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Cardiovascular Disease |
Pontificia Universidade Católica do Paraná, Curitiba, Parana, Brazil
Objective: Metabolic syndrome (MetS) is associated with increased
cardiovascular risk in general population, but data in the dialysis population
are lacking. Monocyte chemoattractant protein (MCP-1) is a chemokine involved
in the early stages of atherogenesis that has been used as a marker of
endothelial dysfunction. The aim of the study was to analyze the association
between MetS components and MCP-1 plasma levels in dialysis patients (pts).
Methods: Clinically stable prevalent hemodialysis (HD) and peritoneal
dialysis (PD) pts were included in the study. All PD pts were on glucose-based
solutions. MetS parameters included fasting glucose, triglycerides, HDL, and
BMI. We also measured the HOMA index, total cholesterol, LDL, and uric acid.
MCP-1 levels were measured by ELISA. Results: We studied 139 pts, 71
in HD and 68 in PD, with a mean age of 55±13 years, 42% diabetics, and
52% males. The plasma MCP-1 levels were 228±86 pg/mL. The prevalence of
MetS was significantly higher in PD pts (54%) when compared to HD (30%,
p<0.005). In a univariate analysis, MCP-1 levels were
significantly higher in pts with MetS, compared to those without
(p<0.005). Pts on PD presented higher levels of MCP-1 when
compared to HD pts, even when adjusted for age, gender, and diabetes
(p<0.0005). There were significant correlations between MCP-1 and
fasting glucose (rho=0.21, p<0.05), HbA1c (rho=0.20,
p<0.05), HOMA index (rho=0.24, p<0.005), total
cholesterol (rho=0.27, p<0.005), LDL (rho=0.24,
p<0.005), triglycerides (rho=0.18, p<0.05), abdominal
waist (rho=0.26, p<0.005), BMI (rho=0.27, p<0.005),
fibrinogen (rho=0.18, p<0.05), and uric acid (rho=0.32,
p<0.0005). In a multivariate analysis, the most important
determinant of MCP-1 levels was PD as the type of dialysis
(R2=0.36, p<0.0001). Conclusions: Several
components of the MetS (which is more prevalent in PD) are associated with
high levels of MCP-1. Moreover, PD is an important determinant of MCP-1
levels. These results suggest that MetS could be involved in the accelerated
atherosclerosis observed in dialysis (particularly PD) in a process mediated
by the expression of MCP-1. The effects of glucose-sparing solutions on this
metabolic/immune response deserve future studies.
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