Severity of thought disorder predicts psychosis in persons at clinical high-risk

AbstractBackgroundImproving predictive accuracy is of paramount importance for early detection and prevention of psychosis. We sought a symptom severity classifier that would improve psychosis risk prediction. MethodsSubjects were from two cohorts of the North American Prodrome Longitudinal Study. A...

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Veröffentlicht in:Schizophrenia research 2015-12, Vol.169 (1), p.169-177
Hauptverfasser: Perkins, Diana O, Jeffries, Clark D, Cornblatt, Barbara A, Woods, Scott W, Addington, Jean, Bearden, Carrie E, Cadenhead, Kristin S, Cannon, Tyrone D, Heinssen, Robert, Mathalon, Daniel H, Seidman, Larry J, Tsuang, Ming T, Walker, Elaine F, McGlashan, Thomas H
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container_end_page 177
container_issue 1
container_start_page 169
container_title Schizophrenia research
container_volume 169
creator Perkins, Diana O
Jeffries, Clark D
Cornblatt, Barbara A
Woods, Scott W
Addington, Jean
Bearden, Carrie E
Cadenhead, Kristin S
Cannon, Tyrone D
Heinssen, Robert
Mathalon, Daniel H
Seidman, Larry J
Tsuang, Ming T
Walker, Elaine F
McGlashan, Thomas H
description AbstractBackgroundImproving predictive accuracy is of paramount importance for early detection and prevention of psychosis. We sought a symptom severity classifier that would improve psychosis risk prediction. MethodsSubjects were from two cohorts of the North American Prodrome Longitudinal Study. All subjects met Criteria of Psychosis-Risk States. In Cohort-1 (n = 296) we developed a classifier that included those items of the Scale of Psychosis-Risk Symptoms that best distinguished subjects who converted to psychosis from nonconverters, with performance initially validated by randomization tests in Cohort-1. Cohort-2 (n = 592) served as an independent test set. ResultsWe derived 2-Item and 4-Item subscales. Both included unusual thought content and suspiciousness; the latter added reduced ideational richness and difficulties with focus/concentration. The Concordance Index (C-Index), a measure of discrimination, was similar for each subscale across cohorts (4-Item subscale Cohort-2: 0.71, 95% CI = [0.64, 0.77], Cohort-1: 0.74, 95% CI = [0.69, 0.80]; 2-Item subscale Cohort-2: 0.68, 95% CI = [0.3, 0.76], Cohort-1: 0.72, 95% CI = [0.66–0.79]). The 4-Item performed better than the 2-Item subscale in 742/1000 random selections of 80% subsets of Cohort-2 subjects (p-value = 1.3E − 55). Subscale calibration between cohorts was proportional (higher scores/lower survival), but absolute conversion risk predicted from Cohort-1 was higher than that observed in Cohort-2, reflecting the cohorts' differences in 2-year conversion rates (Cohort-2: 0.16, 95% CI = [0.13, 0.19]; Cohort-1: 0.30, 95% CI = [0.24, 0.36]). ConclusionSeverity of unusual thought content, suspiciousness, reduced ideational richness, and difficulty with focus/concentration informed psychosis risk prediction. Scales based on these symptoms may have utility in research and, assuming further validation, eventual clinical applications.
