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Long-Term Cardiometabolic Outcomes in Children With Metabolically Healthy and Unhealthy Obesity. 代谢健康和不健康肥胖儿童的长期心脏代谢结局
IF 26.1 1区 医学 Q1 PEDIATRICS Pub Date : 2026-03-23 DOI: 10.1001/jamapediatrics.2026.0343
Resthie R Putri,Pernilla Danielsson,Emilia Hagman,Claude Marcus
ImportanceMetabolically healthy obesity (MHO) in children has been considered a low-risk phenotype, potentially not requiring treatment. However, their long-term cardiometabolic outcomes remain unclear.ObjectiveTo 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 ParticipantsThis 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.ExposuresExposures 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 MeasuresType 2 diabetes, hypertension, dyslipidemia, and mortality up to age 30 years.ResultsA 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 RelevanceResults 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.
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。
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引用次数: 0
COVID-19-Related Changes in Volume of Adolescents and Young Adults With Eating Disorders Requiring Hospitalization. 需要住院治疗的饮食失调青少年和青年人数与covid -19相关的变化
IF 26.1 1区 医学 Q1 PEDIATRICS Pub Date : 2026-03-23 DOI: 10.1001/jamapediatrics.2026.0259
Cassie Burley,Carly E Milliren,Jessica A Lin,Tracy K Richmond
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引用次数: 0
Error in Results. 结果中出现错误。
IF 18 1区 医学 Q1 PEDIATRICS Pub Date : 2026-03-23 DOI: 10.1001/jamapediatrics.2026.0640
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引用次数: 0
Improving Pediatric Patient-Reported Outcome Measure Accessibility-A Call to Action. 提高儿科患者报告结果测量的可及性——行动呼吁。
IF 26.1 1区 医学 Q1 PEDIATRICS Pub Date : 2026-03-23 DOI: 10.1001/jamapediatrics.2026.0256
Christina Zigler,Abigail Rader,Harpreet Chhina
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引用次数: 0
Role of Biomarkers in Acute Brain Injury During ECMO Support. 生物标志物在ECMO支持下急性脑损伤中的作用。
IF 26.1 1区 医学 Q1 PEDIATRICS Pub Date : 2026-03-23 DOI: 10.1001/jamapediatrics.2026.0387
Roberto Lorusso,Eddy Fan
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引用次数: 0
Sleep Health Dimensions From Wearables and Transdiagnostic Mental Health in Young Adolescents. 青少年可穿戴设备的睡眠健康维度和跨诊断心理健康。
IF 26.1 1区 医学 Q1 PEDIATRICS Pub Date : 2026-03-23 DOI: 10.1001/jamapediatrics.2026.0335
Rebecca E Cooper,Amanda E Baker,Allysa D Quick,Lan Yu,Raul Gonzalez,Duncan B Clark,Dana L McMakin,Adriane M Soehner,Maria Jalbrzikowski,Meredith L Wallace
ImportanceSleep behavior markedly shifts in adolescence, increasing vulnerability to mental health disorders. Although sleep health is understood to be multidimensional, adolescent-specific sleep health dimensions have not been empirically validated and their relevance to transdiagnostic mental health outcomes is unknown.ObjectiveTo identify sleep health dimensions using Fitbit devices in a large sample of young adolescents and assess concurrent and prospective associations between sleep health dimensions and transdiagnostic mental health outcomes.Design, Setting, and ParticipantsMulticenter longitudinal cohort study using data from 3393 participants in the Adolescent Brain Cognitive Development (ABCD) Study (Data Release 5.1, collected 2018-2020), including early adolescents (ages 11-13 years) within the US. Exploratory factor analysis (EFA) was used to identify sleep health dimensions and confirmatory factor analysis (CFA) to confirm the factor structure in an independent subsample. Linear mixed-effects models were used to test concurrent and prospective associations between sleep dimensions and mental health outcomes at 1-year follow-up. Statistical analysis was conducted from January to November 2025.ExposuresObjective sleep data collected for up to 21 (range, 7-21) days, using wearable Fitbit devices.Main Outcomes and MeasuresTransdiagnostic mental health outcomes assessed via the Child Behavior Checklist and Brief Problem Monitor (internalizing