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Genvigir et al. J Transl Genet Genom 2020;4:320-55  I  http://dx.doi.org/10.20517/jtgg.2020.37                            Page 347


              Ref.   [22]   [75]    [25]   [71]    [78]         [72]     [80]       [73]       [29]





              Clinical outcomes  No association of IMPDH1 variant with   IMPDH1 rs2278294 G allele was  associated with slower BMI gain   IMPDH2 3757C allele was associated   with increased risk of AR   No association of IMPDH2 variants   with AR or leukopenia  IMPDH2 3757C allele was associated  with increased MPA plasma  concentration (6 h after MMF intake)  and increased IMPDH activity in PBMC   (12 h after MMF intake) No association of IMPDH2 variant with   No associa












             Immunosuppressive   regimen  AR Cyclosporine Tacrolimus  One-year follow-up  Five-year follow-up  One-year follow-up  One-year follow-up  One-year follow-up  AR   One-year follow-up  Calcineurin inhibitors  One-year follow-up   One-year follow-up  Six-month follow-up






                 MMF  Sirolimus  Corticosteroids  MMF  Cyclosporine  Tacrolimus  Corticosteroids  MMF  Cyclosporine  Corticosteroids  MMF  Tacrolimus  Prednisone   MMF  Tacrolimus  Corticosteroids  MMF  Cyclosporine  Tacrolimus  Corticosteroids  MMF  Corticosteroids  MMF  Cyclosporine  Tacrolimus  Corticosteroids  EC-MPS  Cyclosporine  Corticosteroids

                 145 adult patients (Brazil)  190 adult patients  (Poland)  237 adult patients  191 adult patients (USA)  101 adult patients   (Netherlands)  456 adult patients   177 adult patients  (Poland)  1,040 adult patients  189 adult patients

              Population










              Study design          Prospective, multicenter    Prospective (Apomygre and   Prospective, multicenter  (Collaborative Transplant   Prospective, multicenter

                 Retrospective   (Case-control)  Prospective   (CAESAR study)  Retrospective   Prospective  FDCC studies)  Prospective  study)   (Dominos study)






              Allele frequency  rs2278293 A: 47%  rs2278293 A: 45%  rs2278294 A: 30%  3757C: 7%  3757TC+CC: 9%  c.787T: 0.3%  3757C: 7%  rs11706052 C: 9%   rs4974081 G: 24%  3757C: 8%  rs11706052 G: 19%  rs11706052 C: 11%










                                    rs11706052 A>G   (c.819+10T>C, also   known as 3757T>C)  rs121434586   (Leu236Phe,   c.787C>T)  rs4974081   (-3624A>G)
              Variant






              Gene                  IMPDH2
   57   58   59   60   61   62   63   64   65   66   67