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Heart Failure and Ischemic Stroke: A Bidirectional and Multivariable Mendelian Randomization Study
Heart failure (HF) is a potential cause of ischemic stroke (IS), and previous studies have reported an association between HF and IS. This study aimed to analyze the causal link between HF and IS using bidirectional and multivariable Mendelian randomization (MR) studies. Genetic variants significant...
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Published in: | Frontiers in genetics 2021-11, Vol.12, p.771044-771044 |
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creator | Zhang, Luyang Liu, Weishi Sun, Wenxian Wang, Xin Tian, Mengke Pei, Lu-Lu Liu, Kai Liang, Jing Zhou, Lue Lu, Jie Ning, Mingming Buonanno, Ferdinando S Xu, Yuming Song, Bo |
description | Heart failure (HF) is a potential cause of ischemic stroke (IS), and previous studies have reported an association between HF and IS. This study aimed to analyze the causal link between HF and IS using bidirectional and multivariable Mendelian randomization (MR) studies.
Genetic variants significantly associated with HF and IS were selected in the MR analysis from two large genome-wide association studies. Bidirectional and multivariable MR analyses were performed to evaluate the effect of HF on IS or the effect of IS on HF.
Two-sample MR analysis showed causal effects of HF on IS of all causes [odds ratio (OR) = 1.555, 95% confidence interval (CI): 1.343-1.799,
= 3.35 × 10
] and large artery atherosclerosis stroke (LAS) (OR = 1.678, 95% CI: 1.044-2.696,
= 3.03 × 10
), while there was a suggestive effect of HF on cardioembolic stroke (CES) (OR = 3.355, 95% CI: 1.031-10.919,
= 0.044). Genetically predicted HF was not associated with small artery occlusion stroke. Bidirectional MR analysis showed causal effects of IS of all causes (OR = 1.211, 95% CI: 1.040-1.410,
= 0.014) and CES (OR = 1.277, 95% CI: 1.213-1.344,
= 6.73 × 10
) on HF, while there were no causal effects of LAS on HF.
This MR analysis provided evidence of the causal links between genetically predicted HF and IS. Subgroup analysis highlighted the causal or suggestive relationship between genetically predicted HF and LAS or CES. The potential causal links need further investigation with genetic information about other ancestries or etiologies of HF. |
doi_str_mv | 10.3389/fgene.2021.771044 |
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Genetic variants significantly associated with HF and IS were selected in the MR analysis from two large genome-wide association studies. Bidirectional and multivariable MR analyses were performed to evaluate the effect of HF on IS or the effect of IS on HF.
Two-sample MR analysis showed causal effects of HF on IS of all causes [odds ratio (OR) = 1.555, 95% confidence interval (CI): 1.343-1.799,
= 3.35 × 10
] and large artery atherosclerosis stroke (LAS) (OR = 1.678, 95% CI: 1.044-2.696,
= 3.03 × 10
), while there was a suggestive effect of HF on cardioembolic stroke (CES) (OR = 3.355, 95% CI: 1.031-10.919,
= 0.044). Genetically predicted HF was not associated with small artery occlusion stroke. Bidirectional MR analysis showed causal effects of IS of all causes (OR = 1.211, 95% CI: 1.040-1.410,
= 0.014) and CES (OR = 1.277, 95% CI: 1.213-1.344,
= 6.73 × 10
) on HF, while there were no causal effects of LAS on HF.
