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Functional anomalies in healthy individuals with a first degree family history of major depressive disorder
BACKGROUND: Individuals with major depressive disorder (MDD) process information with a bias towards negative stimuli. However, little is known on the link between vulnerability to MDD and brain functional anomalies associated with stimulus bias. METHODS: A cohort of 38 subjects, of which 14 were pa...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3384259/ https://www.ncbi.nlm.nih.gov/pubmed/22738278 http://dx.doi.org/10.1186/2045-5380-2-1 |
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author | Amico, Francesco Carballedo, Angela Lisiecka, Danuta Fagan, Andrew J Boyle, Gerard Frodl, Thomas |
author_facet | Amico, Francesco Carballedo, Angela Lisiecka, Danuta Fagan, Andrew J Boyle, Gerard Frodl, Thomas |
author_sort | Amico, Francesco |
collection | PubMed |
description | BACKGROUND: Individuals with major depressive disorder (MDD) process information with a bias towards negative stimuli. However, little is known on the link between vulnerability to MDD and brain functional anomalies associated with stimulus bias. METHODS: A cohort of 38 subjects, of which 14 were patients with acute MDD and 24 were healthy controls (HC), were recruited and compared. The HC group included 10 healthy participants with a first degree family history of depression (FHP) and 14 volunteers with no family history of any psychiatric disease (FHN). Blood oxygen level dependence signals were acquired from functional magnetic resonance imaging (fMRI) during performance in a dot-probe task using fearful and neutral stimuli. Reaction times and the number of errors were also obtained. RESULTS: Although MDD patients and HC showed no behavioral difference, the MDD group exhibited smaller activation in the left middle cingulum. The MDD group also showed smaller activation in the left insula when compared to the HC group or the FHN group. Finally, FHP participants exhibited higher activation in the right Heschl's gyrus compared to FHN participants. CONCLUSIONS: The present study shows that family risk for MDD is associated with increased activation in the Heschl's gyrus. Our results also suggest that acute MDD is linked to reduced activation in the insula and anterior cingulate cortex during processing of subliminal, not recognizable, masked fearful stimuli. Further research should confirm these results in a larger cohort of participants. |
format | Online Article Text |
id | pubmed-3384259 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-33842592012-06-28 Functional anomalies in healthy individuals with a first degree family history of major depressive disorder Amico, Francesco Carballedo, Angela Lisiecka, Danuta Fagan, Andrew J Boyle, Gerard Frodl, Thomas Biol Mood Anxiety Disord Research BACKGROUND: Individuals with major depressive disorder (MDD) process information with a bias towards negative stimuli. However, little is known on the link between vulnerability to MDD and brain functional anomalies associated with stimulus bias. METHODS: A cohort of 38 subjects, of which 14 were patients with acute MDD and 24 were healthy controls (HC), were recruited and compared. The HC group included 10 healthy participants with a first degree family history of depression (FHP) and 14 volunteers with no family history of any psychiatric disease (FHN). Blood oxygen level dependence signals were acquired from functional magnetic resonance imaging (fMRI) during performance in a dot-probe task using fearful and neutral stimuli. Reaction times and the number of errors were also obtained. RESULTS: Although MDD patients and HC showed no behavioral difference, the MDD group exhibited smaller activation in the left middle cingulum. The MDD group also showed smaller activation in the left insula when compared to the HC group or the FHN group. Finally, FHP participants exhibited higher activation in the right Heschl's gyrus compared to FHN participants. CONCLUSIONS: The present study shows that family risk for MDD is associated with increased activation in the Heschl's gyrus. Our results also suggest that acute MDD is linked to reduced activation in the insula and anterior cingulate cortex during processing of subliminal, not recognizable, masked fearful stimuli. Further research should confirm these results in a larger cohort of participants. BioMed Central 2012-01-12 /pmc/articles/PMC3384259/ /pubmed/22738278 http://dx.doi.org/10.1186/2045-5380-2-1 Text en Copyright ©2012 Amico et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Amico, Francesco Carballedo, Angela Lisiecka, Danuta Fagan, Andrew J Boyle, Gerard Frodl, Thomas Functional anomalies in healthy individuals with a first degree family history of major depressive disorder |
title | Functional anomalies in healthy individuals with a first degree family history of major depressive disorder |
title_full | Functional anomalies in healthy individuals with a first degree family history of major depressive disorder |
title_fullStr | Functional anomalies in healthy individuals with a first degree family history of major depressive disorder |
title_full_unstemmed | Functional anomalies in healthy individuals with a first degree family history of major depressive disorder |
title_short | Functional anomalies in healthy individuals with a first degree family history of major depressive disorder |
title_sort | functional anomalies in healthy individuals with a first degree family history of major depressive disorder |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3384259/ https://www.ncbi.nlm.nih.gov/pubmed/22738278 http://dx.doi.org/10.1186/2045-5380-2-1 |
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