TY - JOUR
T1 - Factor Analysis of Negative Symptom Items in the Structured Interview for Prodromal Syndromes
AU - Azis, Matilda
AU - Strauss, Gregory P.
AU - Walker, Elaine
AU - Revelle, William
AU - Zinbarg, Richard
AU - Mittal, Vijay
N1 - Funding Information:
This work was supported by National Institute of Health (grant numbers NIH RO1MH094650, NIH 1R01MH112545-01, NIH R21/R33MH103231 and NIH R21MH110374 to V.M., and NIH U01 MH081988 to E.W.) and a Translational Areas of Excellence Grant from Binghamton University to G.P.S.
Publisher Copyright:
© 2018 The Author(s) 2018. Published by Oxford University Press on behalf of the Maryland Psychiatric Research Center. All rights reserved. For permissions, please email: journals.permissions@oup.com.
PY - 2019/9/1
Y1 - 2019/9/1
N2 - Background: Negative symptoms occur early in the clinical high risk (CHR) state and indicate increased risk of conversion to psychotic disorder and poor functional outcome. However, while the negative symptom domain has shown to be parsimoniously explained by a 2-factor construct in schizophrenia, there has yet to be an established factor structure of negative symptoms in CHR. Methods: 214 individuals meeting the Structured Interview for Psychosis-Risk Syndromes (SIPS) criteria for CHR were recruited through 3 active research programs in the United States. Exploratory Factor Analysis was conducted on the 6 negative symptom items of the SIPS, and factors were evaluated with respect to functional outcome and depression. Results: Factor analysis indicated a 2-factor hierarchical model with 2 negative symptom dimensions reflecting volition (Occupational Functioning and Avolition) and emotion (Expression of Emotion, Experience of Emotion and Social Anhedonia). Linear Regression showed that the emotion factor was associated with poor social function, and the volition factor was associated with poor role function and depression. Conclusions: Similar to factor solutions identified in adults diagnosed with psychotic disorders, results indicated that the SIPS negative symptom subscale is not a unidimensional construct. Rather, the SIPS negative subscale has 2 distinct factors that have different associations with clinical outcome and should be interpreted independently. Results have significant relevance for informing the valid assessment and conceptual interpretation of early clinical phenomenology in the psychosis prodrome.
AB - Background: Negative symptoms occur early in the clinical high risk (CHR) state and indicate increased risk of conversion to psychotic disorder and poor functional outcome. However, while the negative symptom domain has shown to be parsimoniously explained by a 2-factor construct in schizophrenia, there has yet to be an established factor structure of negative symptoms in CHR. Methods: 214 individuals meeting the Structured Interview for Psychosis-Risk Syndromes (SIPS) criteria for CHR were recruited through 3 active research programs in the United States. Exploratory Factor Analysis was conducted on the 6 negative symptom items of the SIPS, and factors were evaluated with respect to functional outcome and depression. Results: Factor analysis indicated a 2-factor hierarchical model with 2 negative symptom dimensions reflecting volition (Occupational Functioning and Avolition) and emotion (Expression of Emotion, Experience of Emotion and Social Anhedonia). Linear Regression showed that the emotion factor was associated with poor social function, and the volition factor was associated with poor role function and depression. Conclusions: Similar to factor solutions identified in adults diagnosed with psychotic disorders, results indicated that the SIPS negative symptom subscale is not a unidimensional construct. Rather, the SIPS negative subscale has 2 distinct factors that have different associations with clinical outcome and should be interpreted independently. Results have significant relevance for informing the valid assessment and conceptual interpretation of early clinical phenomenology in the psychosis prodrome.
KW - At Risk Mental State
KW - clinical high risk for psychosis
KW - psychosis
KW - schizophrenia
KW - ultra high risk for psychosis
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U2 - 10.1093/schbul/sby177
DO - 10.1093/schbul/sby177
M3 - Article
C2 - 30535399
AN - SCOPUS:85072032507
SN - 0586-7614
VL - 45
SP - 1042
EP - 1050
JO - Schizophrenia Bulletin
JF - Schizophrenia Bulletin
IS - 5
ER -