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DOI 10.3390/genes14112037

Медицинская библиотека · Genes · 2023

Association between NTRK2 Polymorphisms, Hippocampal Volumes and Treatment Resistance in Major Depressive Disorder.

Paolini Marco, Fortaner-Uyà Lidia, Lorenzi Cristina, Spadini Sara, Maccario Melania, Zanardi Raffaella, Colombo Cristina, Poletti Sara, Benedetti Francesco

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

Despite the increasing availability of antidepressant drugs, a high rate of patients with major depression (MDD) does not respond to pharmacological treatments. Brain-derived neurotrophic factor (BDNF)-tyrosine receptor kinase B (TrkB) signaling is thought to influence antidepressant efficacy and hippocampal volumes, robust predictors of treatment resistance. We therefore hypothesized the possible role of BDNF and neurotrophic receptor tyrosine kinase 2 (NTRK2)-related polymorphisms in affecting both hippocampal volumes and treatment resistance in MDD. A total of 121 MDD inpatients underwent 3T structural MRI scanning and blood sampling to obtain genotype information. General linear models and binary logistic regressions were employed to test the effect of genetic variations related to BDNF and NTRK2 on bilateral hippocampal volumes and treatment resistance, respectively. Finally, the possible mediating role of hippocampal volumes on the relationship between genetic markers and treatment response was investigated. A significant association between one NTRK2 polymorphism with hippocampal volumes and antidepressant response was found, with significant indirect effects. Our results highlight a possible mechanistic explanation of antidepressant action, possibly contributing to the understanding of MDD pathophysiology.

Для цитирования: Paolini Marco, Fortaner-Uyà Lidia, Lorenzi Cristina, Spadini Sara, Maccario Melania, Zanardi Raffaella, Colombo Cristina, Poletti Sara, Benedetti Francesco. Association between NTRK2 Polymorphisms, Hippocampal Volumes and Treatment Resistance in Major Depressive Disorder.. Genes. 2023. DOI: 10.3390/genes14112037.

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