4.6 Article

miR-218-5p and miR-320a-5p as Biomarkers for Brain Disorders: Focus on the Major Depressive Disorder and Parkinson's Disease

Journal

MOLECULAR NEUROBIOLOGY
Volume 60, Issue 10, Pages 5642-5654

Publisher

SPRINGER
DOI: 10.1007/s12035-023-03391-y

Keywords

MicroRNA-218-5p; MicroRNA-320a-5p; Parkinson Disease; Depression

Categories

Ask authors/readers for more resources

Depression is a common but often neglected symptom of Parkinson's disease (PD), and there is a need for suitable diagnostic biomarkers. This study aimed to assess the potential of brain-enriched miR-218-5p and miR-320-5p as biomarkers for depression in Chinese PD patients. The results showed downregulation of miR-218-5p and miR-320-5p and upregulation of IL-6 and S100B in depressed PD patients. These miRNAs were negatively correlated with depression scores and IL-6 levels, and positively correlated with PD duration and medication. ROC analysis demonstrated their potential as diagnostic biomarkers. Furthermore, in silico analysis identified key neurological pathways regulated by the targets of these miRNAs. In conclusion, miR-218-5p and miR-320-5p may serve as future biomarkers for depression in PD, aiding in early diagnosis and treatment.
Depression is one of the early and most persistent non-motor symptoms of Parkinson's disease (PD), which remains ignored, resulting in the underdiagnosis of PD. Unfortunately, scarce studies and the non-availability of diagnostic strategies cause countless complications, highlighting the need for appropriate diagnostic biomarkers. Recently, brain-enriched miRNAs regulating vital neurological functions have been proposed as potent biomarkers for therapeutic strategies. Therefore, the present study is aimed to identify the brain-enriched miR-218-5p and miR-320-5p in the serum of the Chinese depressed PD patients (n = 51) than healthy controls (n = 51) to identify their potency as biomarkers. For this purpose, depressive PD patients were recruited based on HAMA and HAMD scores and miR-218-5p and miR-320-5p and IL-6, and S100B levels were analyzed using real-time PCR (qRT-PCR) and ELISA assay, respectively. In silico analysis was performed to identify key biological pathways and hub genes involved in the psychopathology of depression in PD. Here, we found significantly downregulated miR-218-5p and miR-320-5p following higher levels of IL-6 and S100B in depressed PD patients than in control (p < 0.05). The correlation analysis revealed that both miRNAs were negatively correlated with HAMA and HAMD, and IL-6 scores, along with a positive correlation with PD duration and LEDD medication. ROC analysis showed AUC above 75% in both miRNAs in depressed PD patients, and in silico analysis revealed that both miRNA's targets regulate key neurological pathways such as axon guidance, dopaminergic synapse, and circadian rhythm. Additional analysis revealed PIK3R1, ATRX, BM1, PCDHA10, XRCC5, PPP1CB, MLLT3, CBL, PCDHA4, PLCG1, YWHAZ, CDH2, AGO3, PCDHA3, and PCDHA11 as hub-genes in PPI network. In summary, our findings show that miR-218-5p and miR-320-5p can be utilized as future biomarkers for depression in PD patients, which may aid in the early diagnosis and treatment of Parkinson's disease.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available