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Association between statin use, atherosclerosis, and mortality in HIV-infected adults
BACKGROUND: While HIV infection is associated with increased cardiovascular risk, benefit from statin is not well established in HIV-infected adults. We assessed whether statins are associated with a decrease in carotid artery intima-media thickness (cIMT) progression and all-cause mortality in HIV-...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7192415/ https://www.ncbi.nlm.nih.gov/pubmed/32353062 http://dx.doi.org/10.1371/journal.pone.0232636 |
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author | Phan, Binh An P. Ma, Yifei Scherzer, Rebecca Deeks, Steven G. Hsue, Priscilla Y. |
author_facet | Phan, Binh An P. Ma, Yifei Scherzer, Rebecca Deeks, Steven G. Hsue, Priscilla Y. |
author_sort | Phan, Binh An P. |
collection | PubMed |
description | BACKGROUND: While HIV infection is associated with increased cardiovascular risk, benefit from statin is not well established in HIV-infected adults. We assessed whether statins are associated with a decrease in carotid artery intima-media thickness (cIMT) progression and all-cause mortality in HIV-infected adults who are at elevated ASCVD risk and recommended for statins. METHODS: Carotid IMT was measured at baseline and follow-up in 127 HIV-infected adults who meet ACC/AHA criteria to be on statins. Inverse probability of treatment weighting (IPTW) was used to address selection bias. Multivariable models were used to control for baseline characteristics. RESULTS: 28 subjects (22%) were on statins and 99 subjects (78%) were not. Mean cIMT at baseline was 1.2 mm (SD = 0.34) in statin users and 1.1 mm (SD = 0.34) in non-users, and the multivariable adjusted difference was 0.05mm (95%CI -0.11, 0.21 p = 0.53). After 3.2 years of follow-up, average cIMT progression was similar in statin users and non-users (0.062mm/yr vs. 0.058 mm/yr) and the multivariable adjusted difference over the study period was 0.004 mm/yr (95% CI -0.018, 0.025, p = 0.74). All-cause mortality appeared higher in non-statin users compared with statin users, but the difference was not significant (adjusted HR = 0.74, 95%CI 0.17–3.29, p = 0.70). CONCLUSION: In a HIV cohort who had elevated ASCVD risk and meet ACC/AHA criteria for statins, treatment with statins was not associated with a reduction in carotid atherosclerosis progression or total mortality. Future studies are needed to further explore the impact of statins on cardiovascular risk in the HIV-infected population. |
format | Online Article Text |
id | pubmed-7192415 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-71924152020-05-11 Association between statin use, atherosclerosis, and mortality in HIV-infected adults Phan, Binh An P. Ma, Yifei Scherzer, Rebecca Deeks, Steven G. Hsue, Priscilla Y. PLoS One Research Article BACKGROUND: While HIV infection is associated with increased cardiovascular risk, benefit from statin is not well established in HIV-infected adults. We assessed whether statins are associated with a decrease in carotid artery intima-media thickness (cIMT) progression and all-cause mortality in HIV-infected adults who are at elevated ASCVD risk and recommended for statins. METHODS: Carotid IMT was measured at baseline and follow-up in 127 HIV-infected adults who meet ACC/AHA criteria to be on statins. Inverse probability of treatment weighting (IPTW) was used to address selection bias. Multivariable models were used to control for baseline characteristics. RESULTS: 28 subjects (22%) were on statins and 99 subjects (78%) were not. Mean cIMT at baseline was 1.2 mm (SD = 0.34) in statin users and 1.1 mm (SD = 0.34) in non-users, and the multivariable adjusted difference was 0.05mm (95%CI -0.11, 0.21 p = 0.53). After 3.2 years of follow-up, average cIMT progression was similar in statin users and non-users (0.062mm/yr vs. 0.058 mm/yr) and the multivariable adjusted difference over the study period was 0.004 mm/yr (95% CI -0.018, 0.025, p = 0.74). All-cause mortality appeared higher in non-statin users compared with statin users, but the difference was not significant (adjusted HR = 0.74, 95%CI 0.17–3.29, p = 0.70). CONCLUSION: In a HIV cohort who had elevated ASCVD risk and meet ACC/AHA criteria for statins, treatment with statins was not associated with a reduction in carotid atherosclerosis progression or total mortality. Future studies are needed to further explore the impact of statins on cardiovascular risk in the HIV-infected population. Public Library of Science 2020-04-30 /pmc/articles/PMC7192415/ /pubmed/32353062 http://dx.doi.org/10.1371/journal.pone.0232636 Text en © 2020 Phan et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Phan, Binh An P. Ma, Yifei Scherzer, Rebecca Deeks, Steven G. Hsue, Priscilla Y. Association between statin use, atherosclerosis, and mortality in HIV-infected adults |
title | Association between statin use, atherosclerosis, and mortality in HIV-infected adults |
title_full | Association between statin use, atherosclerosis, and mortality in HIV-infected adults |
title_fullStr | Association between statin use, atherosclerosis, and mortality in HIV-infected adults |
title_full_unstemmed | Association between statin use, atherosclerosis, and mortality in HIV-infected adults |
title_short | Association between statin use, atherosclerosis, and mortality in HIV-infected adults |
title_sort | association between statin use, atherosclerosis, and mortality in hiv-infected adults |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7192415/ https://www.ncbi.nlm.nih.gov/pubmed/32353062 http://dx.doi.org/10.1371/journal.pone.0232636 |
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