Association of age at first sexual intercourse and lifetime number of sexual partners with cardiovascular diseases: a bi-directional Mendelian randomization study

BackgroundLimited studies have explored the association between sexual factors [age at first sexual intercourse (AFS) and lifetime number of sexual partners (LNSP)] and cardiovascular diseases (CVDs), leaving the causality inconclusive.MethodsWe performed a bi-directional Mendelian randomization (MR...

Full description

Bibliographic Details
Main Authors: Chengui Zhuo, Lei Chen, Qiqi Wang, Haipeng Cai, Zujin Lin, Huili Pan, Meicui Wu, Yuxiang Jin, Hong Jin, Liangrong Zheng
Format: Article
Language:English
Published: Frontiers Media S.A. 2023-12-01
Series:Frontiers in Cardiovascular Medicine
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fcvm.2023.1267906/full
_version_ 1797401519476178944
author Chengui Zhuo
Lei Chen
Qiqi Wang
Haipeng Cai
Zujin Lin
Huili Pan
Meicui Wu
Yuxiang Jin
Hong Jin
Liangrong Zheng
author_facet Chengui Zhuo
Lei Chen
Qiqi Wang
Haipeng Cai
Zujin Lin
Huili Pan
Meicui Wu
Yuxiang Jin
Hong Jin
Liangrong Zheng
author_sort Chengui Zhuo
collection DOAJ
description BackgroundLimited studies have explored the association between sexual factors [age at first sexual intercourse (AFS) and lifetime number of sexual partners (LNSP)] and cardiovascular diseases (CVDs), leaving the causality inconclusive.MethodsWe performed a bi-directional Mendelian randomization (MR) study to investigate the causality between sexual factors and CVDs, including coronary artery disease, myocardial infarction, atrial fibrillation (AF), heart failure (HF), and ischemic stroke (IS). Single-nucleotide polymorphisms (SNPs) for sexual factors were extracted from the UK Biobank. Statistics for each CVD were derived from two different databases. MR estimates were calculated per outcome database and were combined through meta-analysis. Several complementary sensitivity analyses were also performed.ResultsThe primary analysis suggested that AFS was causally associated with the risk of CVDs; the odds ratios (ORs) ranged from 0.686 [95% confidence interval (CI), 0.611–0.770] for HF to 0.798 (95% CI, 0.719–0.886) for AF. However, the association between AFS and IS (OR, 0.844; 95% CI, 0.632–1.126) was not consistent in the meta-analysis after excluding SNPs related to confounders. Moreover, non-significant associations were found between LNSP and CVDs. Reverse direction MR analysis showed that CVDs were not associated with sexual factors.ConclusionsGenetic evidence suggested that AFS was causally associated with the risk of CVDs except for IS, whereas non-significant association of LNSP with CVDs was detected. Further investigation into AFS could be warranted in preventing the progression of CVDs.
first_indexed 2024-03-09T02:10:19Z
format Article
id doaj.art-f6da2b0967534d79a4055f872c2c1a0b
institution Directory Open Access Journal
issn 2297-055X
language English
last_indexed 2024-03-09T02:10:19Z
publishDate 2023-12-01
publisher Frontiers Media S.A.
record_format Article
series Frontiers in Cardiovascular Medicine
spelling doaj.art-f6da2b0967534d79a4055f872c2c1a0b2023-12-07T13:25:39ZengFrontiers Media S.A.Frontiers in Cardiovascular Medicine2297-055X2023-12-011010.3389/fcvm.2023.12679061267906Association of age at first sexual intercourse and lifetime number of sexual partners with cardiovascular diseases: a bi-directional Mendelian randomization studyChengui Zhuo0Lei Chen1Qiqi Wang2Haipeng Cai3Zujin Lin4Huili Pan5Meicui Wu6Yuxiang Jin7Hong Jin8Liangrong Zheng9Department of Cardiology, Taizhou Central Hospital (Taizhou University Hospital), Taizhou, ChinaDepartment of Cardiology, Taizhou Central Hospital (Taizhou University Hospital), Taizhou, ChinaZhejiang Provincial Center for Drug and Medical Device Procurement, Hangzhou, ChinaDepartment of Cardiology, Taizhou Central Hospital (Taizhou University Hospital), Taizhou, ChinaDepartment of Cardiology, Taizhou Central Hospital (Taizhou University Hospital), Taizhou, ChinaDepartment of Cardiology, Taizhou Central Hospital (Taizhou University Hospital), Taizhou, ChinaDepartment of Cardiology, Taizhou Central Hospital (Taizhou University Hospital), Taizhou, ChinaDepartment of Cardiology, Taizhou Central Hospital (Taizhou University Hospital), Taizhou, ChinaDepartment of Cardiology, Taizhou Central Hospital (Taizhou University Hospital), Taizhou, ChinaDepartment of Cardiology and Atrial Fibrillation Center, the First Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, ChinaBackgroundLimited studies have explored the association between sexual factors [age at first sexual intercourse (AFS) and lifetime number of sexual partners (LNSP)] and cardiovascular diseases (CVDs), leaving the causality inconclusive.MethodsWe performed a bi-directional Mendelian