Cooper D W, Hill J A, Chesley L C, Bryans C I
School of Biological Sciences, Macquarie University, New South Wales, Australia.
Br J Obstet Gynaecol. 1988 Jul;95(7):644-53. doi: 10.1111/j.1471-0528.1988.tb06524.x.
An analysis has been made of 48 pedigrees selected (ascertained) through an affected mother in the first generation. These pedigrees mainly involve cases of eclampsia which occurred before its recent decline in incidence. The data confirm the genetic determination of susceptibility indicated by published data on eclampsia/preeclampsia. There is a suggestion that the fetal genotype can contribute to susceptibility to eclampsia in its mother, in contrast to previous findings that susceptibility to pre-eclampsia is controlled solely by the maternal genotype. An association between eclampsia and miscarriage is shown in the data. We argue that this suggests that the primary mode of action of the gene(s) involved is to affect the interaction between uterine and placental tissue.
对通过第一代患病母亲挑选(确诊)出的48个家系进行了分析。这些家系主要涉及子痫前期发病率近期下降之前发生的子痫病例。数据证实了已发表的子痫/子痫前期数据所表明的易感性的遗传决定因素。有迹象表明,与之前子痫前期易感性仅由母体基因型控制的研究结果相反,胎儿基因型可能会导致其母亲患子痫的易感性增加。数据显示子痫与流产之间存在关联。我们认为,这表明相关基因的主要作用方式是影响子宫与胎盘组织之间的相互作用。