doi_str_mv 10.1016/j.schres.2015.09.008
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We sought a symptom severity classifier that would improve psychosis risk prediction. MethodsSubjects were from two cohorts of the North American Prodrome Longitudinal Study. All subjects met Criteria of Psychosis-Risk States. In Cohort-1 (n = 296) we developed a classifier that included those items of the Scale of Psychosis-Risk Symptoms that best distinguished subjects who converted to psychosis from nonconverters, with performance initially validated by randomization tests in Cohort-1. Cohort-2 (n = 592) served as an independent test set. ResultsWe derived 2-Item and 4-Item subscales. Both included unusual thought content and suspiciousness; the latter added reduced ideational richness and difficulties with focus/concentration. The Concordance Index (C-Index), a measure of discrimination, was similar for each subscale across cohorts (4-Item subscale Cohort-2: 0.71, 95% CI = [0.64, 0.77], Cohort-1: 0.74, 95% CI = [0.69, 0.80]; 2-Item subscale Cohort-2: 0.68, 95% CI = [0.3, 0.76], Cohort-1: 0.72, 95% CI = [0.66–0.79]). The 4-Item performed better than the 2-Item subscale in 742/1000 random selections of 80% subsets of Cohort-2 subjects (p-value = 1.3E − 55). Subscale calibration between cohorts was proportional (higher scores/lower survival), but absolute conversion risk predicted from Cohort-1 was higher than that observed in Cohort-2, reflecting the cohorts' differences in 2-year conversion rates (Cohort-2: 0.16, 95% CI = [0.13, 0.19]; Cohort-1: 0.30, 95% CI = [0.24, 0.36]). ConclusionSeverity of unusual thought content, suspiciousness, reduced ideational richness, and difficulty with focus/concentration informed psychosis risk prediction. Scales based on these symptoms may have utility in research and, assuming further validation, eventual clinical applications.</description><identifier>ISSN: 0920-9964</identifier><identifier>EISSN: 1573-2509</identifier><identifier>DOI: 10.1016/j.schres.2015.09.008</identifier><identifier>PMID: 26441004</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Adolescent ; Cognition Disorders - diagnosis ; Cognition Disorders - etiology ; Cohort Studies ; Female ; High-risk ; Humans ; Male ; Neuropsychological Tests ; Psychiatric Status Rating Scales ; Psychiatric/Mental Health ; Psychosis ; Psychotic Disorders - complications ; Psychotic Disorders - psychology ; Reproducibility of Results ; Risk Factors ; Risk prediction ; ROC Curve ; Schizophrenia ; Survival ; Survival Analysis ; Symptom severity ; Thinking - physiology ; Young Adult</subject><ispartof>Schizophrenia research, 2015-12, Vol.169 (1), p.169-177</ispartof><rights>Elsevier B.V.</rights><rights>2015 Elsevier B.V.</rights><rights>Copyright © 2015 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c588t-c930d9d08041aa05679fb257c730fe22cebdcf26279a6c4e775de685f1e083083</citedby><cites>FETCH-LOGICAL-c588t-c930d9d08041aa05679fb257c730fe22cebdcf26279a6c4e775de685f1e083083</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.schres.2015.09.008$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,780,784,885,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26441004$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Perkins, Diana O</creatorcontrib><creatorcontrib>Jeffries, Clark D</creatorcontrib><creatorcontrib>Cornblatt, Barbara A</creatorcontrib><creatorcontrib>Woods, Scott W</creatorcontrib><creatorcontrib>Addington, Jean</creatorcontrib><creatorcontrib>Bearden, Carrie E</creatorcontrib><creatorcontrib>Cadenhead, Kristin S</creatorcontrib><creatorcontrib>Cannon, Tyrone D</creatorcontrib><creatorcontrib>Heinssen, Robert</creatorcontrib><creatorcontrib>Mathalon, Daniel H</creatorcontrib><creatorcontrib>Seidman, Larry J</creatorcontrib><creatorcontrib>Tsuang, Ming T</creatorcontrib><creatorcontrib>Walker, Elaine F</creatorcontrib><creatorcontrib>McGlashan, Thomas H</creatorcontrib><title>Severity of thought disorder predicts psychosis in persons at clinical high-risk</title><title>Schizophrenia research</title><addtitle>Schizophr Res</addtitle><description>AbstractBackgroundImproving predictive accuracy is of paramount importance for early detection and prevention of psychosis. We sought a symptom severity classifier that would improve psychosis risk prediction. MethodsSubjects were from two cohorts of the North American Prodrome Longitudinal Study. All subjects met Criteria of Psychosis-Risk States. In Cohort-1 (n = 296) we developed a classifier that included those items of the Scale of Psychosis-Risk Symptoms that best distinguished subjects who converted to psychosis from nonconverters, with