A functional variant of ALDH1A2 is associated with hand osteoarthritis in the Chinese population

Abstract Genome‐wide association study identified common variants within the ALDH1A2 gene as the susceptible loci of hand osteoarthritis (HOA) in UK and Iceland populations. Located in chromosome 15, ALDH1A2 encodes aldehyde dehydrogenase family 1 member A2, which is an enzyme that catalyses the syn...

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Published in:International Journal of Immunogenetics
Main Authors: Dai, Jian, Jiang, Haitao, Yang, Zhaoqi, Chen, Chuan, Tang, Xiaoming
Format: Article in Journal/Newspaper
Language:English
Published: Wiley 2024
Subjects:
Online Access:http://dx.doi.org/10.1111/iji.12662
https://onlinelibrary.wiley.com/doi/pdf/10.1111/iji.12662
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spelling crwiley:10.1111/iji.12662 2024-04-07T07:53:33+00:00 A functional variant of ALDH1A2 is associated with hand osteoarthritis in the Chinese population Dai, Jian Jiang, Haitao Yang, Zhaoqi Chen, Chuan Tang, Xiaoming 2024 http://dx.doi.org/10.1111/iji.12662 https://onlinelibrary.wiley.com/doi/pdf/10.1111/iji.12662 en eng Wiley http://onlinelibrary.wiley.com/termsAndConditions#vor International Journal of Immunogenetics ISSN 1744-3121 1744-313X Genetics (clinical) Genetics Molecular Biology General Medicine Immunology journal-article 2024 crwiley https://doi.org/10.1111/iji.12662 2024-03-08T03:55:59Z Abstract Genome‐wide association study identified common variants within the ALDH1A2 gene as the susceptible loci of hand osteoarthritis (HOA) in UK and Iceland populations. Located in chromosome 15, ALDH1A2 encodes aldehyde dehydrogenase family 1 member A2, which is an enzyme that catalyses the synthesis of retinoic acid from retinaldehyde. Our purposes were to replicate the association of functional variant in ALDH1A2 with the development of HOA in the Chinese population. Variant rs12915901 of ALDH1A2 was genotyped in 872 HOA patients and 1223 healthy controls. Subchondral bone samples were collected from 40 patients who had undergone a trapeziectomy, and the tissue expression of ALDH1A2 was analysed. The chi‐square analysis was used to compare the frequency of genotype and risk allele between the HOA cases and controls. The Student t test was used to compare the mRNA expression of ALDH1A2 between patients with genotype AA/AG and those with genotype GG. The frequency of genotype AA was significantly higher in HOA patients than in the controls (7.6% vs. 5.1%, p = .01). The frequency of allele A was significantly higher in the patients than in the controls (28.9% vs. 24.6%, p = .005). The mRNA expression of ALDH1A2 was 1.31‐folds higher in patients with genotype GG than in the patients with genotype AA/AG (0.000617 ± 0.000231 vs. 0.000471 ± 0.000198, p = .04). Variant rs12915901 of ALDH1A2 contributed to the susceptibility of HOA in the Chinese population. Allele A of rs12915901 can add to the risk of HOA possibly via down‐regulation of ALDH1A2 expression. Article in Journal/Newspaper Iceland Wiley Online Library International Journal of Immunogenetics
institution Open Polar
collection Wiley Online Library
op_collection_id crwiley
language English
topic Genetics (clinical)
Genetics
Molecular Biology
General Medicine
Immunology
spellingShingle Genetics (clinical)
Genetics
Molecular Biology
General Medicine
Immunology
Dai, Jian
Jiang, Haitao
Yang, Zhaoqi
Chen, Chuan
Tang, Xiaoming
A functional variant of ALDH1A2 is associated with hand osteoarthritis in the Chinese population
topic_facet Genetics (clinical)
Genetics
Molecular Biology
General Medicine
Immunology
description Abstract Genome‐wide association study identified common variants within the ALDH1A2 gene as the susceptible loci of hand osteoarthritis (HOA) in UK and Iceland populations. Located in chromosome 15, ALDH1A2 encodes aldehyde dehydrogenase family 1 member A2, which is an enzyme that catalyses the synthesis of retinoic acid from retinaldehyde. Our purposes were to replicate the association of functional variant in ALDH1A2 with the development of HOA in the Chinese population. Variant rs12915901 of ALDH1A2 was genotyped in 872 HOA patients and 1223 healthy controls. Subchondral bone samples were collected from 40 patients who had undergone a trapeziectomy, and the tissue expression of ALDH1A2 was analysed. The chi‐square analysis was used to compare the frequency of genotype and risk allele between the HOA cases and controls. The Student t test was used to compare the mRNA expression of ALDH1A2 between patients with genotype AA/AG and those with genotype GG. The frequency of genotype AA was significantly higher in HOA patients than in the controls (7.6% vs. 5.1%, p = .01). The frequency of allele A was significantly higher in the patients than in the controls (28.9% vs. 24.6%, p = .005). The mRNA expression of ALDH1A2 was 1.31‐folds higher in patients with genotype GG than in the patients with genotype AA/AG (0.000617 ± 0.000231 vs. 0.000471 ± 0.000198, p = .04). Variant rs12915901 of ALDH1A2 contributed to the susceptibility of HOA in the Chinese population. Allele A of rs12915901 can add to the risk of HOA possibly via down‐regulation of ALDH1A2 expression.
format Article in Journal/Newspaper
author Dai, Jian
Jiang, Haitao
Yang, Zhaoqi
Chen, Chuan
Tang, Xiaoming
author_facet Dai, Jian
Jiang, Haitao
Yang, Zhaoqi
Chen, Chuan
Tang, Xiaoming
author_sort Dai, Jian
title A functional variant of ALDH1A2 is associated with hand osteoarthritis in the Chinese population
title_short A functional variant of ALDH1A2 is associated with hand osteoarthritis in the Chinese population
title_full A functional variant of ALDH1A2 is associated with hand osteoarthritis in the Chinese population
title_fullStr A functional variant of ALDH1A2 is associated with hand osteoarthritis in the Chinese population
title_full_unstemmed A functional variant of ALDH1A2 is associated with hand osteoarthritis in the Chinese population
title_sort functional variant of aldh1a2 is associated with hand osteoarthritis in the chinese population
publisher Wiley
publishDate 2024
url http://dx.doi.org/10.1111/iji.12662
https://onlinelibrary.wiley.com/doi/pdf/10.1111/iji.12662
genre Iceland
genre_facet Iceland
op_source International Journal of Immunogenetics
ISSN 1744-3121 1744-313X
op_rights http://onlinelibrary.wiley.com/termsAndConditions#vor
op_doi https://doi.org/10.1111/iji.12662
container_title International Journal of Immunogenetics
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