a Department of Psychiatry , Massachusetts General Hospital , Boston , MA , USA.
b Department of Psychiatry , Hospital de Clínicas de Porto Alegre , Porto Alegre , Brasil.
World J Biol Psychiatry. 2018 Aug;19(5):402-409. doi: 10.1080/15622975.2017.1347713. Epub 2017 Jul 12.
Current evidence supports participation of neurotrophic and inflammatory factors in the pathogenesis of major depressive disorder (MDD). Some studies reported an association between the Val66Met polymorphism (rs6265) of brain-derived neurotrophic factor (BDNF) gene with MDD and peripheral BDNF levels. However, no previous studies have examined the association of this polymorphism with inflammation. The present study assessed the association of the Val66Met polymorphism with serum levels of BDNF and inflammatory markers among depressed outpatients.
All participants (n = 73) met DSM-IV criteria for a unipolar depressive episode. The serum levels of BDNF and inflammatory biomarkers (IL-2, IL-4, IL-6, IL-10, TNF-α and IFN-γ) were compared between individuals presenting with at least one Met allele (Met-carriers) and those homozygous for the Val allele.
In our sample (84.9% female, mean age 52.4 ± 10.3 years), 24.7% (n = 18) were Met-carriers. After Bonferroni correction, the Met allele was significantly associated with higher BDNF and lower TNF-α. These associations persisted after adjusting for potential confounders.
The pattern of low BDNF and high inflammation in MDD may be influenced by the Val66Met polymorphism. The association of a polymorphism in the BDNF gene with inflammatory markers in addition to BDNF levels suggests an interaction between these systems.
目前的证据支持神经营养和炎症因子参与重度抑郁症(MDD)的发病机制。一些研究报道脑源性神经营养因子(BDNF)基因 Val66Met 多态性(rs6265)与 MDD 和外周 BDNF 水平之间存在关联。然而,以前的研究尚未探讨该多态性与炎症之间的关系。本研究评估了该多态性与抑郁门诊患者血清 BDNF 和炎症标志物水平之间的关系。
所有参与者(n=73)均符合 DSM-IV 单相抑郁发作标准。比较至少携带一个 Met 等位基因(Met 携带者)和 Val 等位基因纯合子个体之间血清 BDNF 和炎症生物标志物(IL-2、IL-4、IL-6、IL-10、TNF-α和 IFN-γ)的水平。
在我们的样本中(84.9%为女性,平均年龄 52.4±10.3 岁),24.7%(n=18)为 Met 携带者。经 Bonferroni 校正后,Met 等位基因与较高的 BDNF 和较低的 TNF-α显著相关。这些关联在调整潜在混杂因素后仍然存在。
MDD 中低 BDNF 和高炎症的模式可能受 Val66Met 多态性的影响。BDNF 基因多态性与炎症标志物以及 BDNF 水平的关联表明这些系统之间存在相互作用。