van den Bersselaar Lisa M, van de Laar Ingrid M B H, Baars Marieke J H, Baas Annette, Dulfer Eelco, Helderman-van den Enden Apollonia T J M, Hilhorst-Hofstee Yvonne, Kauling Robert M, Kempers Marlies J E, Oudijk Martijn A, Maugeri Alessandra, Brüggenwirth Hennie T, Houweling Arjan C, Demirdas Serwet
Department of Clinical Genetics, Erasmus MC, University Medical Center, Rotterdam, the Netherlands.
Department of Human Genetics, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, the Netherlands.
BJOG. 2025 Mar 19. doi: 10.1111/1471-0528.18142.
We aim to increase knowledge on pregnancy and delivery risks in vascular Ehlers-Danlos Syndrome (vEDS). Our outcomes can contribute to establishing future guidelines for pregnancy and delivery management in women with vEDS.
Retrospective multicentre cohort study.
Women with vEDS due to pathogenic/likely pathogenic (P/LP) COL3A1 variants are at increased risk for arterial dissection and pregnancy-related complications during pregnancy and delivery.
Women with a P/LP COL3A1 variant were included from 2019 until 2021.
Genetic and clinical data was collected through retrospective analysis.
Description of the genotype and pregnancy-related outcomes.
We collected information about 121 pregnancies of 43 women with vEDS, including nine women with a haploinsufficient variant. Neither uterine rupture nor life-threatening or fatal vascular events occurred in the perinatal period. The miscarriage rate was 19% (23/121) and 19.1% of the live births were preterm (18/94). Miscarriages were significantly more frequent in women with a glycine substitution in COL3A1 compared to other COL3A1 variant types (19/23, 82.6%, p = 0.018). Thirty-four women had a vaginal birth (79.1%), including 1/7 with known vEDS. Eight deliveries were complicated by severe perineal tears, and six by postpartum haemorrhage.
No pregnancy-related deaths, arterial dissections or uterine ruptures occurred in our cohort. Since no life-threatening events occurred during pregnancy and delivery, discouragement of pregnancy in all women with vEDS in current guidelines might be too strict. Based on these data, we propose a shared decision-making process.
我们旨在增加对血管型埃勒斯-当洛综合征(vEDS)妊娠和分娩风险的认识。我们的研究结果有助于为vEDS女性建立未来的妊娠和分娩管理指南。
回顾性多中心队列研究。
由于致病性/可能致病性(P/LP)COL3A1变异而患有vEDS的女性在妊娠和分娩期间发生动脉夹层和妊娠相关并发症的风险增加。
纳入2019年至2021年期间携带P/LP COL3A1变异的女性。
通过回顾性分析收集遗传和临床数据。
基因型及妊娠相关结局的描述。
我们收集了43例vEDS女性121次妊娠的信息,其中包括9例携带单倍体不足变异的女性。围产期未发生子宫破裂、危及生命或致命的血管事件。流产率为19%(23/121),19.1%的活产为早产(18/94)。与其他COL3A1变异类型相比,COL3A1中存在甘氨酸替代的女性流产更为频繁(19/23,82.6%,p = 0.018)。34名女性经阴道分娩(79.1%),其中1/7患有已知的vEDS。8例分娩并发严重会阴撕裂,6例并发产后出血。
我们的队列中未发生与妊娠相关的死亡、动脉夹层或子宫破裂。由于妊娠和分娩期间未发生危及生命的事件,当前指南中对所有vEDS女性都不鼓励妊娠可能过于严格。基于这些数据,我们建议采用共同决策的过程。