performance initially validated by randomization tests in Cohort-1. Cohort-2 (n = 592) served as an independent test set. ResultsWe derived 2-Item and 4-Item subscales. Both included unusual thought content and suspiciousness; the latter added reduced ideational richness and difficulties with focus/concentration. The Concordance Index (C-Index), a measure of discrimination, was similar for each subscale across cohorts (4-Item subscale Cohort-2: 0.71, 95% CI = [0.64, 0.77], Cohort-1: 0.74, 95% CI = [0.69, 0.80]; 2-Item subscale Cohort-2: 0.68, 95% CI = [0.3, 0.76], Cohort-1: 0.72, 95% CI = [0.66–0.79]). The 4-Item performed better than the 2-Item subscale in 742/1000 random selections of 80% subsets of Cohort-2 subjects (p-value = 1.3E − 55). Subscale calibration between cohorts was proportional (higher scores/lower survival), but absolute conversion risk predicted from Cohort-1 was higher than that observed in Cohort-2, reflecting the cohorts' differences in 2-year conversion rates (Cohort-2: 0.16, 95% CI = [0.13, 0.19]; Cohort-1: 0.30, 95% CI = [0.24, 0.36]). ConclusionSeverity of unusual thought content, suspiciousness, reduced ideational richness, and difficulty with focus/concentration informed psychosis risk prediction. Scales based on these symptoms may have utility in research and, assuming further validation, eventual clinical applications.</description><subject>Adolescent</subject><subject>Cognition Disorders - diagnosis</subject><subject>Cognition Disorders - etiology</subject><subject>Cohort Studies</subject><subject>Female</subject><subject>High-risk</subject><subject>Humans</subject><subject>Male</subject><subject>Neuropsychological Tests</subject><subject>Psychiatric Status Rating Scales</subject><subject>Psychiatric/Mental Health</subject><subject>Psychosis</subject><subject>Psychotic Disorders - complications</subject><subject>Psychotic Disorders - psychology</subject><subject>Reproducibility of Results</subject><subject>Risk Factors</subject><subject>Risk prediction</subject><subject>ROC Curve</subject><subject>Schizophrenia</subject><subject>Survival</subject><subject>Survival Analysis</subject><subject>Symptom severity</subject><subject>Thinking - physiology</subject><subject>Young Adult</subject><issn>0920-9964</issn><issn>1573-2509</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUk2P0zAQtRCILQv_ACEfuSSMHSe2L0hoxZe0EkgLZ8t1Jo27aVw8SaX-e1K6u3xckCzNwW_ezLz3GHspoBQgmjfbkkKfkUoJoi7BlgDmEVuJWleFrME-ZiuwEgprG3XBnhFtARYk6KfsQjZKCQC1Yl9v8IA5TkeeOj71ad70E28jpdxi5vuMbQwT8T0dQ58oEo8j32OmNBL3Ew9DHGPwA-_jpi9ypNvn7EnnB8IXd_WSff_w_tvVp-L6y8fPV--ui1AbMxXBVtDaFgwo4T3UjbbdWtY66Ao6lDLgug2dbKS2vgkKta5bbEzdCQRTLe-SvT3z7uf1DtuA45T94PY57nw-uuSj-_tnjL3bpINTjRG1UQvB6zuCnH7MSJPbRQo4DH7ENJMTWllrFyQsUHWGhpyIMnYPYwS4kxlu685muJMZDqyDXyu--nPFh6Z79X_fgItQh4h5YYk4hkX0jGFybYr_m_Avwb0ht3hE2qY5j4sJTjiSDtzNKRCnPCwxAKWNqX4C0_Cz2g</recordid><startdate>20151201</startdate><enddate>20151201</enddate><creator>Perkins, Diana O</creator><creator>Jeffries, Clark D</creator><creator>Cornblatt, Barbara A</creator><creator>Woods, Scott W</creator><creator>Addington, Jean</creator><creator>Bearden, Carrie E</creator><creator>Cadenhead, Kristin S</creator><creator>Cannon, Tyrone D</creator><creator>Heinssen, Robert</creator><creator>Mathalon, Daniel H</creator><creator>Seidman, Larry J</creator><creator>Tsuang, Ming T</creator><creator>Walker, Elaine F</creator><creator>McGlashan, Thomas H</creator><general>Elsevier B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20151201</creationdate><title>Severity of thought disorder predicts psychosis in persons at clinical high-risk</title><author>Perkins, Diana O ; Jeffries, Clark D ; Cornblatt, Barbara A ; Woods, Scott W ; Addington, Jean ; Bearden, Carrie E ; Cadenhead, Kristin S ; Cannon, Tyrone D ; Heinssen, Robert ; Mathalon, Daniel H ; Seidman, Larry J ; Tsuang, Ming T ; Walker, Elaine F ; McGlashan, Thomas H</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c588t-c930d9d08041aa05679fb257c730fe22cebdcf26279a6c4e775de685f1e083083</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Adolescent</topic><topic>Cognition Disorders - diagnosis</topic><topic>Cognition Disorders - etiology</topic><topic>Cohort Studies</topic><topic>Female</topic><topic>High-risk</topic><topic>Humans</topic><topic>Male</topic><topic>Neuropsychological Tests</topic><topic>Psychiatric Status Rating Scales</topic><topic>Psychiatric/Mental Health</topic><topic>Psychosis</topic><topic>Psychotic Disorders - complications</topic><topic>Psychotic Disorders - psychology</topic><topic>Reproducibility of Results</topic><topic>Risk Factors</topic><topic>Risk prediction</topic><topic>ROC