Evidence map›Paper›PMID 23644848›Full record

ArticleClinics (Sao Paulo, Brazil)2013

Is there a relationship between endothelial nitric oxide synthase gene polymorphisms and ankylosing spondylitis?

Ismail Sari, Yusuf Ziya Igci, Gercek Can, Ali Taylan, Dilek Solmaz, Bulent Gogebakan, Servet Akar, Zeynep Eslik, Giray Bozkaya, Nurullah Akkoc

Open access · goldAbstract read
In one paragraph

Article in Clinics (Sao Paulo, Brazil), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

10 authors at 3 institutions in 1 country.

Ismail SariDivision of Rheumatology, Department of Internal Medicine, School of Medicine, Dokuz Eylul University, Izmir, Turkey. ismailsari35@gmail.com
Yusuf Ziya Igci
Gercek Can
Ali Taylan
Dilek Solmaz
Bulent Gogebakan
Servet Akar
Zeynep Eslik
Giray Bozkaya
Nurullah Akkoc
Dokuz Eylül University · TRGaziantep University · TRIzmir Bozyaka Eğitim ve Araştırma Hastanesi · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveNitric oxide is produced by endothelial nitric oxide synthase, and its production can be influenced by polymorphisms of the endothelial nitric oxide synthase gene. Because candidate genes responsible for susceptibility to ankylosing spondylitis are mostly unknown and available data suggest that there may be problems related to the nitric oxide pathway, such as endothelial dysfunction and increased asymmetric dimethylarginine, this study aimed to assess the association of common endothelial nitric oxide synthase gene polymorphisms with ankylosing spondylitis.

methodsOne hundred ninety-four unrelated Turkish ankylosing spondylitis patients and 113 healthy without apparent cardiovascular disease, hypertension or diabetes mellitus were included. All individuals were genotyped by PCR-RFLP for two single-nucleotide polymorphisms, namely 786T>C (rs2070744, promoter region) and 786 Glu298Asp (rs1799983, exon 7). Variable numbers of tandem repeat polymorphisms in intron 4 were also studied and investigated by direct electrophoresis on agarose gel following polymerase chain reaction analysis. The Bath ankylosing spondylitis metrology index of the patients was calculated, and human leukocyte antigen B27 was studied.

resultsAll studied polymorphisms satisfied Hardy-Weinberg equilibrium. Sex distributions were similar between the patient and control groups. No significant differences were found in the distributions of allele and genotype frequencies of the studied endothelial nitric oxide synthase polymorphisms between patients and controls. There were no correlations between endothelial nitric oxide synthase polymorphisms, disease duration, Bath ankylosing spondylitis metrology index or human leukocyte antigen B27.

conclusionThe results presented in this study do not support a major role of common endothelial nitric oxide synthase polymorphisms in Turkish ankylosing spondylitis patients.

Indexed as

AdultAnalysis of VarianceCase-Control StudiesFemaleGene FrequencyHumansMaleMiddle AgedNitric Oxide Synthase Type IIIPolymerase Chain ReactionPolymorphism, GeneticRisk FactorsSpondylitis, AnkylosingNitric Oxide Synthase Type III

Identifiers

PMID23644848
PMCPMC3611897
OpenAlexW2031852379

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