Significant interactions occur at the interface between dialysis membranes and blood during every hemodialysis procedure. These interactions result in the activation of the complement system, the coagulation and the kallikrein pathways. Platelets, neutrophils and lymphocytes are also involved in this interaction. Preliminary evidence also suggests the formation of leukotrienes by activated neutrophils during dialysis. These interactions are a function of the type of dialysis membrane used, and a function of reuse of these membranes. Increasing evidence suggests that these interactions have a significant effect on the morbidity and mortality of the more than 50,000 patients on chronic hemodialysis in the United States, with consequent economic implications. The objective of this proposal is to continue the study of the blood-membrane interactions; in particular, we propose the study of the activation of the coagulation pathway, platelet activation and leukotriene production by activated neutrophils. Possible synergism in the activation of these pathways will also be studied. These interactions will also be studied in sheep animal models and will be extended to include in-vitro models, and the use (in-vitro) of specific pharmacological agents to block the activation of these pathways.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
7R01HL036015-01
Application #
3350498
Study Section
Surgery and Bioengineering Study Section (SB)
Project Start
1985-07-01
Project End
1987-06-30
Budget Start
1985-07-01
Budget End
1986-06-30
Support Year
1
Fiscal Year
1985
Total Cost
Indirect Cost
Name
Brigham and Women's Hospital
Department
Type
DUNS #
071723621
City
Boston
State
MA
Country
United States
Zip Code
Himmelfarb, Jonathan; Evanson, James; Hakim, Raymond M et al. (2002) Urea volume of distribution exceeds total body water in patients with acute renal failure. Kidney Int 61:317-23
Himmelfarb, J; McMonagle, E; Holbrook, D et al. (1999) Increased susceptibility to erythrocyte C5b-9 deposition and complement-mediated lysis in chronic renal failure. Kidney Int 55:659-66
Evanson, J A; Ikizler, T A; Wingard, R et al. (1999) Measurement of the delivery of dialysis in acute renal failure. Kidney Int 55:1501-8
Neyra, N R; Ikizler, T A; May, R E et al. (1998) Change in access blood flow over time predicts vascular access thrombosis. Kidney Int 54:1714-9
Hakim, R; Himmelfarb, J (1998) Hemodialysis access failure: a call to action. Kidney Int 54:1029-40
Himmelfarb, J; Tolkoff Rubin, N; Chandran, P et al. (1998) A multicenter comparison of dialysis membranes in the treatment of acute renal failure requiring dialysis. J Am Soc Nephrol 9:257-66
May, R E; Himmelfarb, J; Yenicesu, M et al. (1997) Predictive measures of vascular access thrombosis: a prospective study. Kidney Int 52:1656-62
Becker, B N; Himmelfarb, J; Henrich, W L et al. (1997) Reassessing the cardiac risk profile in chronic hemodialysis patients: a hypothesis on the role of oxidant stress and other non-traditional cardiac risk factors. J Am Soc Nephrol 8:475-86
Hakim, R M; Held, P J; Stannard, D C et al. (1996) Effect of the dialysis membrane on mortality of chronic hemodialysis patients. Kidney Int 50:566-70
Hakim, R M; Wingard, R L; Husni, L et al. (1996) The effect of membrane biocompatibility on plasma beta 2-microglobulin levels in chronic hemodialysis patients. J Am Soc Nephrol 7:472-8

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