PST Linkage Based Analysis in the Family of More Than Two Members With Type 1 Diabetes in Taiwan (PATT)

Chang Gung Medical Foundation

Status: Completed

Conditions: The Genetic Variation of Type 1 Diabetes

Study type: Observational

Funder types: Other

Identifiers

NCT01955746

CMRPG3C1151

Details and patient eligibility

About

The purpose of this study is to explore the susceptible genes for Type 1 diabetes in Taiwan through the new genetic study methods.

Full description

As an unclear autoimmune disorder, the pathogenesis of type 1 diabetes (T1D) remains elusive. Among all the methods for studying diseases pathophysiology, genetic approach has valuable capability as being both hypothesis-testing and hypothesis-generating. Although geo-epidemiological studies show relatively higher prevalence of T1D in Caucasians than in Asians, whether genetic factors identified in T1D of Caucasians are essential for T1D in Asians is not yet clarified. Although the human leukocyte antigen (HLA) genotype variants have been reported to be associated with T1D, the odds ratio (ORs) is relatively low in Taiwan as comparing with western countries, some families are indeed more than one child with T1D. However, the genetic linkage study in T1D is still limited in Taiwan that hampered the drug development or research in T1D. Therefore, we intend to explore the susceptible genes for T1D of Taiwan in this study, which will provide further researcher directions for this disease.

Enrollment: 20 patients

Sex: All

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Type 1 diabetes on the criteria of the American Diabetes Association with a very low C-peptide level (<0.35 ng/mL) with or without the experience of diabetic ketoacidosis.
2. The subjects whose four grandparents are of Chinese Han origin

Exclusion criteria

1. Patients with ages of onset more than 35 years are excluded.
2. The families having any member with known possible type 2 diabetes

Trial design

20 participants in 1 patient group

Type 1 DM