Evidence map›Paper›PMID 24185312›Full record

ArticleInflammatory bowel diseases2013

Lectin-reactive anti-α-gal in patients with Crohn's disease: correlation with clinical phenotypes.

Parham Safaie, Maggie Ham, Peter Kuang, Anand S Mehta, Mengjun Wang, Adam S Cheifetz, Simon Robson, Daryl Lau, Timothy M Block, Alan C Moss

Abstract readComparative Study
In one paragraph

Article in Inflammatory bowel diseases, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact, top 75% 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

3 citing papers in PubMed, 1 citations in OpenAlex.

  1. Article
  2. Review
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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

10 authors at 1 institution in 1 country.

Parham Safaie*Liver Disease Center, Beth Israel Deaconess Medical Center, Boston, Massachusetts; †Center for Inflammatory Bowel Disease, Beth Israel Deaconess Medical Center, Boston, Massachusetts; and ‡Department of Microbiology and Immunology, Drexel College of Medicine, Pennsylvania Biotechnology Center, Philadelphia, Pennsylvania.
Maggie Ham
Peter Kuang
Anand S Mehta
Mengjun Wang
Adam S Cheifetz
Simon Robson
Daryl Lau
Timothy M Block
Alan C Moss
Beth Israel Deaconess Medical Center · US

Funding

Predicting HCC through GlycomicsR01CA120206 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI MEHTA, ANAND S. · 2006 to 2016
$4.3M
Liver Cancer and the Role of Protein Hyper-FucosylationR01CA136607 · NCI · DREXEL UNIVERSITY · PI BLOCK, TIMOTHY M · 2009 to 2013
$2.0M
Aberrantly secreted glycoproteins as markers of liver cancerU01CA168856 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI MEHTA, ANAND S. · 2012 to 2016
$1.5M
Purinergic Pathways in Crohn's DiseaseK23DK084338 · NIDDK · BETH ISRAEL DEACONESS MEDICAL CENTER · PI MOSS, ALAN COLM · 2011 to 2015
$735k
NCI NIH HHS CA136607NCI NIH HHS CA168856-01NCI NIH HHS R01 CA120206NCI NIH HHS R01 CA136607NCI NIH HHS U01 CA168856NIDDK NIH HHS K23 DK084338NIDDK NIH HHS K23DK084338
6 · The paper itself

Abstract

backgroundPatients with inflammatory bowel disease have higher proportions of immunoglobulin G (IgG) antibodies lacking N-galactose, also called agalactosyl IgG, in their serum. Such agalactosyl IgGs have been associated with disease activity and the immunogenicity of biologics. The aim was to describe the relationship between circulating levels of a subset of agalactosyl IgGs (anti-α-Gal) and Crohn's disease (CD) phenotypes.

methodsProspectively collected serum samples of a well-characterized cohort of patients with inflammatory bowel disease and controls were used. Serum anti-α-Gal levels were measured by a high-affinity enzyme-linked immunosorbent assay and referenced to a standard control.

resultsSerum samples from 167 subjects were tested; 62 with CD, 76 with ulcerative colitis, and 29 controls. Agalactosyl anti-α-Gal levels were significantly higher in active CD than in active ulcerative colitis (P = 0.0043) or healthy controls (P < 0.0001). Among patients with CD, agalactosyl anti-α-Gal levels were significantly higher in those with a history of arthritis, than those without (P = 0.0002), but lower in those taking immunomodulators (P = 0.03). There was no correlation between agalactosyl anti-α-Gal levels and indices of Crohn's severity, including C-reactive protein levels or Harvey-Bradshaw index. Patients who were primary or secondary nonresponders to infliximab had similar agalactosyl anti-α-Gal levels to clinical responders.

conclusionsPatients with CD have greater amounts of agalactosylated anti-α-Gal antibodies in their serum, particularly in those with associated joint disease. This increase seems to be independent of indices of disease activity, but is influenced by immunomodulator use.

Indexed as

AdultCase-Control StudiesColitis, UlcerativeC-Reactive ProteinCrohn DiseaseEnzyme-Linked Immunosorbent AssayFemaleFollow-Up StudiesHumansImmunoglobulin GLectinsMalePhenotypePrognosisProspective Studiesagalactosyl IGGC-Reactive ProteinImmunoglobulin GLectins

Identifiers

PMID24185312
PMCPMC4112456
OpenAlexW2331930703

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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.