Impact of comorbidities on atrial fibrillation and sudden cardiac death in hypertrophic cardiomyopathy
Background The impact of comorbid disease states on the development of atrial and ventricular arrhythmias in patients with hypertrophic cardiomyopathy (HCM) remains unresolved. Objective Evaluate the association of comorbidities linked to arrhythmias in other cardiovascular diseases (e.g., obesity,...
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Veröffentlicht in: | Journal of cardiovascular electrophysiology 2022-01, Vol.33 (1), p.20-29 |
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description | Background
The impact of comorbid disease states on the development of atrial and ventricular arrhythmias in patients with hypertrophic cardiomyopathy (HCM) remains unresolved.
Objective
Evaluate the association of comorbidities linked to arrhythmias in other cardiovascular diseases (e.g., obesity, systemic hypertension, diabetes, obstructive sleep apnea, renal disorders, tobacco, and alcohol use) to atrial fibrillation (AF) and sudden cardiac death (SCD) events in a large cohort of HCM patients.
Methods
A total of 2269 patients, 54 ± 15 years of age, 1392 males, were evaluated at the Tufts HCM Institute between 2004 and 2018 and followed for an average of 4 ± 3 years for new‐onset clinical AF and SCD events (appropriate defibrillation for ventricular tachyarrhythmias, resuscitated cardiac arrest, or SCD).
Results
One or more comorbidity was present in 75% of HCM patients, including 50% with ≥2 comorbidities, most commonly obesity (body mass index [BMI] ≥ 30 kg/m2) in 43%. New‐onset atrial fibrillation developed in 11% of our cohort (2.6%/year). On univariate analysis, obesity was associated with a 1.7‐fold increased risk for AF (p = .03) with 12% of obese patients developing AF (3.3%/year) as compared to 7% of patients with BMI .10 for each).
SCD events occurred in 3.3% of patients (0.8%/year) and neither obesity nor other comorbidities were associated with increased risk for SCD (p > .10 for each).
Conclusions
In adult HCM patients comorbidities do not appear to impact AF or SCD risk. Therefore, for most patients with HCM, adverse disease related events of AF and SCD appear to be primarily driven by underlying left ventricular and atrial myopathy as opposed to comorbidities. |
doi_str_mv | 10.1111/jce.15304 |
format | Article |
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The impact of comorbid disease states on the development of atrial and ventricular arrhythmias in patients with hypertrophic cardiomyopathy (HCM) remains unresolved.
Objective
Evaluate the association of comorbidities linked to arrhythmias in other cardiovascular diseases (e.g., obesity, systemic hypertension, diabetes, obstructive sleep apnea, renal disorders, tobacco, and alcohol use) to atrial fibrillation (AF) and sudden cardiac death (SCD) events in a large cohort of HCM patients.
Methods
A total of 2269 patients, 54 ± 15 years of age, 1392 males, were evaluated at the Tufts HCM Institute between 2004 and 2018 and followed for an average of 4 ± 3 years for new‐onset clinical AF and SCD events (appropriate defibrillation for ventricular tachyarrhythmias, resuscitated cardiac arrest, or SCD).
Results
One or more comorbidity was present in 75% of HCM patients, including 50% with ≥2 comorbidities, most commonly obesity (body mass index [BMI] ≥ 30 kg/m2) in 43%. New‐onset atrial fibrillation developed in 11% of our cohort (2.6%/year). On univariate analysis, obesity was associated with a 1.7‐fold increased risk for AF (p = .03) with 12% of obese patients developing AF (3.3%/year) as compared to 7% of patients with BMI < 25 kg/m2 (1.6%/year; p = .006). On multivariate analysis, age and LA transverse dimension emerged as the only variables predictive of AF. Comorbidities, including obesity, were not independently associated with AF development (p > .10 for each).
SCD events occurred in 3.3% of patients (0.8%/year) and neither obesity nor other comorbidities were associated with increased risk for SCD (p > .10 for each).
