Interleukin-1-targeted treatment strategies in inflammatory depression: toward personalized care

被引:50
作者
Ellul, P. [1 ]
Boyer, L. [2 ]
Groc, L. [3 ]
Leboyer, M. [1 ,4 ]
Fond, G. [1 ,4 ]
机构
[1] Paris Est Univ, DHU Pe PSY, Pole Psychiat Addictol, Hop Univ H Mondor,Translat Psychiat Team,INSERM U, Creteil, France
[2] Aix Marseille Univ, Res Unit Publ Hlth Chron Dis & Qual Life EA 3279, Marseille, France
[3] Bordeaux Univ, UMR 5297, Interdisciplinary Inst Neurosci, CNRS, Bordeaux, France
[4] Fdn FondaMental, Creteil, France
关键词
major depressive disorder; treatment resistance; inflammation; interleukin-1; beta; inflammasome; NECROSIS-FACTOR-ALPHA; C-REACTIVE PROTEIN; NLRP3; INFLAMMASOME; BIPOLAR DISORDER; CHILDHOOD MALTREATMENT; PREFRONTAL CORTEX; TRAUMA EXPOSURE; CYTOKINE LEVELS; MOOD DISORDERS; P2RX7; GENE;
D O I
10.1111/acps.12656
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
ObjectivesIt is unknown whether a cytokine signature may help the identification of subgroup of patient who would respond to personalized treatment. As interleukin-1 beta (Il-1) seems to play a major role in mood disorder, a systematic review and meta-analysis of its potential role in major depressive disorder (MDD) was carried out. MethodsA systematic search was performed to identify appropriate MDD vs. control studies pertaining to Il-1. Methodological quality and possible moderators were also assessed. ResultsA total of 1922 studies were identified, and 53 articles were selected. Results showed an association between increased blood IL-1 and MDD in high-quality studies only. No association with age was found. No IL-1 gene-related polymorphisms has been associated with MDD. No effect of antidepressant on IL-1 level has been found, although the antidepressants investigated were various. Qualitative analyses indicate that MDD coupled to a history of childhood trauma may be a subgroup for IL-1 -targeted therapies. No difference in studies utilizing a stimulation method has been identified to date. ConclusionsThe present work has confirmed IL-1 as a biological marker of interest for innovative MDD treatments. However, further studies are needed to clarify the patients with MDD who may benefit from these therapies.
引用
收藏
页码:469 / 484
页数:16
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