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体重指数与超重/肥胖人群黄嘌呤氧化酶活性独立相关。

Body mass index is independently associated with xanthine oxidase activity in overweight/obese population.

机构信息

Center for Laboratory Diagnostics, Primary Health Care Center, Trg Nikole Kovacevica 6, 81000, Podgorica, Montenegro.

Department for Medical Biochemistry, University of Nis-School of Medicine, Nis, Serbia.

出版信息

Eat Weight Disord. 2020 Feb;25(1):9-15. doi: 10.1007/s40519-018-0490-5. Epub 2018 Feb 22.

Abstract

PURPOSE

The pathophysiological mechanism of the relationship between xanthine oxidase (XO) activity and obesity has not been completely elucidated. Since inflammation and oxidative stress are regarded as key determinants of enlarged adipose tissue, we aimed to investigate the association between oxidative stress (as measured with XO activity), inflammation [as measured with high-sensitivity C-reactive protein (hsCRP)] and obesity [as measured with body mass index (BMI)]. In addition, we wanted to examine whether hsCRP itself plays an independent role in XO activity increase or it is only mediated through obesity.

METHODS

A total of 118 overweight/obese volunteers (mean age 54.76 ± 15.13 years) were included in the current cross-sectional study. Anthropometric, biochemical parameters, and blood pressure were obtained.

RESULTS

Significant differences between age, BMI, waist circumference, concentrations of uric acid and hsCRP, as well as xanthine dehydrogenase (XDH) activities were evident among XO tertile groups. Multiple linear regression analysis revealed that BMI (beta = 0.241, p = 0.012) and XDH (beta = - 0.489, p < 0.001) are the independent predictors of XO activity (R-adjusted = 0.333), whereas hsCRP lost its independent role in XO activity prediction.

CONCLUSION

Obesity (as determined with increased BMI) is an independent predictor of high XO activity in overweight/obese population.

LEVEL OF EVIDENCE

Level V: cross-sectional descriptive study.

摘要

目的

黄嘌呤氧化酶(XO)活性与肥胖之间的病理生理机制尚未完全阐明。由于炎症和氧化应激被认为是增大的脂肪组织的关键决定因素,我们旨在研究氧化应激(通过 XO 活性来衡量)、炎症[通过高敏 C 反应蛋白(hsCRP)来衡量]与肥胖(通过体重指数(BMI)来衡量)之间的关联。此外,我们还想研究 hsCRP 本身是否在 XO 活性增加中发挥独立作用,或者它只是通过肥胖起中介作用。

方法

本横断面研究共纳入 118 名超重/肥胖志愿者(平均年龄 54.76±15.13 岁)。记录了人体测量学、生化参数和血压。

结果

在 XO 三分位组之间,年龄、BMI、腰围、尿酸和 hsCRP 浓度以及黄嘌呤脱氢酶(XDH)活性存在显著差异。多元线性回归分析显示,BMI(β=0.241,p=0.012)和 XDH(β=-0.489,p<0.001)是 XO 活性的独立预测因子(调整后的 R ²=0.333),而 hsCRP 在预测 XO 活性方面失去了独立作用。

结论

肥胖(通过 BMI 增加来确定)是超重/肥胖人群中 XO 活性升高的独立预测因子。

证据等级

五级:横断面描述性研究。

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