Increased urinary exosomal microRNAs in children with idiopathic nephrotic syndrome

被引:52
作者
Chen, Tingting [1 ,2 ]
Wang, Cheng [1 ,2 ]
Yu, Hanqing [3 ]
Ding, Meng [2 ]
Zhang, Cuiping [1 ]
Lu, Xiaolan [1 ,2 ]
Zhang, Chen-Yu [2 ]
Zhang, Chunni [1 ,2 ]
机构
[1] Southern Med Univ, Nanjing Sch Clin Med, Jinling Hosp, State Key Lab Analyt Chem Life Sci,Dept Clin Lab, Nanjing, Jiangsu, Peoples R China
[2] Nanjing Univ, Jiangsu Engn Res Ctr MicroRNA Biol & Biotechnol, State Key Lab Pharmaceut Biotechnol, Adv Res Inst Life Sci,Sch Life Sci, Nanjing, Jiangsu, Peoples R China
[3] Nanjing Childrens Hosp, Dept Clin Lab, Nanjing, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Paediatric idiopathic nephrotic syndrome; Urinary exosomes; microRNA; Biomarker; Illumina sequencing via synthesis; RT-qPCR; EXPRESSION; BIOMARKERS; PROFILE; CELLS; SERUM; MIRNA;
D O I
10.1016/j.ebiom.2018.11.018
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Urinary exosomal miRNAs are gaining increasing attention for their potential as ideal non-invasive biomarkers for kidney diseases; however, little is known about their diagnostic ability for paediatric nephrotic syndrome (NS). This study explored the clinical value of urinary exosomal miRNAs for paediatric idiopathic NS. Methods: Urine samples were collected from 129 NS children and 126 age-/sex-matched healthy controls. The miRNA profile of urinary exosomes was analysed by high-throughput Illumina sequencing via synthesis (SBS) technology followed by verification with a quantitative reverse-transcription polymerase chain reaction (RTqPCR) assay arranged in two independent cohorts. Additionally, paired urine samples from 65 of these patients were collected before and after treatment. Findings: The Illumina SBS identified 30 markedly increased urinary exosomal miRNAs in NS children compared with controls (>= 5-fold, P < .05). Fifteen miRNAs were selected for further investigation, of which 5 (miR-194-5p, miR-146b-5p, miR-378a-3p, miR-23b-3p and miR-30a-5p) were verified by RT-qPCR to be significantly and steadily increased in NS (>3-fold, P < .01) and markedly reduced during the clinical remission period (P < .001). Moreover, the concentrations of miR-194-5p and miR-23b-3p were significantly positively correlated with the urine protein content and were markedly higher in the high urine protein group than in the low urine protein group (P < .001 and P < .01, respectively). Interpretations: We identified 5 altered urinary exosomal miRNAs in NS children with disease progression and treatment. These urinary exosomal miRNAs could be promising and non-invasive potential biomarker candidates for diagnosing, monitoring and stratifying paediatric NS. Fund: National Natural Science Foundation of China; Fund of State Key Laboratory of Analytical Chemistry for Life Science; National Basic Research Programme of China; Foundation of Jiangsu Provincial Medical Youth Talent. (c) 2018 The Authors. Published by Elsevier B.V.
引用
收藏
页码:552 / 561
页数:10
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