• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

尿毒症患者血管钙化与血清lncRNA H19及Runx2 mRNA表达的相关性

Association of Vascular Calcification with Serum lncRNA H19 and Runx2 mRNA Expression in Patients with Uremia.

作者信息

Wang Taoxia, Li Guiying, Xu Jinsheng, Bai Yaling, Liu Xiaoli, Jin Jingjing, Cheng Meijuan, Li Jianwei

出版信息

Altern Ther Health Med. 2024 May 3.

PMID:38702154
Abstract

BACKGROUND

The objective of this study was to investigate the relationship between vascular calcification, serum lncRNA H19, and Runt-Related Transcription Factor 2 mRNA expression in patients with uremia.

METHODS

This study is a retrospective study which recruited 146 patients with uremia on dialysis from December 2021 to November 2022. Participants were divided into the VC and non-VC groups based on their chest X-ray calcification ratings. General and clinical data were collected from all patients. Serum H19, Runx2 mRNA, mineral bone disease effectors, and other blood markers were tested. Univariate analysis was performed to compare the changes in each clinical index between these two groups of patients. A multi-factor logistic regression analysis of risk factors for VC was performed. Receiver operating characteristics analyzed the H19 and Runx2 for their diagnostic values for VC. Pearson's test was used to analyze the correlation between the H19 and Runx2 expression and the factors influencing VC.

RESULTS

Patients in the VC group had significantly higher creatinine, serum phosphorus, calcium, BMP-2, FGF-23, OPG, and iPTH levels than those in the non-VC group (P < .05), while their albumin levels were significantly lower than those in the non-VC group (P < .05). The expression of H19 and Runx2 mRNA was significantly upregulated in the serum of VC patients (P < .05). H19 was significantly positively correlated with creatinine, serum phosphorus, calcium, BMP-2, OPG, and iPTH (P < .05). Runx2 mRNA was significantly positively correlated with creatinine, FGF-23, and iPTH (P < .05 ), while there was no significant correlation with other factors(P > .05). Albumin, BMP-2, iPTH, H19, and Runx2 were independent correlative-factors of uremic VC. In addition, the combined H19 and Runx2 test (AUC=0.850; 95% CI: 0.781-0.903) had good diagnostic values for the development of VC.

CONCLUSION

Serum H19 and Runx2 levels are significantly associated with VC-related factors and are independent risk factors for uremic VC, and their levels contribute to the diagnosis of uremic VC.

摘要

背景

本研究旨在探讨尿毒症患者血管钙化、血清长链非编码RNA H19与 runt 相关转录因子 2 mRNA 表达之间的关系。

方法

本研究为回顾性研究,纳入了 2021 年 12 月至 2022 年 11 月期间 146 例接受透析的尿毒症患者。根据胸部 X 线钙化分级将参与者分为血管钙化(VC)组和非 VC 组。收集所有患者的一般资料和临床数据。检测血清 H19、Runx2 mRNA、矿物质骨病效应因子及其他血液标志物。进行单因素分析以比较两组患者各临床指标的变化。对 VC 的危险因素进行多因素逻辑回归分析。采用受试者工作特征曲线分析 H19 和 Runx2 对 VC 的诊断价值。采用 Pearson 检验分析 H19 和 Runx2 表达与影响 VC 的因素之间的相关性。

结果

VC 组患者的肌酐、血清磷、钙、骨形态发生蛋白-2(BMP-2)、成纤维细胞生长因子-23(FGF-23)、骨保护素(OPG)和全段甲状旁腺激素(iPTH)水平显著高于非 VC 组(P < 0.05),而其白蛋白水平显著低于非 VC 组(P < 0.05)。VC 患者血清中 H19 和 Runx2 mRNA 的表达显著上调(P < 0.05)。H19 与肌酐、血清磷、钙、BMP-2、OPG 和 iPTH 显著正相关(P < 0.05)。Runx2 mRNA 与肌酐、FGF-23 和 iPTH 显著正相关(P < 0.05),而与其他因素无显著相关性(P > 0.05)。白蛋白、BMP-2、iPTH、H19 和 Runx2 是尿毒症性 VC 的独立相关因素。此外,联合检测 H19 和 Runx2(AUC = 0.850;95%CI:0.781 - 0.903)对 VC 的发生具有良好的诊断价值。

