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Article: Investigating pleiotropic effects of statins on ischemic heart disease in the UK Biobank using Mendelian randomisation

TitleInvestigating pleiotropic effects of statins on ischemic heart disease in the UK Biobank using Mendelian randomisation
Authors
KeywordsMendelian Randomization Analysis
Instrumental Variable Estimate
Causal Effect
Issue Date2020
PublishereLife Sciences Publications Ltd. The Journal's web site is located at http://elifesciences.org/
Citation
eLife, 2020, v. 9, p. article no. e58567 How to Cite?
AbstractWe examined whether specifically statins, of the major lipid modifiers (statins, proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors and ezetimibe) have pleiotropic effects on ischemic heart disease (IHD) via testosterone in men or women. As a validation, we similarly assessed whether a drug that unexpectedly likely increases IHD also operates via testosterone. Using previously published genetic instruments we conducted a sex-specific univariable and multivariable Mendelian randomization study in the UK Biobank, including 179918 men with 25410 IHD cases and 212080 women with 12511 IHD cases. Of these three lipid modifiers, only genetically mimicking the effects of statins in men affected testosterone, which partly mediated effects on IHD. Correspondingly, genetically mimicking effects of anakinra on testosterone and IHD presented a reverse pattern to that for statins. These insights may facilitate the development of new interventions for cardiovascular diseases as well as highlighting the importance of sex-specific explanations, investigations, prevention and treatment.
Persistent Identifierhttp://hdl.handle.net/10722/287940
ISSN
2023 Impact Factor: 6.4
2023 SCImago Journal Rankings: 3.932
PubMed Central ID
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorSchooling, CM-
dc.contributor.authorZhao, JV-
dc.contributor.authorAu Yeung, SL-
dc.contributor.authorLeung, GM-
dc.date.accessioned2020-10-05T12:05:28Z-
dc.date.available2020-10-05T12:05:28Z-
dc.date.issued2020-
dc.identifier.citationeLife, 2020, v. 9, p. article no. e58567-
dc.identifier.issn2050-084X-
dc.identifier.urihttp://hdl.handle.net/10722/287940-
dc.description.abstractWe examined whether specifically statins, of the major lipid modifiers (statins, proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors and ezetimibe) have pleiotropic effects on ischemic heart disease (IHD) via testosterone in men or women. As a validation, we similarly assessed whether a drug that unexpectedly likely increases IHD also operates via testosterone. Using previously published genetic instruments we conducted a sex-specific univariable and multivariable Mendelian randomization study in the UK Biobank, including 179918 men with 25410 IHD cases and 212080 women with 12511 IHD cases. Of these three lipid modifiers, only genetically mimicking the effects of statins in men affected testosterone, which partly mediated effects on IHD. Correspondingly, genetically mimicking effects of anakinra on testosterone and IHD presented a reverse pattern to that for statins. These insights may facilitate the development of new interventions for cardiovascular diseases as well as highlighting the importance of sex-specific explanations, investigations, prevention and treatment.-
dc.languageeng-
dc.publishereLife Sciences Publications Ltd. The Journal's web site is located at http://elifesciences.org/-
dc.relation.ispartofeLife-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectMendelian Randomization Analysis-
dc.subjectInstrumental Variable Estimate-
dc.subjectCausal Effect-
dc.titleInvestigating pleiotropic effects of statins on ischemic heart disease in the UK Biobank using Mendelian randomisation-
dc.typeArticle-
dc.identifier.emailSchooling, CM: cms1@hkucc.hku.hk-
dc.identifier.emailZhao, JV: janezhao@hku.hk-
dc.identifier.emailAu Yeung, SL: ayslryan@hku.hk-
dc.identifier.emailLeung, GM: gmleung@hku.hk-
dc.identifier.authoritySchooling, CM=rp00504-
dc.identifier.authorityZhao, JV=rp02336-
dc.identifier.authorityAu Yeung, SL=rp02224-
dc.identifier.authorityLeung, GM=rp00460-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.7554/eLife.58567-
dc.identifier.pmid32838838-
dc.identifier.pmcidPMC7449694-
dc.identifier.scopuseid_2-s2.0-85090077149-
dc.identifier.hkuros315524-
dc.identifier.volume9-
dc.identifier.spagearticle no. e58567-
dc.identifier.epagearticle no. e58567-
dc.identifier.isiWOS:000563793400001-
dc.publisher.placeCambridge, UK-
dc.identifier.issnl2050-084X-

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