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Paraoxonase lactonase activity (PON-HTLase), asymmetric dimethylarginine (ADMA) and platelet activating factor-acetylhydrolase (PAF-AH) activity in non-obese women with PCOS

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dc.contributor.author Bayrak, Tulin
dc.contributor.author Dursun, Polat
dc.contributor.author Bayrak, Ahmet
dc.contributor.author Gultekin, Murat
dc.contributor.author Kolusari, Ali
dc.contributor.author Cakir, Erdinc
dc.contributor.author Ozyurt, Merve
dc.contributor.author Zeyneloglu, Hulusi B.
dc.date.accessioned 2024-03-26T07:24:38Z
dc.date.available 2024-03-26T07:24:38Z
dc.date.issued 2012
dc.identifier.citation Bayrak, T., Dursun, P., Bayrak, A., Gültekin, M., Kolusari, A., Çakir, E., Ozyurt, M., Zeyneloglu, HB. (2012). Paraoxonase lactonase activity (PON-HTLase), asymmetric dimethylarginine (ADMA) and platelet activating factor-acetylhydrolase (PAF-AH) activity in non-obese women with PCOS. Gynecol. Endocrinol., 28(11), 874-878. https://doi.org/10.3109/09513590.2012.683068 en_US
dc.identifier.issn 0951-3590
dc.identifier.issn 1473-0766
dc.identifier.uri http://dx.doi.org/10.3109/09513590.2012.683068
dc.identifier.uri https://www.webofscience.com/wos/woscc/full-record/WOS:000309938700011
dc.identifier.uri http://earsiv.odu.edu.tr:8080/xmlui/handle/11489/5303
dc.description WoS Categories: Endocrinology & Metabolism; Obstetrics & Gynecology en_US
dc.description Web of Science Index: Science Citation Index Expanded (SCI-EXPANDED) en_US
dc.description Research Areas: Endocrinology & Metabolism; Obstetrics & Gynecology en_US
dc.description.abstract Objective: Paraoxonase1 (PON1), exhibits both esterase activity (PON1-AREase) and homocysteine thiolactonase activity (PON1-HTLase) which respectively prevent LDL oxidation and detoxify homocysteine thiolactone (HTL). Platelet-activating factor-acetylhydrolase (PAF-AH) is an antioxidant enzyme preventing LDL oxidation by hydrolysis of oxidized phospholipids. Both of these enzymes exhibit a proatherogenic role. ADMA is an endogenous inhibitor of nitric oxide (NO) synthesis causing endothelial dysfunction. The aim was to compare non-obese PCOS patients with a BMI matched control group using the following characteristics: serum PON1-HTLase, ADMA, PAF-AH, and lipid and hormonal parameters. Results: 77 women with PCOS and 25 healthy subject were recruited for this study, The controls were non-obese BMI and age matched with the patients. There were no significant differences with respect to age, BMI, FSH, free testosterone, DHEA, androstenadion, total cholesterol, triglycerides, HDL, LDL, VLDL, fasting glucose/insulin ratio and HOMA-IR among the groups (p > 0.05). However, total testosterone and fasting glucose levels were significantly higher in the PCOS group (p < 0.05). On the other hand, PON1-HTLase levels (39.6 +/- 5.77 vs. 33.8 +/- 8.2, p = 0.02) were significantly lower in the PCOS group while ADMA levels (1.14 +/- 0.6 vs. 3.37 +/- 6.4, p = 0.004) were significantly higher in the PCOS group. However, there was no significant difference in PAF-AH activity among the groups Conclusions: Decreased PON1-HTLase and increased ADMA levels might be a relevant marker for the development of future atherosclerotic heart disease (AHD) in non-obese PCOS patients. Further studies are needed to confirm our results. en_US
dc.language.iso eng en_US
dc.publisher TAYLOR & FRANCIS LTD-ABINGDON en_US
dc.relation.isversionof 10.3109/09513590.2012.683068 en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject PCOS, PON1, homocysteine thiolactonase, ADMA, PAF-AH, atherosclerotic heart disease en_US
dc.subject POLYCYSTIC-OVARY-SYNDROME, OXIDE SYNTHASE INHIBITOR, SERUM PARAOXONASE, RISK-FACTOR, MYOCARDIAL-INFARCTION, INSULIN-RESISTANCE, DIABETES-MELLITUS, PLASMA, ATHEROSCLEROSIS, DISEASE en_US
dc.title Paraoxonase lactonase activity (PON-HTLase), asymmetric dimethylarginine (ADMA) and platelet activating factor-acetylhydrolase (PAF-AH) activity in non-obese women with PCOS en_US
dc.type article en_US
dc.relation.journal GYNECOLOGICAL ENDOCRINOLOGY en_US
dc.contributor.department Ordu Üniversitesi en_US
dc.contributor.authorID 0000-0002-4221-4459 en_US
dc.contributor.authorID 0000-0002-0289-2642 en_US
dc.contributor.authorID 0000-0001-5139-364X en_US
dc.identifier.volume 28 en_US
dc.identifier.issue 11 en_US
dc.identifier.startpage 874 en_US
dc.identifier.endpage 878 en_US


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