Inflammation and remission in older patients with depression treated with electroconvulsive therapy; findings from the MODECT study


Journal

Journal of affective disorders
ISSN: 1573-2517
Titre abrégé: J Affect Disord
Pays: Netherlands
ID NLM: 7906073

Informations de publication

Date de publication:
01 09 2019
Historique:
received: 12 02 2019
revised: 07 05 2019
accepted: 30 06 2019
pubmed: 7 7 2019
medline: 4 6 2020
entrez: 7 7 2019
Statut: ppublish

Résumé

Compelling evidence links elevated levels of C-reactive protein (CRP) and other inflammatory markers to poor treatment outcome of antidepressant medication. Little is known about the contribution of low-grade inflammation to treatment response to electroconvulsive therapy (ECT) in severely depressed patients. Associations between serum levels of CRP, interleukin-6, interleukin-10, and tumour necrosis factor-α as well as remission of depression, time to remission, and speed of decline of depressive symptoms were examined in 95 older (mean age: 73.1 years) depressed patients treated with ECT. Moderately elevated levels of CRP at baseline (3 to 10 mg/L), but no other inflammatory markers, were associated with higher remission rates. In patients with moderately elevated CRP levels, the odds ratio for remission was 3.62 (95% confidence interval [CI], 1.09-11.97; p = 0.04). Time to remission was shorter in those with moderately elevated CRP levels (p = 0.05). Speed of decline was higher in patients with moderately elevated CRP levels as compared with those with low CRP levels (decline of 3.2 Montgomery Åsberg Depression Rating Scale points per administration vs. 2.3 points per administration, p = 0.03). Because of the observational design, residual confounding through other lifestyle or demographic factors cannot be ruled out. Although earlier studies showed that low-grade inflammation contributes to poor treatment response in those treated with antidepressants, our study provides clues that low-grade inflammation does not have such a detrimental effect on the treatment response to ECT. This is underscored by our finding that moderately elevated CRP levels were associated with increased remission rates in depressed patients treated with ECT. Replication studies are warranted.

Sections du résumé

BACKGROUND
Compelling evidence links elevated levels of C-reactive protein (CRP) and other inflammatory markers to poor treatment outcome of antidepressant medication. Little is known about the contribution of low-grade inflammation to treatment response to electroconvulsive therapy (ECT) in severely depressed patients.
METHOD
Associations between serum levels of CRP, interleukin-6, interleukin-10, and tumour necrosis factor-α as well as remission of depression, time to remission, and speed of decline of depressive symptoms were examined in 95 older (mean age: 73.1 years) depressed patients treated with ECT.
RESULTS
Moderately elevated levels of CRP at baseline (3 to 10 mg/L), but no other inflammatory markers, were associated with higher remission rates. In patients with moderately elevated CRP levels, the odds ratio for remission was 3.62 (95% confidence interval [CI], 1.09-11.97; p = 0.04). Time to remission was shorter in those with moderately elevated CRP levels (p = 0.05). Speed of decline was higher in patients with moderately elevated CRP levels as compared with those with low CRP levels (decline of 3.2 Montgomery Åsberg Depression Rating Scale points per administration vs. 2.3 points per administration, p = 0.03).
LIMITATIONS
Because of the observational design, residual confounding through other lifestyle or demographic factors cannot be ruled out.
CONCLUSIONS
Although earlier studies showed that low-grade inflammation contributes to poor treatment response in those treated with antidepressants, our study provides clues that low-grade inflammation does not have such a detrimental effect on the treatment response to ECT. This is underscored by our finding that moderately elevated CRP levels were associated with increased remission rates in depressed patients treated with ECT. Replication studies are warranted.

Identifiants

pubmed: 31279250
pii: S0165-0327(19)30215-0
doi: 10.1016/j.jad.2019.06.040
pii:
doi:

Substances chimiques

Antidepressive Agents 0
Biomarkers 0
IL10 protein, human 0
Interleukin-6 0
TNF protein, human 0
Tumor Necrosis Factor-alpha 0
Interleukin-10 130068-27-8
C-Reactive Protein 9007-41-4

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

509-516

Informations de copyright

Copyright © 2019. Published by Elsevier B.V.

Auteurs

Angela Carlier (A)

GGZ inGeest Specialized Mental Health Care, Department of Old Age Psychiatry, Oldenaller 1, 1081 HJ, Amsterdam, the Netherlands; Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam Public Health research institute and NCA Neuroscience Amsterdam, the Netherlands. Electronic address: a.carlier@ggzingeest.nl.

Johanna G Berkhof (JG)

GGZ inGeest Specialized Mental Health Care, Department of Old Age Psychiatry, Oldenaller 1, 1081 HJ, Amsterdam, the Netherlands.

Maarten Rozing (M)

Section of General Practice, Department of Public Health, University of Copenhagen.

Filip Bouckaert (F)

KU Leuven, University Psychiatric Centre KU Leuven, department of Old Age Psychiatry, Leuven/Kortenberg, Belgium; KU Leuven, University Psychiatric Centre KU Leuven, Academic Center for ECT and Neuromodulation, Leuven/Kortenberg, Belgium.

Pascal Sienaert (P)

KU Leuven, University Psychiatric Centre KU Leuven, Academic Center for ECT and Neuromodulation, Leuven/Kortenberg, Belgium.

Piet Eikelenboom (P)

GGZ inGeest Specialized Mental Health Care, Department of Old Age Psychiatry, Oldenaller 1, 1081 HJ, Amsterdam, the Netherlands.

Robert Veerhuis (R)

Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam Public Health research institute and NCA Neuroscience Amsterdam, the Netherlands; Amsterdam UMC, Vrije Universiteit Amsterdam, Clinical Chemistry department, the Netherlands.

Mathieu Vandenbulcke (M)

KU Leuven, University Psychiatric Centre KU Leuven, department of Old Age Psychiatry, Leuven/Kortenberg, Belgium.

Johannes Berkhof (J)

Amsterdam UMC, Vrije Universiteit Amsterdam, department of Epidemiology & Biostatistics, the Netherlands.

Max L Stek (ML)

GGZ inGeest Specialized Mental Health Care, Department of Old Age Psychiatry, Oldenaller 1, 1081 HJ, Amsterdam, the Netherlands; Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam Public Health research institute and NCA Neuroscience Amsterdam, the Netherlands.

Didi Rhebergen (D)

GGZ inGeest Specialized Mental Health Care, Department of Old Age Psychiatry, Oldenaller 1, 1081 HJ, Amsterdam, the Netherlands; Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam Public Health research institute and NCA Neuroscience Amsterdam, the Netherlands.

Annemiek Dols (A)

GGZ inGeest Specialized Mental Health Care, Department of Old Age Psychiatry, Oldenaller 1, 1081 HJ, Amsterdam, the Netherlands; Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam Public Health research institute and NCA Neuroscience Amsterdam, the Netherlands.

Eric van Exel (EV)

GGZ inGeest Specialized Mental Health Care, Department of Old Age Psychiatry, Oldenaller 1, 1081 HJ, Amsterdam, the Netherlands; Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam Public Health research institute and NCA Neuroscience Amsterdam, the Netherlands.

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Classifications MeSH