Evidence map›Paper›PMID 35737255›Full record

ArticleJournal of clinical immunology2022

Protein-losing Enteropathy as a Complication and/or Differential Diagnosis of Common Variable Immunodeficiency.

Sébastien Sanges, Nicolas Germain, Stéphane Vignes, David Séguy, Sarah Stabler, Nicolas Etienne, Louis Terriou, David Launay, Éric Hachulla, Damien Huglo and 3 more

Erratum issuedAbstract read
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In one paragraph

Article in Journal of clinical immunology, 2022. 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 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

11 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Observational
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  4. Review
  5. Review
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  8. Review
  9. Article
  10. Cryptococcal meningitis and cerebral vasculitis in a patient with primary intestinal lymphangiectasia: a case report.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2023
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 6 institutions in 1 country.

Sébastien Sanges *Université de Lille, UFR Médecine, 59000, Lille, France.
Nicolas Germain *Université de Lille, UFR Médecine, 59000, Lille, France.
Stéphane VignesUnité de Lymphologie, Hôpital Cognacq-Jay, Paris, France.
David SéguyDépartement de Nutrition, CHU Lille, 59000, Lille, France.
Sarah StablerUniversité de Lille, UFR Médecine, 59000, Lille, France.
Nicolas EtienneService de Médecine Interne Et Immunologie Clinique, Centre de Référence Des Maladies Auto-Immunes Systémiques Rares du Nord Et Nord-Ouest de France (CeRAINO), CHU Lille, 59000, Lille, France.
Louis TerriouService de Médecine Interne Et Immunologie Clinique, Centre de Référence Des Maladies Auto-Immunes Systémiques Rares du Nord Et Nord-Ouest de France (CeRAINO), CHU Lille, 59000, Lille, France.
David LaunayUniversité de Lille, UFR Médecine, 59000, Lille, France.
Éric HachullaUniversité de Lille, UFR Médecine, 59000, Lille, France.
Damien HugloUniversité de Lille, UFR Médecine, 59000, Lille, France.
Sylvain DubucquoiUniversité de Lille, UFR Médecine, 59000, Lille, France.
Myriam LabaletteUniversité de Lille, UFR Médecine, 59000, Lille, France.
Guillaume LefèvreUniversité de Lille, UFR Médecine, 59000, Lille, France. guillaume.lefevre@univ-lille.fr.
Centre Hospitalier Universitaire de Lille · FRUniversité de Lille · FRUniversité Lille Nord de France · FRInserm · FRInstitute for Translational Research in InflammationLille Inflammation Research International Center · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As protein-losing enteropathy (PLE) can lead to hypogammaglobulinemia and lymphopenia, and since common variable immunodeficiency (CVID) is associated with digestive complications, we wondered if (1) PLE could occur during CVID and (2) specific features could help determine whether a patient with antibody deficiency has CVID, PLE, or both. Eligible patients were thus classified in 3 groups: CVID + PLE (n = 8), CVID-only (= 19), and PLE-only (n = 13). PLE was diagnosed using fecal clearance of α1-antitrypsin or 111In-labeled albumin. Immunoglobulin (Ig) A, G, and M, naive/memory B and T cell subsets were compared between each group. CVID + PLE patients had multiple causes of PLE: duodenal villous atrophy (5/8), nodular follicular hyperplasia (4/8), inflammatory bowel disease-like (4/8), portal hypertension (4/8), giardiasis (3/8), and pernicious anemia (1/8). Compared to the CVID-only group, CVID + PLE patients had similar serum Ig levels, B cell subset counts, but lower naive T cell proportion and IgG replacement efficiency index. Compared to the CVID-only group, PLE-only patients did not develop infections but had higher serum levels of IgG (p = 0.03), IgA (p < 0.0001), and switched memory B cells (p = 0.001); and decreased naive T cells (CD4

Indexed as

Common Variable ImmunodeficiencyProtein-Losing EnteropathiesDiagnosis, DifferentialHumansImmunoglobulin AImmunoglobulin GImmunoglobulin AImmunoglobulin GAntibody deficiencyCommon variable immunodeficiencyHypogammaglobulinemiaLymphopeniaPrimary intestinal lymphangiectasiaProtein-losing enteropathy

Identifiers

PMID35737255
OpenAlexW4283313782

What OpenQuestion holds

Textmetadata
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.