TY - JOUR
T1 - Soluble E-selectin is an inverse and independent predictor of left ventricular wall thickness in end-stage renal disease patients
AU - Stancanelli, Benedetta
AU - Malatino, Lorenzo S.
AU - Cataliotti, Alessandro
AU - Bellanuova, Ignazio
AU - Mallamaci, Francesca
AU - Tripepi, Giovanni
AU - Benedetto, Frank A.
AU - Leonardis, Daniela
AU - Fatuzzo, Pasquale
AU - Rapisarda, Francesco
AU - Zoccali, Carmine
N1 - Publisher Copyright:
Copyright © 2009 S. Karger AG, Basel.
PY - 2010
Y1 - 2010
N2 - Background: E-selectin is a specific endothelial cell product involved in leukocyte recruitment on the endothelium, which is an important early step in the reparative process following vascular damage. In end-stage renal disease (ESRD), the relationship of E-selectin with left ventricular function has been so far neglected. Methods: We studied 237 patients on chronic dialysis (200 on hemodialysis, 37 on continuous ambulatory peritoneal dialysis) for at least 6 months, without clinical evidence of heart failure. On a midweek non-dialysis day, fasting blood sampling and echocardiography were performed. Results: Left ventricular mass index (LVMI, corrected for height) was inversely related to E-selectin levels, increasing from 56.8 8 18.9 (175th percentile E-selectin tertile) to 66.7 8 20.1 g/m2.7 (!50th percentile E-selectin tertile) (p = 0.002). However, in multiple regression models, including traditional (age, sex, smoking, diabetes, systolic blood pressure, hemoglobin, albumin, previous cardiovascular events) and emerging (asymmetric dimethylarginine, interleukin-6) risk factors associated with ESRD, soluble E-selectin has proved to be a significant inverse and independent predictor of mean wall thickness, but not of LVMI. Conclusion: This study demonstrates that soluble E-selectin is inversely associated with the muscular component of the left ventricle, thereby suggesting that the lack of such a reparative factor may be associated with cardiac remodeling in ESRD patients.
AB - Background: E-selectin is a specific endothelial cell product involved in leukocyte recruitment on the endothelium, which is an important early step in the reparative process following vascular damage. In end-stage renal disease (ESRD), the relationship of E-selectin with left ventricular function has been so far neglected. Methods: We studied 237 patients on chronic dialysis (200 on hemodialysis, 37 on continuous ambulatory peritoneal dialysis) for at least 6 months, without clinical evidence of heart failure. On a midweek non-dialysis day, fasting blood sampling and echocardiography were performed. Results: Left ventricular mass index (LVMI, corrected for height) was inversely related to E-selectin levels, increasing from 56.8 8 18.9 (175th percentile E-selectin tertile) to 66.7 8 20.1 g/m2.7 (!50th percentile E-selectin tertile) (p = 0.002). However, in multiple regression models, including traditional (age, sex, smoking, diabetes, systolic blood pressure, hemoglobin, albumin, previous cardiovascular events) and emerging (asymmetric dimethylarginine, interleukin-6) risk factors associated with ESRD, soluble E-selectin has proved to be a significant inverse and independent predictor of mean wall thickness, but not of LVMI. Conclusion: This study demonstrates that soluble E-selectin is inversely associated with the muscular component of the left ventricle, thereby suggesting that the lack of such a reparative factor may be associated with cardiac remodeling in ESRD patients.
KW - E-selectin
KW - Endothelial cytokines
KW - Inflammation
KW - Left ventricular hypertrophy
KW - Vascular damage
KW - Ventricular remodeling
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U2 - 10.1159/000252806
DO - 10.1159/000252806
M3 - Article
C2 - 19851079
AN - SCOPUS:77952315385
SN - 1660-2110
VL - 114
SP - c74-c80
JO - Nephron - Clinical Practice
JF - Nephron - Clinical Practice
IS - 1
ER -