Investigating the potential role of BDNF and PRL genotypes on antidepressant response in depression patients: A prospective inception cohort study in treatment-free patients; Journal of Affective Disorders; Vol. 259

Bibliografiske detaljer
Parent link:Journal of Affective Disorders
Vol. 259.— 2019.— [P. 432-439]
Institution som forfatter: Национальный исследовательский Томский политехнический университет Инженерная школа неразрушающего контроля и безопасности Отделение контроля и диагностики
Andre forfattere: Ochi T., Vyalova N. N. Nataljya Mikhaylovna, Losenkov I. S. Innokenty Sergeevich, Levchuk L. A. Lyudmila Aleksandrovna, Osmanova D. Z. Diana Zakirovna, Mikhalitskaya E. V., Loonen A. J. M. Anton, Bosker F. J. Fokko, Simutkin G. G. German Gennadjevich, Bokhan N., Wilffert B. Bob, Ivanova S. A. Svetlana Aleksandrovna
Summary:Title screen
Background:Brain-derived neurotrophic factor (BDNF) is associated with response to antidepressant drugs inmood and anxiety disorders. Prolactin (PRL) is a pituitary hormone with behavioural effects, acting as a neu-rotrophic factor within the brain and may be involved in antidepressant response.Objectives:To investigate the relationship betweenBDNFandPRLgenotypes with antidepressant drug response.Methods:Prospective inception cohort of 186 Russian treatment-free participants (28 men and 158 women)between 18 and 70 years clinically diagnosed with depressive disorder who initiated antidepressant medication.DNA polymorphisms were genotyped forPRLrs1341239,BDNFrs6265 and rs7124442. Primary outcome wasmeasured by differences in Hamilton Depression Rating Scale (ΔHAM-D) scores between baseline/week two,week two/week four, and baseline/week four. Linear regression and independentt-test determined the sig-nificance between polymorphisms andΔHAM-D.
Results: Comparisons between genotypes did not reveal any significant differences in scores during thefirst twoweeks of treatment. In the latter two weeks, BDNFrs7124442 homozygous C patients responded significantlyworse in comparison to homozygous T patients during this period. Further analysis within women and in post-menopausal women found a similar comparison between alleles. Limitations: Study lasted four weeks, which may be considered short to associate genuine antidepressant effects.Conclusions:Patients taking tricylic antidepressants were noted to have a significant improvement inΔHAM-Dcompared to patients taking SSRIs. Homozygous CBDNFrs712442 patients were found to respond significantlyworse in the last two weeks of treatment.
Режим доступа: по договору с организацией-держателем ресурса
Sprog:engelsk
Udgivet: 2019
Fag:
Online adgang:https://doi.org/10.1016/j.jad.2019.08.058
Format: MixedMaterials Electronisk Book Chapter
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=661164

MARC

LEADER 00000naa0a2200000 4500
001 661164
005 20250411143558.0
035 |a (RuTPU)RU\TPU\network\31411 
035 |a RU\TPU\network\31217 
090 |a 661164 
100 |a 20191121d2019 k||y0rusy50 ba 
101 0 |a eng 
135 |a drcn ---uucaa 
181 0 |a i  
182 0 |a b 
200 1 |a Investigating the potential role of BDNF and PRL genotypes on antidepressant response in depression patients: A prospective inception cohort study in treatment-free patients  |f T. Ochi [et al.] 
203 |a Text  |c electronic 
300 |a Title screen 
330 |a Background:Brain-derived neurotrophic factor (BDNF) is associated with response to antidepressant drugs inmood and anxiety disorders. Prolactin (PRL) is a pituitary hormone with behavioural effects, acting as a neu-rotrophic factor within the brain and may be involved in antidepressant response.Objectives:To investigate the relationship betweenBDNFandPRLgenotypes with antidepressant drug response.Methods:Prospective inception cohort of 186 Russian treatment-free participants (28 men and 158 women)between 18 and 70 years clinically diagnosed with depressive disorder who initiated antidepressant medication.DNA polymorphisms were genotyped forPRLrs1341239,BDNFrs6265 and rs7124442. Primary outcome wasmeasured by differences in Hamilton Depression Rating Scale (ΔHAM-D) scores between baseline/week two,week two/week four, and baseline/week four. Linear regression and independentt-test determined the sig-nificance between polymorphisms andΔHAM-D. 
330 |a Results: Comparisons between genotypes did not reveal any significant differences in scores during thefirst twoweeks of treatment. In the latter two weeks, BDNFrs7124442 homozygous C patients responded significantlyworse in comparison to homozygous T patients during this period. Further analysis within women and in post-menopausal women found a similar comparison between alleles. Limitations: Study lasted four weeks, which may be considered short to associate genuine antidepressant effects.Conclusions:Patients taking tricylic antidepressants were noted to have a significant improvement inΔHAM-Dcompared to patients taking SSRIs. Homozygous CBDNFrs712442 patients were found to respond significantlyworse in the last two weeks of treatment. 
333 |a Режим доступа: по договору с организацией-держателем ресурса 
461 |t Journal of Affective Disorders 
463 |t Vol. 259  |v [P. 432-439]  |d 2019 
610 1 |a электронный ресурс 
610 1 |a труды учёных ТПУ 
610 1 |a major depressive disorder 
610 1 |a prolactin 
610 1 |a brain derived neurotrophic factor 
610 1 |a rs6265rs7124442 
610 1 |a antidepressant response 
610 1 |a депрессивные расстройства 
610 1 |a антидепрессанты 
701 1 |a Ochi  |b T. 
701 1 |a Vyalova  |b N. N.  |g Nataljya Mikhaylovna 
701 1 |a Losenkov  |b I. S.  |g Innokenty Sergeevich 
701 1 |a Levchuk  |b L. A.  |g Lyudmila Aleksandrovna 
701 1 |a Osmanova  |b D. Z.  |g Diana Zakirovna 
701 1 |a Mikhalitskaya  |b E. V. 
701 1 |a Loonen  |b A. J. M.  |g Anton 
701 1 |a Bosker  |b F. J.  |g Fokko 
701 1 |a Simutkin  |b G. G.  |g German Gennadjevich 
701 1 |a Bokhan  |b N. 
701 1 |a Wilffert  |b B.  |g Bob 
701 1 |a Ivanova  |b S. A.  |c specialist in the field of ecology and life safety  |c Professor of Tomsk Polytechnic University, doctor of medical sciences  |f 1964-  |g Svetlana Aleksandrovna  |3 (RuTPU)RU\TPU\pers\33859 
712 0 2 |a Национальный исследовательский Томский политехнический университет  |b Инженерная школа неразрушающего контроля и безопасности  |b Отделение контроля и диагностики  |3 (RuTPU)RU\TPU\col\23584 
801 2 |a RU  |b 63413507  |c 20191121  |g RCR 
856 4 |u https://doi.org/10.1016/j.jad.2019.08.058 
942 |c CF