Blood Purification Center, Hainan General Hospital (Hai-nan Affiliated Hospital of Hainan Medical University), Haikou, China.
Libyan J Med. 2023 Dec;18(1):2194100. doi: 10.1080/19932820.2023.2194100.
Vascular calcification (VC) is prevalent in uremia patients, lacking effective molecular biomarkers. This study was conducted to explore the role of serum cell division cycle 42 (CDC42) in the diagnosis of uremic VC incidence and progression. We enrolled 104 uremia patients and selected arcus aortae calcification (AAC) as the outcome phenotype. Levels of CDC42, 1,25-dihydroxy vitamin D (1,25(OH) -D), fibroblast growth factor-23 (FGF-23), and other laboratory parameters in the blood were measured. The receiver operator characteristic curve, the Pearson test, and the multivariate Logistic regression were used for the analysis of CDC42 diagnostic values, correlation analysis, and screening of VC risk factors, respectively. CDC42 was higher in the serum of uremia patients with VC and elevated with the increase in AAC level. Serum CDC42 level>1.025 was predictive of VC incidence with 83.58% sensitivity and 56.76% specificity, and CDC42 level>1.280 was predictive of VC progression with 73.33% sensitivity and 68.18% specificity. Serum CDC42 was positively correlated with 1,25(OH) -D and FGF-23. Uremia patients with higher serum CDC42 had a higher probability of VC incidence and progression. Generally, serum CDC42 helped the diagnosis of uremic VC incidence and progression and was an independent risk factor for uremic VC progression.
血管钙化(VC)在尿毒症患者中很常见,缺乏有效的分子生物标志物。本研究旨在探讨血清细胞分裂周期蛋白 42(CDC42)在诊断尿毒症 VC 发病和进展中的作用。我们纳入了 104 例尿毒症患者,并选择弓状动脉钙化(AAC)作为结果表型。测量血液中 CDC42、1,25-二羟维生素 D(1,25(OH)-D)、成纤维细胞生长因子 23(FGF-23)和其他实验室参数的水平。采用受试者工作特征曲线、Pearson 检验和多变量 Logistic 回归分别对 CDC42 的诊断价值、相关性分析和 VC 危险因素进行分析。尿毒症合并 VC 患者血清中 CDC42 水平升高,且随着 AAC 水平的升高而升高。血清 CDC42 水平>1.025 预测 VC 发病的敏感性为 83.58%,特异性为 56.76%,血清 CDC42 水平>1.280 预测 VC 进展的敏感性为 73.33%,特异性为 68.18%。血清 CDC42 与 1,25(OH)-D 和 FGF-23 呈正相关。血清 CDC42 水平较高的尿毒症患者发生 VC 发病和进展的可能性更高。一般来说,血清 CDC42 有助于诊断尿毒症 VC 的发病和进展,是尿毒症 VC 进展的独立危险因素。