Peripheral BDNF–TrkB Expression and Vitamin D Status in Depression, Prediabetes and Type 2 Diabetes: A Cross-Sectional Biomarker Study
Oleksandr Pavlovych, Iryna Ivanivna Kamyshna, Larysa Pavlovych, Oleh Lushchak, Iryna Halabitska, Pavlo Petakh, Oleksandr Kamyshnyi
Bukovinian State Medical University I.Horbachevsky Ternopil National Medical University Kyiv School of Economics Uzhhorod National University
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Background/Objectives: Depression and anxiety cluster with dysglycaemia along a prediabetes–type 2 diabetes continuum, but the signatures of affective and metabolic burden are unclear. We examined whether neurotrophin-related gene expression and 25(OH)D status track symptoms, parameters, or both. Methods: A cross-sectional study of 200 adults (n = 50 each: type 2 diabetes, prediabetes, depressive–anxiety, apparently healthy controls) was conducted. Anthropometry, glycaemic and lipid indices, PHQ-9, GAD-7, serum 25(OH)D and RT-qPCR expression of BDNF, NGF, NTRK1 and NTRK2 in whole peripheral blood were assessed. Multivariable regression, dominance analysis and pre-specified sensitivity analyses were applied. Results: BDNF, NGF and NTRK2 expression progressively decreased from controls to prediabetes and type 2 diabetes and was lowest in the depressive–anxiety group (p < 0.001); NTRK1 expression did not differ. Peripheral BDNF was more closely associated with PHQ-9 and 25(OH)D than with glycaemic or anthropometric indices. Psychiatric variables accounted for approximately 81% of the variance explained by the multivariable model (apparent R2 = 0.257), corresponding to approximately 21% of the total observed variance in log(BDNF). Conclusions: Peripheral BDNF and NTRK2 mRNA and 25(OH)D status were associated with depressive symptom burden more strongly than with metabolic parameters across a prediabetes–type 2 diabetes continuum. These associations describe an exploratory biomarker pattern; they do not establish altered signalling activity, causality or clinical utility, which require prospective validation.
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