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Genetic analysis of families with autoimmune diabetes and thyroiditis: evidence for common and unique genes.
J Clin Endocrinol Metab 2005; 90(8):4904-11JC

Abstract

CONTEXT

Epidemiological data suggest a common genetic susceptibility to type 1 diabetes (T1D) and autoimmune thyroid disease (AITD).

OBJECTIVE

Our objective was to identify the joint susceptibility genes for T1D and AITD.

DESIGN

We conducted a family-based linkage and association study.

SETTING

The study took place at an academic medical center.

PARTICIPANTS

Participants included 55 multiplex families (290 individuals) in which T1D and AITD clustered (T1D-AITD families).

MAIN OUTCOME MEASURES

We conducted tests for linkage and family-based associations (transmission disequilibrium test) with four candidate genes: human leukocyte antigen (HLA), cytotoxic T lymphocyte-associated antigen 4 (CTLA-4), insulin variable number of tandem repeats (VNTR), and thyroglobulin.

RESULTS

Linkage evidence to HLA appeared when subjects with either T1D or AITD were considered affected [maximum LOD score (MLS), 2.2]. The major HLA haplotype contributing to the shared susceptibility was DR3-DQB1*0201, with DR3 conferring most of the shared risk. The CTLA-4 gene showed evidence for linkage only when individuals with both T1D and AITD were considered affected (MLS, 1.7), and the insulin VNTR showed evidence for linkage when individuals with either T1D or AITD were considered affected (MLS, 1.9); i.e. it may contribute to the familial aggregation of T1D and AITD.

CONCLUSIONS

The HLA class II locus contributes to the shared risk for T1D and AITD, and the major HLA haplotype contributing to this association is DR3-DQB1*0201. Additional non-HLA loci contribute to the joint susceptibility to T1D and AITD, and two potential candidates include the CTLA-4 and insulin VNTR loci.

Authors+Show Affiliations

Division of Endocrinology, Diabetes, and Bone Diseases, Department of Medicine, Mount Sinai School of Medicine, New York, New York 10029, USA.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article
Research Support, N.I.H., Extramural
Research Support, U.S. Gov't, P.H.S.

Language

eng

PubMed ID

15928253

Citation

Golden, Brian, et al. "Genetic Analysis of Families With Autoimmune Diabetes and Thyroiditis: Evidence for Common and Unique Genes." The Journal of Clinical Endocrinology and Metabolism, vol. 90, no. 8, 2005, pp. 4904-11.
Golden B, Levin L, Ban Y, et al. Genetic analysis of families with autoimmune diabetes and thyroiditis: evidence for common and unique genes. J Clin Endocrinol Metab. 2005;90(8):4904-11.
Golden, B., Levin, L., Ban, Y., Concepcion, E., Greenberg, D. A., & Tomer, Y. (2005). Genetic analysis of families with autoimmune diabetes and thyroiditis: evidence for common and unique genes. The Journal of Clinical Endocrinology and Metabolism, 90(8), pp. 4904-11.
Golden B, et al. Genetic Analysis of Families With Autoimmune Diabetes and Thyroiditis: Evidence for Common and Unique Genes. J Clin Endocrinol Metab. 2005;90(8):4904-11. PubMed PMID: 15928253.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Genetic analysis of families with autoimmune diabetes and thyroiditis: evidence for common and unique genes. AU - Golden,Brian, AU - Levin,Lara, AU - Ban,Yoshiyuki, AU - Concepcion,Erlinda, AU - Greenberg,David A, AU - Tomer,Yaron, Y1 - 2005/05/31/ PY - 2005/6/2/pubmed PY - 2005/9/15/medline PY - 2005/6/2/entrez SP - 4904 EP - 11 JF - The Journal of clinical endocrinology and metabolism JO - J. Clin. Endocrinol. Metab. VL - 90 IS - 8 N2 - CONTEXT: Epidemiological data suggest a common genetic susceptibility to type 1 diabetes (T1D) and autoimmune thyroid disease (AITD). OBJECTIVE: Our objective was to identify the joint susceptibility genes for T1D and AITD. DESIGN: We conducted a family-based linkage and association study. SETTING: The study took place at an academic medical center. PARTICIPANTS: Participants included 55 multiplex families (290 individuals) in which T1D and AITD clustered (T1D-AITD families). MAIN OUTCOME MEASURES: We conducted tests for linkage and family-based associations (transmission disequilibrium test) with four candidate genes: human leukocyte antigen (HLA), cytotoxic T lymphocyte-associated antigen 4 (CTLA-4), insulin variable number of tandem repeats (VNTR), and thyroglobulin. RESULTS: Linkage evidence to HLA appeared when subjects with either T1D or AITD were considered affected [maximum LOD score (MLS), 2.2]. The major HLA haplotype contributing to the shared susceptibility was DR3-DQB1*0201, with DR3 conferring most of the shared risk. The CTLA-4 gene showed evidence for linkage only when individuals with both T1D and AITD were considered affected (MLS, 1.7), and the insulin VNTR showed evidence for linkage when individuals with either T1D or AITD were considered affected (MLS, 1.9); i.e. it may contribute to the familial aggregation of T1D and AITD. CONCLUSIONS: The HLA class II locus contributes to the shared risk for T1D and AITD, and the major HLA haplotype contributing to this association is DR3-DQB1*0201. Additional non-HLA loci contribute to the joint susceptibility to T1D and AITD, and two potential candidates include the CTLA-4 and insulin VNTR loci. SN - 0021-972X UR - https://www.unboundmedicine.com/medline/citation/15928253/Genetic_analysis_of_families_with_autoimmune_diabetes_and_thyroiditis:_evidence_for_common_and_unique_genes_ L2 - https://academic.oup.com/jcem/article-lookup/doi/10.1210/jc.2004-2236 DB - PRIME DP - Unbound Medicine ER -