Genetics of Type 2 Diabetes in West Africans
NCT00837122 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 10000
Last updated 2026-05-22
Summary
Background:
* Type 2 diabetes (T2D) and associated complications are major contributors to the global disease burden. T2D is already a major health threat in populations in developed countries and is rapidly taking hold in the developing world.
* It is believed that understanding the complex interplay between genetic and lifestyle characteristics in the etiology of T2D and related complications will lead to the development of better preventive and therapeutic strategies. In Addition, the results of this project will facilitate our understanding of causes of diabetes in African Americans, other US and world populations
Objectives:
* To conduct a genome-wide association study (GWAS) to identify susceptibility genetic variants for diabetes among the Yoruba people in Ibadan, Nigeria.
* To enroll and examine 300 unrelated cases of T2D and 300 ethnicity-matched Yoruba controls.
* To conduct resequencing of positional candidate gene/loci to identify likely functional variants in a subset of the cohort.
* To conduct replication studies of the top-100 scoring variants in three independent African and European ancestry samples.
* To investigate whether diabetes-associated variants discovered in European populations increase diabetes risk in West Africans.
Eligibility:
* Patients 18 years of age with confirmed T2D who are newly diagnosed or on treatment of Yoruba ethnicity in Ibadan, Nigeria. Control subjects are nondiabetics ethnically matched to patients.
Design:
* The study design for both patients and controls consists of the following steps:
* Discuss informed consent process and obtain signed informed consent form. Informed consent will be administered by trained clinic staff.
* Assign study ID (barcode)
* Administer questionnaires
* Obtain spot urine sample
* Measure blood pressure
* Obtain anthropometric measurements including body composition
* Perform finger prick for blood glucose level
* Obtain venous blood samples
* Perform eye examination
* On the following day, perform confirmatory blood glucose for the small subset of participants requiring confirmation of previous test result DNA extraction of stored samples will be done at either the National Institutes of Health or the laboratory in Nigeria.
* GWAS will be conducted using publicly available software packages.
Conditions
Sponsors & Collaborators
-
National Human Genome Research Institute (NHGRI)
lead NIH
Principal Investigators
-
Charles N Rotimi, M.D. · National Human Genome Research Institute (NHGRI)
Eligibility
- Min Age
- 18 Years
- Max Age
- 120 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2009-02-03
Countries
- Ghana
- Nigeria
Study Locations
More Related Trials
-
Genes of Hypertension in African Americans
NCT00063505 ·Status: COMPLETED
-
Observational Study of Advanced Data Analytics in Genetic Conditions
NCT05657405 ·Status: RECRUITING
-
Genetic and Metabolic Disease in Children
NCT02650622 ·Status: RECRUITING
-
The Genetics of Kidneys in Diabetes (GoKinD) Study
NCT00024921 ·Status: COMPLETED
-
Genetics of Latent Autoimmune Diabetes in Adults
NCT01793974 ·Status: COMPLETED
-
Study of Inherited Neurological Disorders
NCT00004568 ·Status: RECRUITING
-
Identification and Characterization of Monogenic Diabetes
NCT01481623 ·Status: COMPLETED ·Phase: NA
-
Next Generation to Identify Genetic Causes of Disease in Patients Participating in NICHD Clinical Protocols
NCT01375543 ·Status: COMPLETED
-
Cultural Congruence in International Genetics Research
NCT00767858 ·Status: TERMINATED
-
Genetic Analysis of Hereditary Disorders of Hearing and Balance
NCT00023049 ·Status: COMPLETED
-
Suitability of Some Data Quality Controls Thresholds for Genetic Association Studies of Admixed Population
NCT02770001 ·Status: WITHDRAWN
-
Dissecting the Genetics of Fetal Alcohol Spectrum Disorders
NCT04072809 ·Status: COMPLETED
-
Screening of Healthy Adults for Genetic Variations That Control Fatty Acid Processing
NCT01516125 ·Status: COMPLETED
-
Clinical Integration of Genetic Risk Assessment in Family Medicine
NCT00339794 ·Status: COMPLETED
-
Child Development and Genetic Biomarkers(II): Gene Verification and Data Integration
NCT06532721 ·Status: RECRUITING
-
Clinical and Genetic Evaluation of Individuals With Undiagnosed Disorders Through the Undiagnosed Diseases Network
NCT02450851 ·Status: RECRUITING
-
Clinical and Basic Investigations Into Known and Suspected Congenital Disorders of Glycosylation
NCT02089789 ·Status: RECRUITING
-
Genetic Study of Familial Epilepsy
NCT00006059 ·Status: COMPLETED
-
Study of Glycogen Storage Disease and Associated Disorders
NCT00001342 ·Status: COMPLETED
-
Psychosocial Impact of Disclosing Cancer Predisposition Genetic Testing Results During Childhood
NCT04848142 ·Status: COMPLETED
-
Studies of Children With Metabolic and Other Genetic Disorders
NCT00025870 ·Status: COMPLETED
-
Genetic Variants in Nicotinamide Adenine Dinucleotide (NAD) Synthesis Pathway
NCT03799705 ·Status: COMPLETED
-
Study of Glycogen Storage Disease Expression in Carriers
NCT02057731 ·Status: COMPLETED
-
Genetic Origin of Lipid Disorders
NCT00277121 ·Status: UNKNOWN
-
Mutation Exploration in Non-acquired, Genetic Disorders and Its Impact on Health Economy and Life Quality
NCT02380729 ·Status: COMPLETED