and externalizing symptoms), Prodromal Questionnaire-Brief Child Version (psychoticlike symptoms), and 10-item Mania Scale (mania symptoms).ResultsThe 3393 participants (49% female; median age, 12 years) were split into EFA and CFA subsamples. Six sleep factors were identified using EFA: irregularity, timing, social jetlag, duration, weekend oversleep, and continuity. CFA confirmed this factor structure. All variables loaded strongly (≥0.64) onto at least 1 factor (factor 1 loadings, 0.64-0.98; factor 2, 0.96-0.98; factor 3, 0.95-0.97; factor 4, -0.86 to 1.01; factor 5, 0.68-0.93; factor 6, 0.82-0.94). Greater sleep irregularity was associated with transdiagnostic mental health symptoms cross-sectionally, but not prospectively (β, 0.06 [95% CI, 0.02-0.10] to 0.12 [95% CI, 0.08-0.16]). Shorter duration was associated with total, internalizing, externalizing, and attention symptoms cross-sectionally (β, -0.06 [95% CI, -0.10 to -0.01] to -0.11 [95% CI, -0.15 to -0.06]) and total, attention, and psychotic symptoms 1 year later.Conclusions and RelevanceIn this study, wearable Fitbit data provide empirical support for multidimensional frameworks of sleep health in adolescence. Although effect sizes were small, sleep irregularity and duration emerged as key dimensions with relevance to mental health. These findings establish a foundation for future investigations, including examining within-person patterns of the 6 dimensions, extending to older adolescence, investigating associations with other health outc
睡眠行为在青春期发生显著变化,增加了患心理健康障碍的脆弱性。虽然睡眠健康被认为是多维的,但青少年特定的睡眠健康维度尚未得到经验验证,其与跨诊断精神健康结果的相关性尚不清楚。目的在大量青少年样本中使用Fitbit设备识别睡眠健康维度,并评估睡眠健康维度与跨诊断心理健康结果之间的并发和前瞻性关联。设计、环境和参与者采用来自青少年大脑认知发展(ABCD)研究(数据发布5.1,收集于2018-2020年)的3393名参与者的数据进行多中心纵向队列研究,包括美国的早期青少年(11-13岁)。探索性因子分析(EFA)用于确定睡眠健康维度,验证性因子分析(CFA)用于确认独立子样本中的因素结构。线性混合效应模型用于测试1年随访中睡眠维度与心理健康结果之间的并发和前瞻性关联。统计分析时间为2025年1 - 11月。使用可穿戴Fitbit设备收集多达21天(范围,7-21)的客观睡眠数据。主要结果和测量方法通过儿童行为检查表和简要问题监测表(内化和外化症状)、前驱期问卷-简要儿童版(精神病样症状)和10项躁狂量表(躁狂症状)评估诊断性心理健康结果。结果3393名参与者(49%为女性,中位年龄12岁)被分为EFA和CFA亚样本。使用EFA确定了六个睡眠因素:不规律、时间、社交时差、持续时间、周末睡过头和连续性。CFA证实了这一因素结构。所有变量均强加载(≥0.64)至少1个因子(因子1加载,0.64-0.98;因子2,0.96-0.98;因子3,0.95-0.97;因子4,-0.86 - 1.01;因子5,0.68-0.93;因子6,0.82-0.94)。更严重的睡眠不规律与跨诊断性精神健康症状相关,但与前瞻性无关(β, 0.06 [95% CI, 0.02-0.10]至0.12 [95% CI, 0.08-0.16])。较短的持续时间与总体、内化、外化和注意力症状横断面相关(β, -0.06 [95% CI, -0.10至-0.01]至-0.11 [95% CI, -0.15至-0.06]),以及1年后总体、注意力和精神症状相关。结论与相关性本研究中,可穿戴Fitbit数据为青少年睡眠健康多维框架提供了实证支持。虽然影响大小很小,但睡眠不规律和持续时间成为与心理健康相关的关键因素。这些发现为未来的研究奠定了基础,包括检查6个维度的个人模式,扩展到更大的青春期,调查与其他健康结果的关联,用研究级活动记录仪进行复制,并建议儿科睡眠干预的潜在目标。
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引用次数: 0
JAMA Pediatrics-The Year in Review, 2025. 《美国医学会儿科杂志:2025年回顾》
IF 18 1区 医学 Q1 PEDIATRICS Pub Date : 2026-03-16 DOI: 10.1001/jamapediatrics.2026.0289
Dimitri A Christakis
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引用次数: 0
Generative AI in Adolescence—A Developmental Framework 青少年中的生成式人工智能——一个发展框架
IF 26.1 1区 医学 Q1 PEDIATRICS Pub Date : 2026-03-16 DOI: 10.1001/jamapediatrics.2026.0032
Cindy H. Liu, Tiffany Yip
This Viewpoint describes the engagement of generative artificial intelligence (AI) as a relational partner among adolescents and how to set research priorities in order to pay immediate attention to the developmental risks and benefits.
本观点描述了生成式人工智能(AI)作为青少年关系伙伴的参与,以及如何设定研究重点,以便立即关注其发展风险和益处。
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引用次数: 0
Screens and Youth Sleep. 屏幕与青少年睡眠。
IF 18 1区 医学 Q1 PEDIATRICS Pub Date : 2026-03-16 DOI: 10.1001/jamapediatrics.2026.0253
Lauren Hale, Lauren E Hartstein, Chuan Zhou
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引用次数: 0
Coding Error in Dataset of Study of Behavior Problems in Low-Income Young Children Screened in Pediatric Primary Care. 儿童初级保健筛查中低收入幼儿行为问题研究数据集的编码错误。
IF 26.1 1区 医学 Q1 PEDIATRICS Pub Date : 2026-03-16 DOI: 10.1001/jamapediatrics.2026.0272
Robert T Ammerman
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引用次数: 0
期刊
JAMA Pediatrics
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