The Association of Leptin with Left Ventricular Hypertrophy in End-Stage Kidney Disease Patients on Dialysis

Author:

Coimbra Susana123ORCID,Catarino Cristina12,Sameiro Faria Maria124,Nunes José Pedro L.5,Rocha Susana12ORCID,Valente Maria João126ORCID,Rocha-Pereira Petronila127,Bronze-da-Rocha Elsa12,Bettencourt Nuno5,Beco Ana4,Marques Sofia Homem de Melo4,Oliveira José Gerardo89,Madureira José10,Fernandes João Carlos11,Miranda Vasco12,Belo Luís12,Santos-Silva Alice12

Affiliation:

1. UCIBIO—Applied Molecular Biosciences Unit, Department of Biological Sciences, Faculdade de Farmácia, Universidade do Porto, 4050-313 Porto, Portugal

2. Associate Laboratory i4HB, Institute for Health and Bioeconomy, Faculdade de Farmácia, Universidade do Porto, 4050-313 Porto, Portugal

3. TOXRUN—Toxicology Research Unit, University Institute of Health Sciences, CESPU, CRL, 4585-116 Gandra, Portugal

4. Hemodialysis Clinic Hospital Agostinho Ribeiro, 4610-106 Felgueiras, Portugal

5. Faculty of Medicine, University of Porto, 4200-319 Porto, Portugal

6. National Food Institute, Technical University of Denmark, 2800 Kongens Lyngby, Denmark

7. Health Science Research Centre, University of Beira Interior, 6201-001 Covilhã, Portugal

8. Hemodialysis Clinic of Porto (CHP), 4200-227 Porto, Portugal

9. Center for Health Technology and Services Research (CINTESIS), Faculty of Medicine, University of Porto, 4200-450 Porto, Portugal

10. NefroServe, Hemodialysis Clinic of Barcelos, 4750-110 Barcelos, Portugal

11. NefroServe Hemodialysis Clinic of Viana do Castelo, 4900-281 Viana do Castelo, Portugal

12. Hemodialysis Clinic of Gondomar, 4420-086 Gondomar, Portugal

Abstract

Left ventricular hypertrophy (LVH) is a common cardiovascular complication in end-stage kidney disease (ESKD) patients. We aimed at studying the association of LVH with adiponectin and leptin levels, cardiovascular stress/injury biomarkers and nutritional status in these patients. We evaluated the LV mass (LVM) and calculated the LVM index (LVMI) in 196 ESKD patients on dialysis; the levels of hemoglobin, calcium, phosphorus, parathyroid hormone, albumin, adiponectin, leptin, N-terminal pro B-type natriuretic peptide (NT-proBNP) and growth differentiation factor (GDF)-15 were analyzed. ESKD patients with LVH (n = 131) presented higher NT-proBNP and GDF-15, lower hemoglobin and, after adjustment for gender, lower leptin levels compared with non-LVH patients. LVH females also showed lower leptin than the non-LVH female group. In the LVH group, LVMI presented a negative correlation with leptin and a positive correlation with NT-proBNP. Leptin emerged as an independent determinant of LVMI in both groups, and NT-proBNP in the LVH group. Low hemoglobin and leptin and increased calcium, NT-proBNP and dialysis vintage are associated with an increased risk of developing LVH. In ESKD patients on dialysis, LVH is associated with lower leptin values (especially in women), which are negatively correlated with LVMI, and with higher levels of biomarkers of myocardial stress/injury. Leptin and NT-proBNP appear as independent determinants of LVMI; dialysis vintage, hemoglobin, calcium, NT-proBNP and leptin emerged as predicting markers for LVH development. Further studies are needed to better understand the role of leptin in LVH in ESKD patients.

Funder

FCT/MCTES

Publisher

MDPI AG

Subject

General Biochemistry, Genetics and Molecular Biology,Medicine (miscellaneous)

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