Conclusions
In adult HCM patients comorbidities do not appear to impact AF or SCD risk. Therefore, for most patients with HCM, adverse disease related events of AF and SCD appear to be primarily driven by underlying left ventricular and atrial myopathy as opposed to comorbidities.</description><identifier>ISSN: 1045-3873</identifier><identifier>EISSN: 1540-8167</identifier><identifier>DOI: 10.1111/jce.15304</identifier><identifier>PMID: 34845799</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>Adult ; Apnea ; atrial fibrillation ; Atrial Fibrillation - complications ; Atrial Fibrillation - diagnosis ; Atrial Fibrillation - epidemiology ; Body mass index ; Cardiac arrhythmia ; Cardiomyopathy ; Cardiomyopathy, Hypertrophic - complications ; Cardiomyopathy, Hypertrophic - diagnosis ; Cardiomyopathy, Hypertrophic - epidemiology ; Cardiovascular diseases ; comorbidities ; Comorbidity ; Death, Sudden, Cardiac - epidemiology ; Death, Sudden, Cardiac - etiology ; Diabetes mellitus ; Fibrillation ; Humans ; hypertrophic cardiomyopathy ; Male ; Multivariate analysis ; Myopathy ; Obesity ; Patients ; Risk Factors ; Sleep disorders ; sudden death ; Tachycardia, Ventricular - complications ; Ventricle</subject><ispartof>Journal of cardiovascular electrophysiology, 2022-01, Vol.33 (1), p.20-29</ispartof><rights>2021 Wiley Periodicals LLC</rights><rights>2021 Wiley Periodicals LLC.</rights><rights>2022 Wiley Periodicals LLC</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4444-b6cdbc079690bc22efb0ad698be0b43e4838ae6fd53ae7e8a36234a12e4161a83</citedby><cites>FETCH-LOGICAL-c4444-b6cdbc079690bc22efb0ad698be0b43e4838ae6fd53ae7e8a36234a12e4161a83</cites><orcidid>0000-0002-3953-0143</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fjce.15304$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fjce.15304$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,776,780,881,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34845799$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sridharan, Aadhavi</creatorcontrib><creatorcontrib>Maron, Martin S.</creatorcontrib><creatorcontrib>Carrick, Richard T.</creatorcontrib><creatorcontrib>Madias, Christopher A.</creatorcontrib><creatorcontrib>Huang, Dou</creatorcontrib><creatorcontrib>Cooper, Craig</creatorcontrib><creatorcontrib>Drummond, Jennifer</creatorcontrib><creatorcontrib>Maron, Barry J.</creatorcontrib><creatorcontrib>Rowin, Ethan J.</creatorcontrib><title>Impact of comorbidities on atrial fibrillation and sudden cardiac death in hypertrophic cardiomyopathy</title><title>Journal of cardiovascular electrophysiology</title><addtitle>J Cardiovasc Electrophysiol</addtitle><description>Background
The impact of comorbid disease states on the development of atrial and ventricular arrhythmias in patients with hypertrophic cardiomyopathy (HCM) remains unresolved.
Objective
Evaluate the association of comorbidities linked to arrhythmias in other cardiovascular diseases (e.g., obesity, systemic hypertension, diabetes, obstructive sleep apnea, renal disorders, tobacco, and alcohol use) to atrial fibrillation (AF) and sudden cardiac death (SCD) events in a large cohort of HCM patients.
Methods
A total of 2269 patients, 54 ± 15 years of age, 1392 males, were evaluated at the Tufts HCM Institute between 2004 and 2018 and followed for an average of 4 ± 3 years for new‐onset clinical AF and SCD events (appropriate defibrillation for ventricular tachyarrhythmias, resuscitated cardiac arrest, or SCD).
Results
One or more comorbidity was present in 75% of HCM patients, including 50% with ≥2 comorbidities, most commonly obesity (body mass index [BMI] ≥ 30 kg/m2) in 43%. New‐onset atrial fibrillation developed in 11% of our cohort (2.6%/year). On univariate analysis, obesity was associated with a 1.7‐fold increased risk for AF (p = .03) with 12% of obese patients developing AF (3.3%/year) as compared to 7% of patients with BMI < 25 kg/m2 (1.6%/year; p = .006). On multivariate analysis, age and LA transverse dimension emerged as the only variables predictive of AF. Comorbidities, including obesity, were not independently associated with AF development (p > .10 for each).
SCD events occurred in 3.3% of patients (0.8%/year) and neither obesity nor other comorbidities were associated with increased risk for SCD (p > .10 for each).
