Cargando…

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

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Westergaard, David, Nielsen, Anna Pors, Mortensen, Laust Hvas, Nielsen, Henriette Svarre, Brunak, Søren
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7428533/
https://www.ncbi.nlm.nih.gov/pubmed/32299291
http://dx.doi.org/10.1161/JAHA.119.015069
_version_ 1783571094320447488
author Westergaard, David
Nielsen, Anna Pors
Mortensen, Laust Hvas
Nielsen, Henriette Svarre
Brunak, Søren
author_facet Westergaard, David
Nielsen, Anna Pors
Mortensen, Laust Hvas
Nielsen, Henriette Svarre
Brunak, Søren
author_sort Westergaard, David
collection PubMed
description 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.
format Online
Article
Text
id pubmed-7428533
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-74285332020-08-17 Phenome‐Wide Analysis of Short‐ and Long‐Run Disease Incidence Following Recurrent Pregnancy Loss Using Data From a 39‐Year Period Westergaard, David Nielsen, Anna Pors Mortensen, Laust Hvas Nielsen, Henriette Svarre Brunak, Søren J Am Heart Assoc Original Research 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. John Wiley and Sons Inc. 2020-04-17 /pmc/articles/PMC7428533/ /pubmed/32299291 http://dx.doi.org/10.1161/JAHA.119.015069 Text en © 2020 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Research
Westergaard, David
Nielsen, Anna Pors
Mortensen, Laust Hvas
Nielsen, Henriette Svarre
Brunak, Søren
Phenome‐Wide Analysis of Short‐ and Long‐Run Disease Incidence Following Recurrent Pregnancy Loss Using Data From a 39‐Year Period
title Phenome‐Wide Analysis of Short‐ and Long‐Run Disease Incidence Following Recurrent Pregnancy Loss Using Data From a 39‐Year Period
title_full Phenome‐Wide Analysis of Short‐ and Long‐Run Disease Incidence Following Recurrent Pregnancy Loss Using Data From a 39‐Year Period
title_fullStr Phenome‐Wide Analysis of Short‐ and Long‐Run Disease Incidence Following Recurrent Pregnancy Loss Using Data From a 39‐Year Period
title_full_unstemmed Phenome‐Wide Analysis of Short‐ and Long‐Run Disease Incidence Following Recurrent Pregnancy Loss Using Data From a 39‐Year Period
title_short Phenome‐Wide Analysis of Short‐ and Long‐Run Disease Incidence Following Recurrent Pregnancy Loss Using Data From a 39‐Year Period
title_sort phenome‐wide analysis of short‐ and long‐run disease incidence following recurrent pregnancy loss using data from a 39‐year period
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7428533/
https://www.ncbi.nlm.nih.gov/pubmed/32299291
http://dx.doi.org/10.1161/JAHA.119.015069
work_keys_str_mv AT westergaarddavid phenomewideanalysisofshortandlongrundiseaseincidencefollowingrecurrentpregnancylossusingdatafroma39yearperiod
AT nielsenannapors phenomewideanalysisofshortandlongrundiseaseincidencefollowingrecurrentpregnancylossusingdatafroma39yearperiod
AT mortensenlausthvas phenomewideanalysisofshortandlongrundiseaseincidencefollowingrecurrentpregnancylossusingdatafroma39yearperiod
AT nielsenhenriettesvarre phenomewideanalysisofshortandlongrundiseaseincidencefollowingrecurrentpregnancylossusingdatafroma39yearperiod
AT brunaksøren phenomewideanalysisofshortandlongrundiseaseincidencefollowingrecurrentpregnancylossusingdatafroma39yearperiod