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A Newly Developed Method-Based Xanthine Oxidoreductase Activities in Various Human Liver Diseases.
Sato, Ken; Naganuma, Atsushi; Nagashima, Tamon; Arai, Yosuke; Mikami, Yuka; Nakajima, Yuka; Kanayama, Yuki; Murakami, Tatsuma; Uehara, Sanae; Uehara, Daisuke; Yamazaki, Yuichi; Murase, Takayo; Nakamura, Takashi; Uraoka, Toshio.
Afiliação
  • Sato K; Department of Gastroenterology and Hepatology, Gunma University Graduate School of Medicine, Maebashi 371-8511, Japan.
  • Naganuma A; Department of Hepatology, Heisei Hidaka Clinic, Takasaki 371-0001, Japan.
  • Nagashima T; Department of Healthcare Informatics, Takasaki University of Health and Welfare, Takasaki 370-0033, Japan.
  • Arai Y; Department of Gastroenterology, National Hospital Organization Takasaki General Medical Center, Takasaki 370-0829, Japan.
  • Mikami Y; Department of Gastroenterology, National Hospital Organization Shibukawa Medical Center, Shibukawa 377-0204, Japan.
  • Nakajima Y; Department of Gastroenterology, National Hospital Organization Shibukawa Medical Center, Shibukawa 377-0204, Japan.
  • Kanayama Y; Department of Gastroenterology and Hepatology, Gunma University Graduate School of Medicine, Maebashi 371-8511, Japan.
  • Murakami T; Department of Gastroenterology and Hepatology, Gunma University Graduate School of Medicine, Maebashi 371-8511, Japan.
  • Uehara S; Department of Gastroenterology and Hepatology, Gunma University Graduate School of Medicine, Maebashi 371-8511, Japan.
  • Uehara D; Department of Gastroenterology and Hepatology, Gunma University Graduate School of Medicine, Maebashi 371-8511, Japan.
  • Yamazaki Y; Department of Gastroenterology, National Hospital Organization Takasaki General Medical Center, Takasaki 370-0829, Japan.
  • Murase T; Department of Gastroenterology, National Hospital Organization Takasaki General Medical Center, Takasaki 370-0829, Japan.
  • Nakamura T; Department of Gastroenterology and Hepatology, Gunma University Graduate School of Medicine, Maebashi 371-8511, Japan.
  • Uraoka T; Department of Gastroenterology and Hepatology, Gunma University Graduate School of Medicine, Maebashi 371-8511, Japan.
Biomedicines ; 11(5)2023 May 14.
Article em En | MEDLINE | ID: mdl-37239117
ABSTRACT
Studies evaluating xanthine oxidoreductase (XOR) activities in comprehensive liver diseases are scarce, and different etiologies have previously been combined in groups for comparison. To accurately evaluate XOR activities in liver diseases, the plasma XOR activities in etiology-based comprehensive liver diseases were measured using a novel, sensitive, and accurate assay that is a combination of liquid chromatography and triple quadrupole mass spectrometry to detect [13C2, 15N2]uric acid using [13C2, 15N2]xanthine as a substrate. We also mainly evaluated the association between the plasma XOR activities and parameters of liver tests, purine metabolism-associated markers, oxidative stress markers, and an inflammation marker. In total, 329 patients and 32 controls were enrolled in our study. Plasma XOR activities were generally increased in liver diseases, especially in the active phase, such as in patients with hepatitis C virus RNA positivity, those with abnormal alanine transaminase (ALT) levels in autoimmune liver diseases, and uncured hepatocellular carcinoma patients. Plasma XOR activities were numerically highest in patients with acute hepatitis B. Plasma XOR activities were closely correlated with parameters of liver tests, especially serum ALT levels, regardless of etiology and plasma xanthine levels. Our results indicated that plasma XOR activity might reflect the active phase in various liver diseases.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article