Factors Associated with the Risk of Major Adverse Cardiovascular Events in Patients with Ankylosing Spondylitis: A Nationwide, Population-Based Case-Control Study
Background: Potential risk factors for major adverse cardiovascular events (MACE) in patients with ankylosing spondylitis (AS) requiring medical therapy should be investigated. Methods: We identified newly diagnosed AS patients without previous MACE from 2004 to 2012 using the National Health Insura...
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Veröffentlicht in: | International journal of environmental research and public health 2022-03, Vol.19 (7), p.4098 |
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description | Background: Potential risk factors for major adverse cardiovascular events (MACE) in patients with ankylosing spondylitis (AS) requiring medical therapy should be investigated. Methods: We identified newly diagnosed AS patients without previous MACE from 2004 to 2012 using the National Health Insurance Research Database, matched MACE cases with non-MACE controls at a 1:4 ratio for age, gender, AS duration, and index date, and included 947 AS patients with MACE and 3896 matched controls for final analyses. By using conditional logistic regression analyses, we examined the associations of MACE with low income, urbanisation, comorbidities, common extra-articular manifestations (EAM), and medications, including nonsteroidal anti-inflammatory drugs (NSAID) of three categories (traditional NSAIDs, selective cyclooxygenase-2 inhibitors (COX-2i), and preferential COX-2is) with their annual cumulative defined daily dose (cDDD) within a year before MACE development. Results: MACE development was associated with the use of selective COX-2is (especially with annual cDDD > 132) and corticosteroids, residence in rural regions, and well-known associated comorbidities, but not with the use of traditional NSAIDs, preferential COX-2i, biologics, methotrexate, sulfasalazine, and common EAMs. Conclusions: The risk factors of MACE in newly diagnosed AS patients include residence in rural regions, well-known associated comorbidities, and the use of corticosteroids and selective COX-2is. A major limitation was the lack of information on individual lifestyle patterns and disease activity. |
doi_str_mv | 10.3390/ijerph19074098 |
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Methods: We identified newly diagnosed AS patients without previous MACE from 2004 to 2012 using the National Health Insurance Research Database, matched MACE cases with non-MACE controls at a 1:4 ratio for age, gender, AS duration, and index date, and included 947 AS patients with MACE and 3896 matched controls for final analyses. By using conditional logistic regression analyses, we examined the associations of MACE with low income, urbanisation, comorbidities, common extra-articular manifestations (EAM), and medications, including nonsteroidal anti-inflammatory drugs (NSAID) of three categories (traditional NSAIDs, selective cyclooxygenase-2 inhibitors (COX-2i), and preferential COX-2is) with their annual cumulative defined daily dose (cDDD) within a year before MACE development. Results: MACE development was associated with the use of selective COX-2is (especially with annual cDDD > 132) and corticosteroids, residence in rural regions, and well-known associated comorbidities, but not with the use of traditional NSAIDs, preferential COX-2i, biologics, methotrexate, sulfasalazine, and common EAMs. Conclusions: The risk factors of MACE in newly diagnosed AS patients include residence in rural regions, well-known associated comorbidities, and the use of corticosteroids and selective COX-2is. A major limitation was the lack of information on individual lifestyle patterns and disease activity.