Aripiprazole for Clozapine Associated Medical Morbidity
Aripiprazole for Clozapine Associated Medical Morbidity
批准号:
7151989
负责人:
DAVID C HENDERSON
金额:
$24.19万
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:
2005-01-01 至 2008-11-30
关键词:
AcuteAdverse effectsAffectAgeAntipsychotic AgentsApolipoproteinsAtherosclerosisBiochemicalBody CompositionBody Weight decreasedBody mass indexC-reactive proteinCholesterolClassClinicalClozapineCombined Modality TherapyDiabetes MellitusDiabetic KetoacidosisDiseaseEatingEffectivenessEnd PointEnergy MetabolismFamily history ofFastingGenderGlucoseGlucose IntoleranceHamilton Rating Scale for DepressionHyperglycemiaHyperinsulinismHyperlipidemiaHypertensionImpairmentInsulinInsulin ResistanceIntercellular adhesion molecule 1InterventionIntravenousLabelLipidsLipoproteinsLiteratureLow-Density LipoproteinsMeasurementMeasuresMedicalMethodsModelingMorbidity - disease rateNon obeseNon-Insulin-Dependent Diabetes MellitusObservational StudyParticle SizePatientsPharmaceutical PreparationsPlasminogen ActivatorPopulationRaceRelative (related person)ReportingResistanceRiskRisperidoneSafetySamplingSchizophreniaScoreSecondary toSedation procedureSmoking StatusSymptomsTestingThinkingTriglyceridesWeekWeightWeight Gainaripiprazoleatypical antipsychoticcardiovascular risk factordensitydepressive symptomsdesigndiabetes riskdiet and exerciseglucose metabolismimprovedindexinginsulin sensitivityinsulin sensitivity/resistancelipid metabolismmedical complicationnovelnovel therapeuticsolanzapineplacebo controlled studypreventresponsesexvon Willebrand Factor
中文摘要
描述(申请人提供):氯氮平仍然是治疗难治性精神分裂症人群中最有效的药物。虽然氯氮平产生的锥体外系副作用较少,但它也不是没有副作用,可能包括镇静和体重增加。在一项为期五年的观察性研究中,我们发现,接受氯氮平治疗的82名患者中有30名(36.6%)患上了糖尿病,同时还观察到体重、总胆固醇和甘油三酯的增加。我们最近完成了一项对36名非肥胖型精神分裂症患者的研究,发现接受氯氮平和奥氮平治疗的非肥胖型患者的胰岛素敏感性和葡萄糖利用异常,表明葡萄糖代谢受损,糖尿病风险增加。我们还对10名接受氯氮平治疗的患者进行了一项为期六周的阿立哌唑辅助治疗开放研究,阿立哌唑是一种非典型的抗精神病药物。观察到空腹甘油三酯、总胆固醇、体重和体重指数(BMI)显著下降。方法:我们对70例服用氯氮平的精神分裂症患者进行为期8周的阿立哌唑辅助治疗的安慰剂对照试验,观察阿立哌唑对脂代谢、糖代谢、身体成分和心血管危险因素的影响。我们将进行一系列症状评分表,以检验联合治疗的临床相关性。意义:这项研究的结果应该有助于阐明阿立哌唑辅助治疗氯氮平患者的有效性,以及高脂血症与胰岛素抵抗和体重的关系。临床辅助治疗可能使阿立哌唑成为治疗精神分裂症和氯氮平相关内科疾病的一种新方法。
英文摘要
DESCRIPTION (provided by applicant): Clozapine remains the most effective agent for the treatment-resistant schizophrenia population. Though clozapine produces fewer extrapyramidal side effects, it is not without side effects, which may include sedation and weight gain. In a five year observational study, we found that 30 of 82 (36.6%) patients treated with clozapine developed diabetes mellitus, and increases in weight, total cholesterol and triglyceride was also observed. We recently completed a study of 36 nonobese schizophrenia patients and found abnormalities in insulin sensitivity and glucose utilization in clozapine- and olanzapine- non-obese treated patients suggesting an impairment of glucose metabolism and increased risk of diabetes. We also conducted a six-week open label study of adjunctive therapy with aripiprazole, an atypical antipsychotic agent, in ten clozapine-treated patients. Significant reductions in fasting triglyceride, total cholesterol, weight and body mass index (BMI) were observed. Method: We propose an eight week, placebo-controlled trial of aripiprazole for adjunctive therapy in 70 clozapine-treated schizophrenia subjects to examine aripiprazole's affect on lipid metabolism, glucose metabolism, and body composition and cardiovascular risk factors. We will perform a battery of symptoms scales to exam clinical correlates of combination therapy. Significance: The results of this study should help clarify the usefulness of adjunctive therapy with aripiprazole in clozapine-treated patients and the relationship of hyperlipidemia to insulin resistance and weight. Clinical adjunctive therapy may establish aripiprazole as a new therapeutic approach in schizophrenia and clozapine-associated medical disorders.
