Svensson Anna C, Pawitan Yudi, Cnattingius Sven, Reilly Marie, Lichtenstein Paul
Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
Am J Obstet Gynecol. 2006 Feb;194(2):475-9. doi: 10.1016/j.ajog.2005.08.019.
This study was undertaken to disentangle the maternal genetic, fetal genetic, and environmental effects for the risk of having small-for-gestational-age (SGA) offspring.
By cross-linking the population-based Swedish Multi-Generation and Medical Birth Registers, we extracted 2,193,142 births between 1973 and 2001 with both parents identified. Odds ratios (OR) were calculated to estimate the relative risks, and generalized linear mixed models were used to estimate the contribution of genetic and environmental effects.
Women whose full sisters had an offspring born SGA had a significantly increased risk of having a SGA offspring themselves (OR = 1.8, 95% CI 1.7-1.9), whereas the corresponding risk for brothers was lower (OR = 1.3, 95% CI 1.2-1.4). Thirty-seven percent of the liability was explained by fetal (including both maternal and paternal) genetic effects and 9% by maternal genetic effects.
Genetic factors account for almost half of the liability to have SGA births. These effects are primarily caused by fetal genes.
本研究旨在剖析母亲遗传、胎儿遗传及环境因素对生出小于胎龄儿(SGA)的风险影响。
通过将基于人群的瑞典多代和医疗出生登记册进行交叉关联,我们提取了1973年至2001年间父母双方信息均已确定的2,193,142例出生记录。计算比值比(OR)以估计相对风险,并使用广义线性混合模型来估计遗传和环境因素的贡献。
亲姐妹有SGA后代的女性自身生出SGA后代的风险显著增加(OR = 1.8,95% CI 1.7 - 1.9),而兄弟的相应风险则较低(OR = 1.3,95% CI 1.2 - 1.4)。37%的易感性由胎儿(包括母亲和父亲)遗传因素解释,9%由母亲遗传因素解释。
遗传因素几乎占SGA出生易感性的一半。这些影响主要由胎儿基因引起。