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采用 39 年数据进行的复发性妊娠丢失后短期和长期疾病发病的表型全基因组分析。

Phenome-Wide Analysis of Short- and Long-Run Disease Incidence Following Recurrent Pregnancy Loss Using Data From a 39-Year Period.

机构信息

Novo Nordisk Foundation Center for Protein Research Faculty of Health and Medical Sciences University of Copenhagen Denmark.

Methods and Analysis Statistics Denmark Copenhagen Denmark.

出版信息

J Am Heart Assoc. 2020 Apr 21;9(8):e015069. doi: 10.1161/JAHA.119.015069. Epub 2020 Apr 17.

DOI:10.1161/JAHA.119.015069
PMID:32299291
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7428533/
Abstract

Background It is unclear how recurrent pregnancy loss (RPL) impacts disease risk and whether there is a difference in risk between women with or without a live birth before RPL (primary versus secondary RPL). We investigated the disease risk following RPL, and whether there was a difference between primary and secondary RPL. Methods and Results Using population-wide healthcare registries from Denmark, we identified a cohort of 1 370 896 ever-pregnant women aged 12 to 40 years between 1977 and 2016. Of this cohort, 10 691 (0.77%) fulfilled the criteria for RPL (50.0% primary RPL). Average follow-up was 15.8 years. Incidence rate ratios were calculated in a phenome-wide manner. Diagnoses related to assessment and diagnosis of RPL and those appearing later in life were separated using a mixture model. Primary RPL increased the risk of subsequent cardiovascular disorders, including atherosclerosis, cerebral infarction, heart failure, and pulmonary embolism, as well as systemic lupus erythematosus, chronic obstructive pulmonary disease, anxiety, and obsessive-compulsive disorder. Women with secondary RPL had no increased risk of cardiovascular disorders. However, we observed an increased risk of gastrointestinal disorders such as irritable bowel syndrome and intestinal malabsorption, as well as mental disorders and obstetric complications. Conclusions RPL is a risk factor for a spectrum of disorders, which is different for primary and secondary RPL. Screening following RPL explains some associations, but the remaining findings suggest that RPL influences or shares cause with cardiovascular disorders, autoimmune disorders, and mental disorders. Research into the pathophysiology of RPL and later diseases merits further investigation.

摘要

背景

复发性妊娠丢失(RPL)如何影响疾病风险尚不清楚,以及在有或没有 RPL 活产史的女性(原发性与继发性 RPL)之间风险是否存在差异。我们调查了 RPL 后的疾病风险,以及原发性和继发性 RPL 之间是否存在差异。

方法和结果

我们使用丹麦全人群医疗保健登记处的数据,确定了一个 1977 年至 2016 年期间年龄在 12 至 40 岁之间的 1370896 名曾妊娠女性队列。该队列中有 10691 名(0.77%)符合 RPL 标准(50.0%为原发性 RPL)。平均随访时间为 15.8 年。使用表型全基因组方法计算发病率比值。使用混合模型分离与 RPL 的评估和诊断相关的诊断以及以后生活中出现的诊断。原发性 RPL 增加了随后发生心血管疾病的风险,包括动脉粥样硬化、脑梗死、心力衰竭和肺栓塞,以及系统性红斑狼疮、慢性阻塞性肺疾病、焦虑和强迫症。继发性 RPL 女性发生心血管疾病的风险没有增加。然而,我们观察到胃肠道疾病(如肠易激综合征和肠道吸收不良)以及精神障碍和产科并发症的风险增加。

结论

RPL 是一系列疾病的危险因素,原发性和继发性 RPL 之间的风险不同。RPL 后的筛查可以解释一些关联,但剩余的发现表明 RPL 与心血管疾病、自身免疫性疾病和精神障碍有一定的影响或共同病因。对 RPL 和后续疾病的病理生理学的研究值得进一步调查。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9bf3/7428533/cdc57030579a/JAH3-9-e015069-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9bf3/7428533/1295cbf8fc55/JAH3-9-e015069-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9bf3/7428533/8c0f1fb66c02/JAH3-9-e015069-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9bf3/7428533/cdc57030579a/JAH3-9-e015069-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9bf3/7428533/1295cbf8fc55/JAH3-9-e015069-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9bf3/7428533/8c0f1fb66c02/JAH3-9-e015069-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9bf3/7428533/cdc57030579a/JAH3-9-e015069-g003.jpg

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