Krulewitch C J, Herman A A, Yu K F, Johnson Y R
Pregnancy and Infant Health Branch, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
Paediatr Perinat Epidemiol. 1997 Jan;11 Suppl 1:41-7. doi: 10.1046/j.1365-3016.11.s1.7.x.
An immune reaction initiated by paternal antigens may be necessary for healthy placental development, pregnancy maintenance and infant growth. An inadequate immune response may result in intrauterine growth retardation (IUGR). We hypothesised that a change in paternity may interfere with the immune response and cause poor placentation with resultant IUGR. In this paper we examine the risk of IUGR associated with changes in paternity. We used the Utah Successive Pregnancies Data Set that contains information on women across their pregnancies. We restricted the analysis to 141,817 women with two or three pregnancies. Women who did not have an IUGR infant in the previous pregnancy were at a 20-30% greater risk of developing IUGR if they had changed partners. Women who had a previous IUGR infant were at no increased risk for IUGR after a change in paternity. These results may point to an immune mechanism or may be as a result of residual confounding of unmeasured risk factors for IUGR. Further studies with data that contain more sociodemographic and biological risk factors for IUGR are necessary to exclude residual confounding.
由父系抗原引发的免疫反应可能是胎盘健康发育、维持妊娠及婴儿生长所必需的。免疫反应不足可能导致胎儿宫内生长受限(IUGR)。我们推测,父亲的改变可能会干扰免疫反应,导致胎盘形成不良,进而引发胎儿宫内生长受限。在本文中,我们研究了与父亲改变相关的胎儿宫内生长受限风险。我们使用了犹他州连续妊娠数据集,其中包含了女性整个孕期的信息。我们将分析限制在141,817名有两次或三次妊娠的女性。如果在前次妊娠中没有生出患胎儿宫内生长受限婴儿的女性更换了伴侣,那么她们生出患胎儿宫内生长受限婴儿的风险会增加20%至30%。在前次妊娠中有患胎儿宫内生长受限婴儿的女性,在更换伴侣后,患胎儿宫内生长受限的风险并未增加。这些结果可能指向一种免疫机制,也可能是胎儿宫内生长受限未测量风险因素残余混杂的结果。有必要通过包含更多胎儿宫内生长受限社会人口统计学和生物学风险因素的数据进行进一步研究,以排除残余混杂因素。