Academic Journal
Genes of neurotrophic factors and responsiveness to antidepressive psychopharmacotherapy in patients with depressive disorders
| العنوان: | Genes of neurotrophic factors and responsiveness to antidepressive psychopharmacotherapy in patients with depressive disorders |
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| المؤلفون: | Levchuk, L., Losenkov, I., Pozhidaev, I., Osmanova, D., Simutkin, G., Bokhan, N., Loonen, A., Ivanova, S.A. |
| المصدر: | Levchuk , L , Losenkov , I , Pozhidaev , I , Osmanova , D , Simutkin , G , Bokhan , N , Loonen , A & Ivanova , S A 2019 , ' Genes of neurotrophic factors and responsiveness to antidepressive psychopharmacotherapy in patients with depressive disorders ' , European Neuropsychopharmacology , vol. 29 , no. Supplement 1 , pp. S341-S342 . https://doi.org/10.1016/j.euroneuro.2018.11.532 |
| سنة النشر: | 2019 |
| المجموعة: | University of Groningen research database |
| مصطلحات موضوعية: | antidepressant agent, brain derived neurotrophic factor, endogenous compound, phosphotransferase, prolactin, adult, basic research, chi square test, clinical feature, Clinical Global Impression scale, conference abstract, controlled study, data analysis software, drug therapy, female, gene frequency, gene mutation, genetic association, genetic susceptibility, genotype, Hamilton Depression Rating Scale, human, ICD-10, major clinical study, major depression, male, psychopharmacotherapy, remission, serotoninergic system, treatment response |
| الوصف: | Major depressive disorder (MDD) is a clinically and biologically heterogeneous disorder with a heavy personal and socio-economic burden [1]. The neurotrophic theory of the development of depression most fully explains the morphological changes that occur in the brain of patients [2,3]. Among the various neurotrophic factors brain-derived neurotrophic factor (BDNF) and prolactin play an important role in pathogenesis of depression [4]. Objective of the study was to investigate the association of genes polymorphisms of BDNF and prolactin with responsiveness to therapy in patients with MDD. Methods The study group included 185 MDD patients (F32,F33,ICD-10) and 134 healthy persons. Severity of depressive symptoms on the baseline and on the 14th and 28th day of therapy was assessed using Hamilton Depression Scale (HDRS-17) and Clinical Global Impression – Severity scale (CGI-S). Antidepressive therapy response on the 14th and 28th day of therapy was evaluated using Clinical Global Impression – Improvement scale (CGI-I). Genotyping was carried out on polymorphic variants of BDNF genes (rs6265, rs7124442, rs11030104) and PRL gene (rs1341239). The SPSS software was used for statistical analysis. The Hardy-Weinberg equilibrium (HWE) of genotypic frequencies was tested by the chi-square test. Results The study found no deviation of genotype frequencies from HWE (р > 0.05), except for the SNP rs11030104 in the group of patients (χ2 = 37.540; p = 0.001). Important differences in frequency of genotypes and alleles of SNPs rs11030104 of BDNF and rs1341239 of PRL genes between patients and healthy persons at entry have been found. The final multivariate binary logistic regression analysis shows that the A/A genotype of SNP rs11030104 has a more than 6 times higher risk of developing depression than G/G or G/A genotype (p = 0.009). Allele G of SNP rs1341239 gene was more common in patients (63%) compared to control (59%) (p <0.001). We studied the association between the scores on the HDRS-17, CGI-S and CGI-I scales and ... |
| نوع الوثيقة: | article in journal/newspaper |
| وصف الملف: | application/pdf |
| اللغة: | English |
| Relation: | https://research.rug.nl/en/publications/0fa9e425-801d-46de-a418-60c5004ba49e |
| DOI: | 10.1016/j.euroneuro.2018.11.532 |
| الاتاحة: | https://hdl.handle.net/11370/0fa9e425-801d-46de-a418-60c5004ba49e https://research.rug.nl/en/publications/0fa9e425-801d-46de-a418-60c5004ba49e https://doi.org/10.1016/j.euroneuro.2018.11.532 https://pure.rug.nl/ws/files/76676662/1_s2.0_S0924977X18313798_main.pdf |
| Rights: | info:eu-repo/semantics/openAccess |
| رقم الانضمام: | edsbas.1638D197 |
| قاعدة البيانات: | BASE |
| DOI: | 10.1016/j.euroneuro.2018.11.532 |
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