The spectrum of association in HLA region with rheumatoid arthritis in a diverse Asian population: evidence from the MyEIRA case-control study.


Journal

Arthritis research & therapy
ISSN: 1478-6362
Titre abrégé: Arthritis Res Ther
Pays: England
ID NLM: 101154438

Informations de publication

Date de publication:
30 01 2021
Historique:
received: 04 11 2020
accepted: 19 01 2021
entrez: 30 1 2021
pubmed: 31 1 2021
medline: 22 6 2021
Statut: epublish

Résumé

Fine-mapping of human leukocyte antigen (HLA) region for rheumatoid arthritis (RA) risk factors has identified several HLA alleles and its corresponding amino acid residues as independent signals (i.e., HLA-A, HLA-B, HLA-DPB1, and HLA-DQA1 genes), in addition to the well-established genetic factor in HLA-DRB1 gene. However, this was mainly performed in the Caucasian and East Asian populations, and data from different Asian regions is less represented. We aimed to evaluate whether there are independent RA risk variants in both anti-citrullinated protein antibody (ACPA)-positive and ACPA-negative RA patients from the multi-ethnic Malaysian population, using the fine-mapping of HLA region strategy. We imputed the classical HLA alleles, amino acids, and haplotypes using the Immunochip genotyping data of 1260 RA cases (i.e., 530 Malays, 259 Chinese, 412 Indians, and 59 mixed ethnicities) and 1571 controls (i.e., 981 Malays, 205 Chinese, 297 Indians, and 87 mixed ethnicities) from the Malaysian Epidemiological Investigation of Rheumatoid Arthritis (MyEIRA) population-based case-control study. Stepwise logistic regression was performed to identify the independent genetic risk factors for RA within the HLA region. We confirmed that the HLA-DRB1 amino acid at position 11 with valine residue conferred the strongest risk effect for ACPA-positive RA (OR = 4.26, 95% CI = 3.30-5.49, P Our results demonstrate that the RA-associated genetic factors in the multi-ethnic Malaysian population are similar to those in the Caucasian population, despite significant differences in the genetic architecture of HLA region across populations. A novel and distinct independent association between the HLA-DQB1*03:02 allele and ACPA-positive RA was observed in the Malays. In common with the Caucasian population, there is little risk from HLA region for ACPA-negative RA.

Sections du résumé

BACKGROUND
Fine-mapping of human leukocyte antigen (HLA) region for rheumatoid arthritis (RA) risk factors has identified several HLA alleles and its corresponding amino acid residues as independent signals (i.e., HLA-A, HLA-B, HLA-DPB1, and HLA-DQA1 genes), in addition to the well-established genetic factor in HLA-DRB1 gene. However, this was mainly performed in the Caucasian and East Asian populations, and data from different Asian regions is less represented. We aimed to evaluate whether there are independent RA risk variants in both anti-citrullinated protein antibody (ACPA)-positive and ACPA-negative RA patients from the multi-ethnic Malaysian population, using the fine-mapping of HLA region strategy.
METHODS
We imputed the classical HLA alleles, amino acids, and haplotypes using the Immunochip genotyping data of 1260 RA cases (i.e., 530 Malays, 259 Chinese, 412 Indians, and 59 mixed ethnicities) and 1571 controls (i.e., 981 Malays, 205 Chinese, 297 Indians, and 87 mixed ethnicities) from the Malaysian Epidemiological Investigation of Rheumatoid Arthritis (MyEIRA) population-based case-control study. Stepwise logistic regression was performed to identify the independent genetic risk factors for RA within the HLA region.
RESULTS
We confirmed that the HLA-DRB1 amino acid at position 11 with valine residue conferred the strongest risk effect for ACPA-positive RA (OR = 4.26, 95% CI = 3.30-5.49, P
CONCLUSIONS
Our results demonstrate that the RA-associated genetic factors in the multi-ethnic Malaysian population are similar to those in the Caucasian population, despite significant differences in the genetic architecture of HLA region across populations. A novel and distinct independent association between the HLA-DQB1*03:02 allele and ACPA-positive RA was observed in the Malays. In common with the Caucasian population, there is little risk from HLA region for ACPA-negative RA.

