Evidence map›Paper›PMID 35418742›Full record

ArticleClinical ophthalmology (Auckland, N.Z.)2022

Class II Human Leukocyte Antigen (HLA) and Susceptibility to Polypoidal Choroidal Vasculopathy in Afro-Caribbean Descent.

Harold Merle, Laurence Béral, Maxime Rocher, Mitta Pierre, Albert Jean-Charles, Odile Béra, Laurie-Anne Rosamont, Pierre-Yves Robert, Agnes Lézin

Open access · goldAbstract read
In one paragraph

Article in Clinical ophthalmology (Auckland, N.Z.), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
1.0field-weighted citation impact, top 28% 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

1 citing paper in PubMed, 5 citations in OpenAlex.

  1. Review
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

9 authors at 3 institutions in 3 countries.

Harold MerleDepartment of Ophthalmology, University Hospital of Martinique, Fort de France, French West Indies, France.
Laurence BéralDepartment of Ophthalmology, University Hospital of Guadeloupe, Pointe à Pitre, French West Indies, France.
Maxime RocherDepartment of Ophthalmology, University Hospital of Limoges, France.
Mitta PierreDepartment of Ophthalmology, University Hospital of Martinique, Fort de France, French West Indies, France.
Albert Jean-CharlesDepartment of Ophthalmology, University Hospital of Martinique, Fort de France, French West Indies, France.
Odile BéraDepartment of Genetics, University Hospital of Martinique, Fort de France, French West Indies, France.
Laurie-Anne RosamontDepartment of Genetics, University Hospital of Martinique, Fort de France, French West Indies, France.ORCID 0000-0002-1476-3223
Pierre-Yves RobertDepartment of Ophthalmology, University Hospital of Limoges, France.
Agnes LézinDepartment of Genetics, University Hospital of Martinique, Fort de France, French West Indies, France.
Centre Hospitalier Universitaire de Martinique · MQUniversité de Limoges · FRCentre Hospitalier Universitaire Pointe-à-Pitre · GP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: To evaluate how the HLA genotype is associated to the polypoidal choroidal vasculopathy (PCV) in a population of patients of Afro-Caribbean descent. Methods: Forty-seven patients were diagnosed with PCV. The number of control patients was 457. All affected patients and control patients were of Afro-Caribbean descent and natives to Martinique. HLA typing was based on blood sample, using the polymerase chain reaction technique. Comparison of HLA alleles between the 2 groups was done using chi-2 test, odds ratio (OR) and confidence interval using Woolf's method. The Bonferroni correction was considered significant when p-value ≤0.05. Alleles frequency was analyzed for DRB1 and DQB1 locus. Results: HLA-DRB1*13 allele was significantly associated to PCV (OR = 2.02, CI = [1.3; 3.13], p = 0.003). In group DRB1, the Bonferroni correction significance threshold was <0.004. HLA-DQB1*04 allele was significantly associated to PCV (OR = 3.5, CI = [1.48; 8.3], p = 0.006). In group DQB1, the Bonferroni correction significance threshold was <0.006. Conclusion: Two HLA alleles are positively associated to PCV. The possible association between PCV and certain alleles suggest HLA implication in PCV pathogeny, most likely by modeling the immune system response.

Indexed as

genetic predispositionhuman leucocyte antigenmajor histocompatibility complexpolypoidal choroidal vasculopathy

Identifiers

PMID35418742
PMCPMC8995864
OpenAlexW4225692542

What OpenQuestion holds

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LicenceCC BY-NC
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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.