Impact of Cystic Fibrosis Transmembrane Conductance Regulator Modulators on Maternal Outcomes During and After Pregnancy.

IF 9.5 1区 医学 Q1 CRITICAL CARE MEDICINE Chest Pub Date : 2025-02-01 Epub Date: 2024-09-27 DOI:10.1016/j.chest.2024.09.019
Raksha Jain, Giselle Peng, MinJae Lee, Ashley Keller, Sophia Cosmich, Sarthak Reddy, Natalie E West, Traci M Kazmerski, Jennifer L Goralski, Patrick A Flume, Andrea H Roe, Denis Hadjiliadis, Ahmet Uluer, Sheila Mody, Sigrid Ladores, Jennifer L Taylor-Cousar
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Abstract

Background: Cystic fibrosis (CF) transmembrane conductance regulator (CFTR) modulators are available to the majority of people with CF in the United States; little is known about pregnancy outcomes with modulator use. The aim of this retrospective study was to determine the impact of CFTR modulators on maternal outcomes.

Research question: Does pregnancy differentially affect outcomes in female individuals with CF with and without CFTR modulator exposure?

Study design and methods: Data on pregnancies from 2010 to 2021 were collected from 11 US adult CF centers. Multivariable longitudinal regression analysis was performed to assess whether changes in percent predicted FEV1 (ppFEV1), BMI, pulmonary exacerbations (PEx), and Pseudomonas aeruginosa prevalence differed from prior to, during, and following pregnancy according to CFTR modulator use while adjusting for confounders. Infant outcomes are also described based on maternal modulator use.

Results: Among 307 pregnancies, mean age at conception was 28.5 years (range, 17-42 years), before pregnancy ppFEV1 was 74.2, and BMI was 22.3 kg/m2. A total of 114 pregnancies (37.1%) had CFTR modulator exposure during pregnancy (77 with highly effective modulator therapy [HEMT] and 37 with other modulators). The adjusted mean change in ppFEV1 from before pregnancy to during pregnancy was -2.36 (95% CI, -3.56 to -1.16) in the unexposed group and 2.60 (95% CI, 0.23 to 4.97) in the HEMT group, with no significant change from during pregnancy to 1 year after pregnancy. There was an overall decline in ppFEV1 from before pregnancy to after pregnancy in the no modulator group (-2.56; 95% CI, -3.62 to -1.49) that was not observed in the HEMT group (1.10; 95% CI, -1.13 to 3.34). PEx decreased from before pregnancy to after pregnancy in the HEMT group, and BMI increased from before pregnancy to during pregnancy in all groups but with no significant change after pregnancy. Missing infant outcomes data precluded firm conclusions.

Interpretation: We observed superior pregnancy and after pregnancy pulmonary outcomes in individuals who used HEMT, including a preservation of ppFEV1, compared with those unexposed to HEMT.

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囊性纤维化跨膜传导调节器调节剂对孕产妇孕期和产后结果的影响。
背景:在美国,囊性纤维化跨膜传导调节剂(CFTR)调节剂可供大多数CF患者使用;但人们对使用调节剂后的妊娠结局知之甚少。这项回顾性研究旨在确定 CFTR 调节剂对妊娠结局的影响:研究设计与方法:我们从 11 个美国成人 CF 中心收集了 2010-2021 年间的妊娠数据。我们进行了多变量纵向回归分析,以评估使用 CFTR 调节剂后,预测一秒用力呼气容积百分比(ppFEV1)、体重指数(BMI)、肺部恶化(PEx)和铜绿假单胞菌患病率的变化在怀孕前、怀孕期间和怀孕后是否存在差异,同时对混杂因素进行了调整。我们还根据母亲使用调节剂的情况描述了婴儿的结局:在 307 名孕妇中,平均受孕年龄为 28.5 岁(范围:17-42 岁),孕前 ppFEV1 为 74.2,体重指数为 22.3 kg/m2。114名孕妇(37.1%)在怀孕期间接触过CFTR调节剂(77人使用高效调节剂疗法[HEMT],37人使用其他调节剂)。ppFEV1从怀孕前到怀孕期间的调整后平均变化为:未暴露组-2.36(95%CI:-3.56,-1.16),HEMT组+2.60(95%CI:0.23,4.97),从怀孕期间到怀孕后一年无显著变化。从怀孕前到怀孕后,无调节剂组的ppFEV1总体下降(-2.56;95%CI:-3.62,-1.49),而HEMT组没有出现这种情况(1.10;95%CI:-1.13,3.34)。HEMT 组的 PEx 从孕前到孕后都有所下降,所有组的 BMI 从孕前到孕期都有所上升,但孕后没有显著变化。缺失的婴儿结果数据无法得出确切结论:我们观察到,与未接触 HEMT 的人相比,使用 HEMT 的人在妊娠期和妊娠后的肺部结果更佳,包括 ppFEV1 的保持率。
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来源期刊
Chest
Chest 医学-呼吸系统
CiteScore
13.70
自引率
3.10%
发文量
3369
审稿时长
15 days
期刊介绍: At CHEST, our mission is to revolutionize patient care through the collaboration of multidisciplinary clinicians in the fields of pulmonary, critical care, and sleep medicine. We achieve this by publishing cutting-edge clinical research that addresses current challenges and brings forth future advancements. To enhance understanding in a rapidly evolving field, CHEST also features review articles, commentaries, and facilitates discussions on emerging controversies. We place great emphasis on scientific rigor, employing a rigorous peer review process, and ensuring all accepted content is published online within two weeks.
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