</description><identifier>ISSN: 1660-4601</identifier><identifier>ISSN: 1661-7827</identifier><identifier>EISSN: 1660-4601</identifier><identifier>DOI: 10.3390/ijerph19074098</identifier><identifier>PMID: 35409780</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Angioplasty ; Ankylosing spondylitis ; Anti-inflammatory agents ; Anti-Inflammatory Agents, Non-Steroidal - adverse effects ; Arthritis ; Cardiovascular diseases ; Cardiovascular Diseases - chemically induced ; Case-Control Studies ; Chronic obstructive pulmonary disease ; Codes ; Coronary vessels ; Corticoids ; Corticosteroids ; COX-2 inhibitors ; Cyclooxygenase 2 Inhibitors - adverse effects ; Cyclooxygenase-2 ; Diabetes ; Drug dosages ; Health insurance ; Health risks ; Heart attacks ; Heart failure ; Heart surgery ; Hospitalization ; Humans ; Hypertension ; Inflammation ; Inflammatory bowel disease ; Ischemia ; Methotrexate ; Nonsteroidal anti-inflammatory drugs ; Patients ; Population ; Population studies ; Population-based studies ; Psoriasis ; Regression analysis ; Risk analysis ; Risk Factors ; Risk management ; Rural areas ; Socioeconomic factors ; Spondylitis, Ankylosing - complications ; Spondylitis, Ankylosing - drug therapy ; Spondylitis, Ankylosing - epidemiology ; Sulfasalazine ; Urbanization</subject><ispartof>International journal of environmental research and public health, 2022-03, Vol.19 (7), p.4098</ispartof><rights>2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2022 by the authors. 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c418t-73b2cca3decb65c236338876dee6c0b5a5cb3fbd1a39d175116d3c8119ac8f803</citedby><cites>FETCH-LOGICAL-c418t-73b2cca3decb65c236338876dee6c0b5a5cb3fbd1a39d175116d3c8119ac8f803</cites><orcidid>0000-0002-8135-9554 ; 0000-0002-8409-3237 ; 0000-0002-7304-4587 ; 0000-0002-2863-4350 ; 0000-0002-0887-6432</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8998897/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8998897/$$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/35409780$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kao, Chung-Mao</creatorcontrib><creatorcontrib>Wang, Jun-Sing</creatorcontrib><creatorcontrib>Ho, Wei-Li</creatorcontrib><creatorcontrib>Ko, Tai-Ming</creatorcontrib><creatorcontrib>Chen, Hsian-Min</creatorcontrib><creatorcontrib>Lin, Ching-Heng</creatorcontrib><creatorcontrib>Huang, Wen-Nan</creatorcontrib><creatorcontrib>Chen, Yi-Hsing</creatorcontrib><creatorcontrib>Chen, Hsin-Hua</creatorcontrib><title>Factors Associated with the Risk of Major Adverse Cardiovascular Events in Patients with Ankylosing Spondylitis: A Nationwide, Population-Based Case-Control Study</title><title>International journal of environmental research and public health</title><addtitle>Int J Environ Res Public Health</addtitle><description>Background: Potential risk factors for major adverse cardiovascular events (MACE) in patients with ankylosing spondylitis (AS) requiring medical therapy should be investigated. Methods: We identified newly diagnosed AS patients without previous MACE from 2004 to 2012 using the National Health Insurance Research Database, matched MACE cases with non-MACE controls at a 1:4 ratio for age, gender, AS duration, and index date, and included 947 AS patients with MACE and 3896 matched controls for final analyses. By using conditional logistic regression analyses, we examined the associations of MACE with low income, urbanisation, comorbidities, common extra-articular manifestations (EAM), and medications, including nonsteroidal anti-inflammatory drugs (NSAID) of three categories (traditional NSAIDs, selective cyclooxygenase-2 inhibitors (COX-2i), and preferential COX-2is) with their annual cumulative defined daily dose (cDDD) within a year before MACE development. Results: MACE development was associated with the use of selective COX-2is (especially with annual cDDD > 132) and corticosteroids, residence in rural regions, and well-known associated comorbidities, but not with the use of traditional NSAIDs, preferential COX-2i, biologics, methotrexate, sulfasalazine, and common EAMs. Conclusions: The risk factors of MACE in newly diagnosed AS patients include residence in rural regions, well-known associated comorbidities, and the use of corticosteroids and selective COX-2is. A major limitation was the lack of information on individual lifestyle patterns and disease activity.