Klotho and lean mass as novel cardiovascular risk factors in hemodialysis patients

Author:

Martins Ana Rita12,Azeredo-Lopes Sofia34,Pereira Sofia Azeredo56,Moreira Inês7,Weigert André Luíz127

Affiliation:

1. Nephrology Department, Hospital Santa Cruz, Western Lisbon Hospital Centre , Lisbon , Portugal

2. Institute of Pharmacology, Faculty of Medicine, University of Lisbon , Lisbon , Portugal

3. Comprehensive Health Research Centre (CHRC), NOVA Medical School, Nova University Lisbon , Lisbon , Portugal

4. Department of Statistics and Operational Research, Faculty of Sciences, University of Lisbon , Lisbon , Portugal

5. iNOVA4Health, LS4future, NOVA Medical School|Faculdade de Ciências Médicas, NMS|FCM, Universidade Nova de Lisboa , Lisboa , Portugal

6. Centro Clínico Académico de Lisboa , Lisboa , Portugal

7. Davita, Óbidos , Portugal

Abstract

ABSTRACT Background Patients with chronic kidney disease (CKD) present a higher risk of cardiovascular (CV) morbidity and mortality compared with the general population. While there are several well-established traditional CV risk factors, few studies have addressed novel potential risk factors such as α-Klotho, asymmetric dimethylarginine (ADMA) and lean mass. Methods This was an observational, prospective, single-center, cohort study that included prevalent hemodialysis (online hemodiafiltration) adult patients. By univariate logistic regression models, univariate and multivariate Cox proportional hazards models, and Kaplan–Meier analysis, we evaluated the association between the levels of α-Klotho, ADMA and lean mass, with the risk of peripheral vascular disease (PVD), CV events and all-cause mortality in these patients. Results A total of 200 HD patients was included. We found that increased levels of log-α-Klotho were significantly associated with decreased odds of both PVD [odds ratio (OR) 0.521, 95% confidence interval (CI) 0.270–0.954, P = .034] and CV events (OR 0.415, 95% CI 0.203–0.790, P = .01), whereas increased levels of log-ADMA were only significantly associated with increased odds of PVD (OR 13.482, 95% CI 5.055–41.606, P < .001). We also found that the levels of log-α-Klotho (HR 0.357, 95% CI 0.140–0.906, P < .05) and lean mass (HR 0.187, 95% CI 0.042–0.829, P < .05), but not log-ADMA, were significantly associated with the risk of all-cause mortality, even after adjusting for possible confounding variables. Conclusions Novel long-term clinical associations were generated that support α-Klotho and lean mass as novel CV risk factors in hemodialysis patients.

Funder

Davita Portugal

Publisher

Oxford University Press (OUP)

Subject

Transplantation,Nephrology

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