The Effects of Rosiglitazone in Patients with MCI
The Effects of Rosiglitazone in Patients with MCI
批准号:
7924266
负责人:
SUZANNE CRAFT
金额:
$9.97万
依托单位国家:
美国
项目类别:
财政年份:
2005
资助国家:
美国
项目状态:
已结题
起止时间:
2005-09-30 至 2010-06-30
关键词:
AdultAffectAgonistAlzheimer disease preventionAlzheimer&aposs DiseaseAlzheimer&aposs disease riskAmyloid beta-ProteinAnti-Inflammatory AgentsAnti-inflammatoryAtrophicBiological MarkersBiological MarkersCerebrospinal FluidClinical TrialsCognitionCognitiveControlled Clinical TrialsDataDementiaDiseaseEconomic BurdenEnergy MetabolismEpidemiologic StudiesExhibitsFutureGlucose TransporterHypertensionImpaired cognitionImpairmentInflammationInflammatoryInsulinInsulin ReceptorInsulin ResistanceInterventionLinkMagnetic Resonance ImagingMeasuresMedialMemoryNon-Insulin-Dependent Diabetes MellitusPPAR gammaParticipantPathologyPatientsPeptidesPeripheralPeroxisome Proliferator-Activated ReceptorsPersonsPhasePlacebo ControlPlacebosPlasmaPlayPropertyRandomizedResearchRiskRoleSpinal PunctureStagingStructureTemporal LobeTestingcognitive functionimprovedinsulin sensitivitymild neurocognitive impairmentnovelpreventrosiglitazonesocialtreatment strategy
中文摘要
描述(由申请人提供):拟议的安慰剂对照临床试验将检验罗格列酮,一种具有胰岛素增敏和抗炎特性的过氧化物酶体增殖激活受体- γ (ppar - γ)激动剂,改善遗忘性轻度认知障碍(MCI)患者的记忆的假设。100名参与者将被随机分配接受18个月的罗格列酮或安慰剂治疗,每隔6个月进行一次认知评估。他们还将在治疗前和治疗结束时接受一系列结构磁共振成像(MRI)检查,以确定罗格列酮是否能改善支持记忆的内侧颞叶(MTL)结构的萎缩速度。一部分参与者将在治疗前后接受腰椎穿刺,以确定罗格列酮是否会影响与AD相关的脑脊液(CSF)生物标志物水平。该试验将提供关于改善胰岛素敏感性、降低外周胰岛素水平和减少炎症对遗忘性轻度认知损伤(可能是阿尔茨海默病(AD)的前驱期)的认知功能和生物标志物的影响的有价值的数据。最重要的是,这项试验将阐明一种新的治疗方法的可行性和潜在疗效,这种方法可能预防或推迟AD的发病。这样,我们将为未来ppar - γ激动剂的全面临床试验奠定基础。
英文摘要
DESCRIPTION (provided by applicant): The proposed placebo-controlled clinical trial will test the hypothesis that rosiglitazone, a peroxisome proliferator-activated receptor-gamma (PPAR-gamma) agonist with insulin-sensitizing and anti-inflammatory properties, improves memory in persons with amnestic mild cognitive impairment (MCI). One hundred participants will be randomly assigned to receive 18 months of treatment with rosiglitazone or placebo, with cognitive assessment at 6 month intervals. They will also undergo serial structural magnetic resonance imaging (MRI) prior to and at the end of treatment to determine whether rosiglitazone ameliorates the rate of atrophy in medial temporal lobe (MTL) structures supporting memory. A subset of participants will receive lumbar punctures before and following treatment to determine whether rosiglitazone affects cerebrospinal fluid (CSF) levels of biomarkers associated with AD. This trial will provide valuable data regarding the effects of improved insulin sensitivity, reduced peripheral insulin levels, and reduced inflammation on cognitive function and biological markers in amnestic MCI, a likely prodromal phase of Alzheimer's disease (AD). Most importantly, this trial will elucidate the feasibility and potential efficacy of a novel treatment that may prevent or postpone the onset of AD. In doing so, we will lay the groundwork for future full-scale clinical trials of PPAR-gamma, agonists.
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