C-Reactive Protein (CRP), interferon gamma-inducible protein 10 (IP-10), and lipopolysaccharide (LPS) are associated with risk of tuberculosis after initiation of antiretroviral therapy in resource-limited settings

© 2015 Tenforde et al. Objective The association between pre-antiretroviral (ART) inflammation and immune activation and risk for incident tuberculosis (TB) after ART initiation among adults is uncertain. Design Nested case-control study (n = 332) within ACTG PEARLS trial of three ART regimens among...

Full description

Saved in:
Bibliographic Details
Main Authors: Mark W. Tenforde, Nikhil Gupte, David W. Dowdy, David M. Asmuth, Ashwin Balagopal, Richard B. Pollard, Patcharaphan Sugandhavesa, Javier R. Lama, Sandy Pillay, Sandra W. Cardoso, Jyoti Pawar, Breno Santos, Cynthia Riviere, Noluthando Mwelase, Cecilia Kanyama, Johnstone Kumwenda, James G. Hakim, Nagalingeswaran Kumarasamy, Robert Bollinger, Richard D. Semba, Thomas B. Campbell, Amita Gupta
Format: Journal
Published: 2018
Subjects:
Online Access:https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84923869697&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/54016
Tags: Add Tag
No Tags, Be the first to tag this record!
Institution: Chiang Mai University
id th-cmuir.6653943832-54016
record_format dspace
spelling th-cmuir.6653943832-540162018-09-04T10:08:29Z C-Reactive Protein (CRP), interferon gamma-inducible protein 10 (IP-10), and lipopolysaccharide (LPS) are associated with risk of tuberculosis after initiation of antiretroviral therapy in resource-limited settings Mark W. Tenforde Nikhil Gupte David W. Dowdy David M. Asmuth Ashwin Balagopal Richard B. Pollard Patcharaphan Sugandhavesa Javier R. Lama Sandy Pillay Sandra W. Cardoso Jyoti Pawar Breno Santos Cynthia Riviere Noluthando Mwelase Cecilia Kanyama Johnstone Kumwenda James G. Hakim Nagalingeswaran Kumarasamy Robert Bollinger Richard D. Semba Thomas B. Campbell Amita Gupta Agricultural and Biological Sciences Biochemistry, Genetics and Molecular Biology © 2015 Tenforde et al. Objective The association between pre-antiretroviral (ART) inflammation and immune activation and risk for incident tuberculosis (TB) after ART initiation among adults is uncertain. Design Nested case-control study (n = 332) within ACTG PEARLS trial of three ART regimens among 1571 HIV-infected, treatment-naïve adults in 9 countries. We compared cases (participants with incident TB diagnosed by 96 weeks) to a random sample of controls (participants who did not develop TB, stratified by country and treatment arm). Methods We measured pre-ART C-reactive protein (CRP), EndoCab IgM, ferritin, interferon gamma (IFN-γ), interleukin 6 (IL-6), interferon gamma-inducible protein 10 (IP-10), lipopolysaccharide (LPS), soluble CD14 (sCD14), tumor necrosis factor alpha (TNF-α), and CD4/DR+/38+ and CD8/DR+/38+ T cells. Markers were defined according to established cutoff definitions when available, 75thpercentile of measured values when not, and detectable versus undetectable for LPS. Using logistic regression, we measured associations between biomarkers and incident TB, adjusting for age, sex, study site, treatment arm, baseline CD4 and log10 viral load. We assessed the discriminatory value of biomarkers using receiver operating characteristic (ROC) analysis. Results Seventy-seven persons (4.9%) developed incident TB during follow-up. Elevated baseline CRP (aOR 3.25, 95% CI: 1.55-6.81) and IP-10 (aOR 1.89, 95% CI: 1.05-3.39), detectable plasma LPS (aOR 2.39, 95% CI: 1.13-5.06), and the established TB risk factors anemia and hypoalbuminemia were independently associated with incident TB. In ROC analysis, CRP, albumin, and LPS improved discrimination only modestly for TB risk when added to baseline routine patient characteristics including CD4 count, body mass index, and prior TB. Conclusion Incident TB occurs commonly after ART initiation. Although associated with higher post-ART TB risk, baseline CRP, IP-10, and LPS add limited value to routine patient characteristics in discriminating who develops active TB. Besides determining ideal cutoffs for these biomarkers, additional biomarkers should be sought that predict TB disease in ART initiators. 2018-09-04T10:06:39Z 2018-09-04T10:06:39Z 2015-02-26 Journal 19326203 2-s2.0-84923869697 10.1371/journal.pone.0117424 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84923869697&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/54016
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
topic Agricultural and Biological Sciences
Biochemistry, Genetics and Molecular Biology
spellingShingle Agricultural and Biological Sciences
Biochemistry, Genetics and Molecular Biology
Mark W. Tenforde
Nikhil Gupte
David W. Dowdy
David M. Asmuth
Ashwin Balagopal
Richard B. Pollard
Patcharaphan Sugandhavesa
Javier R. Lama
Sandy Pillay
Sandra W. Cardoso
Jyoti Pawar
Breno Santos
Cynthia Riviere