结论

血清 H19 和 Runx2 水平与 VC 相关因素显著相关,是尿毒症性 VC 的独立危险因素,其水平有助于尿毒症性 VC 的诊断。

相似文献

1
Association of Vascular Calcification with Serum lncRNA H19 and Runx2 mRNA Expression in Patients with Uremia.尿毒症患者血管钙化与血清lncRNA H19及Runx2 mRNA表达的相关性
Altern Ther Health Med. 2024 May 3.
2
Upregulated LncRNA H19 Sponges MiR-106a-5p and Contributes to Aldosterone-Induced Vascular Calcification via Activating the Runx2-Dependent Pathway.上调的长链非编码 RNA H19 海绵 miR-106a-5p,并通过激活 Runx2 依赖性途径促进醛固酮诱导的血管钙化。
Arterioscler Thromb Vasc Biol. 2023 Sep;43(9):1684-1699. doi: 10.1161/ATVBAHA.123.319308. Epub 2023 Jul 6.
3
Progression of Vascular Calcification and Clinical Outcomes in Patients Receiving Maintenance Dialysis.维持性透析患者血管钙化的进展及临床转归。
JAMA Netw Open. 2023 May 1;6(5):e2310909. doi: 10.1001/jamanetworkopen.2023.10909.
4
[Bushen Huoxue Recipe Inhibited Vascular Calcification in Chronic Renal Failure Rats by Regulating BMP-2/Runx2/Osterix Signal Pathway].补肾活血方通过调控BMP-2/Runx2/成骨转录因子信号通路抑制慢性肾衰竭大鼠血管钙化
Zhongguo Zhong Xi Yi Jie He Za Zhi. 2016 Mar;36(3):327-32.
5
Uremic Patients with Increased Vascular Calcification Score Have Serum with High Calcific Potential: Role of Vascular Smooth Muscle Cell Osteoblastic Differentiation and Apoptosis.高血管钙化评分的尿毒症患者具有高钙化潜能的血清:血管平滑肌细胞成骨样分化和凋亡的作用。
Blood Purif. 2019;48(2):142-149. doi: 10.1159/000497229. Epub 2019 Feb 6.
6
Clinical significance of serum CDC42 in the prediction of uremic vascular calcification incidence and progression.血清 CDC42 在预测尿毒症血管钙化发病和进展中的临床意义。
Libyan J Med. 2023 Dec;18(1):2194100. doi: 10.1080/19932820.2023.2194100.
7
LncRNA H19 sponges miR-103-3p to promote the high phosphorus-induced osteoblast phenotypic transition of vascular smooth muscle cells by upregulating Runx2.长链非编码RNA H19通过上调Runx2,吸附miR-103-3p来促进高磷诱导的血管平滑肌细胞成骨细胞表型转变。
Cell Signal. 2022 Mar;91:110220. doi: 10.1016/j.cellsig.2021.110220. Epub 2021 Dec 16.
8
Impact of miR-302b on Calcium-phosphorus Metabolism and Vascular Calcification of Rats with Chronic Renal Failure by Regulating BMP-2/Runx2/Osterix Signaling Pathway.miR-302b 通过调控 BMP-2/Runx2/Osterix 信号通路对慢性肾衰竭大鼠钙磷代谢及血管钙化的影响。
Arch Med Res. 2018 Apr;49(3):164-171. doi: 10.1016/j.arcmed.2018.08.002. Epub 2018 Aug 14.
9
Risk Factors Associated With Altered Circulating Micro RNA -125b and Their Influences on Uremic Vascular Calcification Among Patients With End-Stage Renal Disease.与终末期肾病患者循环 microRNA-125b 改变相关的危险因素及其对尿毒症血管钙化的影响。
J Am Heart Assoc. 2019 Jan 22;8(2):e010805. doi: 10.1161/JAHA.118.010805.
10
The mechanisms of uremic serum-induced expression of bone matrix proteins in bovine vascular smooth muscle cells.尿毒症血清诱导牛血管平滑肌细胞中骨基质蛋白表达的机制。
Kidney Int. 2006 Sep;70(6):1046-53. doi: 10.1038/sj.ki.5001663. Epub 2006 Jul 12.