This MR analysis provided evidence of the causal links between genetically predicted HF and IS. Subgroup analysis highlighted the causal or suggestive relationship between genetically predicted HF and LAS or CES. The potential causal links need further investigation with genetic information about other ancestries or etiologies of HF.</description><identifier>ISSN: 1664-8021</identifier><identifier>EISSN: 1664-8021</identifier><identifier>DOI: 10.3389/fgene.2021.771044</identifier><identifier>PMID: 34912375</identifier><language>eng</language><publisher>Switzerland: Frontiers Media S.A</publisher><subject>Genetics ; heart failure ; ischemic stroke ; mendelian randomization ; single nucleotide polymorphism ; stroke</subject><ispartof>Frontiers in genetics, 2021-11, Vol.12, p.771044-771044</ispartof><rights>Copyright © 2021 Zhang, Liu, Sun, Wang, Tian, Pei, Liu, Liang, Zhou, Lu, Ning, Buonanno, Xu and Song.</rights><rights>Copyright © 2021 Zhang, Liu, Sun, Wang, Tian, Pei, Liu, Liang, Zhou, Lu, Ning, Buonanno, Xu and Song. 2021 Zhang, Liu, Sun, Wang, Tian, Pei, Liu, Liang, Zhou, Lu, Ning, Buonanno, Xu and Song</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c465t-361f4125700928b5ecb4cdc1df82930fd0d9f7be3c6b16cd5efdbbe69c3c2a583</citedby><cites>FETCH-LOGICAL-c465t-361f4125700928b5ecb4cdc1df82930fd0d9f7be3c6b16cd5efdbbe69c3c2a583</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8666512/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8666512/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34912375$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhang, Luyang</creatorcontrib><creatorcontrib>Liu, Weishi</creatorcontrib><creatorcontrib>Sun, Wenxian</creatorcontrib><creatorcontrib>Wang, Xin</creatorcontrib><creatorcontrib>Tian, Mengke</creatorcontrib><creatorcontrib>Pei, Lu-Lu</creatorcontrib><creatorcontrib>Liu, Kai</creatorcontrib><creatorcontrib>Liang, Jing</creatorcontrib><creatorcontrib>Zhou, Lue</creatorcontrib><creatorcontrib>Lu, Jie</creatorcontrib><creatorcontrib>Ning, Mingming</creatorcontrib><creatorcontrib>Buonanno, Ferdinando S</creatorcontrib><creatorcontrib>Xu, Yuming</creatorcontrib><creatorcontrib>Song, Bo</creatorcontrib><title>Heart Failure and Ischemic Stroke: A Bidirectional and Multivariable Mendelian Randomization Study</title><title>Frontiers in genetics</title><addtitle>Front Genet</addtitle><description>Heart failure (HF) is a potential cause of ischemic stroke (IS), and previous studies have reported an association between HF and IS. This study aimed to analyze the causal link between HF and IS using bidirectional and multivariable Mendelian randomization (MR) studies.
Genetic variants significantly associated with HF and IS were selected in the MR analysis from two large genome-wide association studies. Bidirectional and multivariable MR analyses were performed to evaluate the effect of HF on IS or the effect of IS on HF.
Two-sample MR analysis showed causal effects of HF on IS of all causes [odds ratio (OR) = 1.555, 95% confidence interval (CI): 1.343-1.799,
= 3.35 × 10
] and large artery atherosclerosis stroke (LAS) (OR = 1.678, 95% CI: 1.044-2.696,
= 3.03 × 10
), while there was a suggestive effect of HF on cardioembolic stroke (CES) (OR = 3.355, 95% CI: 1.031-10.919,
= 0.044). Genetically predicted HF was not associated with small artery occlusion stroke. Bidirectional MR analysis showed causal effects of IS of all causes (OR = 1.211, 95% CI: 1.040-1.410,
= 0.014) and CES (OR = 1.277, 95% CI: 1.213-1.344,
= 6.73 × 10
) on HF, while there were no causal effects of LAS on HF.
This MR analysis provided evidence of the causal links between genetically predicted HF and IS. Subgroup analysis highlighted the causal or suggestive relationship between genetically predicted HF and LAS or CES. The potential causal links need further investigation with genetic information about other ancestries or etiologies of HF.</description><subject>Genetics</subject><subject>heart failure</subject><subject>ischemic stroke</subject><subject>mendelian randomization</subject><subject>single nucleotide polymorphism</subject><subject>stroke</subject><issn>1664-8021</issn><issn>1664-8021</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNpVkU1P3DAQhi3UCtCWH8ClyrGX3drxR5weKlFUykqgSm05W2N7vJg6MXUSJPrrm92lCHwYWzPvPB77JeSU0RXnuv0YNtjjqqY1WzUNo0IckGOmlFjqOfXmxfmInAzDHZ2XaDnn4pAccdGymjfymNhLhDJWFxDTVLCC3lfrwd1iF131cyz5N36qzqov0ceCboy5h7QTXU9pjA9QItiE1TX2HlOEvvoxF3MX_8JWOxMm__iOvA2QBjx52hfk5uLrr_PL5dX3b-vzs6ulE0qOS65YEKyWDaVtra1EZ4Xzjvmg65bT4KlvQ2ORO2WZcl5i8Naiah13NUjNF2S95_oMd-a-xA7Ko8kQzS6Ry8bMT40uoUEG1NJGgQsgADSAFEzrbQzY-DCzPu9Z95Pt0DvsxwLpFfR1pY-3ZpMfjFZKyflvF-TDE6DkPxMOo-ni4DAl6DFPg6kVoy2jspazlO2lruRhKBier2HUbK02O6vN1mqzt3ruef9yvueO_8byf5dXqCU</recordid><startdate>20211129</startdate><enddate>20211129</enddate><creator>Zhang, Luyang</creator><creator>Liu, Weishi</creator><creator>Sun, Wenxian</creator><creator>Wang, Xin</creator><creator>Tian, Mengke</creator><creator>Pei, Lu-Lu</creator><creator>Liu, Kai</creator><creator>Liang, Jing</creator><creator>Zhou, Lue</creator><creator>Lu, Jie</creator><creator>Ning, Mingming</creator><creator>Buonanno, Ferdinando