Sirolimus therapy for patients with adult polycystic kidney disease: a pilot study

A R Soliman1, E Ismail, S Zamil

  • 1Department of Nephrology, Cairo University, Cairo, Egypt. aminroshdy@gmail.com

Transplantation Proceedings
|November 18, 2009
PubMed

Insights

Sirolimus combined with an ARB may slow kidney volume increase in early autosomal dominant polycystic kidney disease (ADPKD). This pilot study suggests potential benefits for ADPKD patients, though infectious complications occurred.

Area of Science:

  • Nephrology
  • Pharmacology

Background:

  • Autosomal dominant polycystic kidney disease (ADPKD) is a genetic disorder characterized by renal cyst growth.
  • Current treatments for ADPKD primarily focus on managing symptoms and slowing disease progression.

Purpose of the Study:

  • To investigate the effect of sirolimus, an mTOR inhibitor, combined with an angiotensin receptor blocker (ARB) on renal cyst growth in ADPKD patients.
  • To assess the impact on renal function and identify potential adverse events.

Main Methods:

  • A pilot study involving 16 adult ADPKD patients with serum creatinine <2 mg/dL.
  • Eight patients received sirolimus (1 mg/d) plus telmisartan (ARB) for 6 months; 8 controls received telmisartan only.
  • Renal volumes were measured using MRI at baseline and after 6 months.

Main Results:

  • The sirolimus group showed an insignificant rise in kidney volume (2845 to 3221 mL, P=NS), while the control group had a significant increase (2667 to 3590 mL, P<.05).
  • Renal function remained stable or improved in most sirolimus patients (7/8), whereas controls showed more variability (3 stable, 3 worsened, 2 improved).
  • Infectious complications (UTIs, pharyngitis) occurred in 4 sirolimus patients; 2 controls developed UTIs.

Conclusions:

  • Sirolimus, when added to an ARB, may offer a potential therapeutic benefit in slowing renal cyst progression in early-stage ADPKD.
  • Further research is warranted to confirm efficacy and optimize safety profiles for sirolimus in ADPKD management.