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. 2010;14(3):R115.
doi: 10.1186/cc9064. Epub 2010 Jun 14.

Kinetics of plasmatic cytokines and cystatin C during and after hemodialysis in septic shock-related acute renal failure

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Kinetics of plasmatic cytokines and cystatin C during and after hemodialysis in septic shock-related acute renal failure

Nicolas Mayeur et al. Crit Care. 2010.

Abstract

Introduction: Cystatin C could be a relevant residual glomerular filtration rate marker during hemodialysis (HD), and a high cytokine plasma (p) rate is associated with an increase in mortality during sepsis. To the best of our knowledge, cytokines and cystatin C kinetics during and after HD during sepsis have never been studied. In this study, we described p cytokines and cystatin C variations during and after hemodialysis in septic-shock patients with acute kidney injury (AKI).

Methods: Ten patients, from two tertiary ICUs, with septic shock-related AKI, according to RIFLE class F, were studied. In this prospective observational study, blood samples were collected at the start, after 1 hour, 2 hours, and at the end of HD with a polymethymethacrylate (PMMA) hemodialyzer (D0, D1, D2, and endD), and 30, 60, 90, 120, and 180 min after HD (postD0.5, postD1, postD1.5, postD2, and postD3). We measured p interleukins (IL)-6, IL-8, IL-10, cystatin C, and albumin. Results are expressed as variations from D0 (mean +/- SD).

Results: During HD, p[IL-6] did not vary significantly, whereas p[IL-8] and p[IL-10] reductions by D1 were 31.8 +/- 21.2% and 36.3 +/- 26%, respectively (P < 0.05 as compared with D0). At postD3, p[IL-8] and p[IL-10] returned to their initial values. p[Cystatin C] was significantly reduced from D1 to postD1, with a maximal reduction of 30 +/- 6.7% on D2 (P < 0.05). Norepinephrine infusion rate decreased from D0 to postD3 (0.65 +/- 0.39 to 0.49 +/- 0.37 microg/kg/min; P < 0.05).

Conclusions: HD allows a transient and selective decrease in p cytokines, which are known as being correlated with mortality during septic shock. Because of a significant decrease in p cystatin C during HD, this should not be considered as an accurate marker for residual glomerular filtration rate during septic acute renal failure when receiving HD with a PMMA hemodialyzer.

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Figures

Figure 1
Figure 1
Hemodynamic, urea, and kalemia variations during and after hemodialysis. Mean arterial pressure (a) and norepinephrine infusion rate (b) at the start (D0), the end (endD), and 3 hours (postD3) after hemodialysis. Values are expressed as mean ± SEM. Urea (c) and kalemia (d) at the start, the end, 1 hour, and 3 hours after hemodialysis, D0, end D (clear), postD1 and postD2 (dark), respectively. Values are expressed in boxplots. *P < 0.05; Friedman test.
Figure 2
Figure 2
Cytokine variations during hemodialysis. Plasma level of IL-6 (a), lL-8 (b), and IL-10 (c). Results are expressed in percentage of value at D0 during (clear) and after (dark) hemodialysis as mean ± SEM. *P < 0.05 versus D0. Friedman test.
Figure 3
Figure 3
Protein variations during and after hemodialysis. Cystatin C (a) and albumin (b) variations during (clear) and after (dark) hemodialysis. Results are expressed in percentage of value at D0 as mean ± SEM. (c) Ratio of percentage of value at D0 of IL-6, IL-8, and IL-10 versus cystatin C. IL-6 (about 26 kDa), IL-8 (about 8 kDa), cystatin C (about 13 kDa), IL-10 (about 19 kDa), and albumin (about 68.5 kDa). *P < 0.05 versus D0; Friedman test.

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