Relationship between fibroblast growth factor 23, Klotho protein and carotid intima-media thickness in patients with chronic kidney disease
CSTR:
Affiliation:

1.Department of Nephrology, ;2.Department of Cadre Health Care, ;3.Department of Scientific Research, the Affiliated Haici Hospital, Qingdao University, Qingdao, Shandong 266001, China)

Clc Number:

R5

  • Article
  • | |
  • Metrics
  • |
  • Reference [16]
  • |
  • Related [20]
  • | | |
  • Comments
    Abstract:

    Aim To investigate the relationship between serum levels of fibroblast growth factor 23 (FGF-23), Klotho protein and carotid atherosclerosis in non-dialysis patients with chronic kidney disease (CKD) 2-5 stage. Methods 126 CKD 2-5 stage patients were involved in the study. Carotid intima-media thickness (CIMT) was measured by color Doppler ultrasonography. The patients were divided into CIMT thickening group and CIMT normal group according to CIMT. Serum levels of FGF-23 and Klotho protein were determined by enzyme-linked immunosorbent assay, and the general data and clinical biochemical indexes were collected. The relative indexes of the two groups were compared, and the correlation between FGF-23, Klotho protein and carotid atherosclerosis was analyzed. Unconditional Logistic regression analysis was used for multivariate analysis of CIMT influencing factors. Results The serum FGF-23 level in CIMT thickening group was significantly higher than that in CIMT normal group (435.39±221.20 vs 360.22±194.26, P<0.05), and the level of Klotho protein was significantly lower than that in CIMT normal group (446.54±132.49 vs 499.36±121.38, P<0.05). Multivariate stepwise regression analysis showed that Klotho protein was an independent protective factor for CIMT thickening in patients with CKD (OR=1.086, P<0.05), while age increase and FGF-23 were independent risk factors for CIMT thickening in patients with CKD (OR=1.075, P<0.05; OR=1.238, P<0.05). Conclusion CIMT thickening is related to FGF-23 and Klotho proteins in non-dialysis patients with CKD 2-5 stage. FGF-23 and Klotho protein play an important role in the occurrence and development of carotid atherosclerosis.

    Reference
    [1] Collins AJ, Foley RN, Gilbertson DT, et al.United States Renal Data System public health surveillance of chronic kidney disease and end-stage renal disease.Kidney Int Suppl, 5,5(1):2-7.
    [2] Inker LA, Astor BC, Fox CH, et al.KDOQI US commentary on the 2012 KDIGO clinical practice guideline for the evaluation and management of CKD.Am J Kidney Dis, 4,3(5):713-735.
    [3] Heine GH, Nangaku M, Fliser D.Calcium and phosphate impact cardiovascular risk.Eur Heart J, 3,4(15):1 112-121.
    [4] Ikushima M, Rakugi H, Ishikawa K, et al.Anti-apoptotic and anti-senescence effects of Klotho on vascular endothelial cells.Biochem Biophys Res Commun, 6,9(3):827-832.
    [5] Leopold JA.Vascular calcification:Mechanisms of vascular smooth muscle cell calcification.Trends Cardiovasc Med, 5,5(4):267-274.
    [6] Razzaque MS.FGF-23, Klotho and vitamin D interactions:What have we learned from in vivo mouse genetics studies.Adv Exp Med Biol, 2,8:84-91.
    [7] Nabeshima Y, Imura H.Alpha-Klotho:a regulator that integrates calcium homeostasis.Am J Nephrol, 8,8(3):455-464.
    [8] Hu MC, Shi MJ, Zhang JN.Klotho deficiency causes vascular calcification in chronic kidney disease.J Am Soc Nephrol, 1,2(1):124-136.
    [9] Hu MC, Kuro-o M, Moe OW.Klotho and kidney disease.J Nephrol, 0,6(4):S136-S144.
    [10] Faul C, Amaral AP, Oskouei B, et al.FGF-23 induces left ventricular hypertrophy.J Clin Invest, 1,1(11):4 393-408.
    [11] Mirza MA, Hansen T, Johansson L, et al.Ralationship between circulating FGF-23 and total body atherosclerosis in the comminity.Nephrol Dial Transplant, 9,4(10):3 125-131.
    [12] Mirza MA, Larsson A, Melhus H, et al.Serum intact FGF-23 associated with left ventricular mass, hypertrophy and geometry in an elderly population.Atherosclerosis, 9,7(2):546-551.
    [13] Mirza MA, Larsson A, Lind L, et al.Circulating fibroblast growth factor-23 is associated with vascular dysfunction in community.Atherosclerosis, 9,5(2):385-390.
    [14] Donate-Correa J, Mora-Fernández C, Martínez-Sanz R, et al.Expression of FGF-23/KLOTHO system in human vascular tissue.Int J Cardiol, 3,5(1):179-183.
    [15] Yilmaz MI, Sonmez A, Saglam M, et al.Longitudinal analysis of vascular function and biomarkers of metabolic bone disorders before and after renal transplantation.Am J Nephrol, 3,7(2):126-134.
    [16] Larsson TE.The role of FGF-23 in CKD-MBD and cardio-vascular disease:friend or foe?.Nephrol Dial Transplant, 0,5(5):1 376-381.
    Cited by
    Comments
    Comments
    分享到微博
    Submit
Get Citation

CHEN Jin-Yan, HU Yong, SUN Hong, JIANG Ting, LIU Xian-Ying. Relationship between fibroblast growth factor 23, Klotho protein and carotid intima-media thickness in patients with chronic kidney disease[J]. Editorial Office of Chinese Journal of Arteriosclerosis,2017,25(9):919-922.

Copy
Share
Article Metrics
  • Abstract:956
  • PDF: 814
  • HTML: 0
  • Cited by: 0
History
  • Received:July 05,2016
  • Revised:May 02,2017
  • Online: September 29,2017
Article QR Code