Conclusions
In adult HCM patients comorbidities do not appear to impact AF or SCD risk. Therefore, for most patients with HCM, adverse disease related events of AF and SCD appear to be primarily driven by underlying left ventricular and atrial myopathy as opposed to comorbidities.</description><subject>Adult</subject><subject>Apnea</subject><subject>atrial fibrillation</subject><subject>Atrial Fibrillation - complications</subject><subject>Atrial Fibrillation - diagnosis</subject><subject>Atrial Fibrillation - epidemiology</subject><subject>Body mass index</subject><subject>Cardiac arrhythmia</subject><subject>Cardiomyopathy</subject><subject>Cardiomyopathy, Hypertrophic - complications</subject><subject>Cardiomyopathy, Hypertrophic - diagnosis</subject><subject>Cardiomyopathy, Hypertrophic - epidemiology</subject><subject>Cardiovascular diseases</subject><subject>comorbidities</subject><subject>Comorbidity</subject><subject>Death, Sudden, Cardiac - epidemiology</subject><subject>Death, Sudden, Cardiac - etiology</subject><subject>Diabetes mellitus</subject><subject>Fibrillation</subject><subject>Humans</subject><subject>hypertrophic cardiomyopathy</subject><subject>Male</subject><subject>Multivariate analysis</subject><subject>Myopathy</subject><subject>Obesity</subject><subject>Patients</subject><subject>Risk Factors</subject><subject>Sleep disorders</subject><subject>sudden death</subject><subject>Tachycardia, Ventricular - complications</subject><subject>Ventricle</subject><issn>1045-3873</issn><issn>1540-8167</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kUtP3TAQha2KqjzaBX8AWWJTFgE7dpx4haor2oKQuoG15ceE66skDnbSKv--hlBEK3U2tuZ8Ojqjg9AxJec0z8XOwjmtGOHv0AGtOCkaKuq9_Ce8KlhTs310mNKOEMoEqT6gfcYbXtVSHqD2uh-1nXBosQ19iMY7P3lIOAxYT9HrDrfeRN91evJPu8HhNDsHA7Y6Oq8tdqCnLfYD3i4jxCmGcevtqoZ-CWNWl4_ofau7BJ9e3iN0__XqbvO9uP3x7Xrz5bawPE9hhHXGkloKSYwtS2gN0U7IxgAxnAFvWKNBtK5iGmpoNBMl45qWwKmgumFH6HL1HWfTg7MwTFF3aoy-13FRQXv1tzL4rXoIPxUlRJaSiOzw-cUhhscZ0qR6nyzk-wcIc1KlIDkFkZxn9PQfdBfmOOT7MkVrXgspaabOVsrGkFKE9jUNJeqpPpXrU8_1ZfbkbfxX8k9fGbhYgV--g-X_Tupmc7Va_gaqfaZk</recordid><startdate>202201</startdate><enddate>202201</enddate><creator>Sridharan, Aadhavi</creator><creator>Maron, Martin S.</creator><creator>Carrick, Richard T.</creator><creator>Madias, Christopher A.</creator><creator>Huang, Dou</creator><creator>Cooper, Craig</creator><creator>Drummond, Jennifer</creator><creator>Maron, Barry J.</creator><creator>Rowin, Ethan J.</creator><general>Wiley Subscription Services, Inc</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>7QP</scope><scope>K9.</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-3953-0143</orcidid></search><sort><creationdate>202201</creationdate><title>Impact of comorbidities on atrial fibrillation and sudden cardiac death in hypertrophic cardiomyopathy</title><author>Sridharan, Aadhavi ; Maron, Martin S. ; Carrick, Richard T. ; Madias, Christopher A. ; Huang, Dou ; Cooper, Craig ; Drummond, Jennifer ; Maron, Barry J. ; Rowin, Ethan J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4444-b6cdbc079690bc22efb0ad698be0b43e4838ae6fd53ae7e8a36234a12e4161a83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Adult</topic><topic>Apnea</topic><topic>atrial fibrillation</topic><topic>Atrial Fibrillation - complications</topic><topic>Atrial Fibrillation - diagnosis</topic><topic>Atrial Fibrillation - epidemiology</topic><topic>Body mass index</topic><topic>Cardiac arrhythmia</topic><topic>Cardiomyopathy</topic><topic>Cardiomyopathy, Hypertrophic - complications</topic><topic>Cardiomyopathy, Hypertrophic - diagnosis</topic><topic>Cardiomyopathy, Hypertrophic - epidemiology</topic><topic>Cardiovascular diseases</topic><topic>comorbidities</topic><topic>Comorbidity</topic><topic>Death, Sudden, Cardiac - epidemiology</topic><topic>Death, Sudden, Cardiac - etiology</topic><topic>Diabetes mellitus</topic><topic>Fibrillation</topic><topic>Humans</topic><topic>hypertrophic cardiomyopathy</topic><topic>Male</topic><topic>Multivariate analysis</topic><topic>Myopathy</topic><topic>Obesity</topic><topic>Patients</topic><topic>Risk Factors</topic><topic>Sleep disorders</topic><topic>sudden death</topic><topic>Tachycardia, Ventricular - complications</topic><topic>Ventricle</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sridharan, Aadhavi</creatorcontrib><creatorcontrib>Maron, Martin S.