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Does HLA explain the high incidence of childhood-onset type 1 diabetes in the Canary Islands? The role of Asp57 DQB1 molecules.

Authors :
Nóvoa-Medina Y
Marcelino-Rodriguez I
Suárez NM
Barreiro-Bautista M
Rivas-García E
Sánchez-Alonso S
González-Martínez G
Quinteiro-González S
Domínguez Á
Cabrera M
López S
Pavlovic S
Flores C
Wägner AM
Source :
BMC pediatrics [BMC Pediatr] 2024 Sep 06; Vol. 24 (1), pp. 569. Date of Electronic Publication: 2024 Sep 06.
Publication Year :
2024

Abstract

The Canary Islands inhabitants, a recently admixed population with significant North African genetic influence, has the highest incidence of childhood-onset type 1 diabetes (T1D) in Spain and one of the highest in Europe. HLA accounts for half of the genetic risk of T1D.<br />Aims: To characterize the classical HLA-DRB1 and HLA-DQB1 alleles in children from Gran Canaria with and without T1D.<br />Methods: We analyzed classic HLA-DRB1 and HLA-DQB1 alleles in childhood-onset T1D patients (n = 309) and control children without T1D (n = 222) from the island of Gran Canaria. We also analyzed the presence or absence of aspartic acid at position 57 in the HLA-DQB1 gene and arginine at position 52 in the HLA-DQA1 gene. Genotyping of classical HLA-DQB1 and HLA-DRB1 alleles was performed at two-digit resolution using Luminex technology. The chi-square test (or Fisher's exact test) and odds ratio (OR) were computed to assess differences in allele and genotype frequencies between patients and controls. Logistic regression analysis was also used.<br />Results: Mean age at diagnosis of T1D was 7.4 ± 3.6 years (46% female). Mean age of the controls was 7.6 ± 1.1 years (55% female). DRB1*03 (OR = 4.2; p = 2.13 <superscript>-13</superscript> ), DRB1*04 (OR = 6.6; p ≤ 2.00 <superscript>-16</superscript> ), DRB1* 07 (OR = 0.37; p = 9.73 <superscript>-06</superscript> ), DRB1*11 (OR = 0.17; p = 6.72 <superscript>-09</superscript> ), DRB1*12, DRB1*13 (OR = 0.38; p = 1.21 <superscript>-05</superscript> ), DRB1*14 (OR = 0.0; p = 0.0024), DRB1*15 (OR = 0.13; p = 7.78 <superscript>-07</superscript> ) and DRB1*16 (OR = 0.21; p = 0.003) exhibited significant differences in frequency between groups. Among the DQB1* alleles, DQB1*02 (OR: 2.3; p = 5.13 <superscript>-06</superscript> ), DQB1*03 (OR = 1.7; p = 1.89 <superscript>-03</superscript> ), DQB1*05 (OR = 0.64; p = 0.027) and DQB1*06 (OR = 0.19; p = 6.25 <superscript>-14</superscript> ) exhibited significant differences. A total of 58% of the studied HLA-DQB1 genes in our control population lacked aspartic acid at position 57.<br />Conclusions: In this population, the overall distributions of the HLA-DRB1 and HLA-DQB1 alleles are similar to those in other European populations. However, the frequency of the non-Asp-57 HLA-DQB1 molecules is greater than that in other populations with a lower incidence of T1D. Based on genetic, historical and epidemiological data, we propose that a common genetic background might help explain the elevated pediatric T1D incidence in the Canary Islands, North-Africa and middle eastern countries.<br /> (© 2024. The Author(s).)

Details

Language :
English
ISSN :
1471-2431
Volume :
24
Issue :
1
Database :
MEDLINE
Journal :
BMC pediatrics
Publication Type :
Academic Journal
Accession number :
39243072
Full Text :
https://doi.org/10.1186/s12887-024-04983-w