@article{350e4c7ee1ce432bab0a7466fd6a1a11,
title = "Impaired insight in schizophrenia: impact on patient-reported and physician-reported outcome measures in a randomized controlled trial",
abstract = "Background: Impaired insight poses a challenge in the treatment of patients with schizophrenia because of its potential to jeopardize therapeutic engagement and medication adherence. This study explored how insight impairment, graded from none to extreme, is related to patient-reported mental health status, depression, and neurocognition in schizophrenia. Methods: In a post hoc analysis of the Clinical Antipsychotic Trials of Intervention Effectiveness (CATIE) study (NCT00014001), insight was measured using the Positive and Negative Syndrome Scale (PANSS) Item G12 (lack of insight). Additional assessments for this analysis included the 12-Item Short-Form Health Survey (SF-12) Mental Component Summary (MCS), physician- and patient-reported Clinical Global Impression–Severity (CGI-S), MATRICS Consensus Cognitive Battery, and Calgary Depression Scale for Schizophrenia. Relationships between patient-reported outcomes and PANSS total and Item G12 ratings were evaluated. Results: Among 1431 CATIE study participants in this analysis, increasingly impaired insight at baseline was significantly associated with better patient-reported quality of life (QoL), lower baseline depression, and greater divergence between physician- and patient-reported illness severity. Patients with more severely impaired insight reported milder illness compared with physician reports, particularly those with moderate-severe to extreme impairment (PANSS Item G12 rating ≥ 5), approximately 10% (138/1431) of CATIE participants. For the 90% of patients with PANSS Item G12 ratings < 5, patient-reported QoL decreased with increasing symptoms. SF-12 MCS scores were linearly related to baseline PANSS total score only in patients with PANSS total score < 90 (moderately ill or better), and better symptom scores were associated with higher QoL. No significant relationship between insight and neurocognition was observed. Conclusions: In the small subgroup (10%) of CATIE study patients with schizophrenia and PANSS Item G12 ratings ≥5, moderate-severe–severe/extreme insight impairment was associated with significantly more positive perception of QoL and illness severity by the patient versus the treating physician. This was not observed in the remaining 90% of patients with normal to moderately impaired insight, suggesting that poor insight as a threat to the validity of self-report is uncommon.",
keywords = "CATIE schizophrenia trial, Insight, Neurocognition, PANSS, Patient-reported outcome, Quality of life, SF-12, Schizophrenia",
author = "Lysaker, {Paul H.} and Weiden, {Peter J.} and Xiaowu Sun and O{\textquoteright}Sullivan, {Amy K.} and McEvoy, {Joseph P.}",
note = "Funding Information: This study was sponsored by Alkermes, Inc. (Waltham, MA, USA). The study sponsor was involved in the design, collection, and analysis of the data. Interpretation of the results was by the authors, and the decision to submit the manuscript for publication was made by the authors. Funding Information: The data used in the preparation of this manuscript were obtained from the limited-access datasets distributed from the NIH-supported Clinical Antipsychotic Trials of Intervention Effectiveness (CATIE) study (NCT00014001). This was a multisite, clinical trial of persons with schizophrenia comparing the effectiveness of randomly assigned medication treatment. The study was supported by National Institute of Mental Health (NIMH) Contract #N01MH90001 to the University of North Carolina at Chapel Hill. The CATIE study was conducted by investigators from the University of North Carolina, Duke University, Columbia University, the University of Southern California, the University of Rochester, and Yale University along with program staff of the Division of Interventions and Services Research, NIMH, and investigators from each of the 57 research sites in the United States. This manuscript reflects the views of the authors and may not reflect the opinions or views of the CATIE Study Investigators or the NIMH. Funding Information: Medical writing and editorial support for the preparation of this article was provided by Susan Bartko-Winters, PhD, and Esther Tazartes, MS, of Global Outcomes Group, and Gina Daniel, PhD and Kathleen Dorries, PhD of Peloton Advantage, LLC (Parsippany, NJ), an OPEN Health company, and funded by Alkermes, Inc. The data used in the preparation of this manuscript were obtained from the limited-access datasets distributed from the NIH-supported Clinical Antipsychotic Trials of Intervention Effectiveness (CATIE) study (NCT00014001). This was a multisite, clinical trial of persons with schizophrenia comparing the effectiveness of randomly assigned medication treatment. The study was supported by National Institute of Mental Health (NIMH) Contract #N01MH90001 to the University of North Carolina at Chapel Hill. The CATIE study was conducted by investigators from the University of North Carolina, Duke University, Columbia University, the University of Southern California, the University of Rochester, and Yale University along with program staff of the Division of Interventions and Services Research, NIMH, and investigators from each of the 57 research sites in the United States. This manuscript reflects the views of the authors and may not reflect the opinions or views of the CATIE Study Investigators or the NIMH. This study was sponsored by Alkermes, Inc. (Waltham, MA, USA). The study sponsor was involved in the design, collection, and analysis of the data. Interpretation of the results was by the authors, and the decision to submit the manuscript for publication was made by the authors. Funding Information: Medical writing and editorial support for the preparation of this article was provided by Susan Bartko-Winters, PhD, and Esther Tazartes, MS, of Global Outcomes Group, and Gina Daniel, PhD and Kathleen Dorries, PhD of Peloton Advantage, LLC (Parsippany, NJ), an OPEN Health company, and funded by Alkermes, Inc. Publisher Copyright: {\textcopyright} 2022, The Author(s).",
year = "2022",
month = dec,
doi = "10.1186/s12888-022-04190-w",
language = "English (US)",
volume = "22",
journal = "BMC Psychiatry",
issn = "1471-244X",
publisher = "BioMed Central",
number = "1",
}