<?xml version="1.1" encoding="utf-8"?>
<article xsi:noNamespaceSchemaLocation="http://jats.nlm.nih.gov/publishing/1.1/xsd/JATS-journalpublishing1-mathml3.xsd" dtd-version="1.1" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance"><front><journal-meta><journal-id journal-id-type="publisher-id">MRP</journal-id><journal-title-group><journal-title>Medical Research and Practice</journal-title></journal-title-group><issn>2993-9690</issn><eissn>2993-9704</eissn><publisher><publisher-name>Art and Technology</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.61369/MRP.8768</article-id><article-categories><subj-group subj-group-type="heading"><subject>Article</subject></subj-group></article-categories><title>糖尿病肾病患者血清微小RNA-193a水平及其与预后的关系</title><url>https://artdesignp.com/journal/MRP/2/9/10.61369/MRP.8768</url><author>潘志铣,李董平,饶杰</author><pub-date pub-type="publication-year"><year>2024</year></pub-date><volume>2</volume><issue>9</issue><history><date date-type="pub"><published-time>2024-09-20</published-time></date></history><abstract>目的 探讨血清miR-193a在糖尿病肾病（DN）患者中的表达水平及在评估患者预后的临床价值。方法 以我院收治的105例2型糖尿病患者（T2DM）为研究对象，根据尿蛋白排泄率（UAER）分为DM对照组（59例）和DN组（46例），并同期选择105例体检健康人群为对照组。比较三组临床资料、血清miR-193a水平。相关法分析DN患者miR-193a水平与各指标相关性；对DN患者随访3年，根据患者预后分为预后较好组（31例）和预后较差组（15例），比较两组miR-193a水平在评估患者预后中的临床价值。结果 相较于对照组和DM对照组，DN组UA、BUN、SCr、UAER、Cys-C、miR-193a水平更高，而eGFR水平更低（P ＜ 0.05）；相关性分析结果显示，DN患者miR-193a水平与UA、BUN、SCr、UAER、Cys-C水平呈正相关，而与eGFR呈负相关（P ＜ 0.05）；相较于预后较好组，预后较差组miR-193a水平更高（P＜0.05）。结论 DN患者miR-193a水平显著上升，与患者病情密切相关，miR-193a检测可作为辅助指标用于评估患者预后。</abstract><keywords>miR-193a,糖尿病肾病,预后</keywords></article-meta></front><body/><back><ref-list><ref id="B1" content-type="article"><label>1</label><element-citation publication-type="journal"><p>[1]曾静怡，鲍晓荣 . 糖尿病肾病发病机制的研究进展［J］．中国中西医结合肾病杂志，2021，22（5）：461-463.[2]KATO M, NATARAJAN R. Epigenetics and epigenomics in diabetic kidney disease and metabolic memory［J］．Nat Rev Nephrol, 2019, 15(6):327-345.[3]韩敏，郭敬，刘子云．微小RNA-31水平在糖尿病肾病患者外周血中的表达及其与肾小球滤过功能的关系研究［J］．中国医刊，2022，57（8）：789-792. .[4] 祁桠楠，胡江伟，武亮，等．血清TLR-3,miR-181b及URBP联合检测在糖尿病肾病诊断及预后判断的价值研究［J］．现代检验医学杂志，2022，37（2）：37-41.[5]秦凤，张惠莉．糖尿病肾病患者外周血微小RNA-21表达与肾间质损伤的关系及意义［J］．中国免疫学杂志，2019，35(14): 1743-1748.[6]CHEN R Q, NING Y C, ZENG G R, et al. The miR-193a-5p/NCX2/AKT axis promotes invasion and metastasis of osteosarcoma［J］．J Cancer, 2021, 12(19):5903-5913.[7]Gebeshuber CA, Kornauth C, Dong L, et al. Focal segmental glomeruloscleros is induced by microRNA-193a and its down regulation of WT1［J］． Nat Med, 2013,19(4):481-487。[8] 中国2 型糖尿病防治指南（2017年版）［J］． 中国实用内科杂志，2018，38（4）:292-344.[9]Shao Y, Lv C, Yuan Q, Wang Q. Levels of serum 25(OH)VD3, HIF-1&amp;alpha;, VEGF,vWf, and IGF-1 and their correlation in type 2 diabetes patients with different urine albumin creatinine ratio［J］．J Diabetes Res. 2016, 20(2016):1925424.[10] Cankurtaran V, Inanc M, Tekin K, et al. Retinal micro circulation in predicting diabetic nephropathy in type 2 diabetic patients without retinopathy［J］．Ophthalmologica, 2020, 243(4 ):271-279.[11]LEE W C, L LC, NG H Y, et al. Urinary exosomal microRNA signatures in nephrotic, Biopsy-Prove ndiabetic nephropathy［J］．Journal of Clinical Medicine,2020, 9(4):1220.[12]PETERS L J F, FLOEGE J, BIESSEN E A L, et al. MicroRNAs in chronic kidney disease: four candidates for clinical application［J］．International Journal of Molecular Sciences, 2020, 21(18): 6547.[13]Kietzmann L,Guhr SS,Meyer TN, et al. MicroRNA-193a Regulates the Transdifferentiation of Human Parietal Epithelial Cells toward a Podocyte Phenotype.J Am Soc Nephrol. 2015, 26(6):1389-1401.</p><pub-id pub-id-type="doi"/></element-citation></ref></ref-list></back></article>
