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Gut microbial diversity in HIV infection post combined antiretroviral therapy: a key target for prevention of cardiovascular disease

PURPOSE OF REVIEW: Although the HIV-infected population is living longer and getting older under current treatment regimens, significant challenges arise for health management as the infection is associated with various premature aging phenotypes, particularly increased incidence of cardiovascular d...

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Autores principales: El-Far, Mohamed, Tremblay, Cécile L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5718258/
https://www.ncbi.nlm.nih.gov/pubmed/29045253
http://dx.doi.org/10.1097/COH.0000000000000426
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author El-Far, Mohamed
Tremblay, Cécile L.
author_facet El-Far, Mohamed
Tremblay, Cécile L.
author_sort El-Far, Mohamed
collection PubMed
description PURPOSE OF REVIEW: Although the HIV-infected population is living longer and getting older under current treatment regimens, significant challenges arise for health management as the infection is associated with various premature aging phenotypes, particularly increased incidence of cardiovascular diseases (CVDs). Here we review the current understanding of HIV-related gut dysbiosis in association with CVD and advances in clinical trials aiming to restore gut microbial diversity. RECENT FINDING: Identification of a unique signature for gut dysbiosis in HIV infection between different cohorts remains challenging. However, low diversity of microbiota combined with the outgrowth of pathogenic bacterial species together with dysregulated metabolic pathways have been linked to compromised gut immunity, bacterial translocation and systemic inflammation, hence higher CVD risk among different cohorts. Data from recent clinical trials aiming to evaluate the tolerability and efficacy of probiotics in treated HIV+ patients are promising and support a significant increase in microbiota diversity and reduction of systemic inflammation. However, the impact of these microbial and immunological corrections on the prevalence of CVD in HIV+ patients remains unclear. SUMMARY: Positive immunological outcomes following enrichment of the gut microbial diversity have been documented, and further trials are in progress to evaluate the range of patients, with different immunological backgrounds, who might benefit from these treatments.
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spelling pubmed-57182582017-12-20 Gut microbial diversity in HIV infection post combined antiretroviral therapy: a key target for prevention of cardiovascular disease El-Far, Mohamed Tremblay, Cécile L. Curr Opin HIV AIDS THE MICROBIOME IN HIV: Edited by Alan L. Landay, James G. Kublin and Seema N. Desai PURPOSE OF REVIEW: Although the HIV-infected population is living longer and getting older under current treatment regimens, significant challenges arise for health management as the infection is associated with various premature aging phenotypes, particularly increased incidence of cardiovascular diseases (CVDs). Here we review the current understanding of HIV-related gut dysbiosis in association with CVD and advances in clinical trials aiming to restore gut microbial diversity. RECENT FINDING: Identification of a unique signature for gut dysbiosis in HIV infection between different cohorts remains challenging. However, low diversity of microbiota combined with the outgrowth of pathogenic bacterial species together with dysregulated metabolic pathways have been linked to compromised gut immunity, bacterial translocation and systemic inflammation, hence higher CVD risk among different cohorts. Data from recent clinical trials aiming to evaluate the tolerability and efficacy of probiotics in treated HIV+ patients are promising and support a significant increase in microbiota diversity and reduction of systemic inflammation. However, the impact of these microbial and immunological corrections on the prevalence of CVD in HIV+ patients remains unclear. SUMMARY: Positive immunological outcomes following enrichment of the gut microbial diversity have been documented, and further trials are in progress to evaluate the range of patients, with different immunological backgrounds, who might benefit from these treatments. Lippincott Williams & Wilkins 2018-01 2017-12-06 /pmc/articles/PMC5718258/ /pubmed/29045253 http://dx.doi.org/10.1097/COH.0000000000000426 Text en Copyright © 2017 The Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0
spellingShingle THE MICROBIOME IN HIV: Edited by Alan L. Landay, James G. Kublin and Seema N. Desai
El-Far, Mohamed
Tremblay, Cécile L.
Gut microbial diversity in HIV infection post combined antiretroviral therapy: a key target for prevention of cardiovascular disease
title Gut microbial diversity in HIV infection post combined antiretroviral therapy: a key target for prevention of cardiovascular disease
title_full Gut microbial diversity in HIV infection post combined antiretroviral therapy: a key target for prevention of cardiovascular disease
title_fullStr Gut microbial diversity in HIV infection post combined antiretroviral therapy: a key target for prevention of cardiovascular disease
title_full_unstemmed Gut microbial diversity in HIV infection post combined antiretroviral therapy: a key target for prevention of cardiovascular disease
title_short Gut microbial diversity in HIV infection post combined antiretroviral therapy: a key target for prevention of cardiovascular disease
title_sort gut microbial diversity in hiv infection post combined antiretroviral therapy: a key target for prevention of cardiovascular disease
topic THE MICROBIOME IN HIV: Edited by Alan L. Landay, James G. Kublin and Seema N. Desai
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5718258/
https://www.ncbi.nlm.nih.gov/pubmed/29045253
http://dx.doi.org/10.1097/COH.0000000000000426
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