Predictors of Treatment Response Relapse and Recurrence in Major Depression
重度抑郁症治疗反应复发和复发的预测因素
基本信息
- 批准号:8053288
- 负责人:
- 金额:$ 134.35万
- 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
- 起止时间:2008-04-02 至 2013-03-31
- 项目状态:已结题
- 来源:
- 关键词:AchievementAcuteAdultAgeAllelesAntidepressive AgentsAwardBehaviorBehavioralBrain imagingCellular NeurobiologyClinical TrialsCognitive TherapyCombination Drug TherapyCombined Modality TherapyCommunicable DiseasesCommunitiesDSM-IVDepressed moodDepression and SuicideDevelopmentDiseaseDisease remissionDisease susceptibilityEndocrineEnvironmentEscitalopramEvaluationFeelingFunctional Magnetic Resonance ImagingFundingGeneticGenetic PolymorphismGlucocorticoid ReceptorGoalsGrantImageImaging TechniquesImmuneIndividualLifeLong-Term EffectsMaintenanceMajor Depressive DisorderMeasuresMedicalMedicineMental DepressionMolecular ChaperonesMolecular NeurobiologyMorbidity - disease rateNational Institute of Mental HealthNatureNeurosecretory SystemsOutcomePatientsPatternPersonalityPersonality DisordersPharmaceutical PreparationsPharmacotherapyProbabilityPsychotherapyRandomizedRecurrenceRelapseRestRiskSample SizeScanningScienceScience of geneticsSelective Serotonin Reuptake InhibitorSubstance abuse problemSyndromeTimeTreatment ProtocolsVariantWorkarmbasechronic depressiondepressive symptomsdesigndevelopmental neurobiologydisabilityduloxetineimprovedmortalityneurochemistrynon-drugoncologypromoterrelating to nervous systemserotonin transportertreatment effecttreatment programtreatment responsetreatment trial
项目摘要
DESCRIPTION (provided by applicant): Major depression (MDD) is a highly prevalent disorder associated with significant morbidity and mortality and is estimated to be one of the leading causes of disability worldwide. The DSM-IV defined syndrome of MDD is a heterogeneous disorder characterized by a range of distinctive genetic, neural, and neuroendocrine diatheses and abnormalities. At the same time, individuals live and grow within an environment that influences developmental neurobiology, neurochemistry, and patterns of thought, feeling and behavior that further impact their vulnerability to the development of MDD. A variety of antidepressant drugs, psychotherapies, and non- drug somatic therapies have been demonstrated to be efficacious in acute treatment trials. The majority of patients in these trials, however, do not attain remission, increasing the risk for the development of chronic depression, suicide, substance abuse and several serious medical disorders. A major unmet need is the identification of predictors of remission to treatments, as has been utilized in other branches of medicine (e.g., oncology and infectious disease) to improve patient outcome. In view of advances in functional brain imaging, molecular and cellular neurobiology, genetics, and personality disorders and a number of promising findings in small studies, it is propitious to conduct studies to determine whether a concatenation of these factors predict antidepressant treatment remission as well as relapse and recurrence. In this application, we propose two studies. The first study is an expansion of our recently funded NIMH CIDAR 3-arm, 12-week treatment trial; we will increase the CIDAR sample size from 400 to 600 and follow all remitted patients for a total of two years. In this expanded study, 600 treatment na¿ve adult depressed patients will be randomized to one of the following treatments: 1) escitalopram, an SSRI; 2) duloxetine, an SNRI; and 3) CBT. The primary goal of the CIDAR is to employ a multivariate approach to predict remission following acute treatment with a single therapy. The primary purpose of study of this proposal is to identify predictors of relapse and recurrence during the 21 months following remission to these three monotherapy treatments. The second study is designed to study prediction of short-term and long-term effects of additional pharmacotherapy and psychotherapy combination treatments for those who fail to remit with monotherapy. Our group has made a number of advances in identifying imaging procedures (e.g., resting BOLD fMRI), genetic polymorphisms, and personality disorder measures that predict remission, relapse, and recurrence of MDD. In addition, we will employ additional state- of-the-science measures of MDD and its treatment. Statistically, we will seek to determine which measure and/or combination of measures leads to prediction of remission, relapse, and recurrence to the treatments under study. Delineation of predictors of treatment remission, relapse, and recurrence of MDD will dramatically improve patient outcomes and reduce the risk of inadequate treatment. Major Depressive Disorder has a lifetime occurrence rate of 16% and is among the most frequent and debilitating of all medical disorders. Despite considerable advances in understanding the causes, nature, and treatment of depression, we still do not know which treatment will work for an individual patient. As a result of the proposed studies, it is hoped that the community clinician of tomorrow will be able to prescribe a specific treatment for an individual patient with major depression, with confidence that the prescribed treatment will provide effective and lasting relief from the symptoms of depression.
