Hunt Charlotte, Macedo E Cordeiro Thiago, Suchting Robert, de Dios Constanza, Cuellar Leal Valeria A, Soares Jair C, Dantzer Robert, Teixeira Antonio L, Selvaraj Sudhakar
The University of Texas Health Science Center at Houston, McGovern Medical School, 6431 Fannin St, Houston, TX, 77030, USA.
Louis A. Faillace, MD, Department of Psychiatry and Behavioral Sciences, McGovern Medical School, University of Texas Health Science Center at Houston (UTHealth), 1941 East Rd, Houston, TX, 77054, USA.
Neurosci Biobehav Rev. 2020 Nov;118:514-523. doi: 10.1016/j.neubiorev.2020.08.010. Epub 2020 Aug 24.
Dysregulated kynurenine (KYN) pathway has been implicated in the pathophysiology of depression. In this systematic review, we examined the relationship between kynurenine pathway metabolites (KYN, kynurenic acid KYNA, tryptophan TRP, quinolinic acid QUIN, KYN/TRP ratio) and depression symptoms in the context of pro-inflammatory activation and immune response. Out of 5,082 articles, fifteen studies were suitable; ten studies (N = 315 medically ill patients treated with interferon-alpha IFN-α) reported baseline and post-intervention plasma KYN, TRP and KYN/TRP ratios which were included in quantitative meta-analysis. Data from five studies were summarized (IFN-α, interferon-beta IFN-β, and lipopolysaccharide LPS). We found that IFN-α treatment in patients with chronic illnesses was associated with decreased TRP, increased levels of KYN and KYN/TRP ratio and depression scores from baseline to follow-up at both 4 and 24 weeks. Our findings suggest that increased risk of depression observed after immune-activating agents in patients with chronic medical illnesses is likely mediated by the kynurenine pathway. Further prospective studies are required to investigate the exact pathophysiology of the KYN pathway in depression.
犬尿氨酸(KYN)途径失调与抑郁症的病理生理学有关。在这项系统评价中,我们研究了在促炎激活和免疫反应的背景下,犬尿氨酸途径代谢物(KYN、犬尿喹啉酸KYNA、色氨酸TRP、喹啉酸QUIN、KYN/TRP比值)与抑郁症状之间的关系。在5082篇文章中,有15项研究符合要求;10项研究(N = 315名接受α干扰素IFN-α治疗的内科疾病患者)报告了基线和干预后的血浆KYN、TRP和KYN/TRP比值,这些数据被纳入定量荟萃分析。总结了5项研究的数据(IFN-α、β干扰素IFN-β和脂多糖LPS)。我们发现,慢性病患者接受IFN-α治疗后,从基线到4周和24周随访时,TRP降低,KYN水平和KYN/TRP比值升高,抑郁评分增加。我们的研究结果表明,慢性疾病患者在使用免疫激活剂后观察到的抑郁症风险增加可能是由犬尿氨酸途径介导的。需要进一步的前瞻性研究来调查犬尿氨酸途径在抑郁症中的确切病理生理学。