Asymmetric Dimethylarginine Levels in Patients With Cutaneous Anthrax: a Laboratory Analysis

dc.contributor.author Sunnetcioglu, Mahmut
dc.contributor.author Mengeloglu, Zafer
dc.contributor.author Baran, Ali Irfan
dc.contributor.author Karahocagil, Mustafa
dc.contributor.author Tosun, Mehmet
dc.contributor.author Kucukbayrak, Abdulkadir
dc.contributor.author Aypak, Cenk
dc.date.accessioned 2025-05-10T17:45:48Z
dc.date.available 2025-05-10T17:45:48Z
dc.date.issued 2014
dc.description Karahocagil, Mustafa Kasim/0000-0002-5171-7306; Aypak, Cenk/0000-0002-8381-790X; Resat, Mehmet/0000-0001-8063-4836 en_US
dc.description.abstract Background: Asymmetric dimethylarginine (ADMA), the main endogenous inhibitor of nitric oxide synthase, is considered to be associated with endothelial dysfunction. High ADMA levels have been shown to be related with disorders causing vascular inflammation such as hypertension, hypercholesterolemia, atherosclerosis, chronic heart failure, stroke and sepsis. Cutaneous anthrax (CA) is a serious infectious disease which may cause vasculitis. The aim of the study was to investigate the serum ADMA levels in patients with CA. Methods: A total of 35 serum samples of the patients with CA and 18 control sera were tested for ADMA levels using ADMA ELISA kit (Immunodiagnostik AG, Bensheim, Germany). Results: ADMA levels were found to be significantly higher in the patients group than the controls (p < 0.001). In addition, ADMA levels were found to be positively associated with sedimentation rates (R = 0.413; p = 0.026), and inversely associated with international normalized ratio (INR) levels (R = -0.46; p = 0.011). A cut-off value of 0.475 of ADMA had a sensitivity of 74.3%, specificity of 77.8%, and accuracy of 75.5% in the diagnosis of CA. Conclusion: Although the exact mechanism still remains unclear, ADMA levels could be related to immune activation in CA. In addition, these data might suggest the higher ADMA levels in patients could be due to the perivascular inflammation and vasculitis in CA. en_US
dc.identifier.doi 10.1186/1476-0711-13-12
dc.identifier.issn 1476-0711
dc.identifier.scopus 2-s2.0-84899051559
dc.identifier.uri https://doi.org/10.1186/1476-0711-13-12
dc.identifier.uri https://hdl.handle.net/20.500.14720/16468
dc.language.iso en en_US
dc.publisher Bmc en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject Dimethylarginine en_US
dc.subject Infection en_US
dc.subject Anthrax en_US
dc.subject Vasculitis en_US
dc.title Asymmetric Dimethylarginine Levels in Patients With Cutaneous Anthrax: a Laboratory Analysis en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.id Karahocagil, Mustafa Kasim/0000-0002-5171-7306
gdc.author.id Aypak, Cenk/0000-0002-8381-790X
gdc.author.id Resat, Mehmet/0000-0001-8063-4836
gdc.author.scopusid 55950866000
gdc.author.scopusid 35604236100
gdc.author.scopusid 25624686400
gdc.author.scopusid 57204080929
gdc.author.scopusid 10039968300
gdc.author.scopusid 13003677000
gdc.author.scopusid 6701669939
gdc.author.wosid Ceylan, Mehmet/Aaa-3159-2021
gdc.author.wosid Karahocagil, Mustafa/Jvz-6523-2024
gdc.author.wosid Aypak, Cenk/Abf-2552-2021
gdc.author.wosid Baran, Ali/Lnr-6591-2024
gdc.coar.access open access
gdc.coar.type text::journal::journal article
gdc.description.department T.C. Van Yüzüncü Yıl Üniversitesi en_US
gdc.description.departmenttemp [Sunnetcioglu, Mahmut; Baran, Ali Irfan; Karahocagil, Mustafa; Ceylan, Mehmet Resat] Yuzuncu Yil Univ, Fac Med, Dept Infect Dis & Clin Microbiol, Van, Turkey; [Mengeloglu, Zafer] Abant Izzet Baysal Univ, Fac Med, Dept Microbiol, Bolu, Turkey; [Tosun, Mehmet] Abant Izzet Baysal Univ, Fac Med, Dept Med Biochem, Bolu, Turkey; [Kucukbayrak, Abdulkadir; Akdeniz, Hayrettin] Abant Izzet Baysal Univ, Fac Med, Dept Infect Dis & Clin Microbiol, Bolu, Turkey; [Aypak, Cenk] Diskapi Yildirim Beyazit Training & Res Hosp, Dept Family Med, TR-06110 Ankara, Turkey en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q1
gdc.description.volume 13 en_US
gdc.description.woscitationindex Science Citation Index Expanded
gdc.description.wosquality Q1
gdc.identifier.pmid 24669818
gdc.identifier.wos WOS:000334615100001
gdc.index.type WoS
gdc.index.type Scopus
gdc.index.type PubMed

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