Evidence map›Paper›PMID 29430306›Full record

ArticleTuberculosis research and treatment2017

A Pilot Study of Immune Activation and Rifampin Absorption in HIV-Infected Patients without Tuberculosis Infection: A Short Report.

Christopher Vinnard, Isabel Manley, Brittney Scott, Mariana Bernui, Joella Adams, Sheryl Varghese, Isaac Zentner, Michele A Kutzler

Registry-linked trialOpen access · hybridAbstract read
In one paragraph

Article in Tuberculosis research and treatment, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01845298 (Immune Activation and Drug Absorption in HIV-Infected Patients), which is not on this map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 46% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT01845298 nacompletednot on this map

Immune Activation and Drug Absorption in HIV-Infected Patients

TypeinterventionalSponsorDrexel UniversityRan2014 to 2016Enrolled7ConditionsHIV InfectionArmsRifampicin 600 mg
3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 1 country.

Christopher VinnardPublic Health Research Institute, Rutgers, The State University of New Jersey, Newark, NJ, USA.ORCID 0000-0002-0641-7814
Isabel ManleyDivision of Infectious Diseases & HIV Medicine, Department of Medicine, Drexel University College of Medicine, Philadelphia, PA, USA.
Brittney ScottDivision of Infectious Diseases & HIV Medicine, Department of Medicine, Drexel University College of Medicine, Philadelphia, PA, USA.
Mariana BernuiDivision of Infectious Diseases & HIV Medicine, Department of Medicine, Drexel University College of Medicine, Philadelphia, PA, USA.
Joella AdamsBrown University School of Public Health, Providence, RI, USA.
Sheryl VargheseDivision of Infectious Diseases & HIV Medicine, Department of Medicine, Drexel University College of Medicine, Philadelphia, PA, USA.
Isaac ZentnerPublic Health Research Institute, Rutgers, The State University of New Jersey, Newark, NJ, USA.
Michele A KutzlerDivision of Infectious Diseases & HIV Medicine, Department of Medicine, Drexel University College of Medicine, Philadelphia, PA, USA.
Drexel University · USRutgers, The State University of New Jersey · USBrown University · US

Funding

Rifampicin Malabsorption in HIV+ Patients: Mechanisms and Recovery after HAARTK23AI102639 · NIAID · RBHS-NEW JERSEY MEDICAL SCHOOL · PI VINNARD, CHRISTOPHER · 2014 to 2018
$695k
NIAID NIH HHS K23 AI102639
6 · The paper itself

Abstract

backgroundRifampin malabsorption is frequently observed in tuberculosis patients coinfected with human immunodeficiency virus (HIV) but cannot be predicted by patient factors such as CD4+ T cell count or HIV viral load.

methodsWe sought to describe the relationship between HIV-associated immune activation, measures of gut absorptive capacity and permeability, and rifampin pharmacokinetic parameters in a pilot study of 6 HIV-infected, tuberculosis-uninfected patients who were naïve to antiretroviral therapy.

resultsThe median rifampin area under the concentration-versus-time curve during the 8-hour observation period was 42.8 mg·hr/L (range: 21.2 to 57.6), with a median peak concentration of 10.1 mg/L (range: 5.3 to 12.5). We observed delayed rifampin absorption, with a time to maximum concentration greater than 2 hours, in 2 of 6 participants. There was a trend towards increased plasma concentrations of sCD14, a marker of monocyte activation in response to bacterial translocation, among participants with delayed rifampin absorption compared to participants with rapid absorption (

conclusionsDelayed rifampin absorption may be associated with elevated markers of bacterial translocation among HIV-infected individuals naïve to antiretroviral therapy. This trial is registered with NCT01845298.

Identifiers

PMID29430306
PMCPMC5752984
OpenAlexW2780747016

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.