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Advisor(s)
Abstract(s)
Background: Neuroinflammation appears as an important epileptogenic mechanism. MicroRNAs (miRNA) are small non-coding RNA molecules that function as post-transcriptional regulators of gene expression. MicroRNas control different biological process including immune system homeostasis and function. Several evidences, both in patients and animal studies, have demonstrated an abnormal brain expression of miR-146a in Mesial Temporal Lobe Epilepsy. Knowing that miR expression is very stable in biological fluids such as plasma or serum our aim was to characterize miR146a expression in serum of MTLE patients.
Methods: Expression levels of miR146a and U6B small nuclear RNA gene (reference gene) were quantified by Real-Time PCR in serum of 14 MTLE patients all with Hippocampal Sclerosis (6F, 8M, mean age= 44.1±11.7 years, age of onset= 13.5±10.6 years, 7 with Febrile Seizures antecedents). A group of 10 healthy individuals was used as control. Relative expression values were calculated using the 2-ΔΔCt method.
Results: We observed that expression of miR146a was 2 fold higher in MTLE-HS patients than in controls.
Conclusion: The results obtained in serum are in accordance with the results obtained from brain tissue of epileptic patients. This may confirm that miR-146a is a suitable biomarker of epileptogenesis. Additionally, it is thought that miR-146a has a role in fine-tuning the response to cytokines during epileptogenesis. Nevertheless its importance in epilepsy development it is yet not fully understood. The comprehension of this role may be relevant for the development of new therapeutic strategies.
Description
Oral Sessions publicado em: European Journal of Neurology. 2015;22(Suppl.1):21. doi: 10.1111/ene.12805. Disponível em: https://onlinelibrary.wiley.com/doi/abs/10.1111/ene.12805
Keywords
Research Subject Categories::MEDICINE::Microbiology, immunology, infectious diseases::Immunology::Immunobiology Mesial Temporal Lobe Epilepsy Inflammation Epigenetics miRNAs Determinantes da Saúde e da Doença Doenças Genéticas