Identifiants

pubmed: 33514426
doi: 10.1186/s13075-021-02431-z
pii: 10.1186/s13075-021-02431-z
pmc: PMC7847037
doi:

Substances chimiques

Autoantibodies 0
HLA Antigens 0
HLA-DRB1 Chains 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

46

Références

Hum Mol Genet. 2014 Dec 20;23(25):6916-26
pubmed: 25070946
Arthritis Res Ther. 2010;12(2):R62
pubmed: 20370905
Arthritis Rheum. 2005 Nov;52(11):3433-8
pubmed: 16255021
HLA. 2016 Sep;88(3):100-9
pubmed: 27580864
Arthritis Res Ther. 2011 Feb 01;13(1):101
pubmed: 21345260
Arthritis Rheum. 2009 Apr;60(4):924-30
pubmed: 19333936
Am J Hum Genet. 2007 Sep;81(3):559-75
pubmed: 17701901
Scand J Rheumatol. 2008 May-Jun;37(3):183-7
pubmed: 18465452
Ann Rheum Dis. 2016 Oct;75(10):1891-8
pubmed: 26715653
Curr Opin Rheumatol. 2010 May;22(3):293-8
pubmed: 20061955
Nat Genet. 2012 Jan 29;44(3):291-6
pubmed: 22286218
Arthritis Rheum. 1987 Nov;30(11):1205-13
pubmed: 2446635
Int J Immunogenet. 2014 Aug;41(4):312-7
pubmed: 24917237
Am J Hum Genet. 2009 Dec;85(6):762-74
pubmed: 19944404
Hum Immunol. 2016 Oct;77(10):818-819
pubmed: 27370684
Arthritis Rheumatol. 2015 Apr;67(4):877-86
pubmed: 25580908
J Rheumatol. 2007 Apr;34(4):674-80
pubmed: 17309132
Hereditas. 2018 Apr 6;155:19
pubmed: 29636655
Nat Genet. 2011 Nov 06;43(12):1193-201
pubmed: 22057235
Scand J Rheumatol. 1998;27(2):146-8
pubmed: 9572642
PLoS One. 2014 Jun 09;9(6):e99453
pubmed: 24911054
Am J Hum Genet. 2014 Apr 3;94(4):522-32
pubmed: 24656864
Nat Genet. 2013 Jun;45(6):664-9
pubmed: 23603761
Hum Mol Genet. 2014 Aug 15;23(16):4443-51
pubmed: 24698974
Ann Rheum Dis. 2010 Aug;69(8):1569-70
pubmed: 19854714
Arthritis Rheum. 2004 Nov;50(11):3468-75
pubmed: 15529363
Hum Immunol. 2020 Jun;81(6):263-264
pubmed: 32312605
Clin Invest Med. 2016 Dec 01;39(6):E182-E203
pubmed: 27917778
Ann Rheum Dis. 2019 Jun;78(6):773-780
pubmed: 30936065
PLoS One. 2013 Jun 06;8(6):e64683
pubmed: 23762245
Arthritis Rheum. 2006 Jan;54(1):38-46
pubmed: 16385494
Ann Saudi Med. 2017 Jan-Feb;37(1):38-41
pubmed: 28151455
PLoS One. 2011;6(6):e21069
pubmed: 21698259
Arthritis Rheumatol. 2015 Jul;67(7):1744-50
pubmed: 25777156
Hum Immunol. 2019 Nov;80(11):906-907
pubmed: 31558331
Biochem Cell Biol. 2007 Apr;85(2):227-38
pubmed: 17534404
HLA. 2016 Nov;88(5):253-258
pubmed: 27753285
N Engl J Med. 1978 Apr 20;298(16):869-71
pubmed: 147420
Mod Rheumatol. 2012 Aug;22(4):524-31
pubmed: 22006120
J Rheumatol. 2019 Feb;46(2):138-144
pubmed: 30385709

