Association between Plasma Xanthine Oxidoreductase Activity and the Renal Function in a General Japanese Population: The Tohoku Medical Megabank Community-Based Cohort Study.


Journal

Kidney & blood pressure research
ISSN: 1423-0143
Titre abrégé: Kidney Blood Press Res
Pays: Switzerland
ID NLM: 9610505

Informations de publication

Date de publication:
2022
Historique:
received: 09 02 2022
accepted: 10 10 2022
pubmed: 2 11 2022
medline: 27 12 2022
entrez: 1 11 2022
Statut: ppublish

Résumé

Xanthine oxidoreductase (XOR) has been identified as a critical source of reactive oxygen species in various pathophysiological conditions, including hypertension, endothelial dysfunction, and atherosclerosis. This study investigated the association between XOR and renal function in a general Japanese population. The Iwate Tohoku Medical Megabank Organization pooled individual participant data from a community-based cohort study in Iwate prefecture. Chronic kidney disease (CKD) was estimated using the estimated glomerular filtration rate of cystatin C (eGFRcys). Individuals with a history of hyperuricemia or severe renal dysfunction (eGFRcys <15 mL/min/1.73 m2 or undergoing dialysis) were excluded from the study. We performed a multinominal multivariate logistic analysis adjusted for age, blood pressure, uric acid, glycated hemoglobin A1c, low-density lipoprotein cholesterol, and high-density lipoprotein cholesterol to associate XOR activity and renal function. The present study included 4,248 participants (male/female: 1,373/2,875, age: 62.9 ± 11.7 years). When participants were divided according to XOR quartiles, blood pressure, body mass index, uric acid, low-density lipoprotein cholesterol, and glycated hemoglobin A1c were highest in the highest XOR quartile (all p < 0.001). The XOR activity was significantly higher in the subgroup with CKD stage G3 and G4 (G1 vs. G2 vs. G3-G4: 44.8 ± 40.5 vs. 52.0 ± 42.9 vs. 54.1 ± 43.9 pmol/h/mL, p = 0.02). The higher XOR activity was significantly associated with an increase of CKD stage: the odd ratios (95% confidence intervals) per 1 pmol/h/mL increase in XOR activity with CKD stage G1 as a reference were 1.37 (1.13-1.73) in G2 and 1.51 (1.30-1.84) in G3-G4. The present study concluded that high XOR activity was associated with the severity of CKD in a general Japanese population, suggesting that upregulated XOR activity may be involved in advanced renal dysfunction.

Identifiants

pubmed: 36318900
pii: 000527654
doi: 10.1159/000527654
doi:

Substances chimiques

Xanthine Dehydrogenase EC 1.17.1.4
Glycated Hemoglobin 0
Uric Acid 268B43MJ25
Lipoproteins, LDL 0
Cholesterol 97C5T2UQ7J

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

722-728

Informations de copyright

© 2022 The Author(s). Published by S. Karger AG, Basel.

Auteurs

Satoru Taguchi (S)

Department of Biomedical Information Analysis, Institute for Biomedical Sciences, Iwate Medical University, Morioka, Japan, staguchi888@gmail.com.
Division of Cardiology, Department of Internal Medicine, Iwate Medical University, Morioka, Japan, staguchi888@gmail.com.

Takahito Nasu (T)

Department of Biomedical Information Analysis, Institute for Biomedical Sciences, Iwate Medical University, Morioka, Japan.
Division of Cardiology, Department of Internal Medicine, Iwate Medical University, Morioka, Japan.
Iwate Tohoku Medical Megabank Organization, Iwate Medical University, Morioka, Japan.

Mamoru Satoh (M)

Department of Biomedical Information Analysis, Institute for Biomedical Sciences, Iwate Medical University, Morioka, Japan.
Iwate Tohoku Medical Megabank Organization, Iwate Medical University, Morioka, Japan.

Yuka Kotozaki (Y)

Iwate Tohoku Medical Megabank Organization, Iwate Medical University, Morioka, Japan.

Kozo Tanno (K)

Iwate Tohoku Medical Megabank Organization, Iwate Medical University, Morioka, Japan.
Department of Hygiene and Preventive Medicine, Iwate Medical University, Morioka, Japan.

Fumitaka Tanaka (F)

Iwate Tohoku Medical Megabank Organization, Iwate Medical University, Morioka, Japan.
Division of Nephrology and Hypertension, Department of Internal Medicine, Iwate MedicalUniversity, Morioka, Japan.

Koichi Asahi (K)

Iwate Tohoku Medical Megabank Organization, Iwate Medical University, Morioka, Japan.
Division of Nephrology and Hypertension, Department of Internal Medicine, Iwate MedicalUniversity, Morioka, Japan.

Hideki Ohmomo (H)

Department of Biomedical Information Analysis, Institute for Biomedical Sciences, Iwate Medical University, Morioka, Japan.
Iwate Tohoku Medical Megabank Organization, Iwate Medical University, Morioka, Japan.

Hiroto Kikuchi (H)

Department of Biomedical Information Analysis, Institute for Biomedical Sciences, Iwate Medical University, Morioka, Japan.
Division of Cardiology, Department of Internal Medicine, Iwate Medical University, Morioka, Japan.

Takamasa Kobayashi (T)

Division of Cardiology, Department of Internal Medicine, Iwate Medical University, Morioka, Japan.

Yoshihiro Morino (Y)

Division of Cardiology, Department of Internal Medicine, Iwate Medical University, Morioka, Japan.

Atsushi Shimizu (A)

Department of Biomedical Information Analysis, Institute for Biomedical Sciences, Iwate Medical University, Morioka, Japan.
Iwate Tohoku Medical Megabank Organization, Iwate Medical University, Morioka, Japan.

Kenji Sobue (K)

Department of Neuroscience, Institute for Biomedical Science, Iwate Medical University, Morioka, Japan.

Makoto Sasaki (M)

Iwate Tohoku Medical Megabank Organization, Iwate Medical University, Morioka, Japan.
Division of Ultrahigh Field MRI, Institute for Biomedical Science, Iwate Medical University, Morioka, Japan.

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