Prenatal and postnatal nutritional mismatch, reflected by birth weight and adult body mass index, and cardiometabolic disease risk

医学 孟德尔随机化 危险系数 体质指数 低出生体重 比例危险模型 内科学 糖尿病 出生体重 疾病 生理学 内分泌学 怀孕 置信区间 化学 基因型 基因 生物 生物化学 遗传学 遗传变异
作者
Shiping Chen,Ding Ding,Qingmei Cui,Xinquan Zhao,Anping Feng,Yuhan Xia,Qian Xu,Jie Li
出处
期刊:European Journal of Preventive Cardiology [Oxford University Press]
被引量:1
标识
DOI:10.1093/eurjpc/zwaf059
摘要

Abstract Aims This study aimed to investigate how nutritional exposures in early life, represented by birth weight (BW), and in later life, indicated by adult body mass index (BMI), interact to influence cardiometabolic disease (CMD) risk and to examine the underlying causal relationships. Methods and results Included were 254 224 participants of White European ancestry from the UK Biobank. To evaluate the joint associations of BW and adult BMI with CMD risk, BW was categorized as low (LBW, < 2.5 kg) or high (HBW, ≥ 2.5 kg) and BMI as low (LBMI, < 30 kg/m²) or high (HBMI, ≥ 30 kg/m²). Multivariable Cox proportional hazard models and 2 × 2 factorial Mendelian randomization (MR) analyses were employed to assess these associations and the underlying causality. Compared with the participants with HBW-LBMI, the hazard ratio (HR) for atherosclerotic cardiovascular disease (ASCVD) was 1.19 (95% confidence interval: 1.12–1.26) in the LBW-LBMI group, 1.33 (1.28–1.38) in the HBW-HBMI group, and 1.62 (1.50–1.75) in the LBW-HBMI group. The LBW-HBMI group also exhibited higher risks for hypertension [HR: 2.42 (2.26–2.59)], diabetes [HR: 5.16 (4.73–5.63)], and hyperlipidaemia [HR: 1.95 (1.81–2.10)]. Additive interactions between LBW and HBMI were identified for metabolic diseases but not for ASCVD. The causality of these associations was confirmed by MR analysis. Conclusion Combined exposure to LBW and HBMI was most strongly associated with an elevated risk of CMD, underscoring the critical role of the mismatch between early-life and adult nutritional status in shaping long-term cardiometabolic health.
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