Auteurs

Lay Kim Tan (LK)

Immunogenetic Unit, Allergy and Immunology Research Center, Ministry of Health Malaysia, Institute for Medical Research, National Institutes of Health Complex, Shah Alam, Selangor, Malaysia. tanlk@moh.gov.my.
Faculty of Medicine, Universiti Kuala Lumpur Royal College of Medicine Perak, Ipoh, Perak, Malaysia. tanlk@moh.gov.my.
Department of Medicine, Division of Rheumatology, Karolinska Institutet and Karolinska University Hospital, Stockholm, Sweden. tanlk@moh.gov.my.

Chun Lai Too (CL)

Immunogenetic Unit, Allergy and Immunology Research Center, Ministry of Health Malaysia, Institute for Medical Research, National Institutes of Health Complex, Shah Alam, Selangor, Malaysia. toocl@moh.gov.my.
Department of Medicine, Division of Rheumatology, Karolinska Institutet and Karolinska University Hospital, Stockholm, Sweden. toocl@moh.gov.my.

Lina Marcela Diaz-Gallo (LM)

Department of Medicine, Division of Rheumatology, Karolinska Institutet and Karolinska University Hospital, Stockholm, Sweden.

Sulaiman Wahinuddin (S)

Faculty of Medicine, Universiti Kuala Lumpur Royal College of Medicine Perak, Ipoh, Perak, Malaysia.
Department of Medicine, Ministry of Health Malaysia, Hospital Raja Perempuan Bainun, Ipoh, Perak, Malaysia.

Ing Soo Lau (IS)

Department of Medicine, Ministry of Health Malaysia, Selayang Hospital, Selayang, Selangor, Malaysia.

Hussein Heselynn (H)

Department of Medicine, Ministry of Health Malaysia, Putrajaya Hospital, Putrajaya, Malaysia.

Shahril Nor-Shuhaila (S)

Department of Medicine, Ministry of Health Malaysia, Putrajaya Hospital, Putrajaya, Malaysia.

Suk Chyn Gun (SC)

Department of Medicine, Ministry of Health Malaysia, Hospital Tuanku Ja'afar Seremban, Seremban, Negeri Sembilan, Malaysia.

Mageswaran Eashwary (M)

Department of Medicine, Ministry of Health Malaysia, Putrajaya Hospital, Putrajaya, Malaysia.

Mohamed Said Mohd-Shahrir (MS)

Faculty of Medicine, Universiti Kebangsaan Malaysia Medical Center, Kuala Lumpur, Malaysia.

Mohd Mokhtar Ainon (MM)

Department of Medicine, Ministry of Health Malaysia, Tengku Ampuan Afzan Hospital, Kuantan, Pahang, Malaysia.

Rosman Azmillah (R)

Department of Medicine, Ministry of Health Malaysia, Selayang Hospital, Selayang, Selangor, Malaysia.

Othman Muhaini (O)

Department of Medicine, Ministry of Health Malaysia, Hospital Raja Perempuan Bainun, Ipoh, Perak, Malaysia.

Murad Shahnaz (M)

Ministry of Health Malaysia, Federal Government Administrative Center, Putrajaya, Malaysia.

Lars Alfredsson (L)

Institute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden.

Lars Klareskog (L)

Faculty of Medicine, Universiti Kuala Lumpur Royal College of Medicine Perak, Ipoh, Perak, Malaysia.

Leonid Padyukov (L)

Department of Medicine, Division of Rheumatology, Karolinska Institutet and Karolinska University Hospital, Stockholm, Sweden. leonid.padyukov@ki.se.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH