Department of Clinical Sciences Lund, Psychiatry, Faculty of Medicine, Lund University, 221 85 Lund, Sweden.
Office for Psychiatry and Habilitation, Psychiatric Clinic Helsingborg, Region Skåne, 252 23 Helsingborg, Sweden.
Int J Mol Sci. 2021 Feb 6;22(4):1640. doi: 10.3390/ijms22041640.
Treatment of depression is hampered by the failure to identify distinct symptom profiles with distinct pathophysiologies that differentially respond to distinct treatments. We posit that inflammatory depression is a meaningful depression subtype associated with specific symptoms and biological abnormalities. We review several upstream, potentially causative, mechanisms driving low-grade inflammation in this subtype of depression. We also discuss downstream mechanisms mediating the link between inflammation and symptoms of depression, including alterations in dopaminergic neurotransmission and tryptophan metabolism. Finally, we review evidence for several non-pharmacological interventions for inflammatory depression, including probiotics, omega-3 fatty acids, and physical exercise interventions. While some evidence suggests that these interventions may be efficacious in inflammatory depression, future clinical trials should consider enriching patient populations for inflammatory markers, or stratify patients by inflammatory status, to confirm or refute this hypothesis.
抑郁症的治疗受到阻碍,因为未能确定具有不同病理生理学的不同症状特征,这些特征对不同的治疗方法有不同的反应。我们假设炎症性抑郁症是一种有意义的抑郁症亚型,与特定的症状和生物学异常有关。我们回顾了几种可能导致这种亚型抑郁症低度炎症的上游潜在病因机制。我们还讨论了炎症与抑郁症症状之间的下游机制,包括多巴胺能神经递质传递和色氨酸代谢的改变。最后,我们回顾了几种针对炎症性抑郁症的非药物干预措施的证据,包括益生菌、ω-3 脂肪酸和体育锻炼干预。虽然有一些证据表明这些干预措施在炎症性抑郁症中可能有效,但未来的临床试验应考虑为炎症标志物富集患者人群,或根据炎症状态对患者进行分层,以证实或反驳这一假设。