Machine Learning and Personalized Prognosis for Depression Treatment
Machine Learning and Personalized Prognosis for Depression Treatment
批准号:
9168157
负责人:
CHRISTOPHER G BEEVERS
金额:
$23.44万
依托单位国家:
美国
项目类别:
财政年份:
2016
资助国家:
美国
项目状态:
已结题
起止时间:
2016-07-01 至 2018-05-31
关键词:
AdvocateAlgorithmsCitalopramClinicalClinical TrialsCoinComplexDataData SetDatabasesDecision TreesDevelopmentGoalsHealthInternetInterventionLogistic RegressionsMachine LearningMeasuresMental DepressionMental HealthMethodsModelingMulti-Institutional Clinical TrialNoiseOnline SystemsPatientsPharmaceutical PreparationsProbabilityPublic HealthRecommendationSample SizeSamplingSelection for TreatmentsStatistical MethodsSymptomsSystemTechniquesTestingTrainingTreatment CostTreatment EfficacyTreatment outcomeUnited StatesUnited States National Institutes of HealthUpdateValidationabstractingbaseclinical practiceeffective therapyhealth care availabilityimprovedinformation modellearning strategynoveloutcome forecastpersonalized medicineprecision medicinepredicting responsepsychologicresponsesuccesstreatment response
中文摘要
摘要
抑郁症的治疗对大约50%-60%的接受治疗的患者有效,但
在治疗开始之前,成功应答的概率通常是未知的。其结果是,抑郁症
治疗通常以反复试验的方式进行,直到获得满意的反应。我们的
目的是通过应用集成机器学习技术来提供个性化的预测
多个弱预测因子的新颖、非线性组合,共同产生准确的
治疗结果。这种统计方法同时考虑了许多预测变量,并且
迭代地构建复杂的预测模型,该模型通常显著优于传统统计模型
方法:研究方法。目标1是应用随机梯度增强决策树来预测西酞普兰的疗效。
STAR*D临床试验的档案数据。在初步分析中,我们随机选择了1223名患者
训练该模型和另外407名患者独立测试该模型(75:25),并进行调整
通过交叉验证选择的参数,以将原木损失降至最低。对独立测试的结果预测
样本优于无信息率(p<;0.001),总体预测准确率为66%。
尽管这一水平的预测明显好于无信息模型,但我们计划改进
通过以下方式预测模型:1)添加捕捉并发(非
研究)药物使用和2)基于早期反应迹象的更新模型预测。目标2是使用一个
类似的机器学习方法来检查抑郁症患者对基于互联网的CBT的反应。基于互联网的
抑郁症的治疗越来越受欢迎,提供了有效的医疗保健途径,减少了治疗
成本,并有很好的证据证明治疗效果。重要的是,我们有一个大型数据集(N=1,013
以开发基于患者属性预测治疗反应的治疗匹配算法。
研究影响:该项目的总体目标是使用机器学习方法来开发治疗方法
匹配算法。从长远来看,我们可以设想一个系统,根据许多因素对患者进行评估
重要的预测变量,并提供个人化的治疗成功概率。这些概率
然后用于指导治疗选择或在预测到不良反应的情况下修改当前治疗。
开发算法,成功预测一种特定形式的治疗是否可能成功
对于拥有一组给定属性的患者来说,这将是朝着高效和个性化迈出的巨大一步
抑郁症治疗。
英文摘要
Abstract
Depression treatment is effective for approximately 50-60% of patients who receive treatment, but the
probability of a successful response is typically unknown before treatment begins. As a result, depression
treatment is routinely delivered in a trial-and-error fashion until a satisfactory response is achieved. Our
objective is to provide a personalized prognosis by applying ensemble machine learning techniques to discover
novel, non-linear combinations of multiple weak predictors that collectively yield accurate predictions of
treatment outcome. This statistical approach considers many prediction variables simultaneously and
iteratively constructs a complex prediction model that often dramatically outperforms traditional statistical
methods. Aim 1 is to apply stochastic gradient boosted decision trees to predict response to citalopram using
archival data from the STAR*D clinical trial. In preliminary analyses, we randomly selected 1223 patients to
train the model and another 407 patients to independently test the model (a 75-25 split), with tuning
parameters selected by cross-validation to minimize log-loss. The resulting prediction on the independent test
sample was superior to the no-information rate (p < 0.001), with an overall predictive accuracy of 66%.
Although this level of prediction is significantly better than a no information model, we plan to improve the
model's prognostication by 1) adding features that capture the “pharmacological noise” of concurrent (non-
study) medication use and 2) updating model predictions based on early signs of response. Aim 2 is to use a
similar machine learning approach to examine response to internet-based CBT for depression. Internet-based
treatments for depression are growing in popularity, provide efficient access to health care, reduce treatment
costs, and have good evidence for treatment efficacy. Importantly, we have a large dataset (N = 1,013) within
which to develop treatment-matching algorithms that predict treatment response based on patient attributes.
Study Impact: The overarching goal of this project is to use machine learning methods to develop treatment
matching algorithms. In the long term, we can envision a system that evaluates a patient on a number of
important predictor variables and provides a personalized probability of treatment success. These probabilities
would then be used to guide treatment selection or modify current treatment if a poor response is predicted.
Developing algorithms that successfully predict whether a particular form of treatment is likely to be successful
for a patient with a given set of attributes would be a tremendous step towards efficient and personalized
depression treatment.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
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批准号:10726299
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项目类别:
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财政年份:2023
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Perceptual and decisional processes underlying face perception biases in clinical depression
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Genetic Influences on Dual Processing Modes of Reward and Punishment Learning
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Genetic Influences on Dual Processing Modes of Reward and Punishment Learning
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财政年份:2012
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Genetic Influences on Dual Processing Modes of Reward and Punishment Learning
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批准号:8599762
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财政年份:2012
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负责人:CHRISTOPHER G BEEVERS
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依托单位:
Genetic Influences on Dual Processing Modes of Reward and Punishment Learning
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批准号:8478300
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项目类别:
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资助金额:$2.07万
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财政年份:2012
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负责人:CHRISTOPHER G BEEVERS
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依托单位:
Genetic Influences on Dual Processing Modes of Reward and Punishment Learning
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项目类别:
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财政年份:2012
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负责人:CHRISTOPHER G BEEVERS
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依托单位:
Attention Training for Major Depressive Disorder
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批准号:8150366
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项目类别:
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资助金额:$19.05万
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财政年份:2010
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负责人:CHRISTOPHER G BEEVERS
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依托单位:
Attention Training for Major Depressive Disorder
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批准号:8029338
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项目类别:
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资助金额:$23.03万
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财政年份:2010
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负责人:CHRISTOPHER G BEEVERS
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依托单位:
Genetic Associations with Biased Processing of Emotion Cues in MDD
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批准号:7497977
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项目类别:
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资助金额:$26.55万
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财政年份:2007
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负责人:CHRISTOPHER G BEEVERS
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依托单位:
Genetic Associations with Biased Processing of Emotion Cues in MDD
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批准号:7265756
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项目类别:
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资助金额:$27.83万
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财政年份:2007
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负责人:CHRISTOPHER G BEEVERS
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依托单位:
Genetic Associations with Biased Processing of Emotion Cues in MDD
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批准号:7609066
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资助金额:$26.55万
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依托单位:
海外基金