Department of Sports and Health, Institute of Nutrition, Consumption and Health, Paderborn University, Germany; University of Health and Allied Sciences, Ho, Volta Region, Ghana.
Institute of Nutritional and Food Sciences, Nutritional Epidemiology, University of Bonn, Bonn, Germany.
Nutr Metab Cardiovasc Dis. 2021 Jun 30;31(7):2109-2121. doi: 10.1016/j.numecd.2021.03.024. Epub 2021 Apr 7.
Early life exposures could be pertinent risk factors of cardiometabolic diseases in adulthood. We assessed the prospective associations of early life factors with markers of cardiometabolic risk among healthy German adults.
We examined 348 term-born DONALD Study participants with measurement of fasting blood at the age of 18-24 years to assess metabolic indices: fatty liver index (FLI), hepatic steatosis index (HSI), pro-inflammatory score and insulin sensitivity (HOMA2-%S). Early life factors (maternal weight in early pregnancy, maternal early pregnancy BMI, gestational weight gain (GWG), maternal age, birth weight and full breastfeeding (>17 weeks)) were assessed at enrolment of the offspring into the study. Multivariable linear regression models were used to analyze associations between early life factors and markers of cardiometabolic risk in early adulthood with adjustment for potential confounders. A higher early pregnancy BMI was related to notably higher levels of offspring FLI, HSI, pro-inflammatory score and a lower HOMA2-%S (all p < 0.0001). Similarly, a higher gestational weight gain was associated with a higher FLI (p = 0.044), HSI (p = 0.016), pro-inflammatory score (p = 0.032) and a lower HOMA2-%S among females (p = 0.034). Full breastfeeding was associated with a lower adult FLI (p = 0.037). A casual mediation analysis showed that these associations were mediated by offspring adult waist circumference (WC).
This study suggests that early pregnancy BMI, gestational weight gain, and full breastfeeding are relevant for offspring markers of cardiometabolic risk which seems to be mediated by body composition in young adulthood.
生命早期的暴露可能是成年人心血管代谢疾病的相关危险因素。我们评估了生命早期因素与健康德国成年人心血管代谢风险标志物之间的前瞻性关联。
我们检查了 348 名足月出生的 DONALD 研究参与者,他们在 18-24 岁时测量了空腹血液,以评估代谢指标:脂肪肝指数 (FLI)、肝脂肪变性指数 (HSI)、促炎评分和胰岛素敏感性 (HOMA2-%S)。生命早期因素(母亲妊娠早期体重、母亲妊娠早期 BMI、妊娠增重 (GWG)、母亲年龄、出生体重和完全母乳喂养 (>17 周)) 在研究对象入组时进行评估。使用多变量线性回归模型分析生命早期因素与成年早期心血管代谢风险标志物之间的关联,并调整潜在混杂因素。较高的妊娠早期 BMI 与后代 FLI、HSI、促炎评分显著升高和 HOMA2-%S 降低有关(均 p<0.0001)。同样,较高的妊娠增重与女性 FLI(p=0.044)、HSI(p=0.016)、促炎评分(p=0.032)和 HOMA2-%S 降低有关(p=0.034)。完全母乳喂养与成年 FLI 降低有关(p=0.037)。因果中介分析表明,这些关联通过后代成年腰围 (WC) 进行中介。
本研究表明,妊娠早期 BMI、妊娠增重和完全母乳喂养与后代心血管代谢风险标志物相关,这似乎是通过成年早期的身体成分介导的。