HLA-DRB1*15:01 Is Associated and Linked With Kawasaki Disease, With DRB1*14:01 Conferring Risk to Coronary Artery
Hsin Chi1,2,3,4, Horng-Woei Yang4, Yann-Jinn Lee3,4,5,6
1Department of Pediatrics, MacKay Memorial Hospital, Taipei, Taiwan.
Insights
This study found specific HLA-DRB1 gene variants are linked to Kawasaki disease (KD) in children. HLA-DRB1*15:01 is associated with KD, while HLA-DRB1*14:01 and HLA-DRB1*12:02 influence coronary artery abnormalities.
Area of Science:
- Immunogenetics
- Pediatric Vasculitis
Background:
- Kawasaki disease (KD), a leading cause of vasculitis in young children, has an unknown etiology.
- Previous studies investigating the human leukocyte antigen (HLA) complex's association with KD yielded inconclusive results due to small sample sizes.
Purpose of the Study:
- To investigate the association and genetic linkage between the HLA-DRB1 locus and Kawasaki disease (KD), including its complications.
- To identify specific HLA-DRB1 alleles that confer susceptibility or protection against KD and coronary artery abnormalities (CALs).
Main Methods:
- A case-control and family-based study design was employed, including 795 KD patients and 946 healthy controls.
- HLA-DRB1 genotyping was performed using sequence-based typing.
- Transmission/disequilibrium test (TDT) was utilized to confirm genetic linkage between HLA-DRB1 and KD.
Main Results:
- HLA-DRB1*15:01 was significantly associated with KD and KD without coronary artery abnormalities (CALs).
- HLA-DRB1*14:01 was identified as a risk factor for KD with CALs, whereas HLA-DRB1*12:02 showed a protective effect against CALs.
- Family-based analysis confirmed significant overtransmission of HLA-DRB1*15:01 to KD patients, particularly males, and those without CALs.
Conclusions:
- Specific HLA-DRB1 alleles, including *15:01, *14:01, and *12:02, are significantly associated with Kawasaki disease susceptibility and the development of coronary artery abnormalities.
- The findings confirm a genetic linkage between the HLA-DRB1 locus and KD, providing insights into its pathogenesis.
Abstract:
Kawasaki disease (KD), also known as mucocutaneous lymph node syndrome, is a leading cause of vasculitis in children aged < 5 years. The HLA complex has been investigated for its association with KD since 1978 without conclusive results due to limitations such as small sample sizes. This study aimed to evaluate the associations and genetic linkage between HLA-DRB1 and KD, as well as its complications. The case-control and family-based studies enrolled 795 patients with KD and 946 healthy controls. Of the 795 patients, 180 trios were included. Genotypes of HLA-DRB1 were identified by sequence-based typing according to the International ImMunoGeneTics database. Allele frequencies were calculated using PyPop 7.0. The transmission/disequilibrium test (TDT) was used to verify the genetic linkage between HLA-DRB1 and KD. HLA-DRB1*15:01 was significantly associated with KD (OR, 1.44, Pc = 0.03) and with KD without CALs (OR = 1.46, Pc = 0.04). HLA-DRB1*14:01 was a risk factor for KD with CALs (OR = 2.47, Pc = 0.004) whereas HLA-DRB1*12:02 was a protective factor against CALs (OR = 0.49, Pc = 0.01). In the family-based study, HLA-DRB1*15:01 demonstrated significant overtransmission to KD patients (OR = 3.35; 95% CI, 2.20-5.78; Pc = 1.19E-06) and to KD patients without CALs (OR = 4.42; 95% CI, 2.59-10.08; Pc = 6.24E-06). The overtransmission remained significant in male KD patients (OR = 2.81; 95% CI, 1.68-5.58; Pc = 0.003), and in male KD patients without CALs (OR = 3.22; 95% CI, 1.69-8.84; Pc = 0.02). Our study identified significant associations between HLA-DRB1*15:01, *14:01, and *12:02 with KD. The association between HLA-DRB1*15:01 and KD was further verified by TDT, indicating a genetic linkage between the HLA-DRB1 locus and KD susceptibility.
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