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Is HIV Infection a Risk Factor for Multi-Drug Resistant Tuberculosis? A Systematic Review

BACKGROUND: Tuberculosis (TB) is an important cause of human suffering and death. Human immunodeficiency virus (HIV), multi-drug resistant TB (MDR-TB), and extensive drug resistant tuberculosis (XDR-TB) have emerged as threats to TB control. The association between MDR-TB and HIV infection has not y...

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Autores principales: Suchindran, Sujit, Brouwer, Emily S., Van Rie, Annelies
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2680616/
https://www.ncbi.nlm.nih.gov/pubmed/19440304
http://dx.doi.org/10.1371/journal.pone.0005561
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author Suchindran, Sujit
Brouwer, Emily S.
Van Rie, Annelies
author_facet Suchindran, Sujit
Brouwer, Emily S.
Van Rie, Annelies
author_sort Suchindran, Sujit
collection PubMed
description BACKGROUND: Tuberculosis (TB) is an important cause of human suffering and death. Human immunodeficiency virus (HIV), multi-drug resistant TB (MDR-TB), and extensive drug resistant tuberculosis (XDR-TB) have emerged as threats to TB control. The association between MDR-TB and HIV infection has not yet been fully investigated. We conducted a systematic review and meta-analysis to summarize the evidence on the association between HIV infection and MDR-TB. METHODS AND RESULTS: Original studies providing Mycobacterium tuberculosis resistance data stratified by HIV status were identified using MEDLINE and ISI Web of Science. Crude MDR-TB prevalence ratios were calculated and analyzed by type of TB (primary or acquired), region and study period. Heterogeneity across studies was assessed, and pooled prevalence ratios were generated if appropriate. No clear association was found between MDR-TB and HIV infection across time and geographic locations. MDR-TB prevalence ratios in the 32 eligible studies, comparing MDR-TB prevalence by HIV status, ranged from 0.21 to 41.45. Assessment by geographical region or study period did not reveal noticeable patterns. The summary prevalence ratios for acquired and primary MDR-TB were 1.17 (95% CI 0.86, 1.6) and 2.72 (95% CI 2.03, 3.66), respectively. Studies eligible for review were few considering the size of the epidemics. Most studies were not adjusted for confounders and the heterogeneity across studies precluded the calculation of a meaningful overall summary measure. CONCLUSIONS: We could not demonstrate an overall association between MDR-TB and HIV or acquired MDR-TB and HIV, but our results suggest that HIV infection is associated with primary MDR-TB. Future well-designed studies and surveillance in all regions of the world are needed to better clarify the relationship between HIV infection and MDR-TB.
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spelling pubmed-26806162009-05-15 Is HIV Infection a Risk Factor for Multi-Drug Resistant Tuberculosis? A Systematic Review Suchindran, Sujit Brouwer, Emily S. Van Rie, Annelies PLoS One Research Article BACKGROUND: Tuberculosis (TB) is an important cause of human suffering and death. Human immunodeficiency virus (HIV), multi-drug resistant TB (MDR-TB), and extensive drug resistant tuberculosis (XDR-TB) have emerged as threats to TB control. The association between MDR-TB and HIV infection has not yet been fully investigated. We conducted a systematic review and meta-analysis to summarize the evidence on the association between HIV infection and MDR-TB. METHODS AND RESULTS: Original studies providing Mycobacterium tuberculosis resistance data stratified by HIV status were identified using MEDLINE and ISI Web of Science. Crude MDR-TB prevalence ratios were calculated and analyzed by type of TB (primary or acquired), region and study period. Heterogeneity across studies was assessed, and pooled prevalence ratios were generated if appropriate. No clear association was found between MDR-TB and HIV infection across time and geographic locations. MDR-TB prevalence ratios in the 32 eligible studies, comparing MDR-TB prevalence by HIV status, ranged from 0.21 to 41.45. Assessment by geographical region or study period did not reveal noticeable patterns. The summary prevalence ratios for acquired and primary MDR-TB were 1.17 (95% CI 0.86, 1.6) and 2.72 (95% CI 2.03, 3.66), respectively. Studies eligible for review were few considering the size of the epidemics. Most studies were not adjusted for confounders and the heterogeneity across studies precluded the calculation of a meaningful overall summary measure. CONCLUSIONS: We could not demonstrate an overall association between MDR-TB and HIV or acquired MDR-TB and HIV, but our results suggest that HIV infection is associated with primary MDR-TB. Future well-designed studies and surveillance in all regions of the world are needed to better clarify the relationship between HIV infection and MDR-TB. Public Library of Science 2009-05-15 /pmc/articles/PMC2680616/ /pubmed/19440304 http://dx.doi.org/10.1371/journal.pone.0005561 Text en Suchindran 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Suchindran, Sujit
Brouwer, Emily S.
Van Rie, Annelies
Is HIV Infection a Risk Factor for Multi-Drug Resistant Tuberculosis? A Systematic Review
title Is HIV Infection a Risk Factor for Multi-Drug Resistant Tuberculosis? A Systematic Review
title_full Is HIV Infection a Risk Factor for Multi-Drug Resistant Tuberculosis? A Systematic Review
title_fullStr Is HIV Infection a Risk Factor for Multi-Drug Resistant Tuberculosis? A Systematic Review
title_full_unstemmed Is HIV Infection a Risk Factor for Multi-Drug Resistant Tuberculosis? A Systematic Review
title_short Is HIV Infection a Risk Factor for Multi-Drug Resistant Tuberculosis? A Systematic Review
title_sort is hiv infection a risk factor for multi-drug resistant tuberculosis? a systematic review
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2680616/
https://www.ncbi.nlm.nih.gov/pubmed/19440304
http://dx.doi.org/10.1371/journal.pone.0005561
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