| Literature DB >> 34227186 |
Shinji Sakamoto1, Xiaolei Zhu1, Yuto Hasegawa1, Sadik Karma1, Mizuho Obayashi1, Emily Alway1, Atsushi Kamiya1.
Abstract
Although there are a number of clinically effective treatments for depression, many patients exhibit treatment resistance. Recent clinical and preclinical studies reveal that peripheral and brain immune changes and inflammation are involved in the pathophysiology of depression. This 'Inflamed Brain' research provides critical clues for understanding of disease pathophysiology and many candidate molecules that are potentially useful for identifying novel drug targets for the treatment of depression. In this review, we will present clinical evidence on the role of inflammation in the pathophysiology of depression. We will also summarize current clinical trials which test drugs targeting inflammation for the treatment of patients with depression. Furthermore, we will briefly provide preclinical evidence demonstrating altered immune system function and inflammation in stress-induced animal models and will discuss the future potential of inflammation-related drug targets. Collectively, inflammatory signatures identified in clinical and preclinical studies may allow us to stratify depressive patients based on biotypes, contributing to the development of novel mechanism-based interventions that target specific patient populations.Entities:
Keywords: biotype; depression; drug-repositioning; inflammation; stress mouse models
Mesh:
Year: 2021 PMID: 34227186 PMCID: PMC8683253 DOI: 10.1111/pcn.13286
Source DB: PubMed Journal: Psychiatry Clin Neurosci ISSN: 1323-1316 Impact factor: 12.145