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A brief questionnaire measure of multidimensional schizotypy predicts interview-rated symptoms and impairment

The present study employed structured diagnostic interviews to assess the construct validity of the brief version of the Multidimensional Schizotypy Scale (MSS-B), which was developed to assess positive, negative, and disorganized dimensions of schizotypy. It was hypothesized that the MSS-B subscale...

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Autores principales: Kemp, Kathryn C., Bathery, Alyssa J., Barrantes-Vidal, Neus, Kwapil, Thomas R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7416934/
https://www.ncbi.nlm.nih.gov/pubmed/32776979
http://dx.doi.org/10.1371/journal.pone.0237614
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author Kemp, Kathryn C.
Bathery, Alyssa J.
Barrantes-Vidal, Neus
Kwapil, Thomas R.
author_facet Kemp, Kathryn C.
Bathery, Alyssa J.
Barrantes-Vidal, Neus
Kwapil, Thomas R.
author_sort Kemp, Kathryn C.
collection PubMed
description The present study employed structured diagnostic interviews to assess the construct validity of the brief version of the Multidimensional Schizotypy Scale (MSS-B), which was developed to assess positive, negative, and disorganized dimensions of schizotypy. It was hypothesized that the MSS-B subscales would be associated with differential patterns of symptoms and impairment, comparable to findings for the full-length MSS. A total of 177 young adults completed structured diagnostic interviews assessing symptoms and impairment. As hypothesized, MSS-B positive schizotypy was significantly associated with interview ratings of positive (psychotic-like) symptoms, as well as schizotypal and paranoid personality disorder traits. MSS-B negative schizotypy was associated with interview ratings of negative symptoms, as well as schizoid, paranoid, and schizotypal traits. Furthermore, negative schizotypy predicted Cluster A personality disorder diagnoses. MSS-B disorganized schizotypy was associated with interview ratings of disorganized symptoms. All three schizotypy dimensions were associated with impaired functioning. This was the first study to evaluate the validity of the MSS-B using interview measures, and the pattern of findings for each MSS-B subscale was closely comparable to the findings for the full-length MSS. Contrary to our hypothesis, cannabis use was largely unassociated with psychotic-like symptoms and did not moderate the expression of the schizotypy dimensions. The MSS-B has good psychometric properties, high concordance with the full-length MSS, and good construct validity. Thus, it appears to be a promising brief alternative to traditional schizotypy measures.
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spelling pubmed-74169342020-08-19 A brief questionnaire measure of multidimensional schizotypy predicts interview-rated symptoms and impairment Kemp, Kathryn C. Bathery, Alyssa J. Barrantes-Vidal, Neus Kwapil, Thomas R. PLoS One Research Article The present study employed structured diagnostic interviews to assess the construct validity of the brief version of the Multidimensional Schizotypy Scale (MSS-B), which was developed to assess positive, negative, and disorganized dimensions of schizotypy. It was hypothesized that the MSS-B subscales would be associated with differential patterns of symptoms and impairment, comparable to findings for the full-length MSS. A total of 177 young adults completed structured diagnostic interviews assessing symptoms and impairment. As hypothesized, MSS-B positive schizotypy was significantly associated with interview ratings of positive (psychotic-like) symptoms, as well as schizotypal and paranoid personality disorder traits. MSS-B negative schizotypy was associated with interview ratings of negative symptoms, as well as schizoid, paranoid, and schizotypal traits. Furthermore, negative schizotypy predicted Cluster A personality disorder diagnoses. MSS-B disorganized schizotypy was associated with interview ratings of disorganized symptoms. All three schizotypy dimensions were associated with impaired functioning. This was the first study to evaluate the validity of the MSS-B using interview measures, and the pattern of findings for each MSS-B subscale was closely comparable to the findings for the full-length MSS. Contrary to our hypothesis, cannabis use was largely unassociated with psychotic-like symptoms and did not moderate the expression of the schizotypy dimensions. The MSS-B has good psychometric properties, high concordance with the full-length MSS, and good construct validity. Thus, it appears to be a promising brief alternative to traditional schizotypy measures. Public Library of Science 2020-08-10 /pmc/articles/PMC7416934/ /pubmed/32776979 http://dx.doi.org/10.1371/journal.pone.0237614 Text en © 2020 Kemp et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Kemp, Kathryn C.
Bathery, Alyssa J.
Barrantes-Vidal, Neus
Kwapil, Thomas R.
A brief questionnaire measure of multidimensional schizotypy predicts interview-rated symptoms and impairment
title A brief questionnaire measure of multidimensional schizotypy predicts interview-rated symptoms and impairment
title_full A brief questionnaire measure of multidimensional schizotypy predicts interview-rated symptoms and impairment
title_fullStr A brief questionnaire measure of multidimensional schizotypy predicts interview-rated symptoms and impairment
title_full_unstemmed A brief questionnaire measure of multidimensional schizotypy predicts interview-rated symptoms and impairment
title_short A brief questionnaire measure of multidimensional schizotypy predicts interview-rated symptoms and impairment
title_sort brief questionnaire measure of multidimensional schizotypy predicts interview-rated symptoms and impairment
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7416934/
https://www.ncbi.nlm.nih.gov/pubmed/32776979
http://dx.doi.org/10.1371/journal.pone.0237614
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