The Association between Fibroblast Growth Factor-23 and Vascular Calcification Is Mitigated by Inflammation Markers

被引:37
作者
NasrAllah, Mohamed M. [1 ]
El-Shehaby, Amal R. [2 ]
Osman, Noha A. [1 ]
Fayad, Tarek [1 ]
Nassef, Amr [3 ]
Salem, Mona M. [4 ]
El Din, Usama A. A. Sharaf [1 ]
机构
[1] Cairo Univ, Kasr Al Ainy Sch Med, Dept Nephrol, 27,St 305,New Maadi, Cairo, Egypt
[2] Cairo Univ, Kasr Al Ainy Sch Med, Dept Med Biochem, Cairo, Egypt
[3] Cairo Univ, Kasr Al Ainy Sch Med, Dept Radiol, Cairo, Egypt
[4] Cairo Univ, Kasr Al Ainy Sch Med, Dept Endocrinol, Cairo, Egypt
关键词
Fibroblast growth factor-23; Vascular calcification; Chronic kidney disease; Inflammation markers; Uremic toxins;
D O I
10.1159/000356118
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Background: Fibroblast growth factor-23 (FGF-23) has been linked to vascular calcification, ventricular hypertrophy and mortality in chronic kidney disease (CKD), although these links may not be direct and independent. Similar grave outcomes are associated with inflammation and oxidative stress in CKD. Recently, accumulating evidence has linked components of phosphate homeostasis to inflammation and oxidative stress. The interaction between the triad of inflammation, FGF-23 and cardiovascular outcomes is underinvestigated. Methods: We studied 65 patients with stage 5 CKD on hemodialysis. Serum levels of FGF-23, high-sensitivity Creactive protein (hsCRP), endogenous soluble receptor of advanced glycation end products (esRAGE), advanced oxidation protein products (AOPP), parathormone, lipids, calcium and phosphorous were measured. The aortic calcification index (ACI) was determined using noncontrast CT scans of the abdominal aorta. Results: FGF-23 was elevated (mean: 4,681 pg/ml, SD: 3,906) and correlated with hsCRP, esRAGE, AOPP, dialysis vintage and phosphorus in univariate analysis. In multiple regression analysis, hsCRP, AOPP and phosphorus but not esRAGE were all significantly correlated to FGF-23 (R-2 = 0.7, p < 0.001). In univariate analysis, ACI correlated with hsCRP, esRAGE, FGF-23, dialysis vintage, systolic blood pressure (BP) and serum cholesterol. In multiple regression analysis not including inflammation markers, ACI was associated with FGF-23. However, inclusion of inflammation markers in another multiple regression analyses showed that ACI correlated with hsCRP, BP, dialysis vintage and esRAGE but not with FGF-23 (R-2 = 0.65, p < 0.001). Conclusion: FGF-23 is strongly correlated to various markers of inflammation and oxidative stress in hemodialysis patients. The association between FGF-23 and vascular calcification was mitigated when corrected for inflammation markers. (C) 2013 S. Karger AG, Basel
引用
收藏
页码:106 / 112
页数:7
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