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
Hauptverfasser: 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
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container_issue 7
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container_title International journal of environmental research and public health
container_volume 19
creator 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
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 &gt; 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. 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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/). 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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 &gt; 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 ; 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Results: MACE development was associated with the use of selective COX-2is (especially with annual cDDD &gt; 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. 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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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