TY - JOUR
T1 - Self-reported Attenuated Psychotic Symptoms as Forerunners of Severe Mental Disorders Later in Life
AU - Werbeloff, Nomi
AU - Drukker, Marjan
AU - Dohrenwend, Bruce P.
AU - Levav, Itzhak
AU - Yoffe, Rinat
AU - van Os, Jim
AU - Davidson, Michael
AU - Weiser, Mark
PY - 2012/5
Y1 - 2012/5
N2 - Context: It has been suggested that attenuated psychotic symptoms (APSs) reported by people who do not have psychotic disorders signal risk for later severe mental illness. Objective: To investigate this suggestion using follow-up assessments of hospitalization for clinical diagnoses of nonaffective psychotic and other psychiatric disorders. Design: Longitudinal cohort study of self-reported APSs with outcome assessment of severe mental illness obtained through linkage with a national hospitalization case registry. Setting: Israel. Participants: A stratified full probability sample of 4914 persons aged 25 to 34 years who were screened for psychopathology in the 1980s. Main Outcome Measure: Subsequent psychiatric hospitalization was ascertained using the psychiatric hospitalization registry, with a mean follow-up of 24 years. Results: After removing subjects with diagnosable psychotic disorders at baseline, 57.2% of the remaining sample reported at least 1 weak (infrequent) APS and 14.3% reported at least 1 strong (frequent) APS in the year preceding the assessment. Self-reported APSs predicted risk of later hospitalization for nonaffective psychotic disorders, mostly during the 5 years after baseline (adjusted odds ratio=4.31; 95% CI, 2.21-8.41; positive predictive value=1.27%; population attributable risk fraction=33%). Also, APSs increased the risk of later hospitalization for other psychiatric disorders, albeit to a lesser extent (adjusted odds ratio=2.21; 95% CI, 1.02-4.82). Conclusions: Self-reported APSs signal risk for later nonaffective psychotic disorders but are not clinically useful as predictors. The difference between these population-based data and the high-risk literature in terms of the positive predictive value (1% vs 10%, respectively) and the time window of transition (5 years vs 12 months, respectively) can be attributed to the selective enrichment strategies that produce high-risk samples.
AB - Context: It has been suggested that attenuated psychotic symptoms (APSs) reported by people who do not have psychotic disorders signal risk for later severe mental illness. Objective: To investigate this suggestion using follow-up assessments of hospitalization for clinical diagnoses of nonaffective psychotic and other psychiatric disorders. Design: Longitudinal cohort study of self-reported APSs with outcome assessment of severe mental illness obtained through linkage with a national hospitalization case registry. Setting: Israel. Participants: A stratified full probability sample of 4914 persons aged 25 to 34 years who were screened for psychopathology in the 1980s. Main Outcome Measure: Subsequent psychiatric hospitalization was ascertained using the psychiatric hospitalization registry, with a mean follow-up of 24 years. Results: After removing subjects with diagnosable psychotic disorders at baseline, 57.2% of the remaining sample reported at least 1 weak (infrequent) APS and 14.3% reported at least 1 strong (frequent) APS in the year preceding the assessment. Self-reported APSs predicted risk of later hospitalization for nonaffective psychotic disorders, mostly during the 5 years after baseline (adjusted odds ratio=4.31; 95% CI, 2.21-8.41; positive predictive value=1.27%; population attributable risk fraction=33%). Also, APSs increased the risk of later hospitalization for other psychiatric disorders, albeit to a lesser extent (adjusted odds ratio=2.21; 95% CI, 1.02-4.82). Conclusions: Self-reported APSs signal risk for later nonaffective psychotic disorders but are not clinically useful as predictors. The difference between these population-based data and the high-risk literature in terms of the positive predictive value (1% vs 10%, respectively) and the time window of transition (5 years vs 12 months, respectively) can be attributed to the selective enrichment strategies that produce high-risk samples.
U2 - 10.1001/archgenpsychiatry.2011.1580
DO - 10.1001/archgenpsychiatry.2011.1580
M3 - Article
C2 - 22213772
SN - 0003-990X
VL - 69
SP - 467
EP - 475
JO - Archives of General Psychiatry
JF - Archives of General Psychiatry
IS - 5
ER -