Evidence map›Paper›PMID 36382644›Full record

ArticleInternational archives of allergy and immunology2023

The Association of HLA Alleles and Haplotypes with Age of Disease Onset in Pakistani Psoriatic Patients.

Saeeda Munir, Simeen Ber Rahman, Sadia Rehman, Nusrat Saba, Kehkashan Mazhar, Åsa Torinsson Naluai

Open access · hybridAbstract read
In one paragraph

Article in International archives of allergy and immunology, 2023. 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
0.3field-weighted citation impact, top 48% of its field
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 5 citations in OpenAlex.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors at 3 institutions in 2 countries.

Saeeda MunirInstitute of Biomedical and Genetic Engineering, Islamabad, Pakistan, saeedaonline@yahoo.com.
Simeen Ber RahmanSkin and Laser Clinic, Rawalpindi, Pakistan.
Sadia RehmanInstitute of Biomedical and Genetic Engineering, Islamabad, Pakistan.
Nusrat SabaInstitute of Biomedical and Genetic Engineering, Islamabad, Pakistan.
Kehkashan MazharInstitute of Biomedical and Genetic Engineering, Islamabad, Pakistan.
Åsa Torinsson NaluaiInstitute of Biomedicine, Sahlgrenska Academy at the University of Gothenburg, Gothenburg, Sweden.
Institute of Biomedical and Genetic Engineering · PKRawalpindi Medical University · PKUniversity of Gothenburg · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe human leukocyte antigen (HLA) region on chromosome 6p21 is well known to carry the most important genetic factors in susceptibility to psoriasis. Different HLA alleles and haplotypes have been reported to be associated with psoriasis in different populations. Psoriasis has a variable age of onset and, based on this, it can be classified into two types; type I with age of onset before 40 years of age and type II with age of onset after 40 years of age. The objective of this study was to determine the association of HLA class I and class II alleles and haplotypes with disease and stratification using age of onset in Pakistani psoriatic patients.

methodsA group of 603 individuals (326 cases and 277 controls) were analyzed for HLA class I and II alleles and haplotype association by sequence specific PCR. The association was further analyzed according to the age of onset of the patients.

resultsWe found that HLA alleles B*57 and Cw*06:02, DQB1*03:03:02 are strongly associated with early onset psoriasis, while alleles B*15, DRB1*13:02 and DQB1*03:03:02 are associated with late-onset psoriasis. Cw*06:02 allele was not associated with late-onset psoriasis patients. Allele DQB1*03:03:02 had the highest odds ratio in all patients. We found a novel association specifically with late-onset psoriasis samples with the haplotype HLA-A*11; B*15; Cw*04; DRB1*15; DQB1*05 (Pc = 3.60 × 10-7). We also found strong association with previously reported extended haplotype EH-57.1: HLA-B*57; Cw*06:02; DRB1*07:01; DQB1*03:03:02 in all our patients (Pc = 8.34 × 10-07).

conclusionOur results show that different HLA class I and II alleles and haplotypes are associated with psoriasis at different age of onset. In this study, we have reported novel alleles and haplotype association with late-onset psoriasis. Our data confirm the previous strong associations with HLA alleles and haplotypes and also reports novel alleles and haplotype association in Pakistani psoriasis patients.

Indexed as

Histocompatibility Antigens Class IIPsoriasisAdultAllelesGene FrequencyGenetic Predisposition to DiseaseHaplotypesHistocompatibility Antigens Class IHLA-DRB1 ChainsHumansPakistanHistocompatibility Antigens Class IHistocompatibility Antigens Class IIHLA-DRB1 ChainsAutoimmunityHaplotypeHLA allelePsoriasis

Identifiers

PMID36382644
PMCPMC9932843
OpenAlexW4309160676

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LicenceCC BY-NC
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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.