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Hippocampal Volume in Psychiatric Diagnoses: Should Psychiatry Biomarker Research Account for Comorbidities?
BACKGROUND: Many research papers claim that patients with specific psychiatric disorders (major depressive disorder, posttraumatic stress disorder, borderline personality disorder, alcohol use disorder, and others) have smaller hippocampi, but most of those reports compared patients to healthy contr...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7219869/ https://www.ncbi.nlm.nih.gov/pubmed/32440605 http://dx.doi.org/10.1177/2470547020906799 |
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author | Gosnell, Savannah N. Meyer, Matthew J. Jennings, Cassandra Ramirez, Danna Schmidt, Jake Oldham, John Salas, Ramiro |
author_facet | Gosnell, Savannah N. Meyer, Matthew J. Jennings, Cassandra Ramirez, Danna Schmidt, Jake Oldham, John Salas, Ramiro |
author_sort | Gosnell, Savannah N. |
collection | PubMed |
description | BACKGROUND: Many research papers claim that patients with specific psychiatric disorders (major depressive disorder, posttraumatic stress disorder, borderline personality disorder, alcohol use disorder, and others) have smaller hippocampi, but most of those reports compared patients to healthy controls. We hypothesized that if psychiatrically matched controls (psychiatric control, matched for demographics and psychiatric comorbidities) were used, much of the biomarker literature in psychiatric research would not replicate. We used hippocampus and amygdala volume only as examples, as these are very commonly replicated results in psychiatry biomarker research. We propose that psychiatry biomarker research could benefit from using psychiatric controls, as the use of healthy controls results in data that are not disorder-specific. METHOD: Hippocampus/amygdala volumes were compared between major depressive disorder, sex-/age-/race-matched healthy control, and psychiatric control (N = 126/group). Similar comparisons were performed for posttraumatic stress disorder (N = 67), borderline personality disorder (N = 111), and alcohol use disorder (N = 136). RESULTS: Major depressive disorder patients had smaller left (p = 8.79 × 10(−3)) and right (p = 3.13 × 10(−3)) hippocampal volumes than healthy control. Posttraumatic stress disorder had smaller left (p = 0.018) and right (p = 8.64 × 10(−4)) hippocampi than healthy control. Borderline personality disorder had smaller right hippocampus (p = 7.90 × 10(−3)) and amygdala (p = 1.49 × 10(−3)) than healthy control. Alcohol use disorder had smaller right hippocampus (p = 0.034) and amygdala (p = .024) than healthy control. No differences were found between any of the four diagnostic groups and psychiatric control. CONCLUSION: When psychiatric controls were used, there was no difference in hippocampal or amygdalar volume between any of the diagnoses studied and controls. This strategy (keeping all possible relevant variables matched between experimental groups) has been used to advance science for hundreds of years, and we propose should also be used in biomarker psychiatry research. |
format | Online Article Text |
id | pubmed-7219869 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-72198692020-05-21 Hippocampal Volume in Psychiatric Diagnoses: Should Psychiatry Biomarker Research Account for Comorbidities? Gosnell, Savannah N. Meyer, Matthew J. Jennings, Cassandra Ramirez, Danna Schmidt, Jake Oldham, John Salas, Ramiro Chronic Stress (Thousand Oaks) Original Article BACKGROUND: Many research papers claim that patients with specific psychiatric disorders (major depressive disorder, posttraumatic stress disorder, borderline personality disorder, alcohol use disorder, and others) have smaller hippocampi, but most of those reports compared patients to healthy controls. We hypothesized that if psychiatrically matched controls (psychiatric control, matched for demographics and psychiatric comorbidities) were used, much of the biomarker literature in psychiatric research would not replicate. We used hippocampus and amygdala volume only as examples, as these are very commonly replicated results in psychiatry biomarker research. We propose that psychiatry biomarker research could benefit from using psychiatric controls, as the use of healthy controls results in data that are not disorder-specific. METHOD: Hippocampus/amygdala volumes were compared between major depressive disorder, sex-/age-/race-matched healthy control, and psychiatric control (N = 126/group). Similar comparisons were performed for posttraumatic stress disorder (N = 67), borderline personality disorder (N = 111), and alcohol use disorder (N = 136). RESULTS: Major depressive disorder patients had smaller left (p = 8.79 × 10(−3)) and right (p = 3.13 × 10(−3)) hippocampal volumes than healthy control. Posttraumatic stress disorder had smaller left (p = 0.018) and right (p = 8.64 × 10(−4)) hippocampi than healthy control. Borderline personality disorder had smaller right hippocampus (p = 7.90 × 10(−3)) and amygdala (p = 1.49 × 10(−3)) than healthy control. Alcohol use disorder had smaller right hippocampus (p = 0.034) and amygdala (p = .024) than healthy control. No differences were found between any of the four diagnostic groups and psychiatric control. CONCLUSION: When psychiatric controls were used, there was no difference in hippocampal or amygdalar volume between any of the diagnoses studied and controls. This strategy (keeping all possible relevant variables matched between experimental groups) has been used to advance science for hundreds of years, and we propose should also be used in biomarker psychiatry research. SAGE Publications 2020-02-26 /pmc/articles/PMC7219869/ /pubmed/32440605 http://dx.doi.org/10.1177/2470547020906799 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Article Gosnell, Savannah N. Meyer, Matthew J. Jennings, Cassandra Ramirez, Danna Schmidt, Jake Oldham, John Salas, Ramiro Hippocampal Volume in Psychiatric Diagnoses: Should Psychiatry Biomarker Research Account for Comorbidities? |
title | Hippocampal Volume in Psychiatric Diagnoses: Should Psychiatry
Biomarker Research Account for Comorbidities? |
title_full | Hippocampal Volume in Psychiatric Diagnoses: Should Psychiatry
Biomarker Research Account for Comorbidities? |
title_fullStr | Hippocampal Volume in Psychiatric Diagnoses: Should Psychiatry
Biomarker Research Account for Comorbidities? |
title_full_unstemmed | Hippocampal Volume in Psychiatric Diagnoses: Should Psychiatry
Biomarker Research Account for Comorbidities? |
title_short | Hippocampal Volume in Psychiatric Diagnoses: Should Psychiatry
Biomarker Research Account for Comorbidities? |
title_sort | hippocampal volume in psychiatric diagnoses: should psychiatry
biomarker research account for comorbidities? |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7219869/ https://www.ncbi.nlm.nih.gov/pubmed/32440605 http://dx.doi.org/10.1177/2470547020906799 |
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