Evidence map›Paper›PMID 27047767›Full record

ArticleJournal of clinical and translational hepatology2016

Overestimate of Fibrosis by FIBROSpect® II in African Americans Complicates the Management of their Chronic Hepatitis C.

Maher Tama, Paul Naylor, Suhag Patel, Johnny Altawil, Dhiraj Gulati, Fadi Antaki, Milton G Mutchnick, Murray Ehrinpreis

Open access · diamondAbstract read
In one paragraph

Article in Journal of clinical and translational hepatology, 2016. 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
0.5field-weighted citation impact, top 31% 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, 3 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

8 authors at 1 institution in 1 country.

Maher TamaWayne State University School of Medicine, Department of Internal Medicine, Division of Gastroenterology, Detroit, MI, USA.
Paul NaylorWayne State University School of Medicine, Department of Internal Medicine, Division of Gastroenterology, Detroit, MI, USA.
Suhag PatelWayne State University School of Medicine, Department of Internal Medicine, Division of Gastroenterology, Detroit, MI, USA.
Johnny AltawilWayne State University School of Medicine, Department of Internal Medicine, Division of Gastroenterology, Detroit, MI, USA.
Dhiraj GulatiWayne State University School of Medicine, Department of Internal Medicine, Division of Gastroenterology, Detroit, MI, USA.
Fadi AntakiWayne State University School of Medicine, Department of Internal Medicine, Division of Gastroenterology, Detroit, MI, USA.
Milton G MutchnickWayne State University School of Medicine, Department of Internal Medicine, Division of Gastroenterology, Detroit, MI, USA.
Murray EhrinpreisWayne State University School of Medicine, Department of Internal Medicine, Division of Gastroenterology, Detroit, MI, USA.
Wayne State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEvaluation of advanced fibrosis in patients with hepatitis C virus (HCV) infection is used to facilitate decisions on treatment strategy and to initiate additional screening measures. Unfortunately, most studies have predominately Caucasian (Cau) patients and may not be as relevant for African Americans (AA).

aimsThis study specifically addresses the issue of defining minimal vs. significant fibrosis in African Americans (AA) with chronic hepatitis C (CHC) using noninvasive assays.

methodsAll patients (n = 319) seen between 1 January 2008 and 30 June 2013 for whom a FibroSpect II® (FSII) assay was performed and had data for calculation of aspartate aminotransferase (AST) platelet ratio index (APRI) and Fibrosis-4 (FIB-4) were identified using the medical records.

resultsWhen liver biopsy score and FSII assay results for the AA patients with CHC were compared, 31% of AA had advanced FSII fibrosis scores (F2-F4) despite a biopsy score of F0-F1. In contrast, 10% of Cau over-scored. The AA false positive rate was 14% for APRI and 34% for FIB-4. Combining FSII with either APRI (7% false positive) or FIB-4 (10% false positive) improved the false positive rate in AA to 7% (FSII + APRI) and 10% (FSII + FIB-4) but reduced the sensitivity for significant fibrosis.

conclusionsThe FSII assay overestimates fibrosis in AA and should be used with caution since these patients may not have significant fibrosis. If the APRI or FIB-4 assay is combined with the FSII assay, minimal fibrosis in AA can be defined without subjecting the patients to a subsequent biopsy.

Indexed as

African AmericansFibrosisFibrospectHepatitis c

Identifiers

PMID27047767
PMCPMC4807138
OpenAlexW2331450868

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

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.