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Original article
Fine mapping MHC associations in Graves’ disease and its clinical subtypes in Han Chinese
  1. Xun Chu1,2,3,
  2. Minjun Yang3,
  3. Zhen-Ju Song4,
  4. Yan Dong1,2,
  5. Chong Li3,
  6. Min Shen3,
  7. Yong-Qiang Zhu3,
  8. Huai-Dong Song5,
  9. Sai-Juan Chen5,
  10. Zhu Chen5,
  11. Wei Huang3
  1. 1 Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China
  2. 2 Shanghai Key Laboratory of Pediatric Gastroenterology and Nutrition, Shanghai Institute for Pediatric Research, Shanghai, China
  3. 3 Department of Genetics, Shanghai-MOST Key Laboratory of Health and Disease Genomics, Chinese National Human Genome Center and Shanghai Academy of Science & Technology, Shanghai, China
  4. 4 Department of Emergency Medicine, Zhongshan Hospital, Fudan University, Shanghai, China
  5. 5 Shanghai Institute of Hematology, Ruijin Hospital Affiliated to Shanghai Jiaotong University (SJTU) School of Medicine, Shanghai, China, China
  1. Correspondence to Dr Xun Chu, Xinhua Hospital, Shanghai Institute for Pediatric Research, Shanghai Jiao Tong University School of Medicine, Shanghai 200092, China; chuxun{at}xinhuamed.com.cn

Abstract

Background The classical human leucocyte antigen (HLA) genes were the most important genetic determinant for Graves’ disease (GD). The aim of the study was to fine map causal variants of the HLA genes.

Methods We applied imputation with a Pan-Asian HLA reference panel to thoroughly investigate themajor histocompatibility complex (MHC) associations with GD down to the amino acid level of classical HLA genes in 1468 patients with GD and 1490 controls of Han Chinese.

Results The strongest finding across the HLA genes was the association with HLA-DPβ1 position 205 (Pomnibus=2.48×10−33). HLA-DPA1*02:02 was the strongest association among the classical HLA alleles, which was in perfect linkage disequilibrium with HLA-DPα1 residue Met11 (OR=1.90, Pbinary=1.76×10−31). Applying stepwise conditional analysis, we identified amino acid position 205 in HLA-DPβ1, position 66 and 99 in HLA-B and position 28 in HLA-DRβ1 explain majority of the MHC association to GD risk. We further evaluated risk of two clinical subtypes of GD, namely persistent thyroid stimulating hormone receptor antibody -positive (pTRAb+) group and ‘non-persistent TRAb positive’ (pTRAb−) group after antithyroid drug therapy. We found that HLA-B residues Lys66-Arg69-Val76 could drive pTRAb− GD risk alone, while HLA-DPβ1 position 205, HLA-B position 69 and 199 and HLA-DRβ1 position 28 drive pTRAb+ GD risk. The risk heterogeneity between pTRAb+ and pTRAb− GD might be driven by HLA-DPα1 Met11.

Conclusions Four amino acid positions could account for the associations of MHC with GD in Han Chinese. These distinct HLA association patterns indicated the two subtypes have distinct molecular mechanisms of pathogenesis.

  • Graves’ disease
  • MHC
  • HLA
  • genome-wide association studies
  • amino acid position

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Footnotes

  • Contributors XC designed research and wrote the paper; XC, MY, Z-JS and CL analysed data; MS, YD, Y-Q Z, H-DS, S-JC, ZC and WH collected clinical samples and performed experiments.

  • Funding This work was supported by the National Natural Science Foundation of China (31671317, 31471190, 81471840 and 31271343).

  • Competing interests None declared.

  • Patient consent Obtained.

  • Ethics approval Ethical Committee of the Chinese National Human Genome Center at Shanghai.

  • Provenance and peer review Not commissioned; externally peer reviewed.

  • Data sharing statement The snp allele frequencies of the cases and controls could be shared with researchers by contacting corresponding author by email.

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