Noluthando Mwelase
Cecilia Kanyama
Johnstone Kumwenda
James G. Hakim
Nagalingeswaran Kumarasamy
Robert Bollinger
Richard D. Semba
Thomas B. Campbell
Amita Gupta
C-Reactive Protein (CRP), interferon gamma-inducible protein 10 (IP-10), and lipopolysaccharide (LPS) are associated with risk of tuberculosis after initiation of antiretroviral therapy in resource-limited settings
description © 2015 Tenforde et al. Objective The association between pre-antiretroviral (ART) inflammation and immune activation and risk for incident tuberculosis (TB) after ART initiation among adults is uncertain. Design Nested case-control study (n = 332) within ACTG PEARLS trial of three ART regimens among 1571 HIV-infected, treatment-naïve adults in 9 countries. We compared cases (participants with incident TB diagnosed by 96 weeks) to a random sample of controls (participants who did not develop TB, stratified by country and treatment arm). Methods We measured pre-ART C-reactive protein (CRP), EndoCab IgM, ferritin, interferon gamma (IFN-γ), interleukin 6 (IL-6), interferon gamma-inducible protein 10 (IP-10), lipopolysaccharide (LPS), soluble CD14 (sCD14), tumor necrosis factor alpha (TNF-α), and CD4/DR+/38+ and CD8/DR+/38+ T cells. Markers were defined according to established cutoff definitions when available, 75thpercentile of measured values when not, and detectable versus undetectable for LPS. Using logistic regression, we measured associations between biomarkers and incident TB, adjusting for age, sex, study site, treatment arm, baseline CD4 and log10 viral load. We assessed the discriminatory value of biomarkers using receiver operating characteristic (ROC) analysis. Results Seventy-seven persons (4.9%) developed incident TB during follow-up. Elevated baseline CRP (aOR 3.25, 95% CI: 1.55-6.81) and IP-10 (aOR 1.89, 95% CI: 1.05-3.39), detectable plasma LPS (aOR 2.39, 95% CI: 1.13-5.06), and the established TB risk factors anemia and hypoalbuminemia were independently associated with incident TB. In ROC analysis, CRP, albumin, and LPS improved discrimination only modestly for TB risk when added to baseline routine patient characteristics including CD4 count, body mass index, and prior TB. Conclusion Incident TB occurs commonly after ART initiation. Although associated with higher post-ART TB risk, baseline CRP, IP-10, and LPS add limited value to routine patient characteristics in discriminating who develops active TB. Besides determining ideal cutoffs for these biomarkers, additional biomarkers should be sought that predict TB disease in ART initiators.
format Journal
author Mark W. Tenforde
Nikhil Gupte
David W. Dowdy
David M. Asmuth
Ashwin Balagopal
Richard B. Pollard
Patcharaphan Sugandhavesa
Javier R. Lama
Sandy Pillay
Sandra W. Cardoso
Jyoti Pawar
Breno Santos
Cynthia Riviere
Noluthando Mwelase
Cecilia Kanyama
Johnstone Kumwenda
James G. Hakim
Nagalingeswaran Kumarasamy
Robert Bollinger
Richard D. Semba
Thomas B. Campbell
Amita Gupta
author_facet Mark W. Tenforde
Nikhil Gupte
David W. Dowdy
David M. Asmuth
Ashwin Balagopal
Richard B. Pollard
Patcharaphan Sugandhavesa
Javier R. Lama
Sandy Pillay
Sandra W. Cardoso
Jyoti Pawar
Breno Santos
Cynthia Riviere
Noluthando Mwelase
Cecilia Kanyama
Johnstone Kumwenda
James G. Hakim
Nagalingeswaran Kumarasamy
Robert Bollinger
Richard D. Semba
Thomas B. Campbell
Amita Gupta
author_sort Mark W. Tenforde
title C-Reactive Protein (CRP), interferon gamma-inducible protein 10 (IP-10), and lipopolysaccharide (LPS) are associated with risk of tuberculosis after initiation of antiretroviral therapy in resource-limited settings
title_short C-Reactive Protein (CRP), interferon gamma-inducible protein 10 (IP-10), and lipopolysaccharide (LPS) are associated with risk of tuberculosis after initiation of antiretroviral therapy in resource-limited settings
title_full C-Reactive Protein (CRP), interferon gamma-inducible protein 10 (IP-10), and lipopolysaccharide (LPS) are associated with risk of tuberculosis after initiation of antiretroviral therapy in resource-limited settings
title_fullStr C-Reactive Protein (CRP), interferon gamma-inducible protein 10 (IP-10), and lipopolysaccharide (LPS) are associated with risk of tuberculosis after initiation of antiretroviral therapy in resource-limited settings
title_full_unstemmed C-Reactive Protein (CRP), interferon gamma-inducible protein 10 (IP-10), and lipopolysaccharide (LPS) are associated with risk of tuberculosis after initiation of antiretroviral therapy in resource-limited settings
title_sort c-reactive protein (crp), interferon gamma-inducible protein 10 (ip-10), and lipopolysaccharide (lps) are associated with risk of tuberculosis after initiation of antiretroviral therapy in resource-limited settings
publishDate 2018
url https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84923869697&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/54016
_version_ 1681424242563874816