Genetic Determinants: Low HDL, High Triglycerides, Obes*
Genetic Determinants: Low HDL, High Triglycerides, Obes*
批准号:
6535479
负责人:
ROBERT W. MAHLEY
金额:
$18.0万
依托单位国家:
美国
项目类别:
财政年份:
2002
资助国家:
美国
项目状态:
已结题
起止时间:
2002-04-01 至 2004-03-31
关键词:
Middle East cardiovascular disorder risk clinical research diabetes mellitus genetics gender difference genetic mapping genetic polymorphism genetic susceptibility high density lipoproteins human genetic material tag human population genetics human tissue hyperlipidemia insulin sensitivity /resistance metabolic syndrome metabolism disorder obesity racial /ethnic difference reporter genes syndrome tissue /cell culture
中文摘要
点击翻译按钮获取中文摘要
英文摘要
DESCRIPTION (provided by applicant):
Over the past 10 years, extensive studies have been conducted in Turkey to
determine the risk factors for heart disease. Studies involving approximately
10,000 Turkish men and women from six different regions of Turkey have
established that this population is unique in several ways. The Turks have the
lowest plasma levels of high density lipoprotein cholesterol (HDL-C) of almost
any population in the world (75 percent of the men and 50 percent of the women
have HDL-C levels <40 mg/dl). The mean HDL-C levels are 10-15 mg/dl lower
than those in Western European or American populations. In addition, Turks,
especially Turkish women, have a tendency toward obesity [38.8 percent of the
women have body mass index (BMI) >30 kg/M2], and both men and women have a
tendency toward hypertriglyceridemia. The low HDL-C, however, is independent
of obesity or hypertriglyceridemia. Samples from this well-characterized
population provide a unique opportunity to explore the genetic determinants
associated with the high prevalence of low HDL-C, hypertriglyceridemia, and
obesity (characteristics of the metabolic syndrome).
This project will analyze DNA from frozen blood samples to investigate new
candidate gene targets that may provide insights into the abnormalities
characterizing this population. The samples and extensive biodata are
available on all 10,000 participants. In Specific Aim 1, we will identify
polymorphisms in acyl CoA:diacylglycerol acyltranferase (DGAT)- I and -2 and
in ATP-binding cassette A I (ABCA I) genes that are associated with
differences in BMI, HDL-C, and triglyceride concentration, and other
parameters such as blood pressure. These studies will focus significantly on
promoter and coding sequence polymorphisms in DGAT-I and -2 and ABCAL In
Specific Aim 2, we will determine whether the polymorphisms have functional
significance by using a luciferase reporter system to determine expression of
polymorphic forms of DGAT and ABCAI, a cholesterol efflux measurement to
determine the functional significance of ABCAI coding sequence polymorphic
sites, and a triglyceride synthesis assay to determine the functional
significance of DGAT-I and -2 polymorphic sites. The polymorphic site
association studies will be performed on DNA samples from three subgroups of
Turks: (a) individuals likely to have the metabolic syndrome, (b) individuals
with isolated low HDL-C (normal triglycerides), and (c) normolipidemic
unaffected controls.
