Parkinson’s disease (PD) is a widespread neurodegenerative disorder. Despite the intensive studies of this pathology, in general, the picture of the etiopathogenesis has still not been clarified fully. To understand better the mechanisms underlying the pathogenesis of PD, we analyzed the expression of 10 genes in the peripheral blood of treated and untreated patients with PD. 35 untreated patients with PD and 12 treated patients with Parkinson’s disease (Hoehn and Yahr scores 1-2) were studied. An analysis of the mRNA levels ofATP13A2,PARK2,PARK7,PINK1,LRRK2,SNCA,ALDH1A1,PDHB,PPARGC1A, andZNF746genes in the peripheral blood of patients was carried out using reverse transcription followed by real-time PCR. A statistically significant and specific increase by more than 1.5-fold in the expression of theATP13A2,PARK7, andZNF746genes was observed in patients with PD. Based on these results, it can be suggested that the upregulation of the mRNA levels ofATP13A2,PARK7, andZNF746in untreated patients in the earliest clinical stages can also be observed in the preclinical stages of PD, and that these genes can be considered as potential biomarkers of the preclinical stage of PD.
Serum microRNA-30c-5p and microRNA-373 expressions as potential biomarkers for Parkinson's disease