TY - JOUR
T1 - Efficacy of Using Cognitive Status in Predicting Psychosis
T2 - A 7-Year Follow-Up
AU - Riecher-Rössler, Anita
AU - Pflueger, Marlon O.
AU - Aston, Jacqueline
AU - Borgwardt, Stefan J.
AU - Brewer, Warrick J.
AU - Gschwandtner, Ute
AU - Stieglitz, Rolf Dieter
N1 - Funding Information:
Dr. Warrick J. Brewer, Associate Professor, is supported by the National Health & Medical Research Council of Australia and the Colonial Foundation. The other authors reported no biomedical financial interests or potential conflicts of interest. All authors do not have any conflict interests that might be interpreted as influencing its content.
Funding Information:
This project was supported by the Swiss National Science Foundation, Grant No. [3200-057216.99], no. [3200-0572216.99], No. [PBBSB-106936], and No. [3232BO-119382]; the Nora van Meeuwen-Haefliger Stiftung, Basel (CH), and by unconditional grants from the Novartis Foundation, Bristol-Myers Squibb, GmbH (CH), Eli Lilly SA (CH), AstraZeneca AG (CH), Janssen-Cilag AG (CH), and Sanofi-Synthelabo AG (CH).
PY - 2009/12/1
Y1 - 2009/12/1
N2 - Background: Despite extensive early detection research in schizophrenic psychoses, methods for identifying at-risk individuals and predicting their transition to psychosis are still unreliable. Moreover, there are sparse data on long-term prediction. We therefore investigated long-term psychosis transition in individuals with an At Risk Mental State (ARMS) and examined the relative efficacy of clinical and neuropsychological status in optimizing the prediction of transition. Methods: Sixty-four individuals with ARMS for psychosis were identified from all referrals to our early detection clinic between March 1, 2000 and February 29, 2004. Fifty-three (83%) were followed up for up to 7 (mean 5.4) years. Results: Twenty-one of the 53 staying in follow-up developed psychosis, corresponding to a transition rate of .34 (Kaplan-Meier estimates). Median time to transition was 10 months (range <1-55). Six of all transitions (29%) occurred only after 12 months from referral. Best transition predictors within this population were selected attenuated psychotic symptoms (suspiciousness), negative symptoms (anhedonia/asociality), and cognitive deficits (reduced speed of information processing). With these predictors in an integrated model for predicting transition to psychosis, the overall predictive accuracy was 80.9% with a sensitivity of 83.3% and a specificity of 79.3%. Conclusions: Follow-up of ARMS subjects should exceed the usual 12 months. Prediction of transitions could be improved by a stronger weighting of certain early symptoms and by introducing neurocognitive tests into a stepwise risk assessment. Confirmatory research will hopefully further improve risk algorithm, including psychopathology and neuropsychological performance, for clinical application in early detection clinics.
AB - Background: Despite extensive early detection research in schizophrenic psychoses, methods for identifying at-risk individuals and predicting their transition to psychosis are still unreliable. Moreover, there are sparse data on long-term prediction. We therefore investigated long-term psychosis transition in individuals with an At Risk Mental State (ARMS) and examined the relative efficacy of clinical and neuropsychological status in optimizing the prediction of transition. Methods: Sixty-four individuals with ARMS for psychosis were identified from all referrals to our early detection clinic between March 1, 2000 and February 29, 2004. Fifty-three (83%) were followed up for up to 7 (mean 5.4) years. Results: Twenty-one of the 53 staying in follow-up developed psychosis, corresponding to a transition rate of .34 (Kaplan-Meier estimates). Median time to transition was 10 months (range <1-55). Six of all transitions (29%) occurred only after 12 months from referral. Best transition predictors within this population were selected attenuated psychotic symptoms (suspiciousness), negative symptoms (anhedonia/asociality), and cognitive deficits (reduced speed of information processing). With these predictors in an integrated model for predicting transition to psychosis, the overall predictive accuracy was 80.9% with a sensitivity of 83.3% and a specificity of 79.3%. Conclusions: Follow-up of ARMS subjects should exceed the usual 12 months. Prediction of transitions could be improved by a stronger weighting of certain early symptoms and by introducing neurocognitive tests into a stepwise risk assessment. Confirmatory research will hopefully further improve risk algorithm, including psychopathology and neuropsychological performance, for clinical application in early detection clinics.
UR - http://www.scopus.com/inward/record.url?scp=70350719233&partnerID=8YFLogxK
U2 - 10.1016/j.biopsych.2009.07.020
DO - 10.1016/j.biopsych.2009.07.020
M3 - Journal articles
C2 - 19733837
AN - SCOPUS:70350719233
SN - 0006-3223
VL - 66
SP - 1023
EP - 1030
JO - Biological Psychiatry
JF - Biological Psychiatry
IS - 11
ER -