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会议论文
Somatostatin (SST)-GABAergic Interneuron Therapy for Alzheimer's Disease with ApoE4
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批准号:9893103
-
项目类别:
-
资助金额:$98.21万
-
财政年份:2019
-
负责人:ROBERT W. MAHLEY
-
依托单位:
Develop GABAergic Neuron Protectors for Treating ApoE4-Related Alzheimer's Disease
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批准号:10056515
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项目类别:
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资助金额:$107.96万
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财政年份:2019
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负责人:ROBERT W. MAHLEY
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依托单位:
Somatostatin (SST)-GABAergic Interneuron Therapy for Alzheimer's Disease with ApoE4
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批准号:10011752
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项目类别:
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资助金额:$94.86万
-
财政年份:2019
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负责人:ROBERT W. MAHLEY
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依托单位:
ApoE4 Structure Correctors as a Therapeutic Approach for Alzheimers Disease
-
批准号:8460847
-
项目类别:
-
资助金额:$4.55万
-
财政年份:2012
-
负责人:ROBERT W. MAHLEY
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依托单位:
Targeting ApoE4 as a Therapeutic Strategy for Alzheimer's Disease
-
批准号:8549072
-
项目类别:
-
资助金额:$81.86万
-
财政年份:2012
-
负责人:ROBERT W. MAHLEY
-
依托单位:
ApoE4 Structure Correctors as a Therapeutic Approach for Alzheimers Disease
-
批准号:8328029
-
项目类别:
-
资助金额:$4.69万
-
财政年份:2012
-
负责人:ROBERT W. MAHLEY
-
依托单位:
Targeting ApoE4 as a Therapeutic Strategy for Alzheimer's Disease
-
批准号:8420245
-
项目类别:
-
资助金额:$85.22万
-
财政年份:2012
-
负责人:ROBERT W. MAHLEY
-
依托单位:
Role of apoE structure and metabolism in neurodegeneration
-
批准号:8235856
-
项目类别:
-
资助金额:$37.26万
-
财政年份:2008
-
负责人:ROBERT W. MAHLEY
-
依托单位:
Role of apoE structure and metabolism in neurodegeneration
-
批准号:8036997
-
项目类别:
-
资助金额:$37.26万
-
财政年份:2008
-
负责人:ROBERT W. MAHLEY
-
依托单位:
APOLIPOPROTEIN E IN NEUROBIOLOGY: CELLULAR MECHANISMS
-
批准号:7431632
-
项目类别:
-
资助金额:$31.52万
-
财政年份:2007
-
负责人:ROBERT W. MAHLEY
-
依托单位:
Targeting Apolipoprotein E4-related Neuropathology
-
批准号:6752398
-
项目类别:
-
资助金额:$25.15万
-
财政年份:2003
-
负责人:ROBERT W. MAHLEY
-
依托单位:
Targeting Apolipoprotein E4-related Neuropathology
-
批准号:6673321
-
项目类别:
-
资助金额:$21.26万
-
财政年份:2003
-
负责人:ROBERT W. MAHLEY
-
依托单位:
EXTRAMULAR RESEARCH FACILITIES CONSTRUCTION
-
批准号:6718598
-
项目类别:
-
资助金额:$209.38万
-
财政年份:2003
-
负责人:ROBERT W. MAHLEY
-
依托单位:
Genetic Determinants: Low HDL, High Triglycerides, Obes*
-
批准号:6637876
-
项目类别:
-
资助金额:$18.0万
-
财政年份:2002
-
负责人:ROBERT W. MAHLEY
-
依托单位:
APOLIPOPROTEIN E ISOFORM EFFECTS IN TRANSGENIC ANIMALS
-
批准号:6496758
-
项目类别:
-
资助金额:$24.35万
-
财政年份:2001
-
负责人:ROBERT W. MAHLEY
-
依托单位:
CORE--METABOLISM AND PATHOLOGY
-
批准号:6496762
-
项目类别:
-
资助金额:$24.35万
-
财政年份:2001
-
负责人:ROBERT W. MAHLEY
-
依托单位:
CORE--METABOLISM AND PATHOLOGY
-
批准号:6353064
-
项目类别:
-
资助金额:$26.61万
-
财政年份:2000
-
负责人:ROBERT W. MAHLEY
-
依托单位:
APOLIPOPROTEIN E ISOFORM EFFECTS IN TRANSGENIC ANIMALS
-
批准号:6353060
-
项目类别:
-
资助金额:$26.61万
-
财政年份:2000
-
负责人:ROBERT W. MAHLEY
-
依托单位:
APOLIPOPROTEIN E ISOFORM EFFECTS IN TRANSGENIC ANIMALS
-
批准号:6202341
-
项目类别:
-
资助金额:$26.61万
-
财政年份:1999
-
负责人:ROBERT W. MAHLEY
-
依托单位:
CORE--METABOLISM AND PATHOLOGY
-
批准号:6202345
-
项目类别:
-
资助金额:$26.61万
-
财政年份:1999
-
负责人:ROBERT W. MAHLEY
-
依托单位: