SayuriYamagata Ana, Brietzke Elisa, Rosenblat Joshua D, Kakar Ron, McIntyre Roger S
University of São Paulo (USP), São Paulo, Brazil; Research Group in Molecular and Behavioral Neuroscience of Bipolar Disorder, Federal University of São Paulo (Unifesp), São Paulo, Brazil.
Research Group in Molecular and Behavioral Neuroscience of Bipolar Disorder, Federal University of São Paulo (Unifesp), São Paulo, Brazil.
J Affect Disord. 2017 Mar 15;211:99-106. doi: 10.1016/j.jad.2016.12.059. Epub 2017 Jan 4.
Bipolar disorder (BD) is associated with chronic low-grade inflammation, several medical comorbidities and a decreased life expectancy. Metabolic-inflammatory changes have been postulated as one of the main links between BD and medical comorbidity, although there are few studies exploring possible mechanisms underlying this relationship. Therefore, the aims of the current narrative review were 1) synthesize the evidence for metabolic-inflammatory changes that may facilitate the link between medical comorbidity and BD and 2) discuss therapeutic and preventive implications of these pathways.
The PubMed and Google Scholar databases were searched for relevant studies.
Identified studies suggested that there is an increased risk of medical comorbidities, such as autoimmune disorders, obesity, diabetes and cardiovascular disease in patients with BD. The association between BD and general medical comorbidities seems to be bidirectional and potentially mediated by immune dysfunction. Targeting the metabolic-inflammatory-mood pathway may potential yield improved outcomes in BD; however, further study is needed to determine which specific interventions may be beneficial.
The majority of identified studies had cross-sectional designs, small sample sizes and limited measurements of inflammation.
Treatment and prevention of general medical comorbidities in mood disorders should include preferential prescribing of metabolically neutral agents and adjunctive lifestyle modifications including increased physical activity, improved diet and decreased substance abuse. In addition, the use of anti-inflammatory agents could be a relevant therapeutic target in future research.
双相情感障碍(BD)与慢性低度炎症、多种躯体共病以及预期寿命缩短有关。代谢性炎症变化被认为是BD与躯体共病之间的主要联系之一,尽管很少有研究探讨这种关系背后的潜在机制。因此,本叙述性综述的目的是:1)综合可能促进躯体共病与BD之间联系的代谢性炎症变化的证据;2)讨论这些途径的治疗和预防意义。
在PubMed和谷歌学术数据库中检索相关研究。
已确定的研究表明,BD患者发生自身免疫性疾病、肥胖、糖尿病和心血管疾病等躯体共病的风险增加。BD与一般躯体共病之间的关联似乎是双向的,并且可能由免疫功能障碍介导。针对代谢-炎症-情绪途径可能会改善BD的预后;然而,需要进一步研究以确定哪些具体干预措施可能有益。
大多数已确定的研究采用横断面设计,样本量小,炎症测量有限。
情绪障碍中一般躯体共病的治疗和预防应包括优先开具代谢中性药物以及辅助生活方式改变,包括增加体育活动、改善饮食和减少药物滥用。此外,使用抗炎药物可能是未来研究的一个相关治疗靶点。