Key result
An increase in plasma adiponectin concentration was associated with a lower risk of coronary in-stent restenosis in hemodialysis patients (OR 0.651 per 1 microg/ml; 95% CI 0.506-0.839; P=0.001).
Why the study?
Is circulating adiponectin concentration associated with the occurrence of coronary in-stent restenosis in ESRD patients undergoing haemodialysis?
Observational (n=71)
Is circulating adiponectin concentration associated with the occurrence of coronary in-stent restenosis in ESRD patients undergoing haemodialysis?
Odds Ratio: 0.651 (95% CI 0.506–0.839)
p-value: p=0.001
Higher pre-procedural plasma adiponectin concentrations are associated with a significantly lower risk of coronary in-stent restenosis at 6 months in ESRD patients undergoing hemodialysis.
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Adiponectin may serve as a novel prognostic biomarker for in-stent restenosis in hemod.
BACKGROUND: Success of coronary stenting is limited by in-stent restenosis. We aimed to determine whether circulating levels of the cytokines, which have anti-inflammatory properties such as adiponectin or interleukin-10, could be associated with the occurrence of coronary in-stent restenosis in patients with end-stage renal disease (ESRD). METHODS: We enrolled 71 consecutive ESRD patients undergoing haemodialysis (mean age: 64.9+/-8.9 years; 19 women, 52 men; mean haemodialysis duration: 78.2+/-87.5 months), who received stenting for a single coronary lesion. Plasma concentrations of adiponectin and IL-10 were measured within one week before coronary stenting. RESULTS: Of the 71 patients who had received stenting, in-stent restenosis occurred in 37 patients (52.1%) within 6 months after stenting. In univariate logistic analysis, the homeostasis model assessment index of insulin resistance, blood haemoglobin, serum concentrations of high density lipoprotein-cholesterol or triglycerides and plasma concentrations of insulin or adiponectin were significantly associated with coronary in-stent restenosis. In a multiple logistic regression analysis among these variables, however, only the plasma adiponectin concentration was associated with the coronary in-stent restenosis: the odds ratio of the increase in 1 microg/ml of plasma adiponectin concentration for having restenosis was 0.651 (P = 0.001, 95% confidence interval: 0.506-0.839). Patients with restenosis had lower plasma adiponectin concentrations than those without [6.2+/-2.2 microg/ml (2.1-10.4 microg/ml; n = 37) vs 27.2+/-10.8 microg/ml (17.9-79.8 microg/ml; n = 34); P = 0.0001]. CONCLUSIONS: Circulating adiponectin concentrations may be associated with the occurrence of coronary in-stent restenosis in ESRD patients undergoing maintenance haemodialysis.
Nishimura et al. (2006) conducted an observational in End-stage renal disease (ESRD) with coronary stenting (n=71). Plasma adiponectin concentration vs. Per 1 microg/ml increase was evaluated on Coronary in-stent restenosis (OR 0.651, 95% CI 0.506-0.839, p=0.001). An increase in plasma adiponectin concentration was associated with a lower risk of coronary in-stent restenosis in hemodialysis patients (OR 0.651 per 1 microg/ml; 95% CI 0.506-0.839; P=0.001).