Department of Paediatrics, The Hospital for Sick Children, Toronto, Ontario, Canada.
Institute of Health Policy, Management, and Evaluation, University of Toronto, Toronto, Ontario, Canada.
JAMA Pediatr. 2024 Jul 1;178(7):688-698. doi: 10.1001/jamapediatrics.2024.1543.
Hypertension affects 6% of all children, and its prevalence is increasing. Childhood hypertension tracks into adulthood and is associated with subclinical cardiovascular disease; however, there is a lack of evidence linking childhood hypertension to cardiovascular outcomes, which may contribute to underdiagnosis and undertreatment.
To determine the long-term associated risk of major adverse cardiac events (MACE) among children diagnosed with hypertension.
DESIGN, SETTING, AND PARTICIPANTS: This was a population-based, retrospective, matched cohort study conducted from 1996 to 2022. The study included all children (aged 3-18 years) alive in Ontario, Canada, from 1996 to 2021, who were identified using provincial administrative health databases. Children with prior kidney replacement therapy were excluded.
Incident hypertension diagnosis, identified by validated case definitions using diagnostic and physician billing claims. Each case was matched with 5 controls without hypertension by age, sex, birth weight, maternal gestational hypertension, prior comorbidities (chronic kidney disease, diabetes, cardiovascular surgery), and a propensity score for hypertension.
The primary outcome was MACE (a composite of cardiovascular death, stroke, hospitalization for myocardial infarction or unstable angina, or coronary intervention). Time to MACE was evaluated using the Kaplan-Meier method and Cox proportional hazards regression.
A total of 25 605 children (median [IQR] age, 15 [11-17] years; 14 743 male [57.6%]) with hypertension were matched to 128 025 controls without hypertension. Baseline covariates were balanced after propensity score matching, and prior comorbidities were uncommon (hypertension vs control cohort: malignancy, 1451 [5.7%] vs 7908 [6.2%]; congenital heart disease, 1089 [4.3%] vs 5408 [4.2%]; diabetes, 482 [1.9%] vs 2410 [1.9%]). During a median (IQR) of 13.6 (7.8-19.5) years of follow-up, incidence of MACE was 4.6 per 1000 person-years in children with hypertension vs 2.2 per 1000 person-years in controls (hazard ratio, 2.1; 95% CI, 1.9-2.2). Children with hypertension were at higher associated risk of stroke, hospitalization for myocardial infarction or unstable angina, coronary intervention, and congestive heart failure, but not cardiovascular death, compared with nonhypertensive controls.
Children diagnosed with hypertension had a higher associated long-term risk of MACE compared with controls without hypertension. Improved detection, follow-up, and control of pediatric hypertension may reduce the risk of adult cardiovascular disease.
高血压影响了所有儿童的 6%,其发病率正在上升。儿童期高血压会持续到成年期,并与亚临床心血管疾病有关;然而,目前缺乏将儿童期高血压与心血管结局联系起来的证据,这可能导致诊断不足和治疗不足。
确定诊断为高血压的儿童发生主要不良心脏事件(MACE)的长期风险。
设计、地点和参与者:这是一项基于人群的回顾性匹配队列研究,于 1996 年至 2022 年进行。研究纳入了 1996 年至 2021 年期间安大略省所有(年龄 3-18 岁)活着的儿童,这些儿童通过省级行政健康数据库确定。排除了先前接受过肾脏替代治疗的儿童。
通过使用诊断和医生计费索赔进行验证的病例定义,确定高血压的新发病例。每个病例都通过年龄、性别、出生体重、母亲妊娠期高血压、先前的合并症(慢性肾脏疾病、糖尿病、心血管手术)和高血压的倾向评分与 5 名无高血压的对照相匹配。
主要结局是 MACE(心血管死亡、中风、心肌梗死或不稳定型心绞痛住院或冠状动脉介入治疗的复合结局)。使用 Kaplan-Meier 方法和 Cox 比例风险回归评估 MACE 的发生时间。
共纳入 25605 名(中位数[IQR]年龄为 15[11-17]岁;14743 名男性[57.6%])高血压儿童,与 128025 名无高血压的对照组相匹配。在倾向评分匹配后,基线协变量得到平衡,先前的合并症也不常见(高血压与对照组相比:恶性肿瘤,1451[5.7%]比 7908[6.2%];先天性心脏病,1089[4.3%]比 5408[4.2%];糖尿病,482[1.9%]比 2410[1.9%])。在中位数(IQR)为 13.6(7.8-19.5)年的随访期间,高血压儿童的 MACE 发生率为每 1000 人年 4.6 例,而对照组为每 1000 人年 2.2 例(危险比,2.1;95%CI,1.9-2.2)。与非高血压对照组相比,患有高血压的儿童发生中风、心肌梗死或不稳定型心绞痛住院、冠状动脉介入治疗和充血性心力衰竭的风险更高,但心血管死亡风险无差异。
与无高血压的对照组相比,被诊断为高血压的儿童发生 MACE 的长期风险更高。改善儿童期高血压的检测、随访和控制可能会降低成年期心血管疾病的风险。