METABOLIC EFFECTS OF ANTIHYPERTENSIVE DRUGS
METABOLIC EFFECTS OF ANTIHYPERTENSIVE DRUGS
批准号:
7950743
负责人:
RHONDA DEHOFF
金额:
$0.3万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2008
资助国家:
美国
项目状态:
已结题
起止时间:
2008-12-01 至 2009-07-31
关键词:
Angiotensin-Converting Enzyme InhibitorsAntihypertensive AgentsAttenuatedClinical ResearchComputer Retrieval of Information on Scientific Projects DatabaseDataDiabetes MellitusDiureticsFundingFutureGenetic PolymorphismGrantHypertensionInstitutionInsulin ResistanceInvestigationKCNJ1 geneKnowledgeLaboratoriesMetabolicMetabolic syndromePatientsPatternPeptidyl-Dipeptidase APharmacogenomicsRenin-Angiotensin SystemResearchResearch PersonnelResourcesRiskRoleSourceThiazide DiureticsUnited States National Institutes of Healthattenuationbasecohortdesignresponse
中文摘要
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英文摘要
This subproject is one of many research subprojects utilizing the
resources provided by a Center grant funded by NIH/NCRR. The subproject and
investigator (PI) may have received primary funding from another NIH source,
and thus could be represented in other CRISP entries. The institution listed is
for the Center, which is not necessarily the institution for the investigator.
Patients with metabolic syndrome, characterized primarily by insulin resistance are at increased risk of developing diabetes and often have hypertension-HTN. Thiazide diuretics are recommended for treating HTN in patients with metabolic syndrome, despite being associated with metabolic disturbances that result in increased insulin resistance. The major hypothesis of this study is that in patients with metabolic syndrome and HTN, blockade of the renin-angiotensin system-RAS with an angiotensin converting enzyme-ACE inhibitor attenuates the adverse metabolic effects of a thiazide diuretic. Specific aims are designed to investigate whether this attenuation occurs after the addition of ACE inhibitor to diuretic and/or as a consequence of pretreatment with an ACE inhibitor. Also, laboratory based pharmacogenomic investigations will be conducted in a separate cohort of 6000 hypertensive CAD patients to identify polymorphisms associated with diabetes in the ACE, ADD1 and KCNJ1 genes, selected on the basis of their critical role in ACE inhibitor and diuretic response. This research seeks to overcome gaps in knowledge regarding the metabolic impact of antihypertensive drugs in patients with metabolic syndrome and will provide data to influence future prescribing patterns.
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