Brain Derived Neurotropic Factor Gene Val66Met Polymorphism in Alzheimer’s Patients in Northern Turkey
Journal Title: Journal of Neurology and Experimental Neuroscience - Year 2017, Vol 3, Issue 2
Abstract
Objective: The present study aimed to determine the frequency of Brain Derived Neurotropic Factor (BDNF) gene 196 A/G polymorphism in Alzheimer Disease (AD) patients in northern Turkey. Materials and Methods: 184 probable AD patients (according to NINCDS and ADRDA criteria) and 133 healthy controls were included to this study. The genotyping of BDNF gene rs6265 polymorphism were evaluated in the laboratories of our University Medical Faculty Medical Biology department, in the StepOnePlus Real-Time PCR system using by TaqMan SNP genotyping assay according to the manufacturer’s instructions. Results: In all, 54 (29.35%) patients had mild dementia, 72 (39.13%) had moderate dementia, and 58 (31.52%) had advanced-stage dementia. Mean duration of AD was 4.33 years. There was not a significant difference if the frequency of BDNF gene Val66Met polymorphism between the patient and control groups. The patient group included 88 (47.83%) males and 96 (52.17%) females, versus 72 (54.14%) males and 61 (45.86%) females in the control group. Moreover, there was not a significant association between the frequency of BDNF gene Val66Met polymorphism and gender distribution in the patient group. Mean age in the patient group was 75.83 years, versus 74.29 years in the control group; however, there were not any significant changes when correlating BDNF gene Val66Met polymorphism with age. Similarly, there was not a significant association between BDNF gene Val66Met polymorphism and AD stage in the patient group. Conclusion: In conclusion, there was not an association between AD and BDNF gene Val66Met polymorphism in the northern Turkish population.
Authors and Affiliations
Volkan Solmaz, Orhan Sumbul, Aydın Rustemoglu, Durdane Aksoy, Ekrem Hasbek, Betul Cevik, Elmas Pekdas
Review of “Spasticity: Diagnosis and Management, 2nd Edition”
The 2nd edition of the book «Spasticity: Diagnosis and Management» is edited by Dr. Allison Brashear who is an eminent expert and clinician in this field. It is written by a group of contributors (48 authors) with variou...
Proceedings of the Second Neurological Disorders Summit (NDS-2016)
One pathological hallmark in ALS-linked motor neurons (MNs) is axonal accumulation of damaged mitochondria, which produce energy and buffer Ca2+ less efficiently, and initiate apoptotic cascades and axonal degeneration....
Cobalamin C Deficiency: Case Report of Two Different Clinical Presentations
Cobalamin C deficiency (CblC) is the most frequent inborn error of cobalamin (Cbl) metabolism, which has a wide clinical spectrum. Cbl C defect causes the accumulation of methylmalonic acid and homocysteine and decreased...
Sampling an Intrinsic Foot Muscle Improves Electrodiagnostic Sensitivity for Peripheral Neuropathy
Routinely performed electrodiagnostic study may be normal in some subjects with mild peripheral neuropathy such as acral dysesthesia and/or weakness and, therefore, fails to confirm the diagnosis at the early stage. Aimi...
Indomethacin-Responsive Headaches in Pediatric Age: Nosographic Aspects and Limitations on the use of Indomethacin in Pediatric Population
Headaches are a common problem in children and adolescents. Indomethacinresponsive headaches are a poorly known and rare group of primary headaches, with few cases during childhood. These include a heterogeneous group of...