描述(由申请人提供):重度抑郁症(MDD)是一种高度流行的疾病,与显著的发病率和死亡率相关,估计是全球残疾的主要原因之一。DSM-IV定义的MDD综合征是一种异质性疾病,其特征在于一系列独特的遗传、神经和神经内分泌素质和异常。与此同时,个体在影响发育神经生物学、神经化学以及思维、感觉和行为模式的环境中生活和成长,这进一步影响了他们对MDD发展的脆弱性。各种抗抑郁药物、心理疗法和非药物躯体疗法在急性治疗试验中已被证明有效。然而,这些试验中的大多数患者没有获得缓解,增加了慢性抑郁症、自杀、药物滥用和几种严重医学疾病的发展风险。一个主要的未满足的需求是确定治疗缓解的预测因子,如在其他医学分支中所使用的(例如,肿瘤学和传染病)以改善患者结果。鉴于脑功能成像、分子和细胞神经生物学、遗传学和人格障碍的进展,以及小型研究中一些有希望的发现,进行研究以确定这些因素的串联是否预测抗抑郁药治疗缓解以及复发和复发是有利的。在本申请中,我们提出了两项研究。第一项研究是我们最近资助的NIMH CIDAR 3组12周治疗试验的扩展;我们将CIDAR样本量从400增加到600,并对所有缓解患者进行为期两年的随访。在这项扩展研究中,600名未经治疗的成年抑郁症患者将随机接受以下治疗之一:1)艾司西酞普兰,一种SSRI; 2)度洛沙坦,一种SNRI; 3)CBT。CIDAR的主要目标是采用多变量方法预测单一疗法急性治疗后的缓解。本研究的主要目的是确定这三种单药治疗缓解后21个月内复发和复发的预测因素。第二项研究的目的是研究预测短期和长期的影响,额外的药物治疗和心理治疗联合治疗那些谁不能缓解与单药治疗。我们小组在识别成像程序方面取得了许多进展(例如,静息BOLD fMRI)、遗传多态性和人格障碍测量,可预测MDD的缓解、复发和复发。此外,我们将采用其他MDD及其治疗的科学方法。在统计学上,我们将寻求确定哪种测量和/或测量组合导致对所研究的治疗的缓解、复发和复发的预测。描述MDD治疗缓解、复发和复发的预测因子将显著改善患者结局并降低治疗不充分的风险。重度抑郁症的终生发生率为16%,是所有医学疾病中最常见和最令人衰弱的疾病之一。尽管在了解抑郁症的原因、性质和治疗方面取得了相当大的进展,但我们仍然不知道哪种治疗方法对个体患者有效。作为拟议研究的结果,希望明天的社区临床医生能够为重度抑郁症患者开出具体的治疗方案,并相信所开的治疗方案将有效和持久地缓解抑郁症的症状。
项目成果
期刊论文数量(0)
专著数量(0)
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W. EDWARD CRAIGHEAD其他文献
W. EDWARD CRAIGHEAD的其他文献
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{{ truncateString('W. EDWARD CRAIGHEAD', 18)}}的其他基金
Multi-level Mechanisms of Behavioral Activation Therapy for Adolescent Depression
青少年抑郁症行为激活疗法的多层次机制
- 批准号:
10617351 - 财政年份:2022
- 资助金额:
$ 134.35万 - 项目类别:
Multi-level Mechanisms of Behavioral Activation Therapy for Adolescent Depression
青少年抑郁症行为激活疗法的多层次机制
- 批准号:
10453989 - 财政年份:2022
- 资助金额:
$ 134.35万 - 项目类别:
Predictors of Treatment Response Relapse and Recurrence in Major Depression
重度抑郁症治疗反应复发和复发的预测因素
- 批准号:
7599071 - 财政年份:2008
- 资助金额:
$ 134.35万 - 项目类别:
Predictors of Treatment Response Relapse and Recurrence in Major Depression
重度抑郁症治疗反应复发和复发的预测因素
- 批准号:
8249145 - 财政年份:2008
- 资助金额:
$ 134.35万 - 项目类别:
Predictors of Treatment Response Relapse and Recurrence in Major Depression
重度抑郁症治疗反应复发和复发的预测因素
- 批准号:
7793366 - 财政年份:2008
- 资助金额:
$ 134.35万 - 项目类别:
Prevention of depression among adolescents in Iceland
冰岛青少年抑郁症的预防
- 批准号:
6680224 - 财政年份:2003
- 资助金额:
$ 134.35万 - 项目类别:
Prevention of depression among adolescents in Iceland
冰岛青少年抑郁症的预防
- 批准号:
6801115 - 财政年份:2003
- 资助金额:
$ 134.35万 - 项目类别:
PREVENTION OF RECURRENCE OF MAJOR DEPRESSIVE BEHAVIOR
预防重度抑郁行为复发
- 批准号:
6392452 - 财政年份:2000
- 资助金额:
$ 134.35万 - 项目类别:
PREVENTION OF RECURRENCE OF MAJOR DEPRESSIVE BEHAVIOR
预防重度抑郁行为复发
- 批准号:
6130582 - 财政年份:2000
- 资助金额:
$ 134.35万 - 项目类别:
PREVENTION OF RECURRENCE OF MAJOR DEPRESSIVE BEHAVIOR
预防重度抑郁行为复发
- 批准号:
6598491 - 财政年份:2000
- 资助金额:
$ 134.35万 - 项目类别:
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