# Evaluation of the neurotrophic peptide mixture in pathogenetic therapy of patients with Parkinson’s disease

**Authors:** Dmytro Krasnienkov, Iryna Karaban, Nina Karasevych, Nataliia Melnyk, Sergiy Kryzhanovskyi, Kateryna Rozova, Olga Gonchar, Iryna Mankovska, Sofiia Smovzh, Kostiantyn Midlovets, Olexiy Barsukov, Oksana Zabuha, Tetiana Papurina

PMC · DOI: 10.1038/s41531-026-01270-6 · NPJ Parkinson's Disease · 2026-01-23

## TL;DR

This study explores the effects of a neurotrophic peptide mixture on Parkinson's disease patients, showing improvements in motor and non-motor symptoms, along with biological and cognitive changes.

## Contribution

The study introduces a novel neurotrophic peptide therapy and identifies key molecular and cognitive predictors of improvement in Parkinson's disease.

## Key findings

- Improvements in daily activity, cognition, depression, and anxiety were observed after treatment.
- Biological changes included increased platelet δ-granules, mitochondrial counts, and BDNF gene expression.
- Machine learning models identified BDNF and PINK1 expression as key predictors of UPDRS improvement.

## Abstract

This exploratory, single-group, open-label study investigated 17 patients with Parkinson’s disease (PD) using a pre-post design. Motor and non-motor outcomes were assessed through clinical scales, biochemical and genetic analyses, and machine learning models (Gradient Boosting Machines, Random Forests). After treatment with a neurotrophic peptide mixture, improvements were observed in daily activity (16%), cognition (11%), depression (10% reduction), and reactive anxiety (23% reduction). Biological changes included a 45% increase in platelet δ-granules, higher mitochondrial counts, elevated gene expression (notably BDNF in women, p = 0.046), and modulation of oxidative stress markers (17% reduction in TBARS, 30% increase in GSH). Machine learning identified BDNF and PINK1 expression, along with MOCA and MMSE scores, as key predictors of UPDRS improvement. These findings suggest that neurotrophic peptide therapy may influence clinical, structural, and molecular domains in PD. Larger, controlled trials are warranted to confirm therapeutic potential and clarify associations with cognitive and neurotrophic parameters.

## Linked entities

- **Genes:** BDNF (brain derived neurotrophic factor) [NCBI Gene 627], PINK1 (PTEN induced kinase 1) [NCBI Gene 65018]
- **Diseases:** Parkinson’s disease (MONDO:0005180)

## Full-text entities

- **Genes:** BDNF (brain derived neurotrophic factor) [NCBI Gene 627] {aka ANON2, BULN2}, PINK1 (PTEN induced kinase 1) [NCBI Gene 65018] {aka BRPK, PARK6}
- **Diseases:** anxiety (MESH:D001007), PD (MESH:D010300), depression (MESH:D003866)
- **Chemicals:** TBARS (MESH:D017392), neurotrophic (-), GSH (MESH:D005978)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

17 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12932723/full.md

## References

3 references — full list in the complete paper: https://tomesphere.com/paper/PMC12932723/full.md

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Source: https://tomesphere.com/paper/PMC12932723