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Investigation of PON1 activity and MDA levels in patients with epilepsy not receiving antiepileptic treatment
PURPOSE: There are many studies dedicated to researching the etiopathogenesis of epilepsy. In such research, oxidative and antioxidant indicators of etiopathogenesis have also been examined under the scope. Drawing on a group of patients with epilepsy who were receiving no treatment, we have tried t...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4854258/ https://www.ncbi.nlm.nih.gov/pubmed/27175078 http://dx.doi.org/10.2147/NDT.S103336 |
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author | Dönmezdil, Nilüfer Çevik, Mehmet Uğur Özdemir, Hasan Hüseyin Taşin, Muhterem |
author_facet | Dönmezdil, Nilüfer Çevik, Mehmet Uğur Özdemir, Hasan Hüseyin Taşin, Muhterem |
author_sort | Dönmezdil, Nilüfer |
collection | PubMed |
description | PURPOSE: There are many studies dedicated to researching the etiopathogenesis of epilepsy. In such research, oxidative and antioxidant indicators of etiopathogenesis have also been examined under the scope. Drawing on a group of patients with epilepsy who were receiving no treatment, we have tried to evaluate whether or not an increase in oxidative indicators is linked directly with the disorder, independent of epileptic medicaments. METHODS: Thirty people in good health and 30 newly diagnosed with epilepsy and who received ambulatory treatment in the polyclinic of the Neurology Department took part in the study. The tests relating to serum malondialdehyde (MDA) levels and paraoxonase 1 (PON1) activity were carried out in the biochemistry laboratory. RESULTS: Even though the levels of MDA in the patient group (14.34±3.59 nmol/mL) were found to be high compared to those of the control group, which consisted of people in good health (13.53±3.56 nmol/mL), there was no statistically significant difference. PON1 activity in the serum taken from people in the patient group (0.65±0.17) was lower in comparison to that observed in the serum of the control group (0.71±0.17 U/L). Nonetheless, it was not so low as to have significance from a statistical point of view. CONCLUSION: We conclude that such a high level of oxidative parameters should have been related to the disease and that statistically significant findings that emerged in some other studies could have been related to an antiepileptic treatment. |
format | Online Article Text |
id | pubmed-4854258 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-48542582016-05-12 Investigation of PON1 activity and MDA levels in patients with epilepsy not receiving antiepileptic treatment Dönmezdil, Nilüfer Çevik, Mehmet Uğur Özdemir, Hasan Hüseyin Taşin, Muhterem Neuropsychiatr Dis Treat Original Research PURPOSE: There are many studies dedicated to researching the etiopathogenesis of epilepsy. In such research, oxidative and antioxidant indicators of etiopathogenesis have also been examined under the scope. Drawing on a group of patients with epilepsy who were receiving no treatment, we have tried to evaluate whether or not an increase in oxidative indicators is linked directly with the disorder, independent of epileptic medicaments. METHODS: Thirty people in good health and 30 newly diagnosed with epilepsy and who received ambulatory treatment in the polyclinic of the Neurology Department took part in the study. The tests relating to serum malondialdehyde (MDA) levels and paraoxonase 1 (PON1) activity were carried out in the biochemistry laboratory. RESULTS: Even though the levels of MDA in the patient group (14.34±3.59 nmol/mL) were found to be high compared to those of the control group, which consisted of people in good health (13.53±3.56 nmol/mL), there was no statistically significant difference. PON1 activity in the serum taken from people in the patient group (0.65±0.17) was lower in comparison to that observed in the serum of the control group (0.71±0.17 U/L). Nonetheless, it was not so low as to have significance from a statistical point of view. CONCLUSION: We conclude that such a high level of oxidative parameters should have been related to the disease and that statistically significant findings that emerged in some other studies could have been related to an antiepileptic treatment. Dove Medical Press 2016-04-22 /pmc/articles/PMC4854258/ /pubmed/27175078 http://dx.doi.org/10.2147/NDT.S103336 Text en © 2016 Dönmezdil et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Dönmezdil, Nilüfer Çevik, Mehmet Uğur Özdemir, Hasan Hüseyin Taşin, Muhterem Investigation of PON1 activity and MDA levels in patients with epilepsy not receiving antiepileptic treatment |
title | Investigation of PON1 activity and MDA levels in patients with epilepsy not receiving antiepileptic treatment |
title_full | Investigation of PON1 activity and MDA levels in patients with epilepsy not receiving antiepileptic treatment |
title_fullStr | Investigation of PON1 activity and MDA levels in patients with epilepsy not receiving antiepileptic treatment |
title_full_unstemmed | Investigation of PON1 activity and MDA levels in patients with epilepsy not receiving antiepileptic treatment |
title_short | Investigation of PON1 activity and MDA levels in patients with epilepsy not receiving antiepileptic treatment |
title_sort | investigation of pon1 activity and mda levels in patients with epilepsy not receiving antiepileptic treatment |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4854258/ https://www.ncbi.nlm.nih.gov/pubmed/27175078 http://dx.doi.org/10.2147/NDT.S103336 |
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