Treatment Prediction in Adolescent and Adult Depression
Treatment Prediction in Adolescent and Adult Depression
批准号:
7884287
负责人:
UMA RAO
金额:
$31.15万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2004
资助国家:
美国
项目状态:
已结题
起止时间:
2004-06-09 至 2014-03-31
关键词:
AccountingAdolescentAdrenal GlandsAdultAntidepressive AgentsBrainBupropionChildClinicalClinical TreatmentDataDepressed moodDepressive disorderDevelopmentDoseEarly identificationEarly treatmentEconomicsFailureHealth BenefitHumanHydrocortisoneHypothalamic structureIndividualInterventionInvestigationLaboratoriesLife ExperienceLife StressLong-Term EffectsMasksMeasuresMental DepressionMental HealthMood DisordersMorbidity - disease rateNatural HistoryNeurobiologyPatientsPharmaceutical PreparationsPituitary GlandPlacebosPopulationPsychosocial StressPublic HealthREM SleepRecoveryRecurrenceReportingResearch PersonnelResponse LatenciesRiskSelective Serotonin Reuptake InhibitorSleepSocial FunctioningSocial supportStagingStressTimeVariantYouthbasecompliance behaviordepressive symptomseffective interventioneffective therapyimprovedmortalitynovelprogramspsychosocialrapid eye movementresponsetreatment responsetreatment strategyurinary
中文摘要
点击翻译按钮获取中文摘要
英文摘要
Although there is growing evidence for continuities in adolescent and adult depression, with similarities in
clinical presentation and natural history, maturational differences also have been highlighted. Specifically,
several studies reported greater variations in electroencephalographic (EEG) sleep changes, hypothalamic-
pituitary-adrenal (HPA) activity and antidepressant (AD) response in depressed adolescents compared with
the findings in adults. This proposal aims to understand the mechanism(s) underlying these developmental
differences and to develop a strategy for use in identifying those patients, both youngsters and adults, who
might benefit from AD treatment in general, and from bupropion treatment in particular.
Based on the results of preliminary studies conducted in our laboratory, this investigation proposes to predict
AD response to sustained-release bupropion in depressed adolescents and adults by assessing rapid eye
movement (REM) sleep and HPA activity responses to single-dose bupropion administration prior to initiating
treatment. Following completion of the sleep and neuroendrocrine assessments, subjects will receive clinical
treatment with sustained-release bupropion for 8 weeks. In addition to examining the strength of association
between REM sleep (and HPA) response to the bupropion challenge and clinical response to the drug,
psychosocial measures (specifically stressful life experiences and social support) will be obtained in order to
assess their contribution to AD response, both singly and in combination with the neurobiological measures.
Bupropion was selected specifcally because of its relatively subtle effects on REM sleep compared with the
other AD compounds (tricyclic agents and selective serotonin reuptake inhibitors, in particular). The robust
REM sleep suppression induced by the other AD compounds might mask inter-individual variability; inherent
differences in sensitivity that relate to treatment response could be lost due to a "ceiling effect".
Adolescent depression is a major public health problem that not only relates to the younger population, but
also for the long-term mental health and social functioning of adults. Because depression in youngsters is
associated with serious morbidity and mortality, and since it marks the gateway into recurrent mood
disorders in a large proportion of adults, the early identification and effective treatment of depression in
youngsters is of utmost importance. Because the long-term effects of AD agents on the developing human
brain are not known, and because initial treatment can influence subsequent treatment compliance and
clinical course, the identification of depressed youth who would (or would not) benefit from treatment with AD
drugs is crucial. Results of the proposed study should not only be helpful in developing novel and more
effective AD drugs and treatment strategies for youngsters, but also will enhance our understanding of the
neurobiology of inadequate AD response in some adult patients with depression.
期刊论文(0)
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科研奖励(0)
会议论文
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依托单位:
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依托单位:
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依托单位:
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项目类别:
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负责人:UMA RAO
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依托单位:
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依托单位:
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海外基金