Evidence map›Paper›PMID 29099018›Full record

ArticleMedical sciences (Basel, Switzerland)2017

HLA Typing and Celiac Disease in Moroccans.

Daniela Piancatelli, Imane Ben El Barhdadi, Khadija Oumhani, Pierluigi Sebastiani, Alessia Colanardi, Abdellah Essaid

Abstract read
In one paragraph

Article in Medical sciences (Basel, Switzerland), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

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

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Celiac Disease: Fallacies and Facts.The American journal of gastroenterology · 2021
    Review
  9. Article
  10. Article
  11. Article
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

6 authors.

Daniela PiancatelliNational Research Council (CNR)-Institute of Translational Pharmacology, U.O.S. L'Aquila, Via Carducci 32, 67100 L'Aquila, Italy. daniela.piancatelli@cnr.it.ORCID 0000-0002-8518-1378
Imane Ben El BarhdadiMohammed V-Souissi University, 10000 Rabat, Morocco. ouhabiimane@yahoo.fr.
Khadija OumhaniInstitute National d'Hygiene, 10000 Rabat, Morocco. khaoumhani@gmail.com.
Pierluigi SebastianiNational Research Council (CNR)-Institute of Translational Pharmacology, U.O.S. L'Aquila, Via Carducci 32, 67100 L'Aquila, Italy. pierluigi.sebastiani@cnr.it.
Alessia ColanardiNational Research Council (CNR)-Institute of Translational Pharmacology, U.O.S. L'Aquila, Via Carducci 32, 67100 L'Aquila, Italy. alessia.colanardi@cnr.it.
Abdellah EssaidMohammed V-Souissi University, 10000 Rabat, Morocco. feydi2001@yahoo.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genetic and environmental factors are responsible for differences in the prevalence of some diseases across countries. Human leukocyte antigen (HLA) allele frequencies in North African populations show some differences in their distribution compared to Europeans, Mediterraneans, and sub-Saharans, and some specific alleles and haplotypes could be clinically relevant. Celiac disease (CD) has been fast increasing in prevalence in North Africa; but few immunogenetic data are available for this area, in which a high prevalence of the disease has been described. In this report, we assess and discuss results of HLA class II (HLA-DQA1/DQB1/DRB1) typing in Moroccan patients with CD and compare them with a control population from Morocco-genetically well characterized-and with other North African, Mediterranean, and European populations. The classical HLA-DQ associations were confirmed in Moroccans with CD. The high frequency of DQ2.5 homozygosity (45.2%) found in Moroccans with CD was noteworthy as compared with other populations (23%-32%). The genetic risk gradient for CD, identified by previous studies, has been confirmed in Moroccans with some differences, mainly concerning DQ8 genotypes. This study provides the immunogenetic framework of CD in Moroccans and confirms the need to learn more about associations with additional HLA and non-HLA genetic factors.

Indexed as

celiac diseaseHLAMoroccoNorth Africapopulation

Identifiers

PMID29099018
PMCPMC5635774

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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.