randomization (MR) study to investigate the causality between sexual factors and CVDs, including coronary artery disease, myocardial infarction, atrial fibrillation (AF), heart failure (HF), and ischemic stroke (IS). Single-nucleotide polymorphisms (SNPs) for sexual factors were extracted from the UK Biobank. Statistics for each CVD were derived from two different databases. MR estimates were calculated per outcome database and were combined through meta-analysis. Several complementary sensitivity analyses were also performed.ResultsThe primary analysis suggested that AFS was causally associated with the risk of CVDs; the odds ratios (ORs) ranged from 0.686 [95% confidence interval (CI), 0.611–0.770] for HF to 0.798 (95% CI, 0.719–0.886) for AF. However, the association between AFS and IS (OR, 0.844; 95% CI, 0.632–1.126) was not consistent in the meta-analysis after excluding SNPs related to confounders. Moreover, non-significant associations were found between LNSP and CVDs. Reverse direction MR analysis showed that CVDs were not associated with sexual factors.ConclusionsGenetic evidence suggested that AFS was causally associated with the risk of CVDs except for IS, whereas non-significant association of LNSP with CVDs was detected. Further investigation into AFS could be warranted in preventing the progression of CVDs.https://www.frontiersin.org/articles/10.3389/fcvm.2023.1267906/fullage at first sexual intercourselifetime number of sexual partnerscardiovascular diseasescausal associationMendelian randomization
spellingShingle Chengui Zhuo
Lei Chen
Qiqi Wang
Haipeng Cai
Zujin Lin
Huili Pan
Meicui Wu
Yuxiang Jin
Hong Jin
Liangrong Zheng
Association of age at first sexual intercourse and lifetime number of sexual partners with cardiovascular diseases: a bi-directional Mendelian randomization study
Frontiers in Cardiovascular Medicine
age at first sexual intercourse
lifetime number of sexual partners
cardiovascular diseases
causal association
Mendelian randomization
title Association of age at first sexual intercourse and lifetime number of sexual partners with cardiovascular diseases: a bi-directional Mendelian randomization study
title_full Association of age at first sexual intercourse and lifetime number of sexual partners with cardiovascular diseases: a bi-directional Mendelian randomization study
title_fullStr Association of age at first sexual intercourse and lifetime number of sexual partners with cardiovascular diseases: a bi-directional Mendelian randomization study
title_full_unstemmed Association of age at first sexual intercourse and lifetime number of sexual partners with cardiovascular diseases: a bi-directional Mendelian randomization study
title_short Association of age at first sexual intercourse and lifetime number of sexual partners with cardiovascular diseases: a bi-directional Mendelian randomization study
title_sort association of age at first sexual intercourse and lifetime number of sexual partners with cardiovascular diseases a bi directional mendelian randomization study
topic age at first sexual intercourse
lifetime number of sexual partners
cardiovascular diseases
causal association
Mendelian randomization
url https://www.frontiersin.org/articles/10.3389/fcvm.2023.1267906/full
work_keys_str_mv AT chenguizhuo associationofageatfirstsexualintercourseandlifetimenumberofsexualpartnerswithcardiovasculardiseasesabidirectionalmendelianrandomizationstudy
AT leichen associationofageatfirstsexualintercourseandlifetimenumberofsexualpartnerswithcardiovasculardiseasesabidirectionalmendelianrandomizationstudy
AT qiqiwang associationofageatfirstsexualintercourseandlifetimenumberofsexualpartnerswithcardiovasculardiseasesabidirectionalmendelianrandomizationstudy
AT haipengcai associationofageatfirstsexualintercourseandlifetimenumberofsexualpartnerswithcardiovasculardiseasesabidirectionalmendelianrandomizationstudy
AT zujinlin associationofageatfirstsexualintercourseandlifetimenumberofsexualpartnerswithcardiovasculardiseasesabidirectionalmendelianrandomizationstudy
AT huilipan associationofageatfirstsexualintercourseandlifetimenumberofsexualpartnerswithcardiovasculardiseasesabidirectionalmendelianrandomizationstudy
AT meicuiwu associationofageatfirstsexualintercourseandlifetimenumberofsexualpartnerswithcardiovasculardiseasesabidirectionalmendelianrandomizationstudy
AT yuxiangjin associationofageatfirstsexualintercourseandlifetimenumberofsexualpartnerswithcardiovasculardiseasesabidirectionalmendelianrandomizationstudy
AT hongjin associationofageatfirstsexualintercourseandlifetimenumberofsexualpartnerswithcardiovasculardiseasesabidirectionalmendelianrandomizationstudy
AT liangrongzheng associationofageatfirstsexualintercourseandlifetimenumberofsexualpartnerswithcardiovasculardiseasesabidirectionalmendelianrandomizationstudy