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Effects of statins in patients with coronary artery spasm: A nationwide population‐based study
Controversies regarding the benefits of statin treatment on clinical outcomes in coronary artery spasm (CAS) without obstructive coronary artery disease (CAD) persist due to limited data. In this retrospective nationwide population‐based cohort study from the Taiwan National Health Insurance Researc...
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Published in: | Clinical and translational science 2024-11, Vol.17 (11), p.e70087-n/a |
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description | Controversies regarding the benefits of statin treatment on clinical outcomes in coronary artery spasm (CAS) without obstructive coronary artery disease (CAD) persist due to limited data. In this retrospective nationwide population‐based cohort study from the Taiwan National Health Insurance Research Database during the period 2000–2012, the matched cohorts consisted of 12,000 patients with CAS. After propensity score matching with 1:1 ratio, 2216 patients were eligible for outcome analysis in either statin or nonstatin group, with the mean follow‐up duration of 4.8 and 4.6 years, respectively. Statin users versus nonusers had a significantly reduced risk of major adverse cardiovascular events (MACEs) (6.7% vs. 9.5%, hazard ratio [HR] 0.68; 95% confidence interval [CI] 0.55–0.84) and all‐cause mortality (6.0% vs. 7.6%; HR 0.77; 95% CI 0.61–0.96). While the results of MACEs were mainly contributed by cardiovascular death (1.9% vs. 3.2%; HR 0.56; 95% CI 0.38–0.83) and ischemic stroke (3.8% vs. 5.4%; subdistribution HR 0.69; 95% CI 0.52–0.91), they were primarily driven by reductions in ischemic but not hemorrhagic stroke. The benefit of statins was significantly pronounced in patients with hypertension and diabetes. Nevertheless, the effect on MACEs was consistent irrespective of age, sex, dyslipidemia, and mental disorder. Statins significantly reduced the risk of MACEs and all‐cause mortality in CAS patients. The benefit of statin therapy in reducing MACEs appeared to be linear, with greater risk reduction with higher doses and longer duration without upper threshold, reflecting the dose‐dependent relationship of statins with MACEs in CAS patients.
In this retrospective nationwide population‐based cohort study from the Taiwan National Health Insurance Research Database during the period 2000–2012, the matched cohorts consisted of 12,000 patients with CAS. After propensity score matching with 1:1 ratio, 2216 patients were eligible for outcome analysis in either statin or nonstatin group, with the mean follow‐up duration of 4.8 and 4.6 years, respectively. Statin users versus nonusers had a significantly reduced risk of MACEs (6.7% vs. 9.5%), which were mainly contributed by reduced cardiovascular death and ischemic stroke but not hemorrhagic stroke. The benefit of statin therapy appeared to be linear, with greater risk reduction with higher doses and longer duration without upper threshold, reflecting the dose‐dependent relationship of statins with MACEs in |
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In this retrospective nationwide population‐based cohort study from the Taiwan National Health Insurance Research Database during the period 2000–2012, the matched cohorts consisted of 12,000 patients with CAS. After propensity score matching with 1:1 ratio, 2216 patients were eligible for outcome analysis in either statin or nonstatin group, with the mean follow‐up duration of 4.8 and 4.6 years, respectively. Statin users versus nonusers had a significantly reduced risk of MACEs (6.7% vs. 9.5%), which were mainly contributed by reduced cardiovascular death and ischemic stroke but not hemorrhagic stroke. The benefit of statin therapy appeared to be linear, with greater risk reduction with higher doses and longer duration without upper threshold, reflecting the dose‐dependent relationship of statins with MACEs in CAS patients. CAD, coronary artery disease; CAS, coronary artery spasm; MACE, major adverse cardiovascular event.