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Effect of antiretroviral therapy on cardiac risk markers in people living with HIV/AIDS

INTRODUCTION: Chronic HIV infection and antiretroviral therapy (ART) are the major causes of cardiovascular diseases (CVDs) and mortality in HIV patients. This study was conducted to look upon the effect of ART on CVD risk markers in patients on different ART regimens and ART-naïve patients. METHODS...

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Autores principales: Gupta, Pulin Kumar, Tyagi, Saurabh, Sheoran, Ankita, Jain, Princi, Koner, Sai Kiran, Sharma, Lokesh Kumar, Singh, Saurabh Kumar, Khura, Jayanti
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9282697/
https://www.ncbi.nlm.nih.gov/pubmed/35846544
http://dx.doi.org/10.4103/ijstd.ijstd_72_21
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author Gupta, Pulin Kumar
Tyagi, Saurabh
Sheoran, Ankita
Jain, Princi
Koner, Sai Kiran
Sharma, Lokesh Kumar
Singh, Saurabh Kumar
Khura, Jayanti
author_facet Gupta, Pulin Kumar
Tyagi, Saurabh
Sheoran, Ankita
Jain, Princi
Koner, Sai Kiran
Sharma, Lokesh Kumar
Singh, Saurabh Kumar
Khura, Jayanti
author_sort Gupta, Pulin Kumar
collection PubMed
description INTRODUCTION: Chronic HIV infection and antiretroviral therapy (ART) are the major causes of cardiovascular diseases (CVDs) and mortality in HIV patients. This study was conducted to look upon the effect of ART on CVD risk markers in patients on different ART regimens and ART-naïve patients. METHODS: It was a cross-sectional, observational study done on 120 HIV-infected patients. CV risk markers were assessed and correlated with disease-specific factors within individual subgroups differentiated as Group A (ART naïve), Group B (first-line ART), and Group C (second-line ART). Carotid intimal medial thickness (CIMT) and high-sensitivity C reactive protein (hsCRP) were done to classify cases as having CVD. RESULTS: CVD risk parameters were found to be significantly higher in cases on ART, as compared to ART-naïve cases. The mean CIMT among cases in Group C, Group B, and Group A was 0.072 ± 0.01 cm, 0.063 ± 0.01 cm, and 0.055 ± 0.01 cm, respectively (P < 0.01). 95%, 65% and 25% cases in Group C, Group B, and Group A, respectively, had high CIMT (>0.06 cm) and were seen to be directly correlated with disease-related factors, i.e., duration of disease and ART, type of ART, and low CD4 cell counts. hsCRP was significantly increased in 65 out of total 120 cases. The mean hsCRP in Group A, Group B, and Group C was 3.69 ± 3.37, 4.21 ± 3.4, and 5.72 ± 3.54 mg/L, respectively (P < 0.01), which corresponds to the high risk of CVD. CONCLUSION: CVD risk parameters of CIMT and hsCRP are seen to be higher in patients on ART than ART-naive subjects.
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spelling pubmed-92826972022-07-15 Effect of antiretroviral therapy on cardiac risk markers in people living with HIV/AIDS Gupta, Pulin Kumar Tyagi, Saurabh Sheoran, Ankita Jain, Princi Koner, Sai Kiran Sharma, Lokesh Kumar Singh, Saurabh Kumar Khura, Jayanti Indian J Sex Transm Dis AIDS Original Article INTRODUCTION: Chronic HIV infection and antiretroviral therapy (ART) are the major causes of cardiovascular diseases (CVDs) and mortality in HIV patients. This study was conducted to look upon the effect of ART on CVD risk markers in patients on different ART regimens and ART-naïve patients. METHODS: It was a cross-sectional, observational study done on 120 HIV-infected patients. CV risk markers were assessed and correlated with disease-specific factors within individual subgroups differentiated as Group A (ART naïve), Group B (first-line ART), and Group C (second-line ART). Carotid intimal medial thickness (CIMT) and high-sensitivity C reactive protein (hsCRP) were done to classify cases as having CVD. RESULTS: CVD risk parameters were found to be significantly higher in cases on ART, as compared to ART-naïve cases. The mean CIMT among cases in Group C, Group B, and Group A was 0.072 ± 0.01 cm, 0.063 ± 0.01 cm, and 0.055 ± 0.01 cm, respectively (P < 0.01). 95%, 65% and 25% cases in Group C, Group B, and Group A, respectively, had high CIMT (>0.06 cm) and were seen to be directly correlated with disease-related factors, i.e., duration of disease and ART, type of ART, and low CD4 cell counts. hsCRP was significantly increased in 65 out of total 120 cases. The mean hsCRP in Group A, Group B, and Group C was 3.69 ± 3.37, 4.21 ± 3.4, and 5.72 ± 3.54 mg/L, respectively (P < 0.01), which corresponds to the high risk of CVD. CONCLUSION: CVD risk parameters of CIMT and hsCRP are seen to be higher in patients on ART than ART-naive subjects. Wolters Kluwer - Medknow 2022 2022-06-07 /pmc/articles/PMC9282697/ /pubmed/35846544 http://dx.doi.org/10.4103/ijstd.ijstd_72_21 Text en Copyright: © 2022 Indian Journal of Sexually Transmitted Diseases and AIDS https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Original Article
Gupta, Pulin Kumar
Tyagi, Saurabh
Sheoran, Ankita
Jain, Princi
Koner, Sai Kiran
Sharma, Lokesh Kumar
Singh, Saurabh Kumar
Khura, Jayanti
Effect of antiretroviral therapy on cardiac risk markers in people living with HIV/AIDS
title Effect of antiretroviral therapy on cardiac risk markers in people living with HIV/AIDS
title_full Effect of antiretroviral therapy on cardiac risk markers in people living with HIV/AIDS
title_fullStr Effect of antiretroviral therapy on cardiac risk markers in people living with HIV/AIDS
title_full_unstemmed Effect of antiretroviral therapy on cardiac risk markers in people living with HIV/AIDS
title_short Effect of antiretroviral therapy on cardiac risk markers in people living with HIV/AIDS
title_sort effect of antiretroviral therapy on cardiac risk markers in people living with hiv/aids
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9282697/
https://www.ncbi.nlm.nih.gov/pubmed/35846544
http://dx.doi.org/10.4103/ijstd.ijstd_72_21
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