Journal of the Renin-Angiotensin-Aldosterone System (Sep 2015)

insertion/deletion polymorphism (rs1799752) modifies the renoprotective effect of renin-angiotensin system blockade in patients with IgA nephropathy

  • Junya Teranishi,
  • Ryohei Yamamoto,
  • Yasuyuki Nagasawa,
  • Tatsuya Shoji,
  • Hirotsugu Iwatani,
  • Noriyuki Okada,
  • Toshiki Moriyama,
  • Atsushi Yamauchi,
  • Yoshiharu Tsubakihara,
  • Enyu Imai,
  • Hiromi Rakugi,
  • Yoshitaka Isaka

DOI
https://doi.org/10.1177/1470320313515036
Journal volume & issue
Vol. 16

Abstract

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Introduction: Little is known about genetic predictors that modify the renoprotective effect of renin-angiotensin system (RAS) blockade in IgA nephropathy (IgAN). Materials and methods: The present multicenter retrospective observational study examined effect modification between RAS blockade and three RAS-related gene polymorphisms in 237 IgAN patients, including ACE I/D (rs1799752), AT1R A1166C (rs5186) and AGT T704C (rs699). Results: During 9.9 ± 4.2 years of observation, 63 patients progressed to a 50% increase in serum creatinine level. Only ACE I/D predicted the outcome ( ACE DD vs ID/II, hazard ratio 1.86 (95% confidence interval 1.03, 3.33)) and modified the renoprotective effect of RAS blockade ( p for interaction between ACE DD and RAS blockade = 0.087). RAS blockade suppressed progression in ACE DD patients but not in ID/II patients ( ACE ID/II with RAS blockade as a reference; ID/II without RAS blockade 1.45 (0.72, 2.92); DD without RAS blockade 3.06 (1.39, 6.73); DD with RAS blockade 1.51 (0.54, 4.19)), which was ascertained in a model with the outcome of slope of estimated glomerular filtration rate ( p = 0.045 for interaction). Conclusion: ACE I/D predicted the IgAN progression and the renoprotective effect of RAS blockade in IgAN patients whereas neither AT1R A1166C nor AGT T704C did.