</description><identifier>ISSN: 1752-8054</identifier><identifier>ISSN: 1752-8062</identifier><identifier>EISSN: 1752-8062</identifier><identifier>DOI: 10.1111/cts.70087</identifier><identifier>PMID: 39568301</identifier><language>eng</language><publisher>United States: John Wiley & Sons, Inc</publisher><subject>Adult ; Aged ; Cardiovascular disease ; Cardiovascular diseases ; Chronic obstructive pulmonary disease ; Coronary artery disease ; Coronary Vasospasm - drug therapy ; Coronary Vasospasm - epidemiology ; Databases, Factual ; Diabetes mellitus ; Drug dosages ; Dyslipidemia ; Female ; Heart diseases ; Hemorrhage ; Humans ; Hydroxymethylglutaryl-CoA Reductase Inhibitors - therapeutic use ; Ischemia ; Male ; Middle Aged ; Mortality ; Patients ; Population studies ; Propensity Score ; Retrospective Studies ; Risk Factors ; Statins ; Stroke ; Taiwan - epidemiology ; Treatment Outcome</subject><ispartof>Clinical and translational science, 2024-11, Vol.17 (11), p.e70087-n/a</ispartof><rights>2024 The Author(s). published by Wiley Periodicals LLC on behalf of American Society for Clinical Pharmacology and Therapeutics.</rights><rights>2024 The Author(s). Clinical and Translational Science published by Wiley Periodicals LLC on behalf of American Society for Clinical Pharmacology and Therapeutics.</rights><rights>2024. This work is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the "License"). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c3657-5746d43bee3d2e7b9bb6cc15363851a5d47547862253271879179153e90054303</cites><orcidid>0000-0001-5189-9755 ; 0000-0002-9751-6710 ; 0000-0002-6912-7523 ; 0000-0002-2667-9029 ; 0000-0003-3675-7753 ; 0000-0001-6986-9765 ; 0000-0003-4732-0450 ; 0000-0002-9694-5468 ; 0000-0003-1138-5471</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/3132707403/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/3132707403?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,11562,25753,27924,27925,37012,37013,44590,46052,46476,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39568301$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lee, Yu‐Ching</creatorcontrib><creatorcontrib>Hung, Ming‐Jui</creatorcontrib><creatorcontrib>Chen, Tien‐Hsing</creatorcontrib><creatorcontrib>Mao, Chun‐Tai</creatorcontrib><creatorcontrib>Yeh, Chi‐Tai</creatorcontrib><creatorcontrib>Kounis, Nicholas G.</creatorcontrib><creatorcontrib>Chen, Ian Y.</creatorcontrib><creatorcontrib>Hu, Patrick</creatorcontrib><creatorcontrib>Hung, Ming‐Yow</creatorcontrib><title>Effects of statins in patients with coronary artery spasm: A nationwide population‐based study</title><title>Clinical and translational science</title><addtitle>Clin Transl Sci</addtitle><description>Controversies regarding the benefits of statin treatment on clinical outcomes in coronary artery spasm (CAS) without obstructive coronary artery disease (CAD) persist due to limited data. In this retrospective nationwide population‐based cohort study from the Taiwan National Health Insurance Research Database during the period 2000–2012, the matched cohorts consisted of 12,000 patients with CAS. After propensity score matching with 1:1 ratio, 2216 patients were eligible for outcome analysis in either statin or nonstatin group, with the mean follow‐up duration of 4.8 and 4.6 years, respectively. Statin users versus nonusers had a significantly reduced risk of major adverse cardiovascular events (MACEs) (6.7% vs. 9.5%, hazard ratio [HR] 0.68; 95% confidence interval [CI] 0.55–0.84) and all‐cause mortality (6.0% vs. 7.6%; HR 0.77; 95% CI 0.61–0.96). While the results of MACEs were mainly contributed by cardiovascular death (1.9% vs. 3.2%; HR 0.56; 95% CI 0.38–0.83) and ischemic stroke (3.8% vs. 5.4%; subdistribution HR 0.69; 95% CI 0.52–0.91), they were primarily driven by reductions in ischemic but not hemorrhagic stroke. The benefit of statins was significantly pronounced in patients with hypertension and diabetes. Nevertheless, the effect on MACEs was consistent irrespective of age, sex, dyslipidemia, and mental disorder. Statins significantly reduced the risk of MACEs and all‐cause mortality in CAS patients. The benefit of statin therapy in reducing MACEs appeared to be linear, with greater risk reduction with higher doses and longer duration without upper threshold, reflecting the dose‐dependent relationship of statins with MACEs in CAS patients.
