Evidence map›Paper›PMID 34698347›Full record

ArticleClinical infectious diseases : an official publication of the Infectious Diseases Society of America2022

Evolution of Fatty Liver Disease and Relationship With Lipoproteins and Clinical Outcomes in Hepatitis B/Human Immunodeficiency Virus Coinfection.

Mandana Khalili, Wendy C King, David E Kleiner, Raymond T Chung, Atul K Bhan, Marc G Ghany, Mark S Sulkowski, Mauricio Lisker-Melman, Mamta K Jain, Harry L A Janssen and 3 more

Open access · greenAbstract read
In one paragraph

Article in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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

13 authors at 9 institutions in 2 countries.

Mandana KhaliliUniversity of California, San Francisco, San Francisco, California, USA.ORCID 0000-0001-9178-9139
Wendy C KingUniversity of Pittsburgh Graduate School of Public Health, Pittsburgh, Pennsylvania, USA.
David E KleinerNational Institutes of Health, Bethesda, Maryland, USA.
Raymond T ChungMassachusetts General Hospital, Boston, Massachusetts,USA.
Atul K BhanMassachusetts General Hospital, Boston, Massachusetts,USA.
Marc G GhanyNational Institutes of Health, Bethesda, Maryland, USA.
Mark S SulkowskiJohns Hopkins University, Baltimore, Maryland, USA.
Mauricio Lisker-MelmanWashington University School of Medicine and John Cochran Veterans Affairs Medical Center, St Louis, USA.
Mamta K JainUniversity of Texas Southwestern Medical Center, Dallas, Texas, USA.
Harry L A JanssenUniversity Health Network, Toronto, Ontario, Canada.
Amanda S HinermanUniversity of Pittsburgh Graduate School of Public Health, Pittsburgh, Pennsylvania, USA.
Arun J SanyalVirginia Commonwealth University, Richmond, Virginia, USA.
Richard K SterlingVirginia Commonwealth University, Richmond, Virginia, USA.
Harvard University · USNational Institutes of Health · USUniversity of Pittsburgh · USVirginia Commonwealth University · USJohn Cochran VA Medical Center · USJohns Hopkins University · USThe University of Texas Southwestern Medical Center · USUniversity Health Network · CAUniversity of California, San Francisco · US

Funding

Pilot & Feasibility ProgramP30DK043351 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI RAYMOND T CHUNG · 1991 to 2026
$35.3M
WU P&FP30DK020579 · NIDDK · WASHINGTON UNIVERSITY · PI James Alexander Fitzpatrick · 2013 to 2026
$27.1M
Postmortem PathologyZICBC010685 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI KLEINER, DAVID ERWIN · 2009 to 2025
$14.3M
Natural History, Therapy and Pathogenesis of Chronic Viral Hepatitis BZIADK054517 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI GHANY, MARC · 2009 to 2025
$9.6M
Harvard Hepatitis B ConsortiumU01DK082919 · NIDDK · BETH ISRAEL DEACONESS MEDICAL CENTER · PI CHUNG, RAYMOND T, LAU, DARYL T · 2008 to 2019
$4.7M
HBV HIV Coinfection Research NetworkR01DK094818 · NIDDK · VIRGINIA COMMONWEALTH UNIVERSITY · PI STERLING, RICHARD K. · 2013 to 2017
$3.5M
Mentoring Multidisciplinary Patient-Oriented Research in Viral HepatitisK24AA022523 · NIAAA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI KHALILI, MANDANA · 2013 to 2023
$1.9M
Patient-Oriented Research on Hepatitis in Special PopulationsK24DK078772 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI CHUNG, RAYMOND T · 2007 to 2016
$1.6M
Patient Oriented Research in Hepatitis C-infected Injection Drug UsersK24DA034621 · NIDA · JOHNS HOPKINS UNIVERSITY · PI SULKOWSKI, MARK SEBASTIAN · 2012 to 2022
$1.2M
NIAAA NIH HHS K24 AA022523NIDA NIH HHS K24 DA034621NIDDK NIH HHS K24 DK078772NIDDK NIH HHS P30 DK020579NIDDK NIH HHS P30 DK043351NIDDK NIH HHS R01 DK094818NIDDK NIH HHS U01 DK082919
6 · The paper itself

Abstract

backgroundFatty liver disease (FLD) and hepatitis B virus (HBV) infection occur commonly in human immunodeficiency virus (HIV). FLD resolution is associated with improvement in lipoproteins in HIV-uninfected patients. We evaluated changes in FLD in an HBV/HIV-coinfected cohort.

methodsOne hundred eight HBV/HIV-coinfected adults with baseline liver biopsies were followed every 24 weeks (median, 166 weeks) and 60 had follow-up biopsies. Baseline FLD categories (none, ≥5% steatosis, steatohepatitis), their change, and relationships with clinical and lipid/lipoprotein parameters were explored using multivariable modeling.

resultsMedian age was 50 years, and 93% were male. At baseline 30% had FLD. With control for lipid-lowering medications and body mass index, low-density lipoprotein (LDL) cholesterol (LDL-C), LDL particle concentration (LDL-P), and apolipoprotein B (apoB) decreased and adiponectin increased over time (all P < .05); On follow-up (vs baseline), there was no significant difference in FLD category (P = .85); 60% remained without FLD, 17% had unchanged, 12% worsening, and 12% improved FLD. Baseline low-density lipoproteins (LDL-C, LDL-P, small LDL-P) and apoB appeared highest in those with unchanged FLD status (all P < .05). No associations between changes in FLD across follow-up (worsening/improvement vs unchanged) and lipid/lipoproteins changes were identified.

conclusionsIn this cohort, there was no significant change in FLD prevalence over a relatively short timeframe. Baseline atherogenic lipids appeared highest in those with persistent steatosis or steatohepatitis, suggesting potentially increased cardiovascular risk in this group, but an independent relationship between individual-level change in FLD status and lipid/lipoprotein levels across follow-up was not observed.

Indexed as

CoinfectionFatty LiverHepatitis BHIV InfectionsAdultApolipoproteins BCholesterol, LDLFemaleHepatitis B virusHIVHumansLipoproteinsMaleMiddle AgedApolipoproteins BCholesterol, LDLLipoproteinscardiovascular riskinsulin resistancelipidsnonalcoholic fatty liver diseasenonalcoholic steatohepatitis

Identifiers

PMID34698347
PMCPMC9630874
OpenAlexW3209719689

What OpenQuestion holds

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Registered trials

None linked

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.