Insitute of Epidemiology and Medical Biometry, ZIBMT, University of Ulm, Ulm, Germany.
German Center for Diabetes Research (DZD), Munich-Neuherberg, Germany.
PLoS Med. 2023 Jan 13;20(1):e1004165. doi: 10.1371/journal.pmed.1004165. eCollection 2023 Jan.
Children with obesity have an increased risk of cardiometabolic risk factors, but not all children carry a similar risk. Perinatal factors, i.e., gestational age (GA) and birth weight for GA, may affect the risk for metabolic complications. However, there are conflicting data whether the association between birth size and cardiometabolic risk factors is independent among children with obesity. Moreover, differential effects of GA and birth weight for GA on cardiometabolic risk factors in pediatric obesity are still unexplored. We aimed to investigate the association between birth weight for GA and cardiometabolic risk factors in children and adolescents with overweight or obesity and to assess whether the association is modified by prematurity.
We conducted a retrospective study of 2 cohorts, using data from the world's 2 largest registers of pediatric obesity treatment-The Swedish childhood obesity treatment register (BORIS) and The Adiposity Patients Registry (APV) (1991 to 2020). Included were individuals with overweight or obesity between 2 to 18 years of age who had data of birth characteristics and cardiometabolic parameters. Birth data was collected as exposure variable and the first reported cardiometabolic parameters during pediatric obesity treatment as the main outcome. The median (Q1, Q3) age at the outcome measurement was 11.8 (9.4, 14.0) years. The main outcomes were hypertensive blood pressure (BP), impaired fasting glucose, elevated glycated hemoglobin (HbA1c), elevated total cholesterol, elevated low-density lipoprotein (LDL) cholesterol, elevated triglycerides, decreased high-density lipoprotein (HDL) cholesterol, and elevated transaminases. With logistic regression, we calculated the odds ratio (OR) and its 95% confidence interval (CI) for each cardiometabolic parameter. All the analyses were adjusted for sex, age, degree of obesity, migratory background, and register source. In total, 42,760 (51.9% females) individuals were included. Small for GA (SGA) was prevalent in 10.4%, appropriate for GA (AGA) in 72.4%, and large for GA (LGA) in 17.2%. Most individuals (92.5%) were born full-term, 7.5% were born preterm. Median (Q1, Q3) body mass index standard deviation score at follow-up was 2.74 (2.40, 3.11) units. Compared with AGA, children born SGA were more likely to have hypertensive BP (OR = 1.20 [95% CI 1.12 to 1.29], p < 0.001), elevated HbA1c (1.33 [1.06 to 1.66], p = 0.03), and elevated transaminases (1.21 [1.10 to 1.33], p < 0.001) as well as low HDL (1.19 [1.09 to 1.31], p < 0.001). On the contrary, individuals born LGA had lower odds for hypertensive BP (0.88 [0.83 to 0.94], p < 0.001), elevated HbA1c (0.81 [0.67 to 0.97], p < 0.001), and elevated transaminases (0.88 [0.81 to 0.94], p < 0.001). Preterm birth altered some of the associations between SGA and outcomes, e.g., by increasing the odds for hypertensive BP and by diminishing the odds for elevated transaminases. Potential selection bias due to occasionally missing data could not be excluded.
Among children and adolescents with overweight/obesity, individuals born SGA are more likely to possess cardiometabolic risk factors compared to their counterparts born AGA. Targeted screening and treatment of obesity-related comorbidities should therefore be considered in this high-risk group of individuals.
肥胖儿童患心血管代谢危险因素的风险增加,但并非所有儿童都有相似的风险。围产期因素,即胎龄(GA)和 GA 对应的出生体重,可能会影响代谢并发症的风险。然而,关于出生体重与心血管代谢危险因素之间的关联是否在肥胖儿童中具有独立性,目前仍存在争议。此外,GA 和 GA 对应的出生体重对儿科肥胖症中心血管代谢危险因素的影响差异尚未得到探索。我们旨在研究 GA 对应的出生体重与超重或肥胖儿童和青少年心血管代谢危险因素之间的关联,并评估早产是否会改变这种关联。
我们对两个队列进行了回顾性研究,使用了世界上最大的两个儿科肥胖症治疗登记处——瑞典儿童肥胖症治疗登记处(BORIS)和肥胖症患者登记处(APV)的数据(1991 年至 2020 年)。纳入了年龄在 2 至 18 岁之间超重或肥胖的个体,他们的数据包括出生特征和心血管代谢参数。出生数据被收集为暴露变量,儿科肥胖症治疗期间首次报告的心血管代谢参数作为主要结局。结局测量的中位数(Q1,Q3)年龄为 11.8(9.4,14.0)岁。主要结局是高血压血压(BP)、空腹血糖受损、糖化血红蛋白升高(HbA1c)、总胆固醇升高、低密度脂蛋白胆固醇升高、甘油三酯升高、高密度脂蛋白胆固醇降低和转氨酶升高。通过逻辑回归,我们计算了每个心血管代谢参数的比值比(OR)及其 95%置信区间(CI)。所有分析均调整了性别、年龄、肥胖程度、移民背景和登记来源。共纳入 42760 名(51.9%为女性)个体。小胎龄儿(SGA)的患病率为 10.4%,适胎龄儿(AGA)为 72.4%,大胎龄儿(LGA)为 17.2%。大多数个体(92.5%)为足月出生,7.5%为早产。随访时的体重指数标准差评分中位数(Q1,Q3)为 2.74(2.40,3.11)单位。与 AGA 相比,SGA 出生的儿童更有可能患有高血压血压(OR=1.20[95%CI 1.12 至 1.29],p<0.001)、HbA1c 升高(1.33[1.06 至 1.66],p=0.03)和转氨酶升高(1.21[1.10 至 1.33],p<0.001)以及低 HDL(1.19[1.09 至 1.31],p<0.001)。相反,LGA 出生的个体发生高血压血压的几率较低(0.88[0.83 至 0.94],p<0.001)、HbA1c 升高(0.81[0.67 至 0.97],p<0.001)和转氨酶升高(0.88[0.81 至 0.94],p<0.001)。早产改变了 SGA 与结局之间的一些关联,例如,增加了高血压血压的几率,并降低了转氨酶升高的几率。由于偶尔缺少数据,可能存在潜在的选择偏差。
在超重/肥胖的儿童和青少年中,与 AGA 出生的儿童相比,SGA 出生的儿童更有可能存在心血管代谢危险因素。因此,应考虑在这一高危人群中对肥胖相关并发症进行有针对性的筛查和治疗。