Cited 7 times in
Proton Pump Inhibitors and Risk of Cardiovascular Disease: A Self-Controlled Case Series Study
DC Field | Value | Language |
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dc.contributor.author | 김진권 | - |
dc.contributor.author | 유준상 | - |
dc.date.accessioned | 2022-08-23T00:20:24Z | - |
dc.date.available | 2022-08-23T00:20:24Z | - |
dc.date.issued | 2022-07 | - |
dc.identifier.issn | 0002-9270 | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/189381 | - |
dc.description.abstract | Introduction: We investigated cardiovascular risk due to proton pump inhibitor (PPI) treatment using a self-controlled case series (SCCS) study design, a type of case-only design and an approach to overcome between-person confounding in which individuals act as their own control. Methods: We conducted an SCCS study using the National Health Insurance Service-Health Screening cohort in Korea (2002-2015). The cohort included 303,404 adult participants without prior cardiovascular events, who were followed up until December 2015. The primary outcome was a composite of stroke or myocardial infarction. The SCCS method estimated the age-adjusted incidence rate ratio between periods with and without exposure to PPI among patients with primary outcomes. As sensitivity analysis, conventional multivariable Cox proportional regression analyses were performed, which treated the exposure to PPI and H2 blocker during follow-up as time-dependent variables. Results: In the SCCS design, 10,952 (3.6%) patients with primary outcomes were included. There was no association between PPI exposure and primary outcome (incidence rate ratio 0.98, 95% confidence interval [CI] 0.89-1.09). In the time-dependent Cox regression analyses, both PPI (adjusted hazard ratio 1.36, 95% CI 1.24-1.49) and H2 blocker (adjusted hazard ratio 1.46, 95% CI 1.38-1.55) were associated with an increased risk of the primary outcome. Discussion: Negative findings in the SCCS design suggest that association between increased cardiovascular risk and PPI, frequently reported in prior observational studies, is likely due to residual confounding related to conditions with PPI treatment, rather than a true relationship. | - |
dc.description.statementOfResponsibility | restriction | - |
dc.language | English | - |
dc.publisher | Nature Pub. Group | - |
dc.relation.isPartOf | AMERICAN JOURNAL OF GASTROENTEROLOGY | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.subject.MESH | Adult | - |
dc.subject.MESH | Cardiovascular Diseases* / epidemiology | - |
dc.subject.MESH | Cohort Studies | - |
dc.subject.MESH | Histamine H2 Antagonists / adverse effects | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Proton Pump Inhibitors / adverse effects | - |
dc.subject.MESH | Risk Factors | - |
dc.subject.MESH | Stroke* / epidemiology | - |
dc.title | Proton Pump Inhibitors and Risk of Cardiovascular Disease: A Self-Controlled Case Series Study | - |
dc.type | Article | - |
dc.contributor.college | College of Medicine (의과대학) | - |
dc.contributor.department | Dept. of Neurology (신경과학교실) | - |
dc.contributor.googleauthor | Ju-Young Park | - |
dc.contributor.googleauthor | Joonsang Yoo | - |
dc.contributor.googleauthor | Jimin Jeon | - |
dc.contributor.googleauthor | Jinkwon Kim | - |
dc.contributor.googleauthor | Sangwook Kang | - |
dc.identifier.doi | 10.14309/ajg.0000000000001809 | - |
dc.contributor.localId | A01012 | - |
dc.contributor.localId | A02513 | - |
dc.relation.journalcode | J00081 | - |
dc.identifier.eissn | 1572-0241 | - |
dc.identifier.pmid | 35505518 | - |
dc.identifier.url | https://journals.lww.com/ajg/Fulltext/2022/07000/Proton_Pump_Inhibitors_and_Risk_of_Cardiovascular.18.aspx | - |
dc.contributor.alternativeName | Kim, Jin Kwon | - |
dc.contributor.affiliatedAuthor | 김진권 | - |
dc.contributor.affiliatedAuthor | 유준상 | - |
dc.citation.volume | 117 | - |
dc.citation.number | 7 | - |
dc.citation.startPage | 1063 | - |
dc.citation.endPage | 1071 | - |
dc.identifier.bibliographicCitation | AMERICAN JOURNAL OF GASTROENTEROLOGY, Vol.117(7) : 1063-1071, 2022-07 | - |
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