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 |
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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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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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