Evidence map›Paper›PMID 28883647›Full record

ArticleScientific reports2017

Circulating miR-122 and miR-200a as biomarkers for fatal liver disease in ART-treated, HIV-1-infected individuals.

Daniel D Murray, Kazuo Suzuki, Matthew Law, Jonel Trebicka, Jacquie Neuhaus Nordwall, Margaret Johnson, Michael J Vjecha, Anthony D Kelleher, Sean Emery

Abstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

19 citing papers in PubMed, 1 synthesis or guideline pooled it.

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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

9 authors.

Daniel D MurrayThe Kirby Institute for Infection and Immunity in Society, University of New South Wales, Sydney, Australia. dmurray@kirby.unsw.edu.au.
Kazuo SuzukiThe Kirby Institute for Infection and Immunity in Society, University of New South Wales, Sydney, Australia.
Matthew LawThe Kirby Institute for Infection and Immunity in Society, University of New South Wales, Sydney, Australia.
Jonel TrebickaDepartment of Internal Medicine, University of Bonn, Bonn, Germany.ORCID 0000-0002-7028-3881
Jacquie Neuhaus NordwallUniversity of Minnesota, Minneapolis, Minnesota, United States of America.
Margaret JohnsonIan Charleson Day Centre, Royal Free Hampstead NHS Trust, London, United Kingdom.
Michael J VjechaInstitute for Clinical Research, Veterans Affairs Medical Center, Washington D.C., United States of America.
Anthony D KelleherThe Kirby Institute for Infection and Immunity in Society, University of New South Wales, Sydney, Australia.
Sean EmeryThe Kirby Institute for Infection and Immunity in Society, University of New South Wales, Sydney, Australia.

Funding

International Network for Strategic Initiatives in Global HIV Trials (INSIGHT)UM1AI068641 · NIAID · UNIVERSITY OF MINNESOTA · PI NEATON, JAMES DENNIS · 2011 to 2014
$83.5M
COMMUNITY PROGRAMS FOR CLINICAL RESEARCH ON AIDSU01AI046362 · NIAID · SOCIAL AND SCIENTIFIC SYSTEMS, INC. · PI GORDIN, FRED M · 2000 to 2006
$75.9M
INTERNATIONAL PHASE III IL-2 STUDYU01AI046957 · NIAID · UNIVERSITY OF MINNESOTA TWIN CITIES · PI NEATON, JAMES DENNIS · 1999 to 2005
$56.4M
TERRY BEIRN COMMUNITY PROGRAMS FOR CLINICAL RESEARCH ONU01AI042170 · NIAID · UNIVERSITY OF MINNESOTA TWIN CITIES · PI NEATON, JAMES DENNIS · 1997 to 2006
$23.2M
Medical Research Council MC_UU_12023/23NIAID NIH HHS U01 AI042170NIAID NIH HHS U01 AI046362NIAID NIH HHS U01 AI046957NIAID NIH HHS UM1 AI068641
6 · The paper itself

Abstract

Liver disease is one of the main contributors to the increased levels of morbidity and mortality seen in the HIV-1-infected, ART-treated population. Circulating miRNAs, particularly those located inside extracellular vesicles, are seen as promising biomarkers for a number of human disease conditions, including liver-related diseases. Here, we show that serum levels of miR-122 and miR-200a are greater in HIV/HCV co-infected individuals compared to HIV-1 mono-infected individuals. We also show that miR-122 and miR-200a are elevated in ART-treated, HIV-1-infected individuals prior to the development of fatal liver disease, suggesting that these miRNA may have some potential clinical utility as biomarkers. While this study is hypothesis generating, it shows clearly that both miR-122 and miR-200a are promising novel biomarkers for liver disease in the ART-treated, HIV-1-infected population.

Indexed as

AdultAnti-Retroviral AgentsAntiretroviral Therapy, Highly ActiveBiomarkersEnd Stage Liver DiseaseFemaleHepatitis C, ChronicHIV InfectionsHumansMaleMicroRNAsMiddle AgedPrognosisAnti-Retroviral AgentsBiomarkersMicroRNAsMIRN122 microRNA, humanMIRN200 microRNA, human

Identifiers

PMID28883647
PMCPMC5589757

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Registered trials

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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.