Literature DB >> 34273021

Determination of serum methylarginine levels by tandem mass spectrometric method in patients with ankylosing spondylitis.

Duygu Eryavuz Onmaz1, Kevser Isik2, Abdullah Sivrikaya3, Sedat Abusoglu3, İlknur Albayrak Gezer2, Gulsum Abusoglu4, Fatma Humeyra Yerlikaya3, Ali Unlu3.   

Abstract

Our aim in this study was to measure serum levels of methylarginines and related metabolites in patients with ankylosing spondylitis (AS), moreover, to investigate the relationship between these parameters and various clinical and laboratory parameters of patients with AS. The study included 60 patients with AS and 60 healthy volunteers. Serum asymmetric dimethylarginine (ADMA), L-N monomethylarginine (L-NMMA), symmetric dimethylarginine (SDMA), arginine (Arg), homoarginine (hArg), ornithine, and citrulline concentrations were measured with tandem mass spectrometry. In addition, participants were divided into three groups according to the treatment regimen: TNF-α inhibitor group (n = 25), conventional therapy group (n = 35), and control group (n = 60). These groups were compared in terms of serum levels of methylarginine pathway metabolites and various biochemical parameters. It was found that total methylated arginine load significantly increased in patients with AS (p < 0.001), and the Arg/ADMA ratio was positively correlated with HDL levels and negatively correlated with glucose, ESR, total cholesterol, triglyceride, and LDL levels. In addition, serum ADMA, SDMA, total methylated arginine load, and CRP levels were lower (p < 0.05) in the TNF-α group compared to the conventional treatment group. To the best of our knowledge, this is the first study to comprehensively investigate serum methylarginine levels in patients with AS. Elevated total methylated arginine load and decreased global arginine bioavailability ratio (GABR) indicate that NO metabolism is impaired in patients with AS. Therefore, the increased cardiovascular risk in patients with AS may be related to the decreased NO production or bioavailability due to the elevated total methylarginine load.
© 2021. The Author(s), under exclusive licence to Springer-Verlag GmbH Austria, part of Springer Nature.

Entities:  

Keywords:  Ankylosing spondylitis; Asymmetric dimethylarginine; Endothelial dysfunction; Methylarginines

Mesh:

Substances:

Year:  2021        PMID: 34273021     DOI: 10.1007/s00726-021-03046-z

Source DB:  PubMed          Journal:  Amino Acids        ISSN: 0939-4451            Impact factor:   3.520


  36 in total

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Journal:  Mediators Inflamm       Date:  2018-01-18       Impact factor: 4.711

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Journal:  Sci Rep       Date:  2018-09-04       Impact factor: 4.379

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