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Profound and reproducible patterns of reduced regional gray matter characterize major depressive disorder
Reduced gray matter (GM) volume may represent a hallmark of major depressive disorder (MDD) neuropathology, typified by wide-ranging distribution of structural alteration. In the study, we aimed to replicate and extend our previous finding of profound and widespread GM loss in MDD, and evaluate the...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6656728/ https://www.ncbi.nlm.nih.gov/pubmed/31341158 http://dx.doi.org/10.1038/s41398-019-0512-8 |
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author | Hellewell, Sarah C. Welton, Thomas Maller, Jerome J. Lyon, Matthew Korgaonkar, Mayuresh S. Koslow, Stephen H. Williams, Leanne M. Rush, A. John Gordon, Evian Grieve, Stuart M. |
author_facet | Hellewell, Sarah C. Welton, Thomas Maller, Jerome J. Lyon, Matthew Korgaonkar, Mayuresh S. Koslow, Stephen H. Williams, Leanne M. Rush, A. John Gordon, Evian Grieve, Stuart M. |
author_sort | Hellewell, Sarah C. |
collection | PubMed |
description | Reduced gray matter (GM) volume may represent a hallmark of major depressive disorder (MDD) neuropathology, typified by wide-ranging distribution of structural alteration. In the study, we aimed to replicate and extend our previous finding of profound and widespread GM loss in MDD, and evaluate the diagnostic accuracy of a structural biomarker derived from GM volume in an interconnected pattern across the brain. In a sub-study of the International Study to Predict Optimized Treatment in Depression (iSPOT-D), two cohorts of clinically defined MDD participants “Test” (n = 98) and “Replication” (n = 131) were assessed alongside healthy controls (n = 66). Using 3T MRI T1-weighted volumes, GM volume differences were evaluated using voxel-based morphometry. Sensitivity, specificity, and area under the receiver operating characteristic curve were used to evaluate an MDD diagnostic biomarker based on a precise spatial pattern of GM loss constructed using principal component analysis. We demonstrated a highly conserved symmetric widespread pattern of reduced GM volume in MDD, replicating our previous findings. Three bilateral dominant clusters were observed: Cluster 1: midline/cingulate (GM reduction: Test: 6.4%, Replication: 5.3%), Cluster 2: medial temporal lobe (GM reduction: Test: 8.2%, Replication: 11.9%), Cluster 3: prefrontal cortex (GM reduction: Test: 12.1%, Replication: 23.2%). We developed a biomarker reflecting the global pattern of GM reduction, achieving good diagnostic classification performance (AUC: Test = 0.75, Replication = 0.84). This study establishes that a highly specific pattern of reduced GM volume is a feature of MDD, suggestive of a structural basis for this disease. We introduce and validate a novel diagnostic biomarker based on this pattern. |
format | Online Article Text |
id | pubmed-6656728 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-66567282019-08-01 Profound and reproducible patterns of reduced regional gray matter characterize major depressive disorder Hellewell, Sarah C. Welton, Thomas Maller, Jerome J. Lyon, Matthew Korgaonkar, Mayuresh S. Koslow, Stephen H. Williams, Leanne M. Rush, A. John Gordon, Evian Grieve, Stuart M. Transl Psychiatry Article Reduced gray matter (GM) volume may represent a hallmark of major depressive disorder (MDD) neuropathology, typified by wide-ranging distribution of structural alteration. In the study, we aimed to replicate and extend our previous finding of profound and widespread GM loss in MDD, and evaluate the diagnostic accuracy of a structural biomarker derived from GM volume in an interconnected pattern across the brain. In a sub-study of the International Study to Predict Optimized Treatment in Depression (iSPOT-D), two cohorts of clinically defined MDD participants “Test” (n = 98) and “Replication” (n = 131) were assessed alongside healthy controls (n = 66). Using 3T MRI T1-weighted volumes, GM volume differences were evaluated using voxel-based morphometry. Sensitivity, specificity, and area under the receiver operating characteristic curve were used to evaluate an MDD diagnostic biomarker based on a precise spatial pattern of GM loss constructed using principal component analysis. We demonstrated a highly conserved symmetric widespread pattern of reduced GM volume in MDD, replicating our previous findings. Three bilateral dominant clusters were observed: Cluster 1: midline/cingulate (GM reduction: Test: 6.4%, Replication: 5.3%), Cluster 2: medial temporal lobe (GM reduction: Test: 8.2%, Replication: 11.9%), Cluster 3: prefrontal cortex (GM reduction: Test: 12.1%, Replication: 23.2%). We developed a biomarker reflecting the global pattern of GM reduction, achieving good diagnostic classification performance (AUC: Test = 0.75, Replication = 0.84). This study establishes that a highly specific pattern of reduced GM volume is a feature of MDD, suggestive of a structural basis for this disease. We introduce and validate a novel diagnostic biomarker based on this pattern. Nature Publishing Group UK 2019-07-24 /pmc/articles/PMC6656728/ /pubmed/31341158 http://dx.doi.org/10.1038/s41398-019-0512-8 Text en © The Author(s) 2019 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Hellewell, Sarah C. Welton, Thomas Maller, Jerome J. Lyon, Matthew Korgaonkar, Mayuresh S. Koslow, Stephen H. Williams, Leanne M. Rush, A. John Gordon, Evian Grieve, Stuart M. Profound and reproducible patterns of reduced regional gray matter characterize major depressive disorder |
title | Profound and reproducible patterns of reduced regional gray matter characterize major depressive disorder |
title_full | Profound and reproducible patterns of reduced regional gray matter characterize major depressive disorder |
title_fullStr | Profound and reproducible patterns of reduced regional gray matter characterize major depressive disorder |
title_full_unstemmed | Profound and reproducible patterns of reduced regional gray matter characterize major depressive disorder |
title_short | Profound and reproducible patterns of reduced regional gray matter characterize major depressive disorder |
title_sort | profound and reproducible patterns of reduced regional gray matter characterize major depressive disorder |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6656728/ https://www.ncbi.nlm.nih.gov/pubmed/31341158 http://dx.doi.org/10.1038/s41398-019-0512-8 |
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