TY - JOUR
T1 - Associations of circulating xanthine oxidoreductase activity with cardiometabolic risk markers in overweight and obese Japanese men
T2 - a cross-sectional pilot study
AU - Kosaki, Keisei
AU - Yokota, Atsumu
AU - Tanahashi, Koichiro
AU - Myoenzono, Kanae
AU - Park, Jiyeon
AU - Yoshikawa, Toru
AU - Yoshida, Yasuko
AU - Murase, Takayo
AU - Akari, Seigo
AU - Nakamura, Takashi
AU - Maeda, Seiji
N1 - Funding Information:
The authors are grateful to the members of our laboratory (University of Tsukuba) for their technical assistance. This work was supported in part by JSPS KAKENHI Grant Number JP19H03995 from the Ministry of Education, Culture, Sports, Science, and Technology, Japan and MEXT Leading Initiative for Excellent Young Researchers Grant Number JPMXS0320200234.
Publisher Copyright:
©2022 JCBN.
PY - 2022
Y1 - 2022
N2 - Circulating xanthine oxidoreductase (XOR) activity may contribute to the pathogenesis of obesity-related adverse cardiometabolic profiles. This pilot study aimed to examine the cross-sectional associations between plasma XOR activity and cardiometabolic risk (CMR) markers in overweight and obese men. In 64 overweight and obese Japanese men (aged 31–63 years), plasma XOR activity and several CMR markers, such as homeostasis model assessment of insulin resistance (HOMA-IR), and clustered CMR score were measured in each participant. Clustered CMR score was constructed based on waist circumference, triglyceride, blood pressure, fasting plasma glucose, and high-density lipoprotein cholesterol. Plasma XOR activity in overweight and obese men was positively associated with the body mass index, waist circumference, visceral fat area, body fat mass, hemoglobin A1c, serum 8-hydroxy-2'-deoxyguanosine, HOMA-IR, and clustered CMR score and was inversely associated with handgrip strength and high-density lipoprotein cholesterol. Multiple linear regression analysis further demonstrated that the associations of plasma XOR activity with HOMA-IR and the clustered CMR score remained significant after adjustment for covariates including uric acid. Our data demonstrate that circulating XOR activity was independently associated, albeit modestly, with HOMA-IR and the clustered CMR score. These preliminary findings suggest that circulating XOR activity can potentially be one of the preventive targets and biomarkers of cardiometabolic disorders in overweight and obese men.
AB - Circulating xanthine oxidoreductase (XOR) activity may contribute to the pathogenesis of obesity-related adverse cardiometabolic profiles. This pilot study aimed to examine the cross-sectional associations between plasma XOR activity and cardiometabolic risk (CMR) markers in overweight and obese men. In 64 overweight and obese Japanese men (aged 31–63 years), plasma XOR activity and several CMR markers, such as homeostasis model assessment of insulin resistance (HOMA-IR), and clustered CMR score were measured in each participant. Clustered CMR score was constructed based on waist circumference, triglyceride, blood pressure, fasting plasma glucose, and high-density lipoprotein cholesterol. Plasma XOR activity in overweight and obese men was positively associated with the body mass index, waist circumference, visceral fat area, body fat mass, hemoglobin A1c, serum 8-hydroxy-2'-deoxyguanosine, HOMA-IR, and clustered CMR score and was inversely associated with handgrip strength and high-density lipoprotein cholesterol. Multiple linear regression analysis further demonstrated that the associations of plasma XOR activity with HOMA-IR and the clustered CMR score remained significant after adjustment for covariates including uric acid. Our data demonstrate that circulating XOR activity was independently associated, albeit modestly, with HOMA-IR and the clustered CMR score. These preliminary findings suggest that circulating XOR activity can potentially be one of the preventive targets and biomarkers of cardiometabolic disorders in overweight and obese men.
KW - clustered cardiometabolic risk
KW - insulin resistance
KW - obesity
KW - purine metabolism
KW - uric acid
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U2 - 10.3164/jcbn.21-118
DO - 10.3164/jcbn.21-118
M3 - Article
AN - SCOPUS:85142105484
SN - 0912-0009
VL - 71
SP - 122
EP - 128
JO - Journal of Clinical Biochemistry and Nutrition
JF - Journal of Clinical Biochemistry and Nutrition
IS - 2
ER -