Luke Barbara, Fisher Sarah C, Forestieri Nina E, Yazdy Mahsa M, Betancourt Dayana, Sacha Caitlin R, Murugappan Gayathree, Cameron Katie, Baker Valerie L, Purkayastha Mitana, Williams Carrie, Sutcliffe Alastair G, Richard Melissa A, Lupo Philip J
Department of Obstetrics, Gynecology, and Reproductive Biology, College of Human Medicine, Michigan State University, East Lansing, Michigan, USA.; Population, Policy, and Practice Research and Teaching Department, Great Ormond Street Institute of Child Health, University College London, London, UK..
Birth Defects Registry, New York State Department of Health, Albany, New York, USA.
Reprod Biomed Online. 2025 Jun;50(6):104781. doi: 10.1016/j.rbmo.2024.104781. Epub 2024 Dec 24.
Does an association exist between maternal, reproductive and perinatal factors, and the risks of major non-chromosomal birth defects?
This population-based cohort study included 1,126,058 naturally conceived singleton live births (21,644 with and 1,104,414 without a major non-chromosomal defect) who were born between 2004 and 2018 in New York, Texas, Massachusetts and North Carolina. All study children were linked to their respective state birth defect registries to identify major birth defects diagnosed within the first year of life, and to state death records. Children with chromosomal defects were excluded. Genitourinary defects were only evaluated in boys. Placental and bleeding issues included placenta previa, placental abruption, uterine bleeding and other excessive bleeding, and, at delivery, blood transfusion or unplanned hysterectomy. Adjusted odds ratios and 95% confidence intervals were modelled using logistic regression.
Among major non-chromosomal defects, the highest significant risks were with pre-gestational diabetes (adjusted OR 2.48, 95% CI 2.25 to 2.74), followed by placental or bleeding issues (adjusted OR 1.82, 95% CI 1.66 to 1.99); this pattern was also evident for congenital heart defects, blastogenesis defects, orofacial defects, gastrointestinal defects and musculoskeletal defects. Hypertension (pre-gestational and gestational), prior caesarean delivery, older maternal age and higher body mass index were also significant risk factors.
The risk factors most strongly associated with major non-chromosomal birth defects were pre-gestational diabetes and placental or bleeding issues; other significantly increased risks were hypertension (pre-gestational and gestational), prior caesarean delivery, older maternal age and pre-pregnancy body mass index 30 kg/m or above.
孕产妇、生殖及围产期因素与主要非染色体出生缺陷风险之间是否存在关联?
这项基于人群的队列研究纳入了2004年至2018年在纽约、得克萨斯州、马萨诸塞州和北卡罗来纳州自然受孕的1,126,058例单胎活产儿(其中21,644例有主要非染色体缺陷,1,104,414例无主要非染色体缺陷)。所有研究儿童均与各自州的出生缺陷登记处相链接,以确定出生后第一年内诊断出的主要出生缺陷,并与州死亡记录相链接。染色体缺陷患儿被排除。泌尿生殖系统缺陷仅在男孩中进行评估。胎盘和出血问题包括前置胎盘、胎盘早剥、子宫出血及其他大出血情况,以及分娩时输血或计划外子宫切除术。采用逻辑回归模型计算调整后的比值比和95%置信区间。
在主要非染色体缺陷中,最高的显著风险与孕前糖尿病有关(调整后的比值比为2.48,95%置信区间为2.25至2.74),其次是胎盘或出血问题(调整后的比值比为1.82,95%置信区间为1.66至1.99);这种模式在先天性心脏病、胚胎发生缺陷、口面部缺陷、胃肠道缺陷和肌肉骨骼缺陷中也很明显。高血压(孕前和孕期)、既往剖宫产、产妇年龄较大和体重指数较高也是显著的风险因素。
与主要非染色体出生缺陷最密切相关的风险因素是孕前糖尿病和胎盘或出血问题;其他显著增加的风险包括高血压(孕前和孕期)、既往剖宫产、产妇年龄较大以及孕前体重指数30kg/m²或以上。