A single nucleotide polymorphism within HOX Transcript Antisense RNA (HOTAIR) is associated with risk of psoriasis.


Journal

International journal of immunogenetics
ISSN: 1744-313X
Titre abrégé: Int J Immunogenet
Pays: England
ID NLM: 101232337

Informations de publication

Date de publication:
Oct 2020
Historique:
received: 21 12 2019
revised: 22 01 2020
accepted: 10 02 2020
pubmed: 25 2 2020
medline: 10 6 2021
entrez: 25 2 2020
Statut: ppublish

Résumé

Recent studies have shown participation of long non-coding RNAs (lncRNAs) in the pathogenesis of psoriasis. Several mechanisms might be involved in the dysregulation of expression of lncRNAs in patients with psoriasis, among them is the presence of single nucleotide polymorphisms (SNPs) which modulate expression or function of these transcripts. In the present work, we genotyped three SNPs (rs12826786, rs1899663 and rs4759314) of the HOX Transcript Antisense RNA (HOTAIR) in 286 patients with psoriasis and 300 control subjects. The rs12826786 was associated with risk of psoriasis in dominant model (TC + TT vs. CC: OR (95% CI) = 1.59 (0.1.14-2.22), adjusted p-value = .02). In the allelic model, T allele of this SNP significantly increased the risk of psoriasis compared with the C allele (OR (95% CI) = 1.35 (1.06-1.71), adjusted p-value = .04). Other SNPs were not associated with risk of psoriasis in any inheritance model. No significant difference was found in haplotype frequencies between cases and controls. The current work shows association between a genomic variant within HOTAIR and risk of psoriasis. The clinical significance of this finding should be assessed in future studies.

Identifiants

pubmed: 32090437
doi: 10.1111/iji.12482
doi:

Substances chimiques

HOTAIR long untranslated RNA, human 0
RNA, Long Noncoding 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

430-434

Subventions

Organisme : Shahid Beheshti University of Medical Sciences

Informations de copyright

© 2020 John Wiley & Sons Ltd.

Références

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Auteurs

Azadeh Rakhshan (A)

Department of Pathology, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

Nader Zarrinpour (N)

Center for Research and Training in Skin Disease and Leprosy, Tehran University of Medical Sciences, Tehran, Iran.

Afshin Moradi (A)

Cancer Research Center, Faculty of Medicine, Shohada Hospital, Shahid Beheshti University of Medical Science, Tehran, Iran.

Mahsa Ahadi (M)

Cancer Research Center, Faculty of Medicine, Shohada Hospital, Shahid Beheshti University of Medical Science, Tehran, Iran.

Mir Davood Omrani (MD)

Urogenital Stem Cell Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

Soudeh Ghafouri-Fard (S)

Department of Medical Genetics, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

Mohammad Taheri (M)

Urogenital Stem Cell Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

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