Natera, Inc., Austin, Texas; and the University of Connecticut Health Center, Farmington, Connecticut.
Obstet Gynecol. 2023 Nov 1;142(5):1208-1216. doi: 10.1097/AOG.0000000000005318. Epub 2023 Aug 10.
To identify conditions on a reproductive carrier screening panel with the potential for carrier manifestations during pregnancy and review the implications for obstetric care.
This was a retrospective cross-sectional study of consecutive samples from female patients aged 18-55 years submitted to a commercial laboratory for a 274-gene carrier screening panel (January 2020 to September 2022). A literature review was performed to identify genes on the panel with potential for pregnancy complications in carriers. Carrier expression and published recommendations for clinical management were reviewed.
We identified 12 genes with potential for carrier manifestations during pregnancy based on reports in the literature: nine with manifestations irrespective of the fetal genetic status ( ABCB11 , COL4A3 , COL4A4 , COL4A5 , DMD , F9 , F11 , GLA , and OTC ) and three ( CPT1A , CYP19A1 , and HADHA ) with manifestations only if the fetus is affected by the condition. Manifestations included cardiomyopathy, hemorrhage, gestational hypertensive disorders, cholestasis of pregnancy, acute fatty liver, hyperammonemic crisis, and maternal virilization. Published recommendations for carrier management were identified for 11 of the 12 genes. Of 91,637 tests performed during the study period, a pathogenic or likely pathogenic variant was identified in 2,139 (2.3%), giving a carrier frequency for any of the 12 genes of 1 in 43 (95% CI 1/41-45) 1,826 (2.0%) of the study population were identified as carriers for one of the nine genes with the potential for carrier manifestations irrespective of an affected or unaffected fetus.
Approximately 1 in 40 female patients were identified as carriers for a condition with potential for maternal manifestations in pregnancy, including some serious or even life-threatening complications. Obstetric care professionals should be aware of the possibility of pregnancy complications among carriers and the available recommendations for management.
This study was funded by Natera, Inc.
确定生殖携带者筛查面板上存在妊娠时携带者表现的条件,并回顾其对产科护理的影响。
这是一项回顾性的横断面研究,对 2020 年 1 月至 2022 年 9 月期间因商业实验室进行 274 个基因携带者筛查面板而提交的 18-55 岁女性患者的连续样本进行了研究。进行了文献回顾,以确定面板上具有携带者表现潜力的基因。回顾了携带者的表达情况和已发表的临床管理建议。
根据文献报道,我们确定了 12 个在妊娠期间具有潜在携带者表现的基因:9 个无论胎儿遗传状态如何都有表现( ABCB11 、 COL4A3 、 COL4A4 、 COL4A5 、 DMD 、 F9 、 F11 、 GLA 和 OTC ),3 个( CPT1A 、 CYP19A1 和 HADHA )仅在胎儿受该疾病影响时才有表现。表现包括心肌病、出血、妊娠高血压疾病、妊娠肝内胆汁淤积症、急性脂肪性肝炎、高氨血症危象和母体男性化。已为 12 个基因中的 11 个确定了携带者管理的建议。在研究期间进行的 91637 次检测中,发现了 2139 种致病性或可能致病性变异(2.3%),这意味着 12 个基因中的任何一个的携带者频率为 1/43(95%CI 1/41-45),研究人群中有 1826 人(2.0%)被确定为 9 个具有潜在携带者表现的基因之一的携带者,无论胎儿是否受影响。
大约每 40 名女性患者中就有 1 名被确定为携带者,存在妊娠时母体表现的潜在风险,包括一些严重甚至危及生命的并发症。产科护理专业人员应意识到携带者可能出现妊娠并发症,并了解可用的管理建议。
本研究由 Natera, Inc. 资助。