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有和没有尿毒症的患者桡动脉钙化的危险因素。

Risk factors for radial artery calcification in patients with and without uremia.

作者信息

Hao Jian-Bing, Wang Si-Yu, Chen Tong, Yuan Bo, Hao Li-Rong

机构信息

Department of Nephrology, Southern University of Science and Technology Hospital, Shenzhen, China.

Department of Clinical Laboratory, Southern University of Science and Technology Hospital, Shenzhen, China.

出版信息

BMC Nephrol. 2025 Jan 11;26(1):18. doi: 10.1186/s12882-024-03940-0.

Abstract

BACKGROUND

Calcification of the radial artery is one of the main causes of anastomotic stenosis in autogenous arteriovenous fistulas in uremic patients. However, the pathogenesis of calcification is still unknown. This study attempted to screen and validate the risk factors for vascular calcification in patients with uremia.

METHODS

Serum of blood were collected and tissue samples from radial artery were obtained from 60 uremia patients with or without hemodialysis. General biochemical indicators and calcification-related molecules were collected and detected via ELISA or correlation analysis. In addition, pathological changes and calcification-related molecules in the radial artery were evaluated by HE or immunohistochemical staining.

RESULTS

There were differences in total calcium, calcium-phosphorus products, allograft inflammatory factor 1 (AIF-1), intact parathyroid hormone (iPTH), vitamin D (VD), fibroblast growth factor 23 (FGF23) and soluble klotho (sKlotho) in the blood of uremic patients with or without hemodialysis. Furthermore, these factors are related to calcification of the radial artery. The expression of AIF-1, PTHR1, VDR, FGF23 and sKlotho was also increased in the calcified radial artery.

CONCLUSIONS

The levels of AIF-1, PTH, VDR, FGF23 and sKlotho in serum were associated with calcification of the radial artery in patients with uremia. Furthermore, calcification of the radial artery was further aggravated by abnormalities in calcium and phosphorus in maintenance hemodialysis patients.

摘要

背景

桡动脉钙化是尿毒症患者自体动静脉内瘘吻合口狭窄的主要原因之一。然而,钙化的发病机制仍不清楚。本研究试图筛选并验证尿毒症患者血管钙化的危险因素。

方法

收集60例接受或未接受血液透析的尿毒症患者的血液血清和桡动脉组织样本。通过酶联免疫吸附测定法(ELISA)或相关性分析收集并检测一般生化指标和钙化相关分子。此外,通过苏木精-伊红(HE)染色或免疫组织化学染色评估桡动脉的病理变化和钙化相关分子。

结果

接受或未接受血液透析的尿毒症患者血液中的总钙、钙磷乘积、同种异体移植炎症因子1(AIF-1)、全段甲状旁腺激素(iPTH)、维生素D(VD)、成纤维细胞生长因子23(FGF23)和可溶性klotho蛋白(sKlotho)存在差异。此外,这些因素与桡动脉钙化有关。钙化的桡动脉中AIF-1、甲状旁腺激素受体1(PTHR1)、维生素D受体(VDR)、FGF23和sKlotho的表达也增加。

结论

尿毒症患者血清中AIF-1、PTH、VDR、FGF23和sKlotho水平与桡动脉钙化有关。此外,维持性血液透析患者钙磷异常会进一步加重桡动脉钙化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e26/11724451/81757734f461/12882_2024_3940_Fig1_HTML.jpg

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