</description><subject>Angioplasty</subject><subject>Ankylosing spondylitis</subject><subject>Anti-inflammatory agents</subject><subject>Anti-Inflammatory Agents, Non-Steroidal - adverse effects</subject><subject>Arthritis</subject><subject>Cardiovascular diseases</subject><subject>Cardiovascular Diseases - chemically induced</subject><subject>Case-Control Studies</subject><subject>Chronic obstructive pulmonary disease</subject><subject>Codes</subject><subject>Coronary vessels</subject><subject>Corticoids</subject><subject>Corticosteroids</subject><subject>COX-2 inhibitors</subject><subject>Cyclooxygenase 2 Inhibitors - adverse effects</subject><subject>Cyclooxygenase-2</subject><subject>Diabetes</subject><subject>Drug dosages</subject><subject>Health insurance</subject><subject>Health risks</subject><subject>Heart attacks</subject><subject>Heart failure</subject><subject>Heart surgery</subject><subject>Hospitalization</subject><subject>Humans</subject><subject>Hypertension</subject><subject>Inflammation</subject><subject>Inflammatory bowel disease</subject><subject>Ischemia</subject><subject>Methotrexate</subject><subject>Nonsteroidal anti-inflammatory drugs</subject><subject>Patients</subject><subject>Population</subject><subject>Population studies</subject><subject>Population-based studies</subject><subject>Psoriasis</subject><subject>Regression analysis</subject><subject>Risk analysis</subject><subject>Risk Factors</subject><subject>Risk management</subject><subject>Rural areas</subject><subject>Socioeconomic factors</subject><subject>Spondylitis, Ankylosing - complications</subject><subject>Spondylitis, Ankylosing - drug therapy</subject><subject>Spondylitis, Ankylosing - epidemiology</subject><subject>Sulfasalazine</subject><subject>Urbanization</subject><issn>1660-4601</issn><issn>1661-7827</issn><issn>1660-4601</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNpVkU1PHSEUholpUz_abZcNSbeOwmWGARcm04lfiVpT65owwHi5jjAF5pr7d_ylctUa3cAhPDznkBeA7xjtEcLRvl2YMM4xR3WJONsAW5hSVJQU4U_v6k2wHeMCIcJKyr-ATVJlumZoCzweS5V8iLCJ0Ssrk9HwwaY5THMD_9h4B30PL-TCB9jopQnRwFYGbf1SRjUNMsCjpXEpQuvglUz2uX4WNO5uNfho3S28Hr3Tq8EmGw9gAy8z592D1WYXXvkxW9bn4peMuXmb16L1LgU_wOs06dVX8LmXQzTfXvcdcHN89Lc9Lc5_n5y1zXmhSsxSUZNuppQk2qiOVmpGKCGM1VQbQxXqKlmpjvSdxpJwjesKY6qJYhhzqVjPENkBhy_ecerujVb5K0EOYgz2XoaV8NKKjzfOzsWtXwrGOWO8zoKfr4Lg_00mJrHwU3B5ZjGj5ZoiGGdq74VSwccYTP_WASOxzlR8zDQ_-PF-rjf8f4jkCTofosQ</recordid><startdate>20220330</startdate><enddate>20220330</enddate><creator>Kao, Chung-Mao</creator><creator>Wang, Jun-Sing</creator><creator>Ho, Wei-Li</creator><creator>Ko, Tai-Ming</creator><creator>Chen, Hsian-Min</creator><creator>Lin, Ching-Heng</creator><creator>Huang, Wen-Nan</creator><creator>Chen, Yi-Hsing</creator><creator>Chen, Hsin-Hua</creator><general>MDPI AG</general><general>MDPI</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-8135-9554</orcidid><orcidid>https://orcid.org/0000-0002-8409-3237</orcidid><orcidid>https://orcid.org/0000-0002-7304-4587</orcidid><orcidid>https://orcid.org/0000-0002-2863-4350</orcidid><orcidid>https://orcid.org/0000-0002-0887-6432</orcidid></search><sort><creationdate>20220330</creationdate><title>Factors Associated with the Risk of Major Adverse Cardiovascular Events in Patients with Ankylosing Spondylitis: A Nationwide, Population-Based Case-Control Study</title><author>Kao, Chung-Mao ; Wang, Jun-Sing ; Ho, Wei-Li ; Ko, Tai-Ming ; Chen, Hsian-Min ; Lin, Ching-Heng ; Huang, Wen-Nan ; Chen, Yi-Hsing ; Chen, Hsin-Hua</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c418t-73b2cca3decb65c236338876dee6c0b5a5cb3fbd1a39d175116d3c8119ac8f803</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Angioplasty</topic><topic>Ankylosing spondylitis</topic><topic>Anti-inflammatory agents</topic><topic>Anti-Inflammatory Agents, Non-Steroidal - adverse effects</topic><topic>Arthritis</topic><topic>Cardiovascular diseases</topic><topic>Cardiovascular Diseases - chemically induced</topic><topic>Case-Control Studies</topic><topic>Chronic obstructive pulmonary