The overall objective of this study is to determine if genetic, immunological and clinical variables can be utilized to identify black individuals at risk of developing gestational diabetes mellitus (GDM) and for individuals so affected to predict who will subsequently become an insulin-dependent (IDDM) or non-insulin dependent (NIDDM) diabetic or normal. The subjects are the Alabama black population of Jefferson County who receive prenatal care at one of the eight County Public Health Department operated Clinics. This involves approximately 3,600 black women which represents approximately 78% of all black women who receive prenatal care in the county. We will determine if there is an association of major histocompatibility complex genetic markers HLA-A, B,C,DR,C4,Bf and GLO, restriction fragment length polymorphisms of the insulin gene, presence of pancreatic islet cell antibodies, family history of diabetes, maternal age, maternal weight, baby birth weight and/or parity with incidence cases of GDM in our black population compared to non-GDM cohorts presenting to the same clinic. We will analyze whether these variables can be used to predict those individuals at risk for developing GDM. We will also determine if the above variables can be used to predict those GDM individuals who are at risk for developing IDDM and/or NIDDM or remain normal. The GDM subjects will be followed throughout the course of their pregnancy at UAB's Complications Clinic. Following delivery, these individuals will be followed longitudinally for five years and evaluated yearly for the susequent development of overt diabetes. Several risk factors have been recognized for GDM as well as IDDM and NIDDM. However, there is a paucity of data available with regard to risk factors for GDM in the black population. Moreover, the interrelationship of clinical, immunological and genetic risk factors for onset of GDM or their use to predict who will sugsequently develop overt disease or recover has not been investigated. Thus, there is an opportunity to utilize a well defined population within the Jefferson County area to more clearly understand risk factor for GDM and the subsequent development of IDDM and/or NIDDM. This study should also provide an opportunity to more clearly define the etiological factors of diabetes in general.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK032767-05
Application #
3231116
Study Section
Epidemiology and Disease Control Subcommittee 3 (EDC)
Project Start
1983-07-01
Project End
1988-06-30
Budget Start
1987-07-01
Budget End
1988-06-30
Support Year
5
Fiscal Year
1987
Total Cost
Indirect Cost
Name
University of Alabama Birmingham
Department
Type
Schools of Medicine
DUNS #
004514360
City
Birmingham
State
AL
Country
United States
Zip Code
35294
Giger, Joyce Newman; Strickland, Ora L; Weaver, Michael et al. (2005) Genetic predictors of coronary heart disease risk factors in premenopausal African-American women. Ethn Dis 15:221-32
Barton, E H; West, P A; Rivers, C A et al. (2001) Transferrin receptor-2 (TFR2) mutation Y250X in Alabama Caucasian and African American subjects with and without primary iron overload. Blood Cells Mol Dis 27:279-84
Acton, R T; Barton, J C; Bell, D S et al. (2001) HFE mutations in African-American women with non-insulin-dependent diabetes mellitus. Ethn Dis 11:578-84
Go, R C; Desmond, R; Roseman, J M et al. (2001) Prevalence and risk factors of microalbuminuria in a cohort of African-American women with gestational diabetes. Diabetes Care 24:1764-9
Rivers, C A; Barton, J C; Acton, R T (2001) A rapid PCR-SSP assay for the hemochromatosis-associated Tyr250Stop mutation in the TFR2 gene. Genet Test 5:131-4
Barton, J C; Sawada-Hirai, R; Rothenberg, B E et al. (1999) Two novel missense mutations of the HFE gene (I105T and G93R) and identification of the S65C mutation in Alabama hemochromatosis probands. Blood Cells Mol Dis 25:147-55
Barton, J C; Shih, W W; Sawada-Hirai, R et al. (1997) Genetic and clinical description of hemochromatosis probands and heterozygotes: evidence that multiple genes linked to the major histocompatibility complex are responsible for hemochromatosis. Blood Cells Mol Dis 23:135-45; discussion 145a-b
Acton, R T; Bell, D S; Collins, J et al. (1997) Genes within and flanking the major histocompatibility region are risk factors for diabetes, insulin resistance, hypertension, and microalbuminuria in African-American women. Transplant Proc 29:3710-2
Acton, R T (1997) Molecular genetic testing for adult-onset disorders: the evolving laboratory, physician, patient interface. J Clin Lab Anal 11:23-7
Barton, J C; Harmon, L; Rivers, C et al. (1996) Hemochromatosis: association of severity of iron overload with genetic markers. Blood Cells Mol Dis 22:195-204

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