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CLINICAL TRIAL: ARIPIPRAZOLE FOR CLOZAPINE ASSOCIATED MEDICAL MORBIDITY
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批准号:7731263
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项目类别:
-
资助金额:$0.45万
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财政年份:2008
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负责人:DAVID C HENDERSON
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依托单位:
ARIPIPRAZOLE FOR CLOZAPINE ASSOCIATED MEDICAL MORBIDITY
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批准号:7731320
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项目类别:
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资助金额:$0.26万
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财政年份:2008
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负责人:DAVID C HENDERSON
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依托单位:
ARIPIPRAZOLE FOR CLOZAPINE ASSOCIATED MEDICAL MORBIDITY
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批准号:7607075
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项目类别:
-
资助金额:$1.25万
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财政年份:2006
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负责人:DAVID C HENDERSON
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依托单位:
ROSIGLITAZONE FOR CLOZAPINE INDUCED GLUCOSE METABOLISM IMPAIRMENT
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批准号:7607033
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项目类别:
-
资助金额:$0.03万
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财政年份:2006
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负责人:DAVID C HENDERSON
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依托单位:
ARIPIPRAZOLE FOR CLOZAPINE ASSOCIATED MEDICAL MORBIDITY
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批准号:7607116
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项目类别:
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资助金额:$0.58万
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财政年份:2006
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负责人:DAVID C HENDERSON
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依托单位:
ARIPIPRAZOLE FOR CLOZAPINE ASSOCIATED MEDICAL MORBIDITY
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批准号:7374767
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项目类别:
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资助金额:$0.12万
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财政年份:2005
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负责人:DAVID C HENDERSON
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依托单位:
ARIPIPRAZOLE FOR CLOZAPINE ASSOCIATED MEDICAL MORBIDITY
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批准号:7374793
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项目类别:
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资助金额:$1.56万
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财政年份:2005
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负责人:DAVID C HENDERSON
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依托单位:
Aripiprazole for Clozapine Associated Medical Morbidity
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批准号:6999284
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项目类别:
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资助金额:$24.92万
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财政年份:2005
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负责人:DAVID C HENDERSON
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依托单位:
Aripiprazole for Clozapine Associated Medical Morbidity
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批准号:6851846
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项目类别:
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资助金额:$25.52万
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财政年份:2005
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负责人:DAVID C HENDERSON
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依托单位:
INSULIN SENSITIVITY, INSULIN SECRETION & GLUCOSE UTIL IN SCHIZOPHRENIC PATIENTS
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批准号:7205031
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项目类别:
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资助金额:$0.48万
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财政年份:2004
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负责人:DAVID C HENDERSON
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依托单位:
ROSIGLITAZONE FOR CLOZAPINE INDUCED GLUCOSE METABOLISM IMPAIRMENT
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批准号:7205076
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项目类别:
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资助金额:$1.86万
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财政年份:2004
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负责人:DAVID C HENDERSON
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依托单位:
ROSIGLITAZONE FOR CLOZAPINE INDUCED GLUCOSE METABOLISM IMPAIRMENT
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批准号:6982600
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项目类别:
-
资助金额:$0.33万
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财政年份:2003
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负责人:DAVID C HENDERSON
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依托单位:
INSULIN SENSITIVITY, INSULIN SECRETION & GLUCOSE UTIL. IN SCHIZOPHRENIC PATIENTS
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批准号:6982543
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项目类别:
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资助金额:$1.05万
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财政年份:2003
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负责人:DAVID C HENDERSON
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依托单位:
Insulin Sensitivity/Secretion/ Glucose in Schizophrenia
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批准号:6586429
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项目类别:
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资助金额:$20.08万
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财政年份:2002
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负责人:DAVID C HENDERSON
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依托单位:
Insulin Sensitivity/Secretion/ Glucose in Schizophrenia
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批准号:6574396
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项目类别:
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资助金额:$20.08万
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财政年份:2001
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负责人:DAVID C HENDERSON
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依托单位:
Insulin Sensitivity/Secretion/ Glucose in Schizophrenia
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批准号:6505199
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项目类别:
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资助金额:$20.08万
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财政年份:2000
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负责人:DAVID C HENDERSON
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依托单位:
HIGH SPEED SOLUTION SWITCHER FOR ELECTROPHYSIOLOGY
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批准号:2713839
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项目类别:
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资助金额:$9.99万
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批准号:6431890
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批准号:8565320
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项目类别:
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财政年份:--
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负责人:DAVID C HENDERSON
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负责人:DAVID C HENDERSON
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