In this retrospective nationwide population‐based cohort study from the Taiwan National Health Insurance Research Database during the period 2000–2012, the matched cohorts consisted of 12,000 patients with CAS. After propensity score matching with 1:1 ratio, 2216 patients were eligible for outcome analysis in either statin or nonstatin group, with the mean follow‐up duration of 4.8 and 4.6 years, respectively. Statin users versus nonusers had a significantly reduced risk of MACEs (6.7% vs. 9.5%), which were mainly contributed by reduced cardiovascular death and ischemic stroke but not hemorrhagic stroke. The benefit of statin therapy appeared to be linear, with greater risk reduction with higher doses and longer duration without upper threshold, reflecting the dose‐dependent relationship of statins with MACEs in CAS patients. CAD, coronary artery disease; CAS, coronary artery spasm; MACE, major adverse cardiovascular event.</description><subject>Adult</subject><subject>Aged</subject><subject>Cardiovascular disease</subject><subject>Cardiovascular diseases</subject><subject>Chronic obstructive pulmonary disease</subject><subject>Coronary artery disease</subject><subject>Coronary Vasospasm - drug therapy</subject><subject>Coronary Vasospasm - epidemiology</subject><subject>Databases, Factual</subject><subject>Diabetes mellitus</subject><subject>Drug dosages</subject><subject>Dyslipidemia</subject><subject>Female</subject><subject>Heart diseases</subject><subject>Hemorrhage</subject><subject>Humans</subject><subject>Hydroxymethylglutaryl-CoA Reductase Inhibitors - therapeutic use</subject><subject>Ischemia</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Mortality</subject><subject>Patients</subject><subject>Population studies</subject><subject>Propensity Score</subject><subject>Retrospective Studies</subject><subject>Risk Factors</subject><subject>Statins</subject><subject>Stroke</subject><subject>Taiwan - 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drug therapy</topic><topic>Coronary Vasospasm - epidemiology</topic><topic>Databases, Factual</topic><topic>Diabetes mellitus</topic><topic>Drug dosages</topic><topic>Dyslipidemia</topic><topic>Female</topic><topic>Heart diseases</topic><topic>Hemorrhage</topic><topic>Humans</topic><topic>Hydroxymethylglutaryl-CoA Reductase Inhibitors - therapeutic use</topic><topic>Ischemia</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Mortality</topic><topic>Patients</topic><topic>Population studies</topic><topic>Propensity Score</topic><topic>Retrospective Studies</topic><topic>Risk Factors</topic><topic>Statins</topic><topic>Stroke</topic><topic>Taiwan - epidemiology</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lee, Yu‐Ching</creatorcontrib><creatorcontrib>Hung, Ming‐Jui</creatorcontrib><creatorcontrib>Chen, Tien‐Hsing</creatorcontrib><creatorcontrib>Mao, Chun‐Tai</creatorcontrib><creatorcontrib>Yeh, Chi‐Tai</creatorcontrib><creatorcontrib>Kounis, Nicholas G.</creatorcontrib><creatorcontrib>Chen, Ian Y.</creatorcontrib><creatorcontrib>Hu, Patrick</creatorcontrib><creatorcontrib>Hung, Ming‐Yow</creatorcontrib><collection>Wiley Open Access</collection><collection>Wiley Free Archive</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>ProQuest_Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biological Sciences</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest Publicly Available Content database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals at publisher websites</collection><jtitle>Clinical and translational science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lee, Yu‐Ching</au><au>Hung, Ming‐Jui</au><au>Chen, Tien‐Hsing</au><au>Mao, Chun‐Tai</au><au>Yeh, Chi‐Tai</au><au>Kounis, Nicholas G.</au><au>Chen, Ian Y.</au><au>Hu, Patrick</au><au>Hung, Ming‐Yow</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of statins in patients with coronary artery spasm: A nationwide population‐based study</atitle><jtitle>Clinical and translational science</jtitle><addtitle>Clin Transl Sci</addtitle><date>2024-11</date><risdate>2024</risdate><volume>17</volume><issue>11</issue><spage>e70087</spage><epage>n/a</epage><pages>e70087-n/a</pages><issn>1752-8054</issn><issn>1752-8062</issn><eissn>1752-8062</eissn><abstract>Controversies regarding the benefits of statin treatment on clinical outcomes in coronary artery spasm (CAS) without obstructive coronary artery disease (CAD) persist due to limited data. In this retrospective nationwide population‐based cohort study from the Taiwan National Health Insurance Research Database during the period 2000–2012, the matched cohorts consisted of 12,000 patients with CAS. After propensity score matching with 1:1 ratio, 2216 patients were eligible for outcome analysis in either statin or nonstatin group, with the mean follow‐up duration of 4.8 and 4.6 years, respectively. Statin users versus nonusers had a significantly reduced risk of major adverse cardiovascular events (MACEs) (6.7% vs. 9.5%, hazard ratio [HR] 0.68; 95% confidence interval [CI] 0.55–0.84) and all‐cause mortality (6.0% vs. 7.6%; HR 0.77; 95% CI 0.61–0.96). While the results of MACEs were mainly contributed by cardiovascular death (1.9% vs. 3.2%; HR 0.56; 95% CI 0.38–0.83) and ischemic stroke (3.8% vs. 5.4%; subdistribution HR 0.69; 95% CI 0.52–0.91), they were primarily driven by reductions in ischemic but not hemorrhagic stroke. The benefit of statins was significantly pronounced in patients with hypertension and diabetes. Nevertheless, the effect on MACEs was consistent irrespective of age, sex, dyslipidemia, and mental disorder. Statins significantly reduced the risk of MACEs and all‐cause mortality in CAS patients. The benefit of statin therapy in reducing MACEs appeared to be linear, with greater risk reduction with higher doses and longer duration without upper threshold, reflecting the dose‐dependent relationship of statins with MACEs in CAS patients.
