Decreased Serum Paraoxonase and Arylesterase Activities in Patients With Rosacea

dc.contributor.author Takci, Z.
dc.contributor.author Bilgili, S. G.
dc.contributor.author Karadag, A. S.
dc.contributor.author Kucukoglu, M. E.
dc.contributor.author Selek, S.
dc.contributor.author Aslan, M.
dc.date.accessioned 2025-05-10T17:43:49Z
dc.date.available 2025-05-10T17:43:49Z
dc.date.issued 2015
dc.description Selek, Sahabettin/0000-0003-1235-3957; Takci, Zennure/0000-0001-7257-5792 en_US
dc.description.abstract Background: Recent evidence suggests that oxidative stress may be an important phenomenon in the pathophysiology of rosacea. Paraoxonase-1 (PON1) is an antioxidant enzyme with three activities: paraoxonase, arylesterase and dyazoxonase. In this study, we evaluated serum paraoxonase and arylesterase activities, and serum lipid hydroperoxide (LOOH) levels in patients with rosacea in comparison to healthy controls. Material and methodThe study included 39 rosacea patients and healthy controls, consisting of 40 age- and sex-matched healthy volunteers. Serum paraoxonase and arylesterase activities were measured using paraoxon and phenylacetate substrates. Serum LOOH levels were measured with the ferrous ion oxidation-xylenol orange assay. ResultsIn rosacea group mean serum paraoxonase and arylesterase activities were 74.5438.30UL(-1) and 141.29 +/- 22.27kUL(-1) respectively, which were significantly lower than controls (P=0.010, 0.005; respectively). Mean serum LOOH level of rosacea group was 8.17 +/- 1.91molL(-1) which was significantly higher than controls (P=0.009). There were no statistically significant differences between the clinical subtypes of the disease, menopause situation or ocular involvement with the respect to the serum paraoxonase and arylesterase activities and LOOH levels (all; P>0.05). ConclusionsSerum PON1 enzyme activities have decreased significantly in rosacea. These findings support that decreased PON1 activity and increased oxidative stress may play a role in the pathogenesis of rosacea. Further studies are needed to elucidate the role of PON1 activity in the pathophysiology of rosacea. en_US
dc.identifier.doi 10.1111/jdv.12556
dc.identifier.issn 0926-9959
dc.identifier.issn 1468-3083
dc.identifier.scopus 2-s2.0-84921504622
dc.identifier.uri https://doi.org/10.1111/jdv.12556
dc.identifier.uri https://hdl.handle.net/20.500.14720/15992
dc.language.iso en en_US
dc.publisher Wiley en_US
dc.rights info:eu-repo/semantics/closedAccess en_US
dc.title Decreased Serum Paraoxonase and Arylesterase Activities in Patients With Rosacea en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.id Selek, Sahabettin/0000-0003-1235-3957
gdc.author.id Takci, Zennure/0000-0001-7257-5792
gdc.author.scopusid 55257710400
gdc.author.scopusid 17134049200
gdc.author.scopusid 26425048800
gdc.author.scopusid 36170739800
gdc.author.scopusid 56798833200
gdc.author.scopusid 7006409671
gdc.author.wosid Takci, Zennure/Aaa-1069-2020
gdc.author.wosid Karadag, Ayse/V-7974-2018
gdc.author.wosid Selek, Sahabettin/N-9323-2019
gdc.coar.access metadata only access
gdc.coar.type text::journal::journal article
gdc.description.department T.C. Van Yüzüncü Yıl Üniversitesi en_US
gdc.description.departmenttemp [Takci, Z.] Gaziosmanpasa Univ, Dept Dermatol, Fac Med, Tokat, Turkey; [Bilgili, S. G.] Yuzuncuyl Univ, Dept Dermatol, Fac Med, Van, Turkey; [Karadag, A. S.] Istanbul Medeniyet Univ, Goztepe Res & Training Hosp, Fac Med, Dept Dermatol, Istanbul, Turkey; [Kucukoglu, M. E.] Yuzuncuyl Univ, Fac Med, Dept Internal Med, Van, Turkey; [Selek, S.] Bezmialem Univ, Fac Med, Dept Clin Biochem, Istanbul, Turkey; [Aslan, M.] Yuzuncuyl Univ, Fac Med, Dept Internal Med, Van, Turkey en_US
gdc.description.endpage 370 en_US
gdc.description.issue 2 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q1
gdc.description.startpage 367 en_US
gdc.description.volume 29 en_US
gdc.description.woscitationindex Science Citation Index Expanded
gdc.description.wosquality Q1
gdc.identifier.pmid 24854673
gdc.identifier.wos WOS:000348717700024
gdc.index.type WoS
gdc.index.type Scopus
gdc.index.type PubMed

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