Ghidini Alessandro, Salafia Carolyn M
Department of Obstetrics and Gynecology, Georgetown University Hospital, Washington, DC 20007, USA.
BJOG. 2005 Feb;112(2):140-4. doi: 10.1111/j.1471-0528.2004.00308.x.
Rates of several obstetric complications have been reported to vary with fetal gender. We investigated whether a sex difference exists in findings at placental histology of extreme prematurity.
Case-control study.
University Hospital.
Four hundred and thirty-seven consecutive deliveries before 32 weeks of gestation of singleton, liveborn, non-anomalous infants.
Obstetric, neonatal and placental histologic findings were compared between male (n= 232) and female (n= 205) neonates.
Histologic evidence of acute placental inflammation, uteroplacental vascular pathology, intraplacental vascular pathology and chronic placental inflammation.
Male fetuses had similar racial distributions, rate of nulliparity, maternal age, gestational age at delivery, placental weight and fetoplacental weight ratio as female fetuses, but higher birthweight centiles (41 [27] vs 33 [26]). Placental histology showed no association between fetal gender and lesions of acute inflammation (P= 0.08), intraplacental vascular pathology (P= 0.16) or uteroplacental vascular pathology (P= 0.83). However, lesions of chronic inflammation had a significantly higher score in male than in female fetuses (P= 0.001). When we examined the distribution of chronic placental inflammation, significantly more severe lesions were noted in male than in female fetuses at the implantation site (i.e. the area of interstitial trophoblast invasion of the maternal decidua and maternal endovascular trophoblast remodelling), than within the placental villi (chronic villitis) or in the amniochorionic membranes (where interstitial trophoblast invasion is minimal).
In premature deliveries at <32 weeks, male fetal gender is associated with placental lesions suggestive of a maternal immune response against the invading interstitial trophoblast. The immunologic basis of these findings deserves further studies.
据报道,几种产科并发症的发生率会因胎儿性别而异。我们调查了极早早产儿胎盘组织学检查结果是否存在性别差异。
病例对照研究。
大学医院。
32周前连续分娩的437例单胎、活产、无畸形婴儿。
比较男性(n = 232)和女性(n = 205)新生儿的产科、新生儿和胎盘组织学检查结果。
急性胎盘炎症、子宫胎盘血管病变、胎盘内血管病变和慢性胎盘炎症的组织学证据。
男性胎儿在种族分布、初产率、母亲年龄、分娩时的孕周、胎盘重量和胎儿胎盘重量比方面与女性胎儿相似,但出生体重百分位数更高(41 [27] 对 33 [26])。胎盘组织学显示,胎儿性别与急性炎症病变(P = 0.08)、胎盘内血管病变(P = 0.16)或子宫胎盘血管病变(P = 0.83)之间无关联。然而,男性胎儿慢性炎症病变的评分显著高于女性胎儿(P = 0.001)。当我们检查慢性胎盘炎症的分布时,发现男性胎儿在植入部位(即母体蜕膜间质滋养层侵入和母体血管内滋养层重塑的区域)的病变比女性胎儿更严重,而在胎盘绒毛内(慢性绒毛炎)或羊膜绒毛膜(间质滋养层侵入最少的部位)则不然。
在孕周小于32周的早产中,男性胎儿性别与提示母体针对侵入性间质滋养层的免疫反应的胎盘病变有关。这些发现的免疫学基础值得进一步研究。