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Plasma urea cycle metabolite levels and the risk of moyamoya disease

BACKGROUND AND PURPOSE: Urea cycle metabolites are expected to be the biomarkers for cerebrovascular diseases. However, the effects of circulating urea cycle metabolites on the risk of MMD and its subcategories remain unclear. The aim of this study was to prospectively investigate the association be...

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Autores principales: Yu, Xiaofan, Ge, Peicong, Zhai, Yuanren, Liu, Wei, Zhang, Qian, Ye, Xun, Liu, Xingju, Wang, Rong, Zhang, Yan, Zhao, Jizong, Zhang, Dong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10363741/
https://www.ncbi.nlm.nih.gov/pubmed/37492403
http://dx.doi.org/10.3389/fnins.2023.1163733
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author Yu, Xiaofan
Ge, Peicong
Zhai, Yuanren
Liu, Wei
Zhang, Qian
Ye, Xun
Liu, Xingju
Wang, Rong
Zhang, Yan
Zhao, Jizong
Zhang, Dong
author_facet Yu, Xiaofan
Ge, Peicong
Zhai, Yuanren
Liu, Wei
Zhang, Qian
Ye, Xun
Liu, Xingju
Wang, Rong
Zhang, Yan
Zhao, Jizong
Zhang, Dong
author_sort Yu, Xiaofan
collection PubMed
description BACKGROUND AND PURPOSE: Urea cycle metabolites are expected to be the biomarkers for cerebrovascular diseases. However, the effects of circulating urea cycle metabolites on the risk of MMD and its subcategories remain unclear. The aim of this study was to prospectively investigate the association between plasma urea cycle metabolites and the risk of MMD and its subcategories. METHODS: We measured plasma urea cycle metabolite levels for 360 adult MMD patients and 89 matched healthy controls. Clinical and laboratory characteristics were obtained from the medical record. The study was conducted from July 2020 to December 2021. RESULTS: After multivariate adjustment, the risk of MMD increased with each increment in ornithine level (per natural log [ornithine] increment: OR, 3.893; 95% CI, 1.366–11.090). The risk of MMD decreased with each increment in arginine level (per natural log [arginine] increment: OR, 0.109; 95% CI, 0.028–0.427), urea level (per natural log [urea] increment: OR, 0.261; 95% CI, 0.072–0.940), and global arginine bioavailability ratio (GABR) level (per natural log [GABR] increment: OR, 0.189; 95% CI, 0.074–0.484). The addition of plasma arginine (integrated discrimination improvement: 1.76%, p = 0.021) or GABR (integrated discrimination improvement: 1.76%, p = 0.004) to conventional risk factors significantly improved the risk reclassification for MMD. CONCLUSION: Plasma ornithine levels are positively associated with the risk of MMD. By contrast, the levels of arginine, urea, and GABR are inversely related to the risk of MMD. Plasma urea cycle metabolites might be potential biomarkers for the risk of MMD.
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spelling pubmed-103637412023-07-25 Plasma urea cycle metabolite levels and the risk of moyamoya disease Yu, Xiaofan Ge, Peicong Zhai, Yuanren Liu, Wei Zhang, Qian Ye, Xun Liu, Xingju Wang, Rong Zhang, Yan Zhao, Jizong Zhang, Dong Front Neurosci Neuroscience BACKGROUND AND PURPOSE: Urea cycle metabolites are expected to be the biomarkers for cerebrovascular diseases. However, the effects of circulating urea cycle metabolites on the risk of MMD and its subcategories remain unclear. The aim of this study was to prospectively investigate the association between plasma urea cycle metabolites and the risk of MMD and its subcategories. METHODS: We measured plasma urea cycle metabolite levels for 360 adult MMD patients and 89 matched healthy controls. Clinical and laboratory characteristics were obtained from the medical record. The study was conducted from July 2020 to December 2021. RESULTS: After multivariate adjustment, the risk of MMD increased with each increment in ornithine level (per natural log [ornithine] increment: OR, 3.893; 95% CI, 1.366–11.090). The risk of MMD decreased with each increment in arginine level (per natural log [arginine] increment: OR, 0.109; 95% CI, 0.028–0.427), urea level (per natural log [urea] increment: OR, 0.261; 95% CI, 0.072–0.940), and global arginine bioavailability ratio (GABR) level (per natural log [GABR] increment: OR, 0.189; 95% CI, 0.074–0.484). The addition of plasma arginine (integrated discrimination improvement: 1.76%, p = 0.021) or GABR (integrated discrimination improvement: 1.76%, p = 0.004) to conventional risk factors significantly improved the risk reclassification for MMD. CONCLUSION: Plasma ornithine levels are positively associated with the risk of MMD. By contrast, the levels of arginine, urea, and GABR are inversely related to the risk of MMD. Plasma urea cycle metabolites might be potential biomarkers for the risk of MMD. Frontiers Media S.A. 2023-07-10 /pmc/articles/PMC10363741/ /pubmed/37492403 http://dx.doi.org/10.3389/fnins.2023.1163733 Text en Copyright © 2023 Yu, Ge, Zhai, Liu, Zhang, Ye, Liu, Wang, Zhang, Zhao and Zhang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Yu, Xiaofan
Ge, Peicong
Zhai, Yuanren
Liu, Wei
Zhang, Qian
Ye, Xun
Liu, Xingju
Wang, Rong
Zhang, Yan
Zhao, Jizong
Zhang, Dong
Plasma urea cycle metabolite levels and the risk of moyamoya disease
title Plasma urea cycle metabolite levels and the risk of moyamoya disease
title_full Plasma urea cycle metabolite levels and the risk of moyamoya disease
title_fullStr Plasma urea cycle metabolite levels and the risk of moyamoya disease
title_full_unstemmed Plasma urea cycle metabolite levels and the risk of moyamoya disease
title_short Plasma urea cycle metabolite levels and the risk of moyamoya disease
title_sort plasma urea cycle metabolite levels and the risk of moyamoya disease
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10363741/
https://www.ncbi.nlm.nih.gov/pubmed/37492403
http://dx.doi.org/10.3389/fnins.2023.1163733
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