S</creator><creator>Xu, Yuming</creator><creator>Song, Bo</creator><general>Frontiers Media S.A</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20211129</creationdate><title>Heart Failure and Ischemic Stroke: A Bidirectional and Multivariable Mendelian Randomization Study</title><author>Zhang, Luyang ; Liu, Weishi ; Sun, Wenxian ; Wang, Xin ; Tian, Mengke ; Pei, Lu-Lu ; Liu, Kai ; Liang, Jing ; Zhou, Lue ; Lu, Jie ; Ning, Mingming ; Buonanno, Ferdinando S ; Xu, Yuming ; Song, Bo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c465t-361f4125700928b5ecb4cdc1df82930fd0d9f7be3c6b16cd5efdbbe69c3c2a583</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Genetics</topic><topic>heart failure</topic><topic>ischemic stroke</topic><topic>mendelian randomization</topic><topic>single nucleotide polymorphism</topic><topic>stroke</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhang, Luyang</creatorcontrib><creatorcontrib>Liu, Weishi</creatorcontrib><creatorcontrib>Sun, Wenxian</creatorcontrib><creatorcontrib>Wang, Xin</creatorcontrib><creatorcontrib>Tian, Mengke</creatorcontrib><creatorcontrib>Pei, Lu-Lu</creatorcontrib><creatorcontrib>Liu, Kai</creatorcontrib><creatorcontrib>Liang, Jing</creatorcontrib><creatorcontrib>Zhou, Lue</creatorcontrib><creatorcontrib>Lu, Jie</creatorcontrib><creatorcontrib>Ning, Mingming</creatorcontrib><creatorcontrib>Buonanno, Ferdinando S</creatorcontrib><creatorcontrib>Xu, Yuming</creatorcontrib><creatorcontrib>Song, Bo</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Frontiers in genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhang, Luyang</au><au>Liu, Weishi</au><au>Sun, Wenxian</au><au>Wang, Xin</au><au>Tian, Mengke</au><au>Pei, Lu-Lu</au><au>Liu, Kai</au><au>Liang, Jing</au><au>Zhou, Lue</au><au>Lu, Jie</au><au>Ning, Mingming</au><au>Buonanno, Ferdinando S</au><au>Xu, Yuming</au><au>Song, Bo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Heart Failure and Ischemic Stroke: A Bidirectional and Multivariable Mendelian Randomization Study</atitle><jtitle>Frontiers in genetics</jtitle><addtitle>Front Genet</addtitle><date>2021-11-29</date><risdate>2021</risdate><volume>12</volume><spage>771044</spage><epage>771044</epage><pages>771044-771044</pages><issn>1664-8021</issn><eissn>1664-8021</eissn><abstract>Heart failure (HF) is a potential cause of ischemic stroke (IS), and previous studies have reported an association between HF and IS. This study aimed to analyze the causal link between HF and IS using bidirectional and multivariable Mendelian randomization (MR) studies.
Genetic variants significantly associated with HF and IS were selected in the MR analysis from two large genome-wide association studies. Bidirectional and multivariable MR analyses were performed to evaluate the effect of HF on IS or the effect of IS on HF.
Two-sample MR analysis showed causal effects of HF on IS of all causes [odds ratio (OR) = 1.555, 95% confidence interval (CI): 1.343-1.799,
= 3.35 × 10
] and large artery atherosclerosis stroke (LAS) (OR = 1.678, 95% CI: 1.044-2.696,
= 3.03 × 10
), while there was a suggestive effect of HF on cardioembolic stroke (CES) (OR = 3.355, 95% CI: 1.031-10.919,
= 0.044). Genetically predicted HF was not associated with small artery occlusion stroke. Bidirectional MR analysis showed causal effects of IS of all causes (OR = 1.211, 95% CI: 1.040-1.410,
= 0.014) and CES (OR = 1.277, 95% CI: 1.213-1.344,
= 6.73 × 10
) on HF, while there were no causal effects of LAS on HF.
This MR analysis provided evidence of the causal links between genetically predicted HF and IS. Subgroup analysis highlighted the causal or suggestive relationship between genetically predicted HF and LAS or CES. The potential causal links need further investigation with genetic information about other ancestries or etiologies of HF.</abstract><cop>Switzerland</cop><pub>Frontiers Media S.A</pub><pmid>34912375</pmid><doi>10.3389/fgene.2021.771044</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Genetics heart failure ischemic stroke mendelian randomization single nucleotide polymorphism stroke |
title | Heart Failure and Ischemic Stroke: A Bidirectional and Multivariable Mendelian Randomization Study |
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