OXIDATIVE STRESS, INFLAMMATION AND CARDIOVASCULAR MORTALITY IN
HAEMODIALYSIS--ROLE OF SENIORITY AND INTRAVENOUS FERROTHERAPY: ANALYSIS AT 4
YEARS OF FOLLOW-UP
Bayes B, Pastor MC, Bonal J, Foraster
A, Romero R.
Nephrol Dial Transplant. 2006 Apr;21(4):984-90. Epub 2005
Dec
BACKGROUND: Cardiovascular disease is the principal cause
of morbidity and mortality in haemodialysis patients. The classic risk factors
do not account for all cases of elevated cardiovascular disease in this patient
population and it is becoming increasingly clear that other cardiovascular risk
factors are implicated. The objective of this study was to analyse whether or
not C-reactive protein (CRP) and plasma copper oxidized anti-lipoprotein (oxLDL)
antibody titre are risk factors for cardiovascular mortality during 4 years of
follow-up.
METHODS: A prospective follow-up study was carried out in
94 stable, chronic haemodialysis patients for 48 months (July 1999-July 2003)
(gender: 50 males and 44 females; mean age: 67+/-14 years). Eighty-four per cent
of these patients were receiving intravenous erythropoietin and 63% were
receiving intravenous ferrotherapy (iron gluconate). Basal markers of
inflammation and oxidative stress were determined at the beginning of the study.
CRP levels were determined by chemiluminescent enzyme-labelled immunometric
assay. The oxLDL antibody titre was measured by enzyme-linked immunosorbent
assay using native LDL and oxLDL as antigens.
RESULTS: Fifty deaths occurred during the study, 66% (n =
33) of which were due to cardiovascular disease. Patients presented with basal
CRP and oxLDL levels indicative of chronic inflammation and elevated oxidative
stress [CRP median: 5.16 mg/l (25-75% percentile: 0.35-88.7 mg/l); oxLDL
antibodies median: 153 (optical density at 495 nm x 1000) (25-75% percentile:
112-214)]. A positive correlation was found between CRP and age (r = 0.33, P =
0.003). Study of the risk factors demonstrated that age (P = 0.007), oxLDL
antibody titre (P = 0.04) and albumin (P = 0.02) were the only predictors of
cardiovascular mortality at 4 years of follow-up in this patient population. The
Cox proportional hazards model for cardiovascular mortality showed that of the
markers studied, oxLDL antibody titre was an independent risk factor for
cardiovascular mortality.
CONCLUSIONS: Oxidative stress (oxLDL antibody titre) is one
of the principal risk factors for cardiovascular mortality in this population of
haemodialysis patients. Intravenous ferrotherapy, due to its pro-oxidant
properties, probably favours oxidative stress. Serum concentration of CRP was
not a good predictive factor of cardiovascular mortality during 4 years of
follow-up, possibly because of the slight positive correlation that exists
between CRP and age.
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