Curve</topic><topic>Schizophrenia</topic><topic>Survival</topic><topic>Survival Analysis</topic><topic>Symptom severity</topic><topic>Thinking - physiology</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Perkins, Diana O</creatorcontrib><creatorcontrib>Jeffries, Clark D</creatorcontrib><creatorcontrib>Cornblatt, Barbara A</creatorcontrib><creatorcontrib>Woods, Scott W</creatorcontrib><creatorcontrib>Addington, Jean</creatorcontrib><creatorcontrib>Bearden, Carrie E</creatorcontrib><creatorcontrib>Cadenhead, Kristin S</creatorcontrib><creatorcontrib>Cannon, Tyrone D</creatorcontrib><creatorcontrib>Heinssen, Robert</creatorcontrib><creatorcontrib>Mathalon, Daniel H</creatorcontrib><creatorcontrib>Seidman, Larry J</creatorcontrib><creatorcontrib>Tsuang, Ming T</creatorcontrib><creatorcontrib>Walker, Elaine F</creatorcontrib><creatorcontrib>McGlashan, Thomas H</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Schizophrenia research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Perkins, Diana O</au><au>Jeffries, Clark D</au><au>Cornblatt, Barbara A</au><au>Woods, Scott W</au><au>Addington, Jean</au><au>Bearden, Carrie E</au><au>Cadenhead, Kristin S</au><au>Cannon, Tyrone D</au><au>Heinssen, Robert</au><au>Mathalon, Daniel H</au><au>Seidman, Larry J</au><au>Tsuang, Ming T</au><au>Walker, Elaine F</au><au>McGlashan, Thomas H</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Severity of thought disorder predicts psychosis in persons at clinical high-risk</atitle><jtitle>Schizophrenia research</jtitle><addtitle>Schizophr Res</addtitle><date>2015-12-01</date><risdate>2015</risdate><volume>169</volume><issue>1</issue><spage>169</spage><epage>177</epage><pages>169-177</pages><issn>0920-9964</issn><eissn>1573-2509</eissn><abstract>AbstractBackgroundImproving predictive accuracy is of paramount importance for early detection and prevention of psychosis. We sought a symptom severity classifier that would improve psychosis risk prediction. MethodsSubjects were from two cohorts of the North American Prodrome Longitudinal Study. All subjects met Criteria of Psychosis-Risk States. In Cohort-1 (n = 296) we developed a classifier that included those items of the Scale of Psychosis-Risk Symptoms that best distinguished subjects who converted to psychosis from nonconverters, with performance initially validated by randomization tests in Cohort-1. Cohort-2 (n = 592) served as an independent test set. ResultsWe derived 2-Item and 4-Item subscales. Both included unusual thought content and suspiciousness; the latter added reduced ideational richness and difficulties with focus/concentration. The Concordance Index (C-Index), a measure of discrimination, was similar for each subscale across cohorts (4-Item subscale Cohort-2: 0.71, 95% CI = [0.64, 0.77], Cohort-1: 0.74, 95% CI = [0.69, 0.80]; 2-Item subscale Cohort-2: 0.68, 95% CI = [0.3, 0.76], Cohort-1: 0.72, 95% CI = [0.66–0.79]). The 4-Item performed better than the 2-Item subscale in 742/1000 random selections of 80% subsets of Cohort-2 subjects (p-value = 1.3E − 55). Subscale calibration between cohorts was proportional (higher scores/lower survival), but absolute conversion risk predicted from Cohort-1 was higher than that observed in Cohort-2, reflecting the cohorts' differences in 2-year conversion rates (Cohort-2: 0.16, 95% CI = [0.13, 0.19]; Cohort-1: 0.30, 95% CI = [0.24, 0.36]). ConclusionSeverity of unusual thought content, suspiciousness, reduced ideational richness, and difficulty with focus/concentration informed psychosis risk prediction. Scales based on these symptoms may have utility in research and, assuming further validation, eventual clinical applications.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>26441004</pmid><doi>10.1016/j.schres.2015.09.008</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
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identifier ISSN: 0920-9964
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language eng
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source MEDLINE; Access via ScienceDirect (Elsevier)
subjects Adolescent
Cognition Disorders - diagnosis
Cognition Disorders - etiology
Cohort Studies
Female
High-risk
Humans
Male
Neuropsychological Tests
Psychiatric Status Rating Scales
Psychiatric/Mental Health
Psychosis
Psychotic Disorders - complications
Psychotic Disorders - psychology
Reproducibility of Results
Risk Factors
Risk prediction
ROC Curve
Schizophrenia
Survival
Survival Analysis
Symptom severity
Thinking - physiology
Young Adult
title Severity of thought disorder predicts psychosis in persons at clinical high-risk
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