scholarly journals Polymorphisms in type I and II inosine monophosphate dehydrogenase genes and association with clinical outcome in patients on mycophenolate mofetil

2010 ◽  
Vol 20 (9) ◽  
pp. 537-543 ◽  
Author(s):  
Olivier Gensburger ◽  
Ron H.N. Van Schaik ◽  
Nicolas Picard ◽  
Yannick Le Meur ◽  
Annick Rousseau ◽  
...  
Keyword(s):  
Mycophenolate Mofetil ◽  
Clinical Outcome ◽  
Type I ◽  
Inosine Monophosphate Dehydrogenase ◽  
Inosine Monophosphate ◽  
Monophosphate Dehydrogenase

scholarly journals Regulation of the Human Inosine Monophosphate Dehydrogenase Type I Gene

1997 ◽  
Vol 272 (7) ◽  
pp. 4458-4466 ◽  
Author(s):  
Jing Jin Gu ◽  
Jozef Spychala ◽  
Beverly S. Mitchell
Keyword(s):  
Type I ◽  
Inosine Monophosphate Dehydrogenase ◽  
Inosine Monophosphate ◽  
I Gene ◽  
Monophosphate Dehydrogenase

Recombinant human inosine monophosphate dehydrogenase type I and type II proteins

1995 ◽  
Vol 49 (9) ◽  
pp. 1323-1329 ◽  
Author(s):  
Paul W. Hager ◽  
Frank R. Collart ◽  
Eliezer Huberman ◽  
Beverly S. Mitchell
Keyword(s):  
Type I ◽  
Type Ii ◽  
Inosine Monophosphate Dehydrogenase ◽  
Inosine Monophosphate ◽  
Monophosphate Dehydrogenase

Mycophenolate mofetil, an inhibitor of inosine monophosphate dehydrogenase, causes a paradoxical elevation of GTP in erythrocytes of renal transplant patients

2004 ◽  
Vol 107 (1) ◽  
pp. 63-68 ◽  
Author(s):  
David GOLDSMITH ◽  
Elizabeth A. CARREY ◽  
Stephen EDBURY ◽  
Ryszard T. SMOLENSKI ◽  
Piotr. JAGODZINSKI ◽  
...  
Keyword(s):  
Mycophenolate Mofetil ◽  
Renal Transplantation ◽  
Renal Transplant ◽  
Plasma Metabolites ◽  
Renal Transplant Recipients ◽  
Inosine Monophosphate Dehydrogenase ◽  
Inosine Monophosphate ◽  
Transplant Patients ◽  
Renal Transplant Patients ◽  
Monophosphate Dehydrogenase

The immunosuppressant MMF (mycophenolate mofetil) has increasingly replaced AZA (azathioprine) in renal transplantation. MMF is a prodrug of MPA (mycophenolic acid), which inhibits lymphocyte IMPDH (inosine monophosphate dehydrogenase), thereby drastically decreasing GTP concentrations essential to lymphocyte proliferation in vitro and in vivo. Erythrocyte GTP concentrations are commonly elevated in severe renal disease, but normalize following successful engraftment. Consequently, elevated GTP in renal transplant recipients might signal impending loss of immunosuppression and graft failure. In the present study, we compared erythrocyte nucleotides and plasma metabolites in two groups of 25 patients after renal transplantation, both receiving prednisolone and cyclosporin A, but one group receiving MMF and the other AZA. No patients had recent allograft biopsy evidence of rejection. Erythrocyte GTP concentrations at MMF commencement were 50.4±23.4 μmol/l. An increase occurred during the first 3 months after transplant when MMF was used de novo, stabilizing at 146.7±62.9 μmol/l after 4 months. This was significantly higher (P=2.5×10−6) than erythrocyte GTP (40.4±15.9 μmol/l) in the AZA group, which was essentially unchanged from values immediately after successful transplantation. The effect of MMF on erythrocyte GTP levels was reversible, since GTP levels fell when MMF therapy was terminated. The results demonstrate paradoxically high GTP concentrations in erythrocytes of renal transplant patients receiving MMF. MPA may stabilize reticulocyte IMPDH, allowing the protein to persist during erythropoiesis. This behaviour is in marked contrast with the decrease in GTP levels seen in white blood cells of patients on chronic MMF therapy.

The Practical Synthesis of a Methylenebisphosphonate Analogue of Benzamide Adenine Dinucleotide:  Inhibition of Human Inosine Monophosphate Dehydrogenase (Type I and II)1

1997 ◽  
Vol 40 (8) ◽  
pp. 1287-1291 ◽  
Author(s):  
Krzysztof W. Pankiewicz ◽  
Krystyna Lesiak ◽  
Andrzej Zatorski ◽  
Barry M. Goldstein ◽  
Stephen F. Carr ◽  
...  
Keyword(s):  
Type I ◽  
Inosine Monophosphate Dehydrogenase ◽  
Inosine Monophosphate ◽  
Practical Synthesis ◽  
Monophosphate Dehydrogenase
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