Evidence map›Paper›PMID 21134375›Full record

ArticleGastroenterology2011

Incidence and risk factors for steatosis progression in adults coinfected with HIV and hepatitis C virus.

Tinsay A Woreta, Catherine G Sutcliffe, Shruti H Mehta, Todd T Brown, Yvonne Higgins, David L Thomas, Michael S Torbenson, Richard D Moore, Mark S Sulkowski

Registry-linked trialOpen access · bronzeAbstract read
In one paragraph

Article in Gastroenterology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01423643 (HCV/HIV Coinfection), which is not on this map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.8field-weighted citation impact, top 16% 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.

NCT01423643 completednot on this map

HCV/HIV Coinfection: Antiviral Therapy and Fibrosis

TypeobservationalSponsorJohns Hopkins UniversityRan2001 to 2015Enrolled1,250ConditionsHIV Infection, Hepatitis C
3 · Its place in the literature

Who cites it

23 citing papers in PubMed, 51 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. HIV and the liver.Topics in antiviral medicine · 2019
    Article
  10. Fatty liver disease in persons with HIV infection.Topics in antiviral medicine · 2019
    Article
  11. Observational
  12. Article
  13. Review
  14. Acrolein enhances epigenetic modifications, FasL expression and hepatocyte toxicity induced by anti-HIV drug Zidovudine.Toxicology in vitro : an international journal published in association with BIBRA · 2016
    Article
  15. Article
  16. Review
  17. Liver steatosis in hepatitis C patients.World journal of hepatology · 2015
    Review
  18. Article
  19. Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Tinsay A WoretaThe Johns Hopkins Hospital/University School of Medicine, Baltimore, Maryland 21287, USA. tworeta1@jhmi.edu
Catherine G Sutcliffe
Shruti H Mehta
Todd T Brown
Yvonne Higgins
David L Thomas
Michael S Torbenson
Richard D Moore
Mark S Sulkowski
Johns Hopkins University · USJohns Hopkins Hospital · US

Funding

North American AIDS Cohorts on Collaboration and Design (NAACCORD)U01AI069918 · NIAID · JOHNS HOPKINS UNIVERSITY · PI Keri Nicole Althoff, RICHARD Douglas MOORE · 2006 to 2026
$65.2M
ZINC THERAPY FOR SCLERODERMA--PHASE I STUDYM01RR002719 · NCRR · JOHNS HOPKINS UNIVERSITY · PI EARLEY, CHRISTOPHER J · 1986 to 2007
$20.2M
Johns Hopkins HIV Clinical CohortU01DA036935 · NIDA · JOHNS HOPKINS UNIVERSITY · PI MOORE, RICHARD DOUGLAS · 2014 to 2024
$14.9M
HIV DISEASE OUTCOMES IN DRUG USERS IN CLINICAL PRACTICER01DA011602 · NIDA · JOHNS HOPKINS UNIVERSITY · PI MOORE, RICHARD DOUGLAS · 1998 to 2013
$10.8M
The Impact of HCV Treatment in HIV/HCV coinfected and HCV monoinfected Incarcerated Persons on HCV EliminationR01DA013806 · NIDA · JOHNS HOPKINS UNIVERSITY · PI IRVIN, RISHA, THOMAS, DAVID L · 2000 to 2024
$8.7M
Management/Hepatitis C/HIV-infected and Uninfected IDU'sR01DA016065 · NIDA · JOHNS HOPKINS UNIVERSITY · PI SULKOWSKI, MARK SEBASTIAN · 2003 to 2018
$8.0M
HIV HCV Coinfection Antiviral Therapy and FibrosisR37DA013806 · NIDA · JOHNS HOPKINS UNIVERSITY · PI THOMAS, DAVID L · 2010 to 2019
$7.0M
MID CAREER INVESTIGATOR AWARDK24DA000432 · NIDA · JOHNS HOPKINS UNIVERSITY · PI MOORE, RICHARD DOUGLAS · 2000 to 2009
$1.5M
Alcohol and HIV Treatment and Clinical ProgressionR01AA016893 · NIAAA · JOHNS HOPKINS UNIVERSITY · PI MOORE, RICHARD DOUGLAS · 2008 to 2011
$1.3M
Patient Oriented Research in Hepatitis C-infected Injection Drug UsersK24DA034621 · NIDA · JOHNS HOPKINS UNIVERSITY · PI SULKOWSKI, MARK SEBASTIAN · 2012 to 2022
$1.2M
Fish oil, inflammation, &metabolic complications in HIVK23AT002862 · NCCIH · JOHNS HOPKINS UNIVERSITY · PI BROWN, TODD T · 2005 to 2009
$650k
OUTCOMES OF PHARMACEUTICAL THERAPY OF HIV DISEASER01HS007809 · AHRQ · JOHNS HOPKINS UNIVERSITY · PI MOORE, RICHARD DOUGLAS · 1993 to 1997
–
AHRQ HHS HS 07-809NCCIH NIH HHS K23 AT002862NCRR NIH HHS M01 RR002719NCRR NIH HHS M01RR-02719NIAAA NIH HHS AA016893NIAAA NIH HHS R01 AA016893NIAID NIH HHS U01 AI069918NIDA NIH HHS DA-11602NIDA NIH HHS DA-13806NIDA NIH HHS DA-16065NIDA NIH HHS K24 DA000432NIDA NIH HHS K24DA00432NIDA NIH HHS K24 DA034621NIDA NIH HHS R01 DA011602NIDA NIH HHS R01 DA013806NIDA NIH HHS R01 DA016065NIDA NIH HHS R37 DA013806NIDA NIH HHS U01 DA036935
6 · The paper itself

Abstract

BACKGROUND &

aimsHepatic steatosis is a common histologic finding in patients coinfected with human immunodeficiency virus (HIV) and hepatitis C virus (HCV), although little is known about its natural history. We prospectively examined the natural history of steatosis in patients coinfected with HIV and HCV who attended an urban HIV clinic.

methodsThe study cohort consisted of 222 coinfected patients (87% black, 94% with HCV genotype 1 infection) who had at least 2 liver biopsies performed between 1993 and 2008. Biopsy specimens were scored by a single pathologist; samples were classified as having trivial (<5% of hepatocytes affected) or significant (>5%) levels of fat (steatosis). We characterized progression to significant levels of fat among patients whose first biopsy samples had no or trivial levels of fat, and regression among those with significant fat, using logistic regression.

resultsInitial biopsy specimens from most patients (88%) had no or trivial amounts of fat. Among second biopsy samples, 74% had no or trivial fat and 13% had significant amounts of fat. The strongest risk factors for progression of steatosis were alcohol abuse and overweight/obesity; cumulative exposure to antiretroviral therapy between biopsies and high counts of CD4(+) T cells were associated with reduced progression of steatosis. Among the 28 patients whose initial biopsy specimen had significant fat levels, most (75%) regressed.

conclusionsAntiretroviral therapy and high counts of CD4(+) T cells are associated with reduced progression of steatosis in patients coinfected with HIV and HCV. Efforts to diagnose and prevent steatosis should focus on persons with a high body mass index and excessive alcohol intake.

Indexed as

AdultAlcohol DrinkingAnti-Retroviral AgentsBaltimoreBiopsyBody Mass IndexCD4 Lymphocyte CountChi-Square DistributionDisease ProgressionFatty LiverFemaleHepatitis CHIVHIV InfectionsHumansIncidenceAnti-Retroviral AgentsRNA, Viral

Identifiers

PMID21134375
PMCPMC3073565
OpenAlexW1995487268

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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.