Department of Obstetrics and Gynecology, and the Edith Wolfson Medical Center, Affiliated with Sackler Faculty of Medicine, Tel Aviv University, P.O. Box 5, Holon, 58100, Israel.
Department of Obstetrics and Gynecology, and the Edith Wolfson Medical Center, Affiliated with Sackler Faculty of Medicine, Tel Aviv University, P.O. Box 5, Holon, 58100, Israel.
Placenta. 2022 May;122:23-28. doi: 10.1016/j.placenta.2022.03.123. Epub 2022 Mar 25.
An increased risk of an unfavorable obstetric outcome has been reported in relation with Müllerian anomalies (MA). We evaluated whether placental lesions are more frequent among patients with MA and correlates with adverse pregnancy outcomes.
The medical records and placental histopathologyy of consecutive patients with MA between 2007 and 2020 were reviewed. A control group matched for maternal age and pregnancy complications was selected in a 1:1 ratio. Characteristics were then compared between the MA and control groups.
The study group included 110 patients with MA. Patients in the MA group gave birth at earlier gestational age as (35.8 ± 3.3 vs 39.1 ± 1.3 weeks, respectively, P < 0.001). Placental weight <10th percentile was significantly more frequent in the MA cohort compared with controls (31% vs. 6%, respectively, p < 0.001). Higher rates of vascular and villous lesions of maternal vascular malperfusion (MVM) were also detected in the MA group (P = 0.04, P = 0.01, respectively). On multivariable analysis the presence of MA was an independent predictor of composite placental MVM lesions (OR 3.9, 95% CI 2.2, 6, p = 0.04). Using multivariate logistic regression models, the presence of MA was also found to be an independent predictor of small for gestational age (SGA), (OR 4.2, 95% CI 2.7, 11.7, p = 0.01).
MA are associated with placental MVM lesions and SGA independent of background confounders including gestational age - suggesting a placental involvement in the association between MA and adverse pregnancy outcomes. Prospective studies among larger cohorts are needed to corroborate our results.
有研究报道,Müllerian 异常(MA)与不良产科结局风险增加有关。我们评估了 MA 患者的胎盘病变是否更频繁,并与不良妊娠结局相关。
回顾了 2007 年至 2020 年间连续 MA 患者的病历和胎盘组织病理学。以 1:1 的比例选择了年龄和妊娠并发症相匹配的对照组。然后比较 MA 组和对照组的特征。
研究组包括 110 例 MA 患者。MA 组患者的分娩孕周较早,分别为(35.8±3.3 与 39.1±1.3 周,P<0.001)。MA 组胎盘重量<第 10 百分位数的比例明显高于对照组(分别为 31%和 6%,P<0.001)。MA 组还发现更高的血管和绒毛病变的母体血管灌注不良(MVM)发生率(分别为 P=0.04 和 P=0.01)。多变量分析显示,MA 的存在是复合胎盘 MVM 病变的独立预测因子(OR 3.9,95%CI 2.2,6,P=0.04)。使用多变量逻辑回归模型,MA 的存在也被发现是胎儿生长受限(SGA)的独立预测因子(OR 4.2,95%CI 2.7,11.7,P=0.01)。
MA 与胎盘 MVM 病变和 SGA 独立于背景混杂因素有关,包括孕周-提示 MA 与不良妊娠结局之间的关联存在胎盘参与。需要更大队列的前瞻性研究来证实我们的结果。