首页> 外文期刊>Clinical kidney journal. >Obesity and chronic kidney disease progression—the role of a new adipocytokine: C1q/tumour necrosis factor-related protein-1
【24h】

Obesity and chronic kidney disease progression—the role of a new adipocytokine: C1q/tumour necrosis factor-related protein-1

机译:肥胖和慢性肾脏疾病的进展-一种新的脂肪细胞因子的作用:C1q /肿瘤坏死因子相关蛋白-1

获取原文
       

摘要

Background Obesity is a risk factor for incident chronic kidney disease (CKD) in the general population. C1q/tumour necrosis factor-related protein 1 (CTRP1) is a new adipokine with multiple vascular and metabolic effects and may modulate the association between obesity and vascular diseases. The aim of the study is to explore potential links between obesity, CTRP1 levels and CKD progression. Methods Patients with Stages 3 and 4 CKD without previous cardiovascular events were enrolled and divided into two groups according to body mass index (BMI). Demographic, clinical and analytical data and CTRP1 levels were collected at baseline. During follow-up, renal events [defined as dialysis initiation, serum creatinine doubling or a 50% decrease in estimated glomerular filtration rate (Modification of Diet in Renal Disease)] were registered. Results A total of 71 patients with CKD were divided into two groups: 25 obese (BMI 30?kg/msup2/sup) and 46 non-obese. CTRP1 in plasma at baseline was higher in obese patients [median (interquartile range) 360 (148) versus 288 (188) ng/mL, P?=?0.041]. No significant association was found between CTRP1 levels and CKD stage, presence of diabetes, aldosterone and renin levels, or blood pressure. Obese patients had higher systolic blood pressure (P?=?0.018) and higher high-sensitivity C-reactive protein (P?=?0.019) and uric acid (P?=?0.003) levels, without significant differences in the percentage of diabetic patients or albuminuria. During a mean follow-up of 65?months, 14 patients had a renal event. Patients with CTRP1 in the lowest tertile had more renal events, both in the overall sample (log rank: 5.810, P?=?0.016) and among obese patients (log rank: 5.405, P?=?0.020). Higher CTRP1 levels were associated with slower renal progression (hazard ratio 0.992, 95% confidence interval 0.986–0.998; P?=?0.001) in a model adjusted for obesity, aspirin, albuminuria and renal function. Conclusions CTRP1 levels are higher in obese than in non-obese patients with CKD. High CTRP1 levels may have a renal protective role since they were associated with slower kidney disease progression. Interventional studies are needed to explore this hypothesis.
机译:背景肥胖是普通人群中发生慢性肾脏病(CKD)的危险因素。 C1q /肿瘤坏死因子相关蛋白1(CTRP1)是一种新的脂肪因子,具有多种血管和代谢作用,可能调节肥胖与血管疾病之间的关联。这项研究的目的是探索肥胖,CTRP1水平和CKD进展之间的潜在联系。方法纳入没有心血管事件的第3期和第4期CKD患者,并根据体重指数(BMI)分为两组。在基线时收集了人口统计学,临床和分析数据以及CTRP1水平。在随访期间,记录了肾脏事件[定义为开始透析,血清肌酐加倍或肾小球滤过率估计降低50%(肾脏疾病饮食的改变)]。结果71例CKD患者分为两组:肥胖25例(BMI> 30?kg / m 2 )和46例非肥胖。肥胖患者在基线时血浆中的CTRP1较高[中位(四分位间距)360(148)对288(188)ng / mL,P1 =?0.041]。在CTRP1水平和CKD阶段,糖尿病,醛固酮和肾素水平或血压之间未发现显着相关性。肥胖患者的收缩压较高(P <= 0.018),高敏C反应蛋白(P = 0.019)和尿酸(P = 0.003)水平较高,糖尿病患者的百分比无明显差异患者或蛋白尿。在平均65个月的随访期间,有14名患者发生了肾脏事件。三分位数最低的CTRP1患者在总样本中(对数等级:5.810,P <= 0.016)和肥胖患者(对数等级:5.405,P <= 0.020)都有更多的肾脏事件。在针对肥胖,阿司匹林,蛋白尿和肾功能调整的模型中,较高的CTRP1水平与较慢的肾脏进展相关(危险比0.992,95%置信区间0.986-0.998; P <= 0.001)。结论肥胖患者的CTRP1水平高于非肥胖CKD患者。高CTRP1水平可能与肾脏疾病进展较慢有关,因此具有肾脏保护作用。需要介入研究来探索该假设。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号