Journal of nephrology · 2026
The Interplay Between Klotho, Aldosterone, and Vascular Damage in Chronic Kidney Disease: Insights from a Cross-Sectional Study.
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Tartaglione Lida, Rotondi Silverio, Pasquali Marzia, Perrotta Adolfo, Tinti Francesca, Zaccaria Antonella, Quiñonez Viviana Beatriz, Andreetti Federico, Fassino Valeria, Lai Silvia, Letizia Claudio, Petramala Luigi, Circosta Francesco, Zaza Gianluigi, Mazzaferro Sandro
Аннотация
BACKGROUND: Patients with chronic kidney disease (CKD) are at increased risk of vascular calcification and cardiovascular mortality. Reduced Klotho levels have been associated with vascular damage in CKD through both direct and indirect mechanisms. Klotho deficiency, a hallmark of CKD, has been suggested to contribute to the hyperaldosteronism observed in CKD. This study aimed to evaluate the relationship between serum Klotho (s-Klotho), aldosterone, and vascular damage in CKD.
METHODS: We studied 55 patients with CKD stages G1-5 (52.0, IQR: 39.0-63.0 y; 27 M/28 F; eGFR 53.1±31.7 ml/min). Vascular damage was assessed non-invasively using the cardio-ankle vascular index (CAVI), ankle-brachial index (ABI), and intima-media thickness (IMT). s-Klotho and aldosterone levels were measured. A control group of 38 age- and sex-matched hypertensive patients without CKD was used for comparison of vascular parameters.
RESULTS: CAVI values in CKD patients were pathological (8.4±1.2) but did not differ from controls. s-Klotho levels progressively declined across CKD stages (p for trend <0.001) and correlated positively with eGFR, while showing negative associations with age and vascular parameters (CAVI, ABI, and IMT). s-Klotho also correlated with aldosterone, whose levels were elevated only in advanced CKD (stages G4-5) and showed no association with vascular parameters. Multivariate analysis identified age as the only independent determinant of CAVI; s-Klotho emerged as an independent predictor only in models excluding age.
CONCLUSION: s-Klotho levels progressively decline in CKD and are associated with vascular damage, supporting an association between Klotho deficiency and vascular damage that appears independent of aldosterone.
METHODS: We studied 55 patients with CKD stages G1-5 (52.0, IQR: 39.0-63.0 y; 27 M/28 F; eGFR 53.1±31.7 ml/min). Vascular damage was assessed non-invasively using the cardio-ankle vascular index (CAVI), ankle-brachial index (ABI), and intima-media thickness (IMT). s-Klotho and aldosterone levels were measured. A control group of 38 age- and sex-matched hypertensive patients without CKD was used for comparison of vascular parameters.
RESULTS: CAVI values in CKD patients were pathological (8.4±1.2) but did not differ from controls. s-Klotho levels progressively declined across CKD stages (p for trend <0.001) and correlated positively with eGFR, while showing negative associations with age and vascular parameters (CAVI, ABI, and IMT). s-Klotho also correlated with aldosterone, whose levels were elevated only in advanced CKD (stages G4-5) and showed no association with vascular parameters. Multivariate analysis identified age as the only independent determinant of CAVI; s-Klotho emerged as an independent predictor only in models excluding age.
CONCLUSION: s-Klotho levels progressively decline in CKD and are associated with vascular damage, supporting an association between Klotho deficiency and vascular damage that appears independent of aldosterone.