In this retrospective nationwide population‐based cohort study from the Taiwan National Health Insurance Research Database during the period 2000–2012, the matched cohorts consisted of 12,000 patients with CAS. After propensity score matching with 1:1 ratio, 2216 patients were eligible for outcome analysis in either statin or nonstatin group, with the mean follow‐up duration of 4.8 and 4.6 years, respectively. Statin users versus nonusers had a significantly reduced risk of MACEs (6.7% vs. 9.5%), which were mainly contributed by reduced cardiovascular death and ischemic stroke but not hemorrhagic stroke. The benefit of statin therapy appeared to be linear, with greater risk reduction with higher doses and longer duration without upper threshold, reflecting the dose‐dependent relationship of statins with MACEs in CAS patients. CAD, coronary artery disease; CAS, coronary artery spasm; MACE, major adverse cardiovascular event.</abstract><cop>United States</cop><pub>John Wiley & Sons, Inc</pub><pmid>39568301</pmid><doi>10.1111/cts.70087</doi><tpages>16</tpages><orcidid>https://orcid.org/0000-0001-5189-9755</orcidid><orcidid>https://orcid.org/0000-0002-9751-6710</orcidid><orcidid>https://orcid.org/0000-0002-6912-7523</orcidid><orcidid>https://orcid.org/0000-0002-2667-9029</orcidid><orcidid>https://orcid.org/0000-0003-3675-7753</orcidid><orcidid>https://orcid.org/0000-0001-6986-9765</orcidid><orcidid>https://orcid.org/0000-0003-4732-0450</orcidid><orcidid>https://orcid.org/0000-0002-9694-5468</orcidid><orcidid>https://orcid.org/0000-0003-1138-5471</orcidid><oa>free_for_read</oa></addata></record> |
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recordid | cdi_doaj_primary_oai_doaj_org_article_7e8cca68fb7143ffb7995d9251eb5815 |
source | PubMed Central database; Wiley Open Access; ProQuest Publicly Available Content database |
subjects | Adult Aged Cardiovascular disease Cardiovascular diseases Chronic obstructive pulmonary disease Coronary artery disease Coronary Vasospasm - drug therapy Coronary Vasospasm - epidemiology Databases, Factual Diabetes mellitus Drug dosages Dyslipidemia Female Heart diseases Hemorrhage Humans Hydroxymethylglutaryl-CoA Reductase Inhibitors - therapeutic use Ischemia Male Middle Aged Mortality Patients Population studies Propensity Score Retrospective Studies Risk Factors Statins Stroke Taiwan - epidemiology Treatment Outcome |
title | Effects of statins in patients with coronary artery spasm: A nationwide population‐based study |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-05T11%3A00%3A58IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Effects%20of%20statins%20in%20patients%20with%20coronary%20artery%20spasm:%20A%20nationwide%20population%E2%80%90based%20study&rft.jtitle=Clinical%20and%20translational%20science&rft.au=Lee,%20Yu%E2%80%90Ching&rft.date=2024-11&rft.volume=17&rft.issue=11&rft.spage=e70087&rft.epage=n/a&rft.pages=e70087-n/a&rft.issn=1752-8054&rft.eissn=1752-8062&rft_id=info:doi/10.1111/cts.70087&rft_dat=%3Cproquest_doaj_%3E3131498827%3C/proquest_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c3657-5746d43bee3d2e7b9bb6cc15363851a5d47547862253271879179153e90054303%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=3132707403&rft_id=info:pmid/39568301&rfr_iscdi=true |