关键词: ACE I/D AGT T704C AT1R A1166C Candidate gene approach PREDICT-IgAN interaction renal prognosis

Mesh : Adult Biopsy Blood Pressure / drug effects Creatinine / blood Female Glomerulonephritis, IGA / drug therapy enzymology genetics physiopathology Humans INDEL Mutation / genetics Kidney / drug effects pathology Male Polymorphism, Single Nucleotide / genetics Protective Agents / pharmacology therapeutic use Renin-Angiotensin System / drug effects

来  源:   DOI:10.1177/1470320313515036   PDF(Sci-hub)

Abstract:
BACKGROUND: Little is known about genetic predictors that modify the renoprotective effect of renin-angiotensin system (RAS) blockade in IgA nephropathy (IgAN).
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).
CONCLUSIONS: 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.
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