4.6 Article

Pharmacokinetics of anakinra in subjects with different levels of renal function

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CLINICAL PHARMACOLOGY & THERAPEUTICS
卷 74, 期 1, 页码 85-94

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WILEY
DOI: 10.1016/S0009-9236(03)00094-8

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Objective: Our objective was to assess the effects of decreased renal function and dialysis on anakinra pharmacokinetics. Methods: In 2 separate studies anakinra (1 mg/kg) was given intravenously to 12 healthy subjects and 20 subjects with end-stage renal disease undergoing dialysis. In a third study anakinra (100 mg) was given subcutaneously to 30 subjects who had been assigned to 5 groups according to renal function, as follows: normal (creatinine clearance [CLCR] >80 mL/min), mildly impaired (CLCR = 50-80 mL/min), moderately impaired (CLCR = 30-49 mL/min), severely impaired (CLCR <30 mL/min), and end-stage renal disease undergoing hemodialysis. Plasma samples were collected up to 96 hours after dosing for anakinra measurement by enzyme-linked immunoassay. Results: The mean plasma clearance (CL) of anakinra after intravenous administration was reduced from 137 21 mL/min in the healthy subjects to approximately 20 mL/min for the subjects with end-stage renal disease (P <.0001). The removal of anakinra by dialysis was less than 2.5% of the dose administered. Compared with mean anakinra clearance (CL/F) after subcutaneous administration in the group with normal renal function (170 37 mL/min), CL/F was reduced by 16% in the mildly impaired group (142 +/- 59 mL/min), by 50% in the moderately impaired group (84.5 +/- 24.7 mL/min, P <.05), by 70% in the severely impaired group (51.5 +/- 8.4 mL/min, P <.05), and by 75% in the group with end-stage renal disease (42.7 +/- 4.7 mL/min, P <.05). A significant correlation between anakinra CL/F and CLCR was observed [log(CL/ F)=1.65 +0.0062(.)CL(CR); r(2) =0.718]. Conclusion: Anakinra is predominantly cleared renally in humans; the plasma clearance of anakinra decreased with decreasing renal function. The dialysis process has a minimal effect on the removal of anakinra. Our results suggest that a dose or schedule adjustment is indicated for persons with severe renal impairment or end-stage renal disease.

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