QT Dispersion in HIV-Infected Patients Receiving Combined Antiretroviral Therapy

© 2014 Wiley Periodicals, Inc. Background A higher prevalence of QT prolongation has been reported among human immunodeficiency virus (HIV)-infected patients. Previous studies have demonstrated that QT dispersion is a better predictor of serious ventricular tachyarrhythmia and cardiac mortality than...

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Main Authors: Wanwarang Wongcharoen, Somkhuan Suaklin, Nualnit Tantisirivit, Arintaya Phrommintikul, Nipon Chattipakorn
Format: Journal
Published: 2018
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http://cmuir.cmu.ac.th/jspui/handle/6653943832/45494
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spelling th-cmuir.6653943832-454942018-01-24T06:11:17Z QT Dispersion in HIV-Infected Patients Receiving Combined Antiretroviral Therapy Wanwarang Wongcharoen Somkhuan Suaklin Nualnit Tantisirivit Arintaya Phrommintikul Nipon Chattipakorn © 2014 Wiley Periodicals, Inc. Background A higher prevalence of QT prolongation has been reported among human immunodeficiency virus (HIV)-infected patients. Previous studies have demonstrated that QT dispersion is a better predictor of serious ventricular tachyarrhythmia and cardiac mortality than corrected QT (QTc) interval. However, data of QT dispersion in HIV-infected patients receiving a combined antiretroviral therapy (cART) is limited. We sought to assess QTc interval and QT dispersion in HIV-infected patients receiving cART. The association between QT parameters and heart rate variability (HRV) was also examined. Methods Ninety-one HIV-infected patients receiving cART (male = 33, mean age = 44 ± 10 years) and 70 HIV-seronegative subjects (male = 25, mean age = 44 ± 8 years) were enrolled in the study. In a resting 12-lead electrocardiogram, QT interval was measured by the tangent method in all leads with well-defined T waves. The QT dispersion was defined as the difference between maximum and minimum QTc intervals in any of 12 leads. Results The baseline characteristics were not different between the two groups. We demonstrated the significantly longer mean QTc interval (420 ± 21 vs. 409 ± 21 ms, P < 0.001), and greater QT dispersion in HIV-infected group compared to the control group (85 ± 29 vs. 55 ± 23 ms, P < 0.001). Among the HIV-infected patients, those who had lower CD4 lymphocyte count ( < 350 cells/mm < sup > 3 < /sup > ) tended to have greater QT dispersion (92 ± 28 vs. 81 ± 29 ms, P = 0.098). There were no associations between QT parameters and either HRV or cART regimens. Conclusions HIV-infected patients receiving cART were associated with prolonged QTc interval and increased QT dispersion, independent of autonomic dysfunction and antiretroviral drugs, which may have led to the potentially higher risk of ventricular arrhythmia and cardiac mortality. 2018-01-24T06:11:17Z 2018-01-24T06:11:17Z 2014-01-01 Journal 1542474X 1082720X 2-s2.0-84937511083 10.1111/anec.12162 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84937511083&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/45494
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
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description © 2014 Wiley Periodicals, Inc. Background A higher prevalence of QT prolongation has been reported among human immunodeficiency virus (HIV)-infected patients. Previous studies have demonstrated that QT dispersion is a better predictor of serious ventricular tachyarrhythmia and cardiac mortality than corrected QT (QTc) interval. However, data of QT dispersion in HIV-infected patients receiving a combined antiretroviral therapy (cART) is limited. We sought to assess QTc interval and QT dispersion in HIV-infected patients receiving cART. The association between QT parameters and heart rate variability (HRV) was also examined. Methods Ninety-one HIV-infected patients receiving cART (male = 33, mean age = 44 ± 10 years) and 70 HIV-seronegative subjects (male = 25, mean age = 44 ± 8 years) were enrolled in the study. In a resting 12-lead electrocardiogram, QT interval was measured by the tangent method in all leads with well-defined T waves. The QT dispersion was defined as the difference between maximum and minimum QTc intervals in any of 12 leads. Results The baseline characteristics were not different between the two groups. We demonstrated the significantly longer mean QTc interval (420 ± 21 vs. 409 ± 21 ms, P < 0.001), and greater QT dispersion in HIV-infected group compared to the control group (85 ± 29 vs. 55 ± 23 ms, P < 0.001). Among the HIV-infected patients, those who had lower CD4 lymphocyte count ( < 350 cells/mm < sup > 3 < /sup > ) tended to have greater QT dispersion (92 ± 28 vs. 81 ± 29 ms, P = 0.098). There were no associations between QT parameters and either HRV or cART regimens. Conclusions HIV-infected patients receiving cART were associated with prolonged QTc interval and increased QT dispersion, independent of autonomic dysfunction and antiretroviral drugs, which may have led to the potentially higher risk of ventricular arrhythmia and cardiac mortality.
format Journal
author Wanwarang Wongcharoen
Somkhuan Suaklin
Nualnit Tantisirivit
Arintaya Phrommintikul
Nipon Chattipakorn
spellingShingle Wanwarang Wongcharoen
Somkhuan Suaklin
Nualnit Tantisirivit
Arintaya Phrommintikul
Nipon Chattipakorn
QT Dispersion in HIV-Infected Patients Receiving Combined Antiretroviral Therapy
author_facet Wanwarang Wongcharoen
Somkhuan Suaklin
Nualnit Tantisirivit
Arintaya Phrommintikul
Nipon Chattipakorn
author_sort Wanwarang Wongcharoen
title QT Dispersion in HIV-Infected Patients Receiving Combined Antiretroviral Therapy
title_short QT Dispersion in HIV-Infected Patients Receiving Combined Antiretroviral Therapy
title_full QT Dispersion in HIV-Infected Patients Receiving Combined Antiretroviral Therapy
title_fullStr QT Dispersion in HIV-Infected Patients Receiving Combined Antiretroviral Therapy
title_full_unstemmed QT Dispersion in HIV-Infected Patients Receiving Combined Antiretroviral Therapy
title_sort qt dispersion in hiv-infected patients receiving combined antiretroviral therapy
publishDate 2018
url https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84937511083&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/45494
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