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Methods for quantifying the heterogeneity of psychopathology

OBJECTIVES: Specifiers for a major depressive disorder (MDE) are supposed to reduce diagnostic heterogeneity. However, recent literature challenges the idea that the atypical and melancholic specifiers identify more homogenous or coherent subgroups. We introduce the usage of distance metrics to char...

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Autores principales: Buss, John F., Watts, Ashley L., Lorenzo-Luaces, Lorenzo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10690966/
https://www.ncbi.nlm.nih.gov/pubmed/38037069
http://dx.doi.org/10.1186/s12888-023-05377-5
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author Buss, John F.
Watts, Ashley L.
Lorenzo-Luaces, Lorenzo
author_facet Buss, John F.
Watts, Ashley L.
Lorenzo-Luaces, Lorenzo
author_sort Buss, John F.
collection PubMed
description OBJECTIVES: Specifiers for a major depressive disorder (MDE) are supposed to reduce diagnostic heterogeneity. However, recent literature challenges the idea that the atypical and melancholic specifiers identify more homogenous or coherent subgroups. We introduce the usage of distance metrics to characterize symptom heterogeneity. We attempt to replicate prior findings and explore whether symptom heterogeneity is reduced using specifier subgroups. METHODS: We used data derived from the National Epidemiological Survey on Alcohol and Related Conditions (NESARC Wave I; N = 5,749) and the Sequenced Treatment Alternatives to Relieve Depression study (STAR*D; N = 2,498). We computed Hamming and Manhattan distances from study participants’ unique symptom profiles. Distances were standardized from 0-1 and compared by their within- and between-group similarities to their non-specifier counterparts for the melancholic and atypical specifiers. RESULTS: There was no evidence of statistically significant differences in heterogeneity for specifier (i.e., melancholic or atypical) vs. non-specifier designations (i.e., non-melancholic vs. non-atypical). CONCLUSION: Replicating prior work, melancholic and atypical depression specifiers appear to have limited utility in reducing heterogeneity. The current study does not support the claim that specifiers create more coherent subgroups as operationalized by similarity in the number of symptoms and their severity. Distance metrics are useful for quantifying symptom heterogeneity.
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spelling pubmed-106909662023-12-02 Methods for quantifying the heterogeneity of psychopathology Buss, John F. Watts, Ashley L. Lorenzo-Luaces, Lorenzo BMC Psychiatry Research OBJECTIVES: Specifiers for a major depressive disorder (MDE) are supposed to reduce diagnostic heterogeneity. However, recent literature challenges the idea that the atypical and melancholic specifiers identify more homogenous or coherent subgroups. We introduce the usage of distance metrics to characterize symptom heterogeneity. We attempt to replicate prior findings and explore whether symptom heterogeneity is reduced using specifier subgroups. METHODS: We used data derived from the National Epidemiological Survey on Alcohol and Related Conditions (NESARC Wave I; N = 5,749) and the Sequenced Treatment Alternatives to Relieve Depression study (STAR*D; N = 2,498). We computed Hamming and Manhattan distances from study participants’ unique symptom profiles. Distances were standardized from 0-1 and compared by their within- and between-group similarities to their non-specifier counterparts for the melancholic and atypical specifiers. RESULTS: There was no evidence of statistically significant differences in heterogeneity for specifier (i.e., melancholic or atypical) vs. non-specifier designations (i.e., non-melancholic vs. non-atypical). CONCLUSION: Replicating prior work, melancholic and atypical depression specifiers appear to have limited utility in reducing heterogeneity. The current study does not support the claim that specifiers create more coherent subgroups as operationalized by similarity in the number of symptoms and their severity. Distance metrics are useful for quantifying symptom heterogeneity. BioMed Central 2023-11-30 /pmc/articles/PMC10690966/ /pubmed/38037069 http://dx.doi.org/10.1186/s12888-023-05377-5 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Buss, John F.
Watts, Ashley L.
Lorenzo-Luaces, Lorenzo
Methods for quantifying the heterogeneity of psychopathology
title Methods for quantifying the heterogeneity of psychopathology
title_full Methods for quantifying the heterogeneity of psychopathology
title_fullStr Methods for quantifying the heterogeneity of psychopathology
title_full_unstemmed Methods for quantifying the heterogeneity of psychopathology
title_short Methods for quantifying the heterogeneity of psychopathology
title_sort methods for quantifying the heterogeneity of psychopathology
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10690966/
https://www.ncbi.nlm.nih.gov/pubmed/38037069
http://dx.doi.org/10.1186/s12888-023-05377-5
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