</creatorcontrib><creatorcontrib>Carrick, Richard T.</creatorcontrib><creatorcontrib>Madias, Christopher A.</creatorcontrib><creatorcontrib>Huang, Dou</creatorcontrib><creatorcontrib>Cooper, Craig</creatorcontrib><creatorcontrib>Drummond, Jennifer</creatorcontrib><creatorcontrib>Maron, Barry J.</creatorcontrib><creatorcontrib>Rowin, Ethan J.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of cardiovascular electrophysiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sridharan, Aadhavi</au><au>Maron, Martin S.</au><au>Carrick, Richard T.</au><au>Madias, Christopher A.</au><au>Huang, Dou</au><au>Cooper, Craig</au><au>Drummond, Jennifer</au><au>Maron, Barry J.</au><au>Rowin, Ethan J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Impact of comorbidities on atrial fibrillation and sudden cardiac death in hypertrophic cardiomyopathy</atitle><jtitle>Journal of cardiovascular electrophysiology</jtitle><addtitle>J Cardiovasc Electrophysiol</addtitle><date>2022-01</date><risdate>2022</risdate><volume>33</volume><issue>1</issue><spage>20</spage><epage>29</epage><pages>20-29</pages><issn>1045-3873</issn><eissn>1540-8167</eissn><abstract>Background
The impact of comorbid disease states on the development of atrial and ventricular arrhythmias in patients with hypertrophic cardiomyopathy (HCM) remains unresolved.
Objective
Evaluate the association of comorbidities linked to arrhythmias in other cardiovascular diseases (e.g., obesity, systemic hypertension, diabetes, obstructive sleep apnea, renal disorders, tobacco, and alcohol use) to atrial fibrillation (AF) and sudden cardiac death (SCD) events in a large cohort of HCM patients.
Methods
A total of 2269 patients, 54 ± 15 years of age, 1392 males, were evaluated at the Tufts HCM Institute between 2004 and 2018 and followed for an average of 4 ± 3 years for new‐onset clinical AF and SCD events (appropriate defibrillation for ventricular tachyarrhythmias, resuscitated cardiac arrest, or SCD).
Results
One or more comorbidity was present in 75% of HCM patients, including 50% with ≥2 comorbidities, most commonly obesity (body mass index [BMI] ≥ 30 kg/m2) in 43%. New‐onset atrial fibrillation developed in 11% of our cohort (2.6%/year). On univariate analysis, obesity was associated with a 1.7‐fold increased risk for AF (p = .03) with 12% of obese patients developing AF (3.3%/year) as compared to 7% of patients with BMI < 25 kg/m2 (1.6%/year; p = .006). On multivariate analysis, age and LA transverse dimension emerged as the only variables predictive of AF. Comorbidities, including obesity, were not independently associated with AF development (p > .10 for each).
SCD events occurred in 3.3% of patients (0.8%/year) and neither obesity nor other comorbidities were associated with increased risk for SCD (p > .10 for each).
Conclusions
In adult HCM patients comorbidities do not appear to impact AF or SCD risk. Therefore, for most patients with HCM, adverse disease related events of AF and SCD appear to be primarily driven by underlying left ventricular and atrial myopathy as opposed to comorbidities.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>34845799</pmid><doi>10.1111/jce.15304</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-3953-0143</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adult Apnea atrial fibrillation Atrial Fibrillation - complications Atrial Fibrillation - diagnosis Atrial Fibrillation - epidemiology Body mass index Cardiac arrhythmia Cardiomyopathy Cardiomyopathy, Hypertrophic - complications Cardiomyopathy, Hypertrophic - diagnosis Cardiomyopathy, Hypertrophic - epidemiology Cardiovascular diseases comorbidities Comorbidity Death, Sudden, Cardiac - epidemiology Death, Sudden, Cardiac - etiology Diabetes mellitus Fibrillation Humans hypertrophic cardiomyopathy Male Multivariate analysis Myopathy Obesity Patients Risk Factors Sleep disorders sudden death Tachycardia, Ventricular - complications Ventricle |
title | Impact of comorbidities on atrial fibrillation and sudden cardiac death in hypertrophic cardiomyopathy |
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