Risk Factors Associated With Altered Circulating MicroRNA-125b and Their Influences on Uremic Vascular Calcification Among Patients With End-Stage Renal Disease

被引:27
作者
Chao, Chia-Ter [1 ,2 ,3 ]
Yuan, Tzu-Hang [4 ]
Yeh, Hsiang-Yuan [5 ]
Chen, Hsuan-Yu [6 ]
Huang, Jenq-Wen [3 ]
Chen, Huei-Wen [4 ]
机构
[1] Natl Taiwan Univ Hosp, BeiHu Branch, Dept Med, Taipei, Taiwan
[2] Natl Taiwan Univ Hosp, BeiHu Branch, Geriatr & Community Med Res Ctr, Taipei, Taiwan
[3] Natl Taiwan Univ Hosp, Dept Internal Med, Nephrol Div, Taipei, Taiwan
[4] Natl Taiwan Univ, Grad Inst Toxicol, Taipei, Taiwan
[5] Soochow Univ, Sch Big Data Management, Taipei, Taiwan
[6] Acad Sinica, Inst Stat Sci, Taipei, Taiwan
来源
JOURNAL OF THE AMERICAN HEART ASSOCIATION | 2019年 / 8卷 / 02期
关键词
biomarker; chronic kidney disease; end-stage renal disease; fibroblast growth factor-23; microRNA-125b; osteoprotegerin; vascular calcification; AORTIC-ARCH CALCIFICATION; CHRONIC KIDNEY-DISEASE; SMOOTH-MUSCLE-CELLS; CARDIOVASCULAR RISK; OSTEOPROTEGERIN; EXPRESSION; SERUM; POPULATION; BIOMARKERS; VESICLES;
D O I
10.1161/JAHA.118.010805
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background MicroRNA-125b (miR-125b) has been shown to regulate vascular calcification (VC), and serum miR-125b levels are a potential biomarker for estimating the risk of uremic VC status. However, it is unknown whether clinical features, including chronic kidney disease mineral bone disorder molecules, affect serum miR-125b levels. Methods and Results Patients receiving chronic dialysis for >= 3 months were recruited from different institutes. Serum miR-125b and chronic kidney disease mineral bone disorder effectors, including intact parathyroid hormone, 25-OH-D, fibroblast growth factor-23, osteoprotegerin, and fetuin-A, were quantified. We used multivariate regression analyses to identify factors associated with low serum miR-125b levels and an area under receiver operating characteristic curve curve to derive optimal cutoffs for factors exhibiting close associations. Further regression analyses evaluated the influence of miR-125b on VC risk. Among 223 patients receiving chronic dialysis (mean age, 67.3 years; mean years of dialysis, 5.2), 54 (24.2%) had high serum miR-125b levels. Osteoprotegerin (P=0.013), fibroblast growth factor-23 (P=0.006), and fetuin-A (P=0.036) were linearly associated with serum miR-125b levels. High osteoprotegerin levels independently correlated with high serum miR-125 levels. Adding serum miR-125b levels and serum osteoprotegerin levels (>400 pg/mL) into models estimating the risk of uremic VC increased the area under receiver operating characteristic curve values (for models without miR-125b/osteoprotegerin, with miR-125b, and both: 0.74, 0.79, and 0.81, respectively). Conclusions Serum osteoprotegerin levels >= 400 pg/mL and serum miR-125b levels synergistically increased the accuracy of estimating VC risk among patients receiving chronic dialysis. Taking miR-125b and osteoprotegerin levels into consideration when estimating VC risk may be recommended.
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页数:12
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