Activated L-arginine/nitric oxide pathway in pediatric cystic fibrosis and its association with pancreatic insufficiency, liver involvement and nourishment

  • Cystic fibrosis (CF; OMIM 219700) is a rare genetic disorder caused by a chloride channel defect, resulting in lung disease, pancreas insufficiency and liver impairment. Altered L-arginine (Arg)/nitric oxide (NO) metabolism has been observed in CF patients' lungs and in connection with malnutrition. The aim of the present study was to investigate markers of the Arg/NO pathway in the plasma and urine of CF patients and to identify possible risk factors, especially associated with malnutrition. We measured the major NO metabolites nitrite and nitrate, Arg, a semi-essential amino acid and NO precursor, the NO synthesis inhibitor asymmetric dimethylarginine (ADMA) and its major urinary metabolite dimethylamine (DMA) in plasma and urine samples of 70 pediatric CF patients and 78 age-matched healthy controls. Biomarkers were determined by gas chromatography–mass spectrometry and high-performance liquid chromatography. We observed higher plasma Arg (90.3 vs. 75.6 \(\mu\)M, \(\it p\) < 0.0001), ADMA (0.62 vs. 0.57 \(\mu\)M, \(\it p\) = 0.03), Arg/ADMA ratio (148 vs. 135, \(\it p\) = 0.01), nitrite (2.07 vs. 1.95 \(\mu\)M, \(\it p\) = 0.03) and nitrate (43.3 vs. 33.1 \(\mu\)M, \(\it p\) < 0.001) concentrations, as well as higher urinary DMA (57.9 vs. 40.7 \(\mu\)M/mM creatinine, \(\it p\) < 0.001) and nitrate (159 vs. 115 \(\mu\)M/mM creatinine, \(\it p\) = 0.001) excretion rates in the CF patients compared to healthy controls. CF patients with pancreatic sufficiency showed plasma concentrations of the biomarkers comparable to those of healthy controls. Malnourished CF patients had lower Arg/ADMA ratios (\(\it p\) = 0.02), indicating a higher NO synthesis capacity in sufficiently nourished CF patients. We conclude that NO production, protein-arginine dimethylation, and ADMA metabolism is increased in pediatric CF patients. Pancreas and liver function influence Arg/NO metabolism. Good nutritional status is associated with higher NO synthesis capacity and lower protein-arginine dimethylation.

Download full text files

Export metadata

Additional Services

Share in Twitter Search Google Scholar
Metadaten
Author:Folke BrinkmannORCiDGND, Beatrice HanuschGND, Manfred BallmannORCiDGND, Sebene MayorandanGND, Alexander BollenbachGND, Kristine Chobanyan-JürgensGND, Kathrin JansenGND, Anjona Schmidt-ChoudhuryGND, Nico DerichsGND, Dimitrios TsikasORCiDGND, Thomas LückeGND
URN:urn:nbn:de:hbz:294-75891
DOI:https://doi.org/10.3390/jcm9062012
Parent Title (English):Journal of Clinical Medicine
Subtitle (English):an overview and new results
Publisher:MDPI
Place of publication:Basel
Document Type:Article
Language:English
Date of Publication (online):2020/10/22
Date of first Publication:2020/06/26
Publishing Institution:Ruhr-Universität Bochum, Universitätsbibliothek
Tag:L-arginine; cystic fibrosis; liver disease; malnutrition; nitric oxide; nitric oxide synthases; nutritional status; pancreatic disease
Volume:9
Issue:6, Article 2012
First Page:2012-1
Last Page:2012-21
Institutes/Facilities:Katholisches Klinikum Bochum, Klinik für Kinder- und Jugendmedizin
open_access (DINI-Set):open_access
Licence (English):License LogoCreative Commons - CC BY 4.0 - Attribution 4.0 International