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Lower Locus Coeruleus MRI intensity in patients with late-life major depression

Authors :
Andrés Guinea-Izquierdo
Mónica Giménez
Ignacio Martínez-Zalacaín
Inés del Cerro
Pol Canal-Noguer
Gerard Blasco
Jordi Gascón
Ramon Reñé
Inmaculada Rico
Angels Camins
Carlos Aguilera
Mikel Urretavizcaya
Isidre Ferrer
José Manuel Menchón
Virginia Soria
Carles Soriano-Mas
Source :
PeerJ, Vol 9, p e10828 (2021)
Publication Year :
2021
Publisher :
PeerJ Inc., 2021.

Abstract

Background The locus coeruleus (LC) is the major noradrenergic source in the central nervous system. Structural alterations in the LC contribute to the pathophysiology of different neuropsychiatric disorders, which may increase to a variable extent the likelihood of developing neurodegenerative conditions. The characterization of such alterations may therefore help to predict progression to neurodegenerative disorders. Despite the LC cannot be visualized with conventional magnetic resonance imaging (MRI), specific MRI sequences have been developed to infer its structural integrity. Methods We quantified LC signal Contrast Ratios (LCCRs) in late-life major depressive disorder (MDD) (n = 37, 9 with comorbid aMCI), amnestic Mild Cognitive Impairment (aMCI) (n = 21, without comorbid MDD), and healthy controls (HCs) (n = 31), and also assessed the putative modulatory effects of comorbidities and other clinical variables. Results LCCRs were lower in MDD compared to aMCI and HCs. While no effects of aMCI comorbidity were observed, lower LCCRs were specifically observed in patients taking serotonin/norepinephrine reuptake inhibitors (SNRIs). Conclusion Our results do not support the hypothesis that lower LCCRs characterize the different clinical groups that may eventually develop a neurodegenerative disorder. Conversely, our results were specifically observed in patients with late-life MDD taking SNRIs. Further research with larger samples is warranted to ascertain whether medication or particular clinical features of patients taking SNRIs are associated with changes in LC neurons.

Details

Language :
English
ISSN :
21678359
Volume :
9
Database :
Directory of Open Access Journals
Journal :
PeerJ
Publication Type :
Academic Journal
Accession number :
edsdoj.721a4f1a04c4c9f8ce7d1b6a839cd08
Document Type :
article
Full Text :
https://doi.org/10.7717/peerj.10828