Chaiworapongsa Tinnakorn, Romero Roberto, Korzeniewski Steven J, Chaemsaithong Piya, Hernandez-Andrade Edgar, Segars James H, DeCherney Alan H, McCoy M Cathleen, Kim Chong Jai, Yeo Lami, Hassan Sonia S
a Perinatology Research Branch, Program for Perinatal Research and Obstetrics, Division of Intramural Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health , Bethesda, MD and Detroit , MI , USA .
b Department of Obstetrics and Gynecology , Wayne State University , Detroit , MI , USA .
J Matern Fetal Neonatal Med. 2016 Mar;29(6):855-62. doi: 10.3109/14767058.2015.1022864. Epub 2015 Apr 20.
Massive perivillous fibrin deposition of the placenta (MPFD) or maternal floor infarction (MFI) is a serious condition associated with recurrent complications including fetal death and severe fetal growth restriction. There is no method to evaluate the risk of adverse outcome in subsequent pregnancies, or effective prevention. Recent observations suggest that MFI is characterized by an imbalance in angiogenic/anti-angiogenic factors in early pregnancy; therefore, determination of these biomarkers may identify the patient at risk for recurrence. We report the case of a pregnant woman with a history of four consecutive pregnancy losses, the last of which was affected by MFI. Abnormalities of the anti-angiogenic factor, sVEGFR-1, and soluble endoglin (sEng) were detected early in the index pregnancy, and treatment with pravastatin corrected the abnormalities. Treatment resulted in a live birth infant at 34 weeks of gestation who had normal biometric parameters and developmental milestones at the age of 2. This is the first reported successful use of pravastatin to reverse an angiogenic/anti-angiogenic imbalance and prevent fetal death.
胎盘大量绒毛周围纤维蛋白沉积(MPFD)或母体底蜕膜梗死(MFI)是一种严重病症,与包括胎儿死亡和严重胎儿生长受限在内的反复并发症相关。目前尚无评估后续妊娠不良结局风险的方法,也没有有效的预防措施。最近的观察表明,MFI的特征是妊娠早期血管生成/抗血管生成因子失衡;因此,测定这些生物标志物可能识别出有复发风险的患者。我们报告了一例有连续四次妊娠丢失史的孕妇病例,最后一次妊娠受MFI影响。在本次索引妊娠早期检测到抗血管生成因子sVEGFR-1和可溶性内皮糖蛋白(sEng)异常,普伐他汀治疗纠正了这些异常。治疗使孕34周时活产一婴儿,该婴儿在2岁时生物测量参数和发育指标正常。这是首次报道成功使用普伐他汀逆转血管生成/抗血管生成失衡并预防胎儿死亡。