Course of Pregnancies and Occurrence of Acute Pancreatitis in Women with Chylomicronemia.

Miriam Larouche, Jean Bergeron, Diane Brisson, Nathalie Laflamme, Noémie Audet-Verreault, Claire Sharon, Sybil Charrière, Melanie Rama, Delphine Collin-Chavagnac, Philippe Moulin, Daniel Gaudet
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Abstract

Objective: Chylomicronemia is characterized by extreme hypertriglyceridemia (triglycerides values >10 mmol/L). It may be caused by bi-allelic combination of pathogenic variant (familial chylomicronemia syndrome (FCS)) or by genetic susceptibility combined with comorbidities and environmental factors (multifactorial chylomicronemia syndrome (MCS)). Acute pancreatitis (AP) is the most serious complication of CM. In the general population, the prevalence of AP during pregnancy is estimated to be <0.35%. As triglycerides levels significantly increase during pregnancy, it may affect the course of pregnancy and further increase the risk of AP in women with chylomicronemia.

Methods: 116 pregnancies involving 49 European and North American women with history of chylomicronemia (20 FCS, 29 MCS) were retrospectively reviewed. The occurrence of AP, the course of pregnancy, fetal development and delivery were evaluated.

Results: 42% of FCS and 10% of MCS women experienced at least one AP episode during pregnancy (p=0.01). Compared to MCS, women with FCS presented a higher percentage of pregnancies with AP (17% vs 5%, p=0.02). Among all reviewed pregnancy-related AP, 56% occurred in primigravida FCS women compared to 0% in MCS. Premature deliveries were elevated in both groups although more frequent in FCS (56%) vs MCS (19%) (p=0.01). The percentage of miscarriages (11.8% vs 10.7%) and fetal failure to thrive (5.9% vs 9.2%) were not significantly different between the two cohorts.

Conclusions: In this study, pregnant women with chylomicronemia had 30-fold (MCS) to 120-fold (FCS) higher occurrence of AP compared to the general population. Chylomicronemia per se does not seem to influence fetal development.

乳糜微粒血症妇女的妊娠过程和急性胰腺炎的发生。
目的:乳糜微粒血症的特点是极度高甘油三酯血症(甘油三酯值bbb10 mmol/L)。它可能是由致病变异的双等位基因组合(家族性乳糜微粒血症综合征(FCS))或遗传易感性结合合并症和环境因素(多因子乳糜微粒血症综合征(MCS))引起的。急性胰腺炎(AP)是CM最严重的并发症。在一般人群中,妊娠期AP的患病率估计为:方法:回顾性分析116例妊娠,涉及49例欧洲和北美有乳糜小铁血症史的妇女(20例FCS, 29例MCS)。观察AP的发生情况、妊娠进程、胎儿发育及分娩情况。结果:42%的FCS妇女和10%的MCS妇女在妊娠期间至少经历过一次AP发作(p=0.01)。与MCS相比,FCS的孕妇患AP的比例更高(17%比5%,p=0.02)。在所有回顾的妊娠相关AP中,56%发生在初生FCS女性中,而MCS中为0%。两组早产发生率均升高,但FCS组早产发生率(56%)高于MCS组(19%)(p=0.01)。流产率(11.8% vs 10.7%)和胎儿发育不全率(5.9% vs 9.2%)在两组间无显著差异。结论:在本研究中,乳糜微粒血症孕妇的AP发生率比一般人群高30倍(MCS)至120倍(FCS)。乳糜微粒血症本身似乎并不影响胎儿发育。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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