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脑源性神经营养因子基因变异体Rs6265与未接受抗抑郁治疗的抑郁症患者抑郁严重程度之间的关联

Association Between BDNF Gene Variant Rs6265 and the Severity of Depression in Antidepressant Treatment-Free Depressed Patients.

作者信息

Losenkov Innokentiy S, Mulder Nathaniël J V, Levchuk Lyudmila A, Vyalova Natalya M, Loonen Anton J M, Bosker Fokko J, Simutkin German G, Boiko Anastasiia S, Bokhan Nikolay A, Wilffert Bob, Hak Eelko, Schmidt Amand F, Ivanova Svetlana A

机构信息

Mental Health Research Institute, Tomsk National Research Medical Center of the Russian Academy of Sciences, Tomsk, Russia.

Unit of PharmacoTherapy, -Epidemiology & -Economics, Groningen Research Institute of Pharmacy, University of Groningen, Groningen, Netherlands.

出版信息

Front Psychiatry. 2020 Feb 12;11:38. doi: 10.3389/fpsyt.2020.00038. eCollection 2020.

Abstract

BACKGROUND

Brain-derived neurotrophic factor (BDNF) plays an important role in neuronal plasticity, and its dysregulation has been associated with the pathogenesis of mood and anxiety disorders. Prolactin (PRL) is a pituitary hormone which is also produced as a cytokine by immune cells and could be a neurotrophic factor regulating the functional activity of stress-related mechanisms.

AIM

To investigate the possible relationship between depressive state and BDNF and PRL genotypes or levels with special reference to severity of depression.

METHODS

Participants of 18-70 years with a clinical diagnosis of depressive disorder of at least moderate severity were included. These patients had not been treated with antidepressant drugs before admission to hospital during the preceding period of the last 6 months, and 54.5% had never been treated with antidepressant drugs during their entire life. The DNA was genotyped for rs1341239 within the prolactin and for rs6265, rs7124442, and rs11030104 within the BDNF gene. Rs11030104 violated the Hardy-Weinberg equilibrium distribution and was excluded from further analyses. BDNF and prolactin concentration was measured in serum by MAGPIX multiplex analyzer (Luminex, USA) using MILLIPLEX MAP kit (Merck, Germany). Genetic associations were determined by sequentially regressing prolactin, BDNF, 17-items Hamilton's Depression (HAMD-17) and Clinical Global Impression scale, Severity (CGI-S) ratings, and depression (absent/present) on the available SNPs. Genetic associations were evaluated assuming an additive model.

RESULTS

A total of 186 depressed patients (of which 169 were women) and 94 healthy controls (67 women) were genotyped. After excluding subjects without genetic information on all three study SNPs, 217 remained of whom 138 suffered from depression. Within depressed patients we observed an association of rs6265 with HAMD-17: mean difference (MD) 2.33 (95%CI 0.49; 4.16; = 0.014) and CGI-S: MD 0.38 (95%CI 0.09; 0.66; = 0.011). No significant association was observed between the prolactin SNP rs1341239 and prolactin levels. Similarly the mean differences of BDNF SNPs did not show an association with BDNF: rs6265 -0.042 ln(pg/ml) (95%CI -0.198; 0.113), and rs7124442 0.006 ln(pg/ml) (95%CI -0.117; 0.130). No other association reached statistical significance.

CONCLUSION

We observed a significant association between BDNF gene variant rs6265 and the severity of depression in newly admitted, antidepressant treatment-free, depressed patients. Actual PRL and BDNF levels were not elevated sufficiently in depressed patients to reach statistical significance and were not associated with the studied genotypes.

摘要

背景

脑源性神经营养因子(BDNF)在神经元可塑性中起重要作用,其失调与情绪和焦虑障碍的发病机制有关。催乳素(PRL)是一种垂体激素,免疫细胞也可将其作为细胞因子产生,它可能是调节应激相关机制功能活动的神经营养因子。

目的

研究抑郁状态与BDNF和PRL基因类型或水平之间的可能关系,特别关注抑郁的严重程度。

方法

纳入年龄在18 - 70岁、临床诊断为至少中度严重程度抑郁症的参与者。这些患者在入院前的前6个月内未接受过抗抑郁药物治疗,54.5%的患者一生中从未接受过抗抑郁药物治疗。对催乳素基因内的rs1341239以及BDNF基因内的rs6265、rs7124442和rs11030104进行基因分型。rs11030104违反了哈迪 - 温伯格平衡分布,被排除在进一步分析之外。使用MILLIPLEX MAP试剂盒(德国默克公司)通过MAGPIX多重分析仪(美国Luminex公司)测定血清中的BDNF和催乳素浓度。通过将催乳素、BDNF、17项汉密尔顿抑郁量表(HAMD - 17)评分、临床总体印象量表严重程度(CGI - S)评分以及抑郁状态(存在/不存在)依次对可用的单核苷酸多态性(SNP)进行回归分析来确定基因关联。采用加性模型评估基因关联。

结果

共对186例抑郁症患者(其中169例为女性)和94例健康对照者(67例女性)进行了基因分型。在排除所有三个研究SNP均无遗传信息的受试者后,剩下217例,其中138例患有抑郁症。在抑郁症患者中,我们观察到rs6265与HAMD - 17之间存在关联:平均差异(MD)为2.33(95%置信区间0.49;4.16;P = 0.014),与CGI - S之间也存在关联:MD为0.38(95%置信区间0.09;0.66;P = 0.011)。未观察到催乳素SNP rs1341239与催乳素水平之间存在显著关联。同样,BDNF SNP的平均差异与BDNF也未显示出关联:rs6265为 - 0.042 ln(pg/ml)(95%置信区间 - 0.198;0.113),rs7124442为0.006 ln(pg/ml)(95%置信区间 - 0.117;0.130)。没有其他关联达到统计学显著性。

结论

我们观察到BDNF基因变体rs6265与新入院、未接受抗抑郁治疗的抑郁症患者的抑郁严重程度之间存在显著关联。抑郁症患者的实际PRL和BDNF水平升高幅度未达到统计学显著性,且与所研究的基因类型无关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6bd/7028755/6223f502fa27/fpsyt-11-00038-g001.jpg

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