Nadja R. Ging-Jehli , Manuel Kuhn , Jacob M. Blank , Pranavan Chanthrakumar , David C. Steinberger , Zeyang Yu , Todd M. Herrington , Daniel G. Dillon , Diego A. Pizzagalli , Michael J. Frank
{"title":"利用计算建模和神经认知测试研究抑郁症状、厌世症状和情感状态的认知特征。","authors":"Nadja R. Ging-Jehli , Manuel Kuhn , Jacob M. Blank , Pranavan Chanthrakumar , David C. Steinberger , Zeyang Yu , Todd M. Herrington , Daniel G. Dillon , Diego A. Pizzagalli , Michael J. Frank","doi":"10.1016/j.bpsc.2024.02.005","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><p>Deeper phenotyping may improve our understanding of depression. Because depression is heterogeneous, extracting cognitive signatures associated with severity of depressive symptoms, anhedonia, and affective states is a promising approach.</p></div><div><h3>Methods</h3><p>Sequential sampling models decomposed behavior from an adaptive approach-avoidance conflict task into computational parameters quantifying latent cognitive signatures. Fifty unselected participants completed clinical scales and the approach-avoidance conflict task by either approaching or avoiding trials offering monetary rewards and electric shocks.</p></div><div><h3>Results</h3><p>Decision dynamics were best captured by a sequential sampling model with linear collapsing boundaries varying by net offer values, and with drift rates varying by trial-specific reward and aversion, reflecting net evidence accumulation toward approach or avoidance. Unlike conventional behavioral measures, these computational parameters revealed distinct associations with self-reported symptoms. Specifically, passive avoidance tendencies, indexed by starting point biases, were associated with greater severity of depressive symptoms (<em>R</em> = 0.34, <em>p</em> = .019) and anhedonia (<em>R</em> = 0.49, <em>p</em> = .001). Depressive symptoms were also associated with slower encoding and response execution, indexed by nondecision time (<em>R</em> = 0.37, <em>p</em> = .011). Higher reward sensitivity for offers with negative net values, indexed by drift rates, was linked to more sadness (<em>R</em> = 0.29, <em>p</em> = .042) and lower positive affect (<em>R</em> = −0.33, <em>p</em> = .022). Conversely, higher aversion sensitivity was associated with more tension (<em>R</em> = 0.33, <em>p</em> = .025). Finally, less cautious response patterns, indexed by boundary separation, were linked to more negative affect (<em>R</em> = −0.40, <em>p</em> = .005).</p></div><div><h3>Conclusions</h3><p>We demonstrated the utility of multidimensional computational phenotyping, which could be applied to clinical samples to improve characterization and treatment selection.</p></div>","PeriodicalId":54231,"journal":{"name":"Biological Psychiatry-Cognitive Neuroscience and Neuroimaging","volume":"9 7","pages":"Pages 726-736"},"PeriodicalIF":5.7000,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Cognitive Signatures of Depressive and Anhedonic Symptoms and Affective States Using Computational Modeling and Neurocognitive Testing\",\"authors\":\"Nadja R. Ging-Jehli , Manuel Kuhn , Jacob M. Blank , Pranavan Chanthrakumar , David C. Steinberger , Zeyang Yu , Todd M. Herrington , Daniel G. Dillon , Diego A. Pizzagalli , Michael J. Frank\",\"doi\":\"10.1016/j.bpsc.2024.02.005\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background</h3><p>Deeper phenotyping may improve our understanding of depression. Because depression is heterogeneous, extracting cognitive signatures associated with severity of depressive symptoms, anhedonia, and affective states is a promising approach.</p></div><div><h3>Methods</h3><p>Sequential sampling models decomposed behavior from an adaptive approach-avoidance conflict task into computational parameters quantifying latent cognitive signatures. Fifty unselected participants completed clinical scales and the approach-avoidance conflict task by either approaching or avoiding trials offering monetary rewards and electric shocks.</p></div><div><h3>Results</h3><p>Decision dynamics were best captured by a sequential sampling model with linear collapsing boundaries varying by net offer values, and with drift rates varying by trial-specific reward and aversion, reflecting net evidence accumulation toward approach or avoidance. Unlike conventional behavioral measures, these computational parameters revealed distinct associations with self-reported symptoms. Specifically, passive avoidance tendencies, indexed by starting point biases, were associated with greater severity of depressive symptoms (<em>R</em> = 0.34, <em>p</em> = .019) and anhedonia (<em>R</em> = 0.49, <em>p</em> = .001). Depressive symptoms were also associated with slower encoding and response execution, indexed by nondecision time (<em>R</em> = 0.37, <em>p</em> = .011). Higher reward sensitivity for offers with negative net values, indexed by drift rates, was linked to more sadness (<em>R</em> = 0.29, <em>p</em> = .042) and lower positive affect (<em>R</em> = −0.33, <em>p</em> = .022). Conversely, higher aversion sensitivity was associated with more tension (<em>R</em> = 0.33, <em>p</em> = .025). Finally, less cautious response patterns, indexed by boundary separation, were linked to more negative affect (<em>R</em> = −0.40, <em>p</em> = .005).