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Screening of mutations in PARK2 gene and Dopamine levels in Parkinson’s disease (PD) patients in Coimbatore population, India

I. Iyer, V. Venkatesan, V. Vellingiri (Coimbatore, India)

Meeting: MDS Virtual Congress 2020

Abstract Number: 534

Keywords: Dopamine, Parkin, Parkinsonism

Category: Parkinson's Disease: Molecular Mechanisms of Disease

Objective: The aim of the present study was to perform the mutational screening of PARK2 gene and dopamine level in PD patients of Coimbatore population, Tamil Nadu, India.

Background: Parkinson’s disease (PD) is a neurodegenerative disorder accompanied by depletion of dopamine and loss of dopaminergic neurons (DA) in the brain that is believed to be responsible for the motor and non-motor symptoms of PD. Parkin belongs to the RBR family of E3 ubiquitin ligase, which is involved in varied cytosolic and mitochondrial functions. Parkin mutations lead to early synaptic damage and appear as a crucial gene having a vast functioning area in PD.

Method: Totally 36 samples were selected including 16 PD patients and 16 Controls. PD subjects were interviewed using Unified Parkinson’s Disease Rating Scale (UPDRS) questionnaire and informed consent has been obtained from the PD subjects and controls. Institutional ethical clearance was obtained. Family history was considered positive if PD was reported in a first or second degree relative, depending on the pedigree. Genomic DNA was isolated from blood samples followed by PCR and sequencing in PD and control subjects.

Results: Higher degree of PARK2 gene point mutation was observed in PD patients compared to controls. In addition, decreased level of dopamine was measured in PD subjects.

Conclusion: Hence, an increased number of mutational studies of PARK2 mutations in PD patients are reported, but the present study is the first to evaluate the polymorphic frequency in Coimbatore patients.

References: 1. Jayaramayya Kaavya, Iyer Mahalaxmi, Venkatesan Dhivya, Balasubramanian Venkatesh, Narayanaswamy Arul, Subramaniam Mohana Devi, Ssang Goo Cho, Vellingiri Balachandar. Unraveling correlative roles of Dopamine transporter (DAT) and Parkin in Parkinson’s disease (PD)-A road to discovery? Brain Research Bulletin. 2020, https://doi.org/10.1016/j.brainresbull.2020.02.001. 2. Mohana Devi S, Mahalaxmi I, Aswathy NP, Dhivya V, Balachandar V. Does retina play a role in Parkinson’s Disease? Acta Neurol Belg, 2020. 10.1007/s13760-020-01274-w. 3. Mackie, P., Lebowitz, J., Saadatpour, L., Nickoloff, E., Gaskill, P., Khoshbouei, H., 2018. The dopamine transporter: An unrecognized nexus for dysfunctional peripheral immunity and signaling in Parkinson’s Disease. Brain. Behav. Immun. 70, 21–35. https://doi.org/10.1016/j.bbi.2018.03.020

To cite this abstract in AMA style:

I. Iyer, V. Venkatesan, V. Vellingiri. Screening of mutations in PARK2 gene and Dopamine levels in Parkinson’s disease (PD) patients in Coimbatore population, India [abstract]. Mov Disord. 2020; 35 (suppl 1). https://www.mdsabstracts.org/abstract/screening-of-mutations-in-park2-gene-and-dopamine-levels-in-parkinsons-disease-pd-patients-in-coimbatore-population-india-2/. Accessed May 18, 2025.
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