Obesity Clinical Trial
To assess the association of immunogenetic factors with onset of coronary heart disease and the interrelationship of these factors with standard coronary heart disease risk factors.
BACKGROUND:
Although the familial clustering of coronary heart disease has been well documented, it is
unclear as to whether the familial clustering can be explained by shared environmental
factors by members of a family or by clustering of risk factors having a genetic component
such as blood pressure, familial hyperlipidemia and/or diabetes. Studies indicate that a
family history of coronary disease may be an independent risk factor. Major
histocompatibility complex genetic markers to identify individuals at risk within a family
may be useful. In 1985 when the study began, there was a paucity of data dealing with the
interrelationship of family history, genetic markers, immunological markers, and traditional
risk factors.
DESIGN NARRATIVE:
In this case-control study, the study population consisted of incident cases who presented
to the Georgia Heart Clinic in La Grange, Georgia with coronary heart disease. The majority
of the subjects were from three counties in mideastern Alabama and from counties in
midwestern Georgia. All subjects had undergone diagnostic coronary angiography. A
determination was made in patients and controls of the association of major
histocompatibility complex genetic markers HLA-A, -B, -C, -DR, C4 and BF, C3, the
restriction fragment length polymorphisms (RFLP's) flanking the apolipoprotein AI and
insulin genes, presence of autoantibodies, and family history of coronary disease, diabetes,
or hypothyroidism. The frequency of these variables was compared with the standard coronary
risk factors of family history, hypertension, lipid abnormalities, lifestyle, Type A
behavior, obesity and with diseases such as diabetes and hypothyroidism. An analysis was
made of the strength of these variables for predicting those individuals at risk and whether
there were variables which predict severity of disease based on 1, 2, or 3 vessel
involvement.
The study completion date listed in this record was obtained from the "End Date" entered in
the Protocol Registration and Results System (PRS) record.
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