期刊论文详细信息
BMC Medicine
Differential effect of pre-pregnancy low BMI on fetal macrosomia: a population-based cohort study
Yuhan Xing1  Zhenhong Zhang2  Yao Wang2  Qing Liu3  Jun Zhang3  Wenjing Chen3  Li Gao4  Guolan Wang4  Guoju Li4  Qin Wu4  Wei Ni4  Na Jiao4  Quansheng Xing4 
[1] Department of Paediatrics, Faculty of Medicine, The Chinese University of Hong Kong, Hong Kong, China;Public Health School, Medical College of Qingdao University, Qingdao, China;Qingdao Women and Children’s Health Care and Family Planning Service Center, Qingdao, Shandong Province, China;Qingdao Women and Children’s Hospital, Qingdao University, No.6 Tongfu Road, 266000, Qingdao, Shandong Province, China;
关键词: Macrosomia;    Pre-pregnancy BMI;    Gestational diabetes mellitus;    Parity;    Maternal age;   
DOI  :  10.1186/s12916-021-02046-w
来源: Springer
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【 摘 要 】

BackgroundThe differential effect of pre-pregnancy low BMI on macrosomia has not been fully addressed. Herein, we conducted a city-wide population-based cohort study to illuminate the association between pre-pregnancy low BMI and macrosomia, stratifying by maternal age, parity, and GDM status.MethodsAll pregnant women who paid their first prenatal visit to the hospital in Qingdao during August 1, 2018, to June 30, 2020, were recruited to this study. The interactive effect of maternal age and pre-pregnancy low BMI on macrosomia was evaluated using logistic regression models, followed by strata-specific analyses.ResultsA total of 105,768 mother-child pairs were included, and the proportion of fetal macrosomia was 11.66%. The interactive effect of maternal pre-pregnancy BMI and age was statistically significant on macrosomia irrespective of parity (nullipara: Padjusted=0.0265; multipara: Padjusted=0.0356). The protective effect of low BMI on macrosomia was most prominent among nullipara aged 35 years and above (aOR=0.16, 95% CI 0.05–0.49) and multipara aged 25 years and below (aOR=0.17, 95% CI 0.05–0.55). In nullipara without GDM, the risk estimates gradually declined with increasing conception age (20-to-24 years: aOR=0.64, 95% CI 0.51–0.80; 25-to-29 years: aOR=0.43 95% CI 0.36–0.52; 30-to-34 years: aOR=0.40 95% CI 0.29–0.53; and ≥35 years: aOR=0.19, 95% CI 0.06–0.60). A similar pattern could also be observed in nullipara with GDM, where the aOR for low BMI on macrosomia decreased from 0.54 (95% CI 0.32–0.93) in pregnant women aged 25–29 years to 0.30 (95% CI 0.12–0.75) among those aged 30–34 years. However, younger multiparous mothers, especially those aged 25 years and below without GDM (aOR=0.21, 95% CI 0.06–0.68), were more benefited from a lower BMI against the development of macrosomia.ConclusionsMaternal low BMI is inversely associated with macrosomia irrespective of maternal age and parity. The impact of pre-pregnancy low BMI on macrosomia varied by maternal age and parity. The protective effect of a lower maternal BMI against fetal macrosomia was more prominent in nulliparous mothers aged 35 years and above, whereas multiparous mothers younger than 25 years of age were more benefited.

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