Abnormal C-reactive protein blood levels as a specific biomarker of major depression and non-remission under antidepressants in schizophrenia.


Journal

Progress in neuro-psychopharmacology & biological psychiatry
ISSN: 1878-4216
Titre abrégé: Prog Neuropsychopharmacol Biol Psychiatry
Pays: England
ID NLM: 8211617

Informations de publication

Date de publication:
08 03 2020
Historique:
received: 26 05 2019
revised: 26 10 2019
accepted: 28 10 2019
pubmed: 5 11 2019
medline: 20 1 2021
entrez: 3 11 2019
Statut: ppublish

Résumé

C-reactive protein (CRP) is a general marker of peripheral inflammation and has been shown to be a good marker of neuroinflammation. CRP has been found to be elevated in patients with mood disorders (especially unipolar disorders (UD) and in schizophrenia (SZ)) but also to be lowered by antidepressants. The objectives were (i) to determine the prevalence of major depression, antidepressant prescription and remission under antidepressant in a stabilized population of SZ and UD patients consulting in a daily hospital, and (ii) to determine if CRP was a marker of major depression and remission under antidepressant in these SZ and UD populations. Abnormal CRP was defined by a CRP blood level ≥ 3 mg/L. Depressive symptoms were assessed by the Calgary Depression Rating Scale score. The clinicians were blinded of the CRP status of the patient. 411 patients were included (272 SZ and 139 UD). 171 (41.6%) were diagnosed with current major depression (74 (27.2%) for SZ and 97 (69.8%) for UD). 86 SZ (31.6%) and 119 UD (85.6%) were treated by antidepressant. Only 28/74 (37.8%) of the SZ subjects with major depression were administered antidepressants vs. 87/97 (89.7%) for UD. The non-remission rate under antidepressant was 28/86(32.6%) for SZ and 87/119 (73.1%) for UD. Overall, 105 (40.1%) of SZ and 39 (28.1%) of UD patients were found to have abnormal CRP blood levels. Abnormal CRP levels were significantly associated with increased MDD and more strongly with increased rates of non-remission under antidepressants in SZ patients, independently of age, gender, psychotic symptomatology, functioning, tobacco smoking and metabolic syndrome. This result was not replicated in UD patients, which suggests that CRP may be a specific marker of major depression and remission under antidepressant in SZ patients. The development of biomarkers in psychiatry may orientate specific etiologic therapies in patients with mental disorders. The present findings suggest that major depression is frequent in SZ patients and that increased CRP levels are associated with non-remission under antidepressants in this population. Anti-inflammatory strategies may be particularly useful in this specific population.

Sections du résumé

BACKGROUND
C-reactive protein (CRP) is a general marker of peripheral inflammation and has been shown to be a good marker of neuroinflammation. CRP has been found to be elevated in patients with mood disorders (especially unipolar disorders (UD) and in schizophrenia (SZ)) but also to be lowered by antidepressants.
OBJECTIVE
The objectives were (i) to determine the prevalence of major depression, antidepressant prescription and remission under antidepressant in a stabilized population of SZ and UD patients consulting in a daily hospital, and (ii) to determine if CRP was a marker of major depression and remission under antidepressant in these SZ and UD populations.
METHODS
Abnormal CRP was defined by a CRP blood level ≥ 3 mg/L. Depressive symptoms were assessed by the Calgary Depression Rating Scale score. The clinicians were blinded of the CRP status of the patient.
RESULTS
411 patients were included (272 SZ and 139 UD). 171 (41.6%) were diagnosed with current major depression (74 (27.2%) for SZ and 97 (69.8%) for UD). 86 SZ (31.6%) and 119 UD (85.6%) were treated by antidepressant. Only 28/74 (37.8%) of the SZ subjects with major depression were administered antidepressants vs. 87/97 (89.7%) for UD. The non-remission rate under antidepressant was 28/86(32.6%) for SZ and 87/119 (73.1%) for UD. Overall, 105 (40.1%) of SZ and 39 (28.1%) of UD patients were found to have abnormal CRP blood levels. Abnormal CRP levels were significantly associated with increased MDD and more strongly with increased rates of non-remission under antidepressants in SZ patients, independently of age, gender, psychotic symptomatology, functioning, tobacco smoking and metabolic syndrome. This result was not replicated in UD patients, which suggests that CRP may be a specific marker of major depression and remission under antidepressant in SZ patients.
CONCLUSION
The development of biomarkers in psychiatry may orientate specific etiologic therapies in patients with mental disorders. The present findings suggest that major depression is frequent in SZ patients and that increased CRP levels are associated with non-remission under antidepressants in this population. Anti-inflammatory strategies may be particularly useful in this specific population.

Identifiants

pubmed: 31676465
pii: S0278-5846(19)30449-X
doi: 10.1016/j.pnpbp.2019.109800
pii:
doi:

Substances chimiques

Antidepressive Agents 0
Biomarkers 0
C-Reactive Protein 9007-41-4

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

109800

Informations de copyright

Copyright © 2019 Elsevier Inc. All rights reserved.

Auteurs

G Fond (G)

Department of Psychiatry, La Conception University Hospital, 13005 Marseille, France; EA 3279 - EA 3279: CEReSS, Health Service Research and Quality of Life Center, 27 Boulevard Jean Moulin, 13005 Marseille, France. Electronic address: guillaume.fond@ap-hm.fr.

J A Micoulaud-Franchi (JA)

Department of Psychiatry, La Conception University Hospital, 13005 Marseille, France; SHU Adult Psychiatry, Sainte Marguerite University Hospital, 13274 Marseille, France.

M Faugere (M)

Department of Psychiatry, La Conception University Hospital, 13005 Marseille, France; EA 3279 - EA 3279: CEReSS, Health Service Research and Quality of Life Center, 27 Boulevard Jean Moulin, 13005 Marseille, France.

L Boyer (L)

Department of Psychiatry, La Conception University Hospital, 13005 Marseille, France; EA 3279 - EA 3279: CEReSS, Health Service Research and Quality of Life Center, 27 Boulevard Jean Moulin, 13005 Marseille, France.

C Faget-Agius (C)

Department of Psychiatry, La Conception University Hospital, 13005 Marseille, France; EA 3279 - EA 3279: CEReSS, Health Service Research and Quality of Life Center, 27 Boulevard Jean Moulin, 13005 Marseille, France.

C Lançon (C)

Department of Psychiatry, La Conception University Hospital, 13005 Marseille, France; EA 3279 - EA 3279: CEReSS, Health Service Research and Quality of Life Center, 27 Boulevard Jean Moulin, 13005 Marseille, France.

R Richieri (R)

Department of Psychiatry, La Conception University Hospital, 13005 Marseille, France; EA 3279 - EA 3279: CEReSS, Health Service Research and Quality of Life Center, 27 Boulevard Jean Moulin, 13005 Marseille, France.

M Cermolacce (M)

SHU Adult Psychiatry, Sainte Marguerite University Hospital, 13274 Marseille, France; Institut de Neurosciences des Systèmes (INS, INSERM UMR 1106), Aix-Marseille University, Marseilles, France.

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