The Genetics of Diabetes in Southern California Chinese Americans
Recruitment status was Recruiting
- Full Text View
- Tabular View
- No Study Results Posted
- Disclaimer
- How to Read a Study Record
Purpose
The purpose of this research study is to investigate the genetic causes of diabetes. Specifically, we are interested in the mitochondrial genome and how variants in the mitochondrial genome influence a person's risk to develop diabetes and metabolic syndrome.
| Condition |
|---|
|
Diabetes Mellitus, Type 1 Diabetes Mellitus, Type 2 Metabolic Syndrome |
| Study Type: | Observational |
| Study Design: | Observational Model: Case Control Time Perspective: Cross-Sectional |
| Official Title: | Mitochondria and Metabolic Syndrome in a Southern California Chinese Cohort |
whole blood and serum
| Estimated Enrollment: | 500 |
| Study Start Date: | January 2006 |
| Estimated Study Completion Date: | November 2010 |
| Estimated Primary Completion Date: | November 2010 (Final data collection date for primary outcome measure) |
| Groups/Cohorts |
|---|
|
1
Individuals with diabetes
|
|
2
Individuals without diabetes
|
Detailed Description:
Since our laboratory's initial linkage of Type 2 diabetes to a mtDNA rearrangement in a three generation maternal pedigree 13 years ago, there has been increasing support for our hypothesis that mitochondrial dysfunction plays an important role in the etiology of Type 2 Diabetes Mellitus (DM) and the overlapping Metabolic Syndrome (MS). With this study we are planning an extensive investigation of defects in mitochondrial oxidative phosphorylation (OXPHOS) caused potentially by deleterious sequence variants in the mitochondrial DNA (mtDNA). As the primary objective we are trying to further substantiate 2 hypotheses: 1) that these diabetogenic mtDNA variants, which are proposed to range from recent, relatively severe, mutations will result in substantial OXPHOS defects with familial DM & MS and 2) that ancient, relatively mild polymorphisms result in partial OXPHOS defects and an increase in the risk to develop DM & MS.
Eligibility| Ages Eligible for Study: | 40 Years to 65 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
| Sampling Method: | Non-Probability Sample |
We are currently recruiting Chinese Americans living in Southern California, espcially in Orange and Los Angeles Counties. We are particularly in need of Chinese American men and women with diabetes as well as healthy male controls. We can arrange for offsite weekend trips to cities within LA or Orange Counties for eligible groups of 10 or more people.
Inclusion Criteria:
- Chinese or Taiwanese ancestry
- Resident of Southern California
- Age between 40 and 65
- Both people with and without diabetes are welcome to enroll.
Exclusion Criteria:
- Younger than 40 years or older than 65 years
- Ancestry is not Chinese or Taiwanese
- Not a resident of Southern California
Contacts and Locations| Contact: Julia Platt, MS | 949-824-9232 | jplatt@uci.edu |
| Contact: Shiqin Xu, PhD | 949-892-7645 | shiqinx@uci.edu |
| United States, California | |
| UC Irvine General Clinical Research Center | Recruiting |
| Irvine, California, United States, 92697 | |
| Contact: Julia Platt, MS 949-824-9232 jplatt@uci.edu | |
| Principal Investigator: | Douglas C Wallace, PhD | UC Irvine Center for Mitochondrial Medicine |
More Information
No publications provided
| Responsible Party: | Douglas C. Wallace, Ph.D / Principal Investigator, UC Irvine Center for Mitochondrial Medicine and Genetics |
| ClinicalTrials.gov Identifier: | NCT00824395 History of Changes |
| Other Study ID Numbers: | 2005-4675 |
| Study First Received: | January 15, 2009 |
| Last Updated: | February 2, 2011 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by University of California, Irvine:
|
diabetes type 1 type 2 metabolic syndrome mitochondria |
Additional relevant MeSH terms:
|
Diabetes Mellitus Diabetes Mellitus, Type 1 Diabetes Mellitus, Type 2 Metabolic Syndrome X Glucose Metabolism Disorders Metabolic Diseases |
Endocrine System Diseases Autoimmune Diseases Immune System Diseases Insulin Resistance Hyperinsulinism |
ClinicalTrials.gov processed this record on June 18, 2013