2012
DOI: 10.1007/s11255-012-0214-0
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The effects of mammalian target of rapamycin inhibitors on serum uric acid levels in renal transplant patients

Abstract: Switch from CNI to mTORi-based regimen provides better control of UA levels and improves renal functions.

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Cited by 2 publications
(2 citation statements)
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“…The mechanism underlying this NH 4 + -independent acidification response is not clear and requires further investigation. The higher serum uric acid found in the tacrolimus vs. the sirolimus group was expected [14] and may be implicated in reduced graft survival [15]. Fractional excretion of calcium was higher in the tacrolimus patients with dRTA and, although expected, was not detected in the sirolimus patients with the same condition.…”
Section: Discussionmentioning
confidence: 85%
“…The mechanism underlying this NH 4 + -independent acidification response is not clear and requires further investigation. The higher serum uric acid found in the tacrolimus vs. the sirolimus group was expected [14] and may be implicated in reduced graft survival [15]. Fractional excretion of calcium was higher in the tacrolimus patients with dRTA and, although expected, was not detected in the sirolimus patients with the same condition.…”
Section: Discussionmentioning
confidence: 85%
“…The effects of the mTOR inhibitor rapamycin (Sirolimus) on serum uric acid levels were studied in renal transplant patients. Immunosuppressive therapy with calcineurin inhibitors elevated uric acid levels, whereas the switch to a Sirolimus-based regimen reversed the rise in serum uric acid levels in these patients [51]. These results, albeit indirectly, suggest that inhibition of the mTOR pathway is important for reducing XOR activity.…”
Section: Molecular Pathways and Pharmacological Agentsmentioning
confidence: 89%