Evidence map›Paper›PMID 30161179›Full record

ArticlePloS one2018

Serum Wisteria floribunda agglutinin-positive Mac-2-binding protein levels predict the presence of fibrotic nonalcoholic steatohepatitis (NASH) and NASH cirrhosis.

Naim Alkhouri, Casey Johnson, Leon Adams, Sachiko Kitajima, Chikayuki Tsuruno, Tracey L Colpitts, Kazuki Hatcho, Eric Lawitz, Rocio Lopez, Ariel E Feldstein

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

12 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
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  11. End-points for drug treatment in NASH.Hepatology international · 2019
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 5 institutions in 3 countries.

Naim AlkhouriThe Texas Liver Institute, University of Texas (UT) Health Science Center, San Antonio, Texas, United States of America.ORCID 0000-0001-9872-2391
Casey JohnsonDepartment of Pediatrics, University of California - San Diego, La Jolla, California, United States of America.
Leon AdamsThe University of Western Australia, Crawley, Australia.
Sachiko KitajimaSysmex Corporation, Kobe, Japan.
Chikayuki TsurunoSysmex Corporation, Kobe, Japan.
Tracey L ColpittsSysmex Corporation R&D Center of Americas, Lincolnshire, Illinois, United States of America.
Kazuki HatchoSysmex Corporation R&D Center of Americas, Lincolnshire, Illinois, United States of America.
Eric LawitzThe Texas Liver Institute, University of Texas (UT) Health Science Center, San Antonio, Texas, United States of America.
Rocio LopezDigestive Disease and Surgery Institute, Cleveland Clinic, Cleveland, Ohio, United States of America.
Ariel E FeldsteinDepartment of Pediatrics, University of California - San Diego, La Jolla, California, United States of America.
Sysmex (Japan) · JPTexas Liver Institute · USUniversity of California San Diego · USCleveland Clinic · USThe University of Western Australia · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe race for finding effective treatments for nonalcoholic fatty liver disease (NAFLD) has been slowed down by the high screen-failure rate for including patients in trials due to the lack of a noninvasive biomarker that can identify patients with significant disease. Recently, Wisteria floribunda agglutinin-positive Mac-2-binding protein (WFA+ -M2BP) has shown promise in predicting liver fibrosis. The aims of this study were to evaluate the utility of WFA+ -M2BP as a biomarker to sub-classify patients with NAFLD according to their disease severity and to assess its correlation with histologic features of NAFLD.

methodsPatients undergoing biopsy for clinical suspicion of NAFLD and healthy controls were included. Patients with NAFLD were classified into: NAFL, early NASH (F0-F1), fibrotic NASH (F2-F3), and NASH cirrhosis (F4). Levels of WFA+ -M2BP in sera was measured by a HISCL™ M2BPGi™ assay kit using an automated immunoanalyzer (HISCL™-800; Sysmex, Kobe, Japan). Analysis of covariance was used to assess difference in WFA+ -M2BP between the groups and Spearman's correlation coefficients were used to assess correlation with histological features.

resultsOur cohort consisted of 20 healthy controls and 198 patients with biopsy-proven NAFLD divided as follows: 52 with NAFL, 62 with early NASH, 52 with fibrotic NASH, and 32 with NASH cirrhosis. WFA+ -M2BP level was found to be significantly increased in the fibrotic NASH and NASH cirrhosis groups compared to healthy controls and those with early NAFLD after adjusting for age, gender and BMI. Furthermore, patients with NASH cirrhosis had significantly higher WFA+ -M2BP levels (2.4[1.5, 4.2] C.O.I (Cut-off Index)) than those with fibrotic NASH (1.2[0.79, 1.9]), p < 0.001. WFA+ -M2BP level had moderate correlation with inflammation, ballooning and NAFLD activity score and strong correlation with fibrosis stage. Additionally, ROC curve analysis demonstrated that WFA+ -M2BP accurately differentiated F2-4 from F0-F1.

conclusionIn a large cohort of patients with the full spectrum of NAFLD, WFA+ -M2BP levels predicted the presence of advanced disease and correlated strongly with fibrosis stage.

Indexed as

AdultAgedAntigens, NeoplasmBiomarkersCase-Control StudiesCohort StudiesFemaleHumansLiver CirrhosisMaleMembrane GlycoproteinsMiddle AgedNon-alcoholic Fatty Liver DiseasePlant LectinsReceptors, N-AcetylglucosamineAntigens, NeoplasmBiomarkersMembrane GlycoproteinsPlant LectinsReceptors, N-AcetylglucosamineTAA90K protein, humanwisteria lectin

Identifiers

PMID30161179
PMCPMC6116978
OpenAlexW2889009981

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.