Reduced plasma Fetuin-A is a promising biomarker of depression in the elderly.


Journal

European archives of psychiatry and clinical neuroscience
ISSN: 1433-8491
Titre abrégé: Eur Arch Psychiatry Clin Neurosci
Pays: Germany
ID NLM: 9103030

Informations de publication

Date de publication:
Oct 2020
Historique:
received: 01 04 2019
accepted: 11 12 2019
pubmed: 22 12 2019
medline: 29 6 2021
entrez: 22 12 2019
Statut: ppublish

Résumé

Depression affects 7% of the elderly population, and it often remains misdiagnosed or untreated. Peripheral biomarkers might aid clinicians by allowing more accurate and well-timed recognition of the disease. We sought to determine if plasma protein levels predict the severity of depressive symptomatology or distinguish patients from healthy individuals. The severity of depressive symptoms and global cognitive functioning were assessed by the Geriatric Depression Scale (GDS) and Mini-Mental State Examination (MMSE) in 152 elderly subjects, 76 of which with major depressive disorder (MDD). Plasma levels of 24 proteins were measured by multiplexing and analyzed as continuous predictors or dichotomized using the median value. The association between individual plasma proteins and MDD risk or depressive symptoms severity was investigated using multiple logistic and linear regressions including relevant covariates. Sensitivity analyses were performed excluding cognitively impaired individuals or non-acute patients with MDD. After adjusting for possible confounders and false discovery rate (FDR) correction, we found lower Fetuin-A levels in MDD patients vs. controls (p

Identifiants

pubmed: 31863164
doi: 10.1007/s00406-019-01090-1
pii: 10.1007/s00406-019-01090-1
doi:

Substances chimiques

AHSG protein, human 0
Biomarkers 0
alpha-2-HS-Glycoprotein 0
Prolactin 9002-62-4

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

901-910

Subventions

Organisme : Korean Health Technology R&D Project, Ministry of Health & Welfare
ID : HC15C1405

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Auteurs

Giuseppe Fanelli (G)

Department of Biomedical and Neuromotor Sciences, University of Bologna, Bologna, Italy.

Francesco Benedetti (F)

Psychiatry and Clinical Psychobiology Unit, Division of Neuroscience, San Raffaele Scientific Institute, Milan, Italy.

Sheng-Min Wang (SM)

Department of Psychiatry, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.

Soo-Jung Lee (SJ)

Department of Psychiatry, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.

Tae-Youn Jun (TY)

Department of Psychiatry, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.

Prakash S Masand (PS)

Global Medical Education, New York, NY, USA.

Ashwin A Patkar (AA)

Department of Psychiatry and Behavioural Sciences, Duke University Medical Center, Durham, NC, USA.

Changsu Han (C)

Department of Psychiatry, College of Medicine, Korea University, Seoul, Republic of Korea.

Alessandro Serretti (A)

Department of Biomedical and Neuromotor Sciences, University of Bologna, Bologna, Italy.

Chi-Un Pae (CU)

Department of Psychiatry, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea. pae@catholic.ac.kr.
Department of Psychiatry and Behavioural Sciences, Duke University Medical Center, Durham, NC, USA. pae@catholic.ac.kr.
Cell Death Disease Research Center, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea. pae@catholic.ac.kr.
Department of Psychiatry, Bucheon St. Mary's Hospital, The Catholic University of Korea, 327 Sosa-ro, Wonmi-gu, Bucheon, 14647, South Korea. pae@catholic.ac.kr.

Chiara Fabbri (C)

Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.

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