Neuroimaging Heterogeneity in Psychosis: Neurobiological Underpinnings and Opportunities for Prognostic and Therapeutic Innovation

Heterogeneity in symptom presentation, outcomes, and treatment response has long been problematic for researchers aiming to identify biological markers of schizophrenia or psychosis. However, there is increasing recognition that there may likely be no such general illness markers, which is consisten...

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Published inBiological psychiatry (1969) Vol. 88; no. 1; pp. 95 - 102
Main Authors Voineskos, Aristotle N., Jacobs, Grace R., Ameis, Stephanie H.
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.07.2020
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Abstract Heterogeneity in symptom presentation, outcomes, and treatment response has long been problematic for researchers aiming to identify biological markers of schizophrenia or psychosis. However, there is increasing recognition that there may likely be no such general illness markers, which is consistent with the notion of a group of schizophrenia(s) that may have both shared and unique neurobiological pathways. Instead, strategies aiming to capitalize on or leverage such heterogeneity may help uncover neurobiological pathways that may then be used to stratify groups of patients for prognostic purposes or for therapeutic trials. A shift toward larger sample sizes with adequate statistical power to overcome small effect sizes and disentangle the shared variance among different brain-imaging or behavioral variables has become a priority for the field. In addition, recognition that two individuals with the same clinical diagnosis may be more different from each other (at brain, genetic, and behavioral levels) than from another individual in a different disorder or nonclinical control group—coupled with computational advances—has catapulted data-driven efforts forward. Emerging challenges for this new approach include longitudinal stability of new subgroups, demonstration of validity, and replicability. The “litmus test” will be whether computational approaches that are successfully identifying groups of patients who share features in common, more than current DSM diagnostic constructs, also provide better prognostic accuracy over time and in addition lead to enhancements in treatment response and outcomes. These are the factors that matter most to patients, families, providers, and payers.
AbstractList Heterogeneity in symptom presentation, outcomes, and treatment response has long been a thorn in the side of researchers aiming to identify biological markers of schizophrenia or psychosis. However, there is increasing recognition that there may likely be no such general illness markers, consistent with the notion of a group of schizophrenia(s) that may have both shared and unique neurobiological pathways. Instead, strategies aiming to capitalize or leverage such heterogeneity may help uncover neurobiological pathways that can then be used to stratify groups of patients for prognostic purposes, or for therapeutic trials. A shift toward larger sample sizes with adequate statistical power to overcome small effect sizes and disentangle the shared variance among different brain imaging or behavioral variables has become a priority for the field. In addition, recognition that two individuals with the same clinical diagnosis may be more different from each other (at brain, genetic, behavioral-levels) than another in a different disorder or non-clinical control group, coupled with computational advances, has catapulted data-driven efforts forward. Emerging challenges for this new approach include longitudinal stability of new subgroups, demonstration of validity, and replicability. The ‘litmus test’ will be whether computational approaches that are successfully identifying groups of patients who share features in common more than current DSM diagnostic constructs, also provide better prognostic accuracy over time, and in addition lead to enhancements in treatment response and outcomes. These are the factors that matter most to patients, families, providers, and payers.
Heterogeneity in symptom presentation, outcomes, and treatment response has long been problematic for researchers aiming to identify biological markers of schizophrenia or psychosis. However, there is increasing recognition that there may likely be no such general illness markers, which is consistent with the notion of a group of schizophrenia(s) that may have both shared and unique neurobiological pathways. Instead, strategies aiming to capitalize on or leverage such heterogeneity may help uncover neurobiological pathways that may then be used to stratify groups of patients for prognostic purposes or for therapeutic trials. A shift toward larger sample sizes with adequate statistical power to overcome small effect sizes and disentangle the shared variance among different brain-imaging or behavioral variables has become a priority for the field. In addition, recognition that two individuals with the same clinical diagnosis may be more different from each other (at brain, genetic, and behavioral levels) than from another individual in a different disorder or nonclinical control group—coupled with computational advances—has catapulted data-driven efforts forward. Emerging challenges for this new approach include longitudinal stability of new subgroups, demonstration of validity, and replicability. The “litmus test” will be whether computational approaches that are successfully identifying groups of patients who share features in common, more than current DSM diagnostic constructs, also provide better prognostic accuracy over time and in addition lead to enhancements in treatment response and outcomes. These are the factors that matter most to patients, families, providers, and payers.
Author Jacobs, Grace R.
Ameis, Stephanie H.
Voineskos, Aristotle N.
AuthorAffiliation 1 Campbell Family Mental Health Institute, Centre for Addiction and Mental Health, Toronto, Canada
3 Brain and Mental Health Program, Hospital for Sick Children, Toronto, Canada
2 Department of Psychiatry, University of Toronto, Toronto, Canada
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Issue 1
Keywords Brain–Behavior
Neuroimaging
Psychosis
Heterogeneity
Computation
Schizophrenia
Data Driven
Multivariate
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Snippet Heterogeneity in symptom presentation, outcomes, and treatment response has long been problematic for researchers aiming to identify biological markers of...
Heterogeneity in symptom presentation, outcomes, and treatment response has long been a thorn in the side of researchers aiming to identify biological markers...
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SubjectTerms Bipolar Disorder
Brain–Behavior
Computation
Data Driven
Heterogeneity
Humans
Multivariate
Neuroimaging
Prognosis
Psychosis
Psychotic Disorders - diagnostic imaging
Psychotic Disorders - therapy
Schizophrenia
Schizophrenia - diagnostic imaging
Schizophrenia - therapy
Title Neuroimaging Heterogeneity in Psychosis: Neurobiological Underpinnings and Opportunities for Prognostic and Therapeutic Innovation
URI https://dx.doi.org/10.1016/j.biopsych.2019.09.004
https://www.ncbi.nlm.nih.gov/pubmed/31668548
https://search.proquest.com/docview/2310725214
https://pubmed.ncbi.nlm.nih.gov/PMC7075720
Volume 88
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