4.7 Article

Klotho as a biomarker of subclinical atherosclerosis in patients with moderate to severe chronic kidney disease

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SCIENTIFIC REPORTS
卷 11, 期 1, 页码 -

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NATURE PORTFOLIO
DOI: 10.1038/s41598-021-95488-4

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  1. Instituto de Salud Carlos III, Fondo Europeo de Desarrollo Regional, Una manera de hacer Europa [PI16/00024, PI19/00035, RD16/0009/0022]
  2. ACINEF
  3. Instituto de Salud Carlos III (ISCIII) [CP20/00122]
  4. Agencia Canaria de Investigacion, Innovacion y Sociedad de la Informacion (ACIISI), Consejeria de Economia, Industria, Comercio y Conocimiento, Gobierno de Canarias [TESIS2018010110]
  5. Fondo Social Europeo (FSE)
  6. ISCIII [RD16/0009/0022]

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The study demonstrates an association between decreased levels of Klotho protein and subclinical atherosclerosis in patients with chronic kidney disease (CKD). Both serum and peripheral blood cells (PBCs) expression levels of Klotho were found to be significantly lower in patients with subclinical atherosclerosis, and were independent determinants for arterial stiffness markers. This suggests that maintaining or elevating Klotho levels may have potential therapeutic benefits in reducing cardiovascular disease risk in CKD patients.
Chronic kidney disease (CKD) has been associated with a higher risk of cardiovascular disease (CVD). CKD patients present a decrease in the levels of the protein Klotho that accompanies the decrease in kidney function. This protein has been related to protective effects against CVD. However, it is unclear whether circulating Klotho, and its expression in peripheral blood cells (PBCs) are also associated with subclinical atherosclerosis in CKD. The present study aimed to study the relationship between Klotho and subclinical atherosclerosis in a population of patients with moderate to severe CKD. We determined the serum levels and gene expression in PBCs levels of Klotho and three inflammatory cytokines in 103 patients with CKD and investigated their relationship with two surrogate markers of subclinical atherosclerotis: ankle-brachial index (ABI) and carotid intima-media thickness (CIMT). Patients with subclinical atherosclerosis presented lower serum and PBCs expression levels of Klotho. Both variables were associated with the presence of subclinical atherosclerosis, being directly related with ABI and inversely with CIMT (P<0.0001 for both). Multiple regression analysis demonstrated that both variables were significant determinants for ABI (adjusted R-2=0.511, P<0.0001) and CIMT (adjusted R-2=0.445, P<0.0001), independently of traditional and emergent cardiovascular risk factors. Moreover, both constituted protective factors against subclinical atherosclerosis [OR: 0.993 (P=0.002) and 0.231 (P=0.025), respectively]. Receiver operating characteristic analysis pointed to the utility of serum Klotho (area under the curve [AUC]: 0.817, 95% CI: 0.736-0.898, P<0.001) and its gene expression in PBCs (AUC: 0.742, 95% CI: 0.647-0.836, P<0.001) to distinguish subclinical atherosclerosis. The reductions in serum and PBCs expression levels of Klotho in CKD patients are independently associated with the presence of for subclinical atherosclerosis. Further research exploring whether therapeutic approaches to maintain or elevate Klotho could reduce the impact of CVD in CKD patients is warranted.

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