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Hippocampal Volume as a Putative Marker of Resilience or Compensation to Minor Depressive Symptoms in a Nonclinical Sample

Case-control studies in major depression have established patterns of regional gray matter loss, including the hippocampus, which might show state-related effects dependent on disease stage. However, there is still limited knowledge on compensation effects that might occur in people resilient to dep...

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Autores principales: Besteher, Bianca, Squarcina, Letizia, Spalthoff, Robert, Bellani, Marcella, Gaser, Christian, Brambilla, Paolo, Nenadić, Igor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6639426/
https://www.ncbi.nlm.nih.gov/pubmed/31354542
http://dx.doi.org/10.3389/fpsyt.2019.00467
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author Besteher, Bianca
Squarcina, Letizia
Spalthoff, Robert
Bellani, Marcella
Gaser, Christian
Brambilla, Paolo
Nenadić, Igor
author_facet Besteher, Bianca
Squarcina, Letizia
Spalthoff, Robert
Bellani, Marcella
Gaser, Christian
Brambilla, Paolo
Nenadić, Igor
author_sort Besteher, Bianca
collection PubMed
description Case-control studies in major depression have established patterns of regional gray matter loss, including the hippocampus, which might show state-related effects dependent on disease stage. However, there is still limited knowledge on compensation effects that might occur in people resilient to depression showing only subclinical symptoms. We used voxel-based morphometry on a multicenter data set of 409 healthy nonclinical subjects to test the hypothesis that local hippocampal volume would be inversely correlated with subclinical depressive symptoms [Symptom Checklist 90-Revised (SCL-90-R) depression scores]. Our region-of-interest results show a significant (p = 0.042, FWE cluster-level corrected) positive correlation of SCL-90-R scores for depression and a left hippocampus cluster. Additionally, we provide an exploratory finding of gyrification, a surface-based morphometric marker, correlating with a right postcentral gyrus cluster [p = 0.031, family-wise error (FWE) cluster-level corrected]. Our findings provide first preliminary evidence of an inverse relationship for subjects in the absence of clinical depression and might thus point to processes related to compensation. Similar effects have been observed in remission from major depression and thus deserve further study to evaluate hippocampal volume not only as a state-dependent marker of disease but also of resilience.
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spelling pubmed-66394262019-07-26 Hippocampal Volume as a Putative Marker of Resilience or Compensation to Minor Depressive Symptoms in a Nonclinical Sample Besteher, Bianca Squarcina, Letizia Spalthoff, Robert Bellani, Marcella Gaser, Christian Brambilla, Paolo Nenadić, Igor Front Psychiatry Psychiatry Case-control studies in major depression have established patterns of regional gray matter loss, including the hippocampus, which might show state-related effects dependent on disease stage. However, there is still limited knowledge on compensation effects that might occur in people resilient to depression showing only subclinical symptoms. We used voxel-based morphometry on a multicenter data set of 409 healthy nonclinical subjects to test the hypothesis that local hippocampal volume would be inversely correlated with subclinical depressive symptoms [Symptom Checklist 90-Revised (SCL-90-R) depression scores]. Our region-of-interest results show a significant (p = 0.042, FWE cluster-level corrected) positive correlation of SCL-90-R scores for depression and a left hippocampus cluster. Additionally, we provide an exploratory finding of gyrification, a surface-based morphometric marker, correlating with a right postcentral gyrus cluster [p = 0.031, family-wise error (FWE) cluster-level corrected]. Our findings provide first preliminary evidence of an inverse relationship for subjects in the absence of clinical depression and might thus point to processes related to compensation. Similar effects have been observed in remission from major depression and thus deserve further study to evaluate hippocampal volume not only as a state-dependent marker of disease but also of resilience. Frontiers Media S.A. 2019-07-12 /pmc/articles/PMC6639426/ /pubmed/31354542 http://dx.doi.org/10.3389/fpsyt.2019.00467 Text en Copyright © 2019 Besteher, Squarcina, Spalthoff, Bellani, Gaser, Brambilla and Nenadić http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Psychiatry
Besteher, Bianca
Squarcina, Letizia
Spalthoff, Robert
Bellani, Marcella
Gaser, Christian
Brambilla, Paolo
Nenadić, Igor
Hippocampal Volume as a Putative Marker of Resilience or Compensation to Minor Depressive Symptoms in a Nonclinical Sample
title Hippocampal Volume as a Putative Marker of Resilience or Compensation to Minor Depressive Symptoms in a Nonclinical Sample
title_full Hippocampal Volume as a Putative Marker of Resilience or Compensation to Minor Depressive Symptoms in a Nonclinical Sample
title_fullStr Hippocampal Volume as a Putative Marker of Resilience or Compensation to Minor Depressive Symptoms in a Nonclinical Sample
title_full_unstemmed Hippocampal Volume as a Putative Marker of Resilience or Compensation to Minor Depressive Symptoms in a Nonclinical Sample
title_short Hippocampal Volume as a Putative Marker of Resilience or Compensation to Minor Depressive Symptoms in a Nonclinical Sample
title_sort hippocampal volume as a putative marker of resilience or compensation to minor depressive symptoms in a nonclinical sample
topic Psychiatry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6639426/
https://www.ncbi.nlm.nih.gov/pubmed/31354542
http://dx.doi.org/10.3389/fpsyt.2019.00467
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