</p></div><div><h3>Conclusions</h3><p>We demonstrated the utility of multidimensional computational phenotyping, which could be applied to clinical samples to improve characterization and treatment selection.</p></div>\",\"PeriodicalId\":54231,\"journal\":{\"name\":\"Biological Psychiatry-Cognitive Neuroscience and Neuroimaging\",\"volume\":\"9 7\",\"pages\":\"Pages 726-736\"},\"PeriodicalIF\":5.7000,\"publicationDate\":\"2024-07-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Biological Psychiatry-Cognitive Neuroscience and Neuroimaging\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2451902224000569\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"NEUROSCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biological Psychiatry-Cognitive Neuroscience and Neuroimaging","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2451902224000569","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
Cognitive Signatures of Depressive and Anhedonic Symptoms and Affective States Using Computational Modeling and Neurocognitive Testing
Background
Deeper phenotyping may improve our understanding of depression. Because depression is heterogeneous, extracting cognitive signatures associated with severity of depressive symptoms, anhedonia, and affective states is a promising approach.
Methods
Sequential sampling models decomposed behavior from an adaptive approach-avoidance conflict task into computational parameters quantifying latent cognitive signatures. Fifty unselected participants completed clinical scales and the approach-avoidance conflict task by either approaching or avoiding trials offering monetary rewards and electric shocks.
Results
Decision dynamics were best captured by a sequential sampling model with linear collapsing boundaries varying by net offer values, and with drift rates varying by trial-specific reward and aversion, reflecting net evidence accumulation toward approach or avoidance. Unlike conventional behavioral measures, these computational parameters revealed distinct associations with self-reported symptoms. Specifically, passive avoidance tendencies, indexed by starting point biases, were associated with greater severity of depressive symptoms (R = 0.34, p = .019) and anhedonia (R = 0.49, p = .001). Depressive symptoms were also associated with slower encoding and response execution, indexed by nondecision time (R = 0.37, p = .011). Higher reward sensitivity for offers with negative net values, indexed by drift rates, was linked to more sadness (R = 0.29, p = .042) and lower positive affect (R = −0.33, p = .022). Conversely, higher aversion sensitivity was associated with more tension (R = 0.33, p = .025). Finally, less cautious response patterns, indexed by boundary separation, were linked to more negative affect (R = −0.40, p = .005).
Conclusions
We demonstrated the utility of multidimensional computational phenotyping, which could be applied to clinical samples to improve characterization and treatment selection.
期刊介绍:
Biological Psychiatry: Cognitive Neuroscience and Neuroimaging is an official journal of the Society for Biological Psychiatry, whose purpose is to promote excellence in scientific research and education in fields that investigate the nature, causes, mechanisms, and treatments of disorders of thought, emotion, or behavior. In accord with this mission, this peer-reviewed, rapid-publication, international journal focuses on studies using the tools and constructs of cognitive neuroscience, including the full range of non-invasive neuroimaging and human extra- and intracranial physiological recording methodologies. It publishes both basic and clinical studies, including those that incorporate genetic data, pharmacological challenges, and computational modeling approaches. The journal publishes novel results of original research which represent an important new lead or significant impact on the field. Reviews and commentaries that focus on topics of current research and interest are also encouraged.