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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
Main Authors: Lee, Yu‐Ching, Hung, Ming‐Jui, Chen, Tien‐Hsing, Mao, Chun‐Tai, Yeh, Chi‐Tai, Kounis, Nicholas G., Chen, Ian Y., Hu, Patrick, Hung, Ming‐Yow
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creator Lee, Yu‐Ching
Hung, Ming‐Jui
Chen, Tien‐Hsing
Mao, Chun‐Tai
Yeh, Chi‐Tai
Kounis, Nicholas G.
Chen, Ian Y.
Hu, Patrick
Hung, Ming‐Yow
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 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. 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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 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. 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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 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. 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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