disease</topic><topic>Codes</topic><topic>Coronary vessels</topic><topic>Corticoids</topic><topic>Corticosteroids</topic><topic>COX-2 inhibitors</topic><topic>Cyclooxygenase 2 Inhibitors - adverse effects</topic><topic>Cyclooxygenase-2</topic><topic>Diabetes</topic><topic>Drug dosages</topic><topic>Health insurance</topic><topic>Health risks</topic><topic>Heart attacks</topic><topic>Heart failure</topic><topic>Heart surgery</topic><topic>Hospitalization</topic><topic>Humans</topic><topic>Hypertension</topic><topic>Inflammation</topic><topic>Inflammatory bowel disease</topic><topic>Ischemia</topic><topic>Methotrexate</topic><topic>Nonsteroidal anti-inflammatory drugs</topic><topic>Patients</topic><topic>Population</topic><topic>Population studies</topic><topic>Population-based studies</topic><topic>Psoriasis</topic><topic>Regression analysis</topic><topic>Risk analysis</topic><topic>Risk Factors</topic><topic>Risk management</topic><topic>Rural areas</topic><topic>Socioeconomic factors</topic><topic>Spondylitis, Ankylosing - 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Methods: We identified newly diagnosed AS patients without previous MACE from 2004 to 2012 using the National Health Insurance Research Database, matched MACE cases with non-MACE controls at a 1:4 ratio for age, gender, AS duration, and index date, and included 947 AS patients with MACE and 3896 matched controls for final analyses. By using conditional logistic regression analyses, we examined the associations of MACE with low income, urbanisation, comorbidities, common extra-articular manifestations (EAM), and medications, including nonsteroidal anti-inflammatory drugs (NSAID) of three categories (traditional NSAIDs, selective cyclooxygenase-2 inhibitors (COX-2i), and preferential COX-2is) with their annual cumulative defined daily dose (cDDD) within a year before MACE development. Results: MACE development was associated with the use of selective COX-2is (especially with annual cDDD > 132) and corticosteroids, residence in rural regions, and well-known associated comorbidities, but not with the use of traditional NSAIDs, preferential COX-2i, biologics, methotrexate, sulfasalazine, and common EAMs. Conclusions: The risk factors of MACE in newly diagnosed AS patients include residence in rural regions, well-known associated comorbidities, and the use of corticosteroids and selective COX-2is. A major limitation was the lack of information on individual lifestyle patterns and disease activity.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>35409780</pmid><doi>10.3390/ijerph19074098</doi><orcidid>https://orcid.org/0000-0002-8135-9554</orcidid><orcidid>https://orcid.org/0000-0002-8409-3237</orcidid><orcidid>https://orcid.org/0000-0002-7304-4587</orcidid><orcidid>https://orcid.org/0000-0002-2863-4350</orcidid><orcidid>https://orcid.org/0000-0002-0887-6432</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Angioplasty Ankylosing spondylitis Anti-inflammatory agents Anti-Inflammatory Agents, Non-Steroidal - adverse effects Arthritis Cardiovascular diseases Cardiovascular Diseases - chemically induced Case-Control Studies Chronic obstructive pulmonary disease Codes Coronary vessels Corticoids Corticosteroids COX-2 inhibitors Cyclooxygenase 2 Inhibitors - adverse effects Cyclooxygenase-2 Diabetes Drug dosages Health insurance Health risks Heart attacks Heart failure Heart surgery Hospitalization Humans Hypertension Inflammation Inflammatory bowel disease Ischemia Methotrexate Nonsteroidal anti-inflammatory drugs Patients Population Population studies Population-based studies Psoriasis Regression analysis Risk analysis Risk Factors Risk management Rural areas Socioeconomic factors Spondylitis, Ankylosing - complications Spondylitis, Ankylosing - drug therapy Spondylitis, Ankylosing - epidemiology Sulfasalazine Urbanization |
title | Factors Associated with the Risk of Major Adverse Cardiovascular Events in Patients with Ankylosing Spondylitis: A Nationwide, Population-Based Case-Control Study |
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