Dissecting the genetic susceptibility to graves' disease in a cohort of patients of Italian origin

Angela Lombardi, Francesca Menconi, David Greenberg, Erlinda Concepcion, Marenza Leo, Roberto Rocchi, Michele Marinó, Mehdi Keddache, Yaron Tomer

Research output: Contribution to journalArticle

18 Citations (Scopus)

Abstract

Graves' disease (GD) is an autoimmune oligogenic disorder with a strong hereditary component. Several GD susceptibility genes have been identified and confirmed during the last two decades. However, there are very few studies that evaluated susceptibility genes for GD in specific geographic subsets. Previously, we mapped a new locus on chromosome 3q that was unique to GD families of Italian origin. In the present study, we used association analysis of single-nucleotide polymorphism (SNPs) at the 3q locus in a cohort of GD patients of Italian origin in order to prioritize the best candidates among the known genes in this locus to choose the one(s) best supported by the association. DNA samples were genotyped using the Illumina GoldenGate genotyping assay analyzing 690 SNP in the linked 3q locus covering all 124 linkage disequilibrium blocks in this locus. Candidate non-HLA (human-leukocyte-antigen) genes previously reported to be associated with GD and/or other autoimmune disorders were analyzed separately. Three SNPs in the 3q locus showed a nominal association (p <0.05): Rs13097181, rs763313, and rs6792646. Albeit these could not be further validated by multiple comparison correction, we were prioritizing candidate genes at a locus already known to harbor a GD-related gene, not hypothesis testing. Moreover, we found significant associations with the thyroid-stimulating hormone receptor (TSHR) gene, the cytotoxic T-lymphocyte antigen-4 (CTLA-4) gene, and the thyroglobulin (TG) gene. In conclusion, we identified three SNPs on chromosome 3q that may map a new GD susceptibility gene in this region which is unique to the Italian population. Furthermore, we confirmed that the TSHR, the CTLA-4, and the TG genes are associated with GD in Italians. Our findings highlight the influence of ethnicity and geographic variations on the genetic susceptibility to GD.

Original languageEnglish (US)
Article number21
JournalFrontiers in Endocrinology
Volume7
Issue numberMAR
DOIs
StatePublished - Mar 8 2016
Externally publishedYes

Fingerprint

Graves Disease
Genetic Predisposition to Disease
Genes
Single Nucleotide Polymorphism
CTLA-4 Antigen
Thyrotropin Receptors
Thyroglobulin
Disease Susceptibility
Chromosomes
Linkage Disequilibrium
HLA Antigens

Keywords

  • Genetic predisposition to disease
  • Graves' disease
  • Italian patients
  • SNP association study
  • Thyroid diseases

ASJC Scopus subject areas

  • Endocrinology, Diabetes and Metabolism

Cite this

Dissecting the genetic susceptibility to graves' disease in a cohort of patients of Italian origin. / Lombardi, Angela; Menconi, Francesca; Greenberg, David; Concepcion, Erlinda; Leo, Marenza; Rocchi, Roberto; Marinó, Michele; Keddache, Mehdi; Tomer, Yaron.

In: Frontiers in Endocrinology, Vol. 7, No. MAR, 21, 08.03.2016.

Research output: Contribution to journalArticle

Lombardi, Angela ; Menconi, Francesca ; Greenberg, David ; Concepcion, Erlinda ; Leo, Marenza ; Rocchi, Roberto ; Marinó, Michele ; Keddache, Mehdi ; Tomer, Yaron. / Dissecting the genetic susceptibility to graves' disease in a cohort of patients of Italian origin. In: Frontiers in Endocrinology. 2016 ; Vol. 7, No. MAR.
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