international peer-reviewed publication and a part of the JAMA Network. Published weekly online and in 12 issues annually, it garners over 8.4 million article views and downloads yearly. All research articles become freely accessible online after 12 months without any author fees, and through the WHO's HINARI program, the online version is accessible to institutions in developing countries. With a focus on advancing the health of infants, children, and adolescents, JAMA Pediatrics serves as a platform for discussing crucial issues and policies in child and adolescent health care. Leveraging the latest technology, it ensures timely access to information for its readers worldwide.
×
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
小红书