02567nas a2200325 4500000000100000008004100001100001500042700001400057700001800071700001200089700001600101700001500117700001600132700001300148700001400161700001400175700001000189700001400199700001300213700001400226700001600240700001900256700001500275700001500290245010400305250001500409490002000424520174600444020005102190 2016 d1 aZoungas S.1 aCooper M.1 aWoodward Mark1 aWong M.1 aMatthews D.1 aPoulter N.1 aWilliams B.1 aHamet P.1 aMancia G.1 aHarrap S.1 aLi Q.1 aHeller S.1 aMarre M.1 aRodgers A1 aChalmers J.1 aPerkovic Vlado1 aNeal Bruce1 aMacmahon S00aLong-term Benefits of Intensive Glucose Control for Preventing End-Stage Kidney Disease: ADVANCE-ON a2016/03/240 vpii: dc152322. 3 a

OBJECTIVE: The Action in Diabetes and Vascular Disease: Preterax and Diamicron Modified Released Controlled Evaluation (ADVANCE) trial reported that intensive glucose control prevents end-stage kidney disease (ESKD) in patients with type 2 diabetes, but uncertainty about the balance between risks and benefits exists. Here, we examine the long-term effects of intensive glucose control on risk of ESKD and other outcomes. RESEARCH DESIGN AND METHODS: Survivors, previously randomized to intensive or standard glucose control, were invited to participate in post-trial follow-up. ESKD, defined as the need for dialysis or kidney transplantation, or death due to kidney disease, was documented overall and by baseline CKD stage, along with hypoglycemic episodes, major cardiovascular events, and death from other causes. RESULTS: A total of 8,494 ADVANCE participants were followed for a median of 5.4 additional years. In-trial HbA1c differences disappeared by the first post-trial visit. The in-trial reductions in the risk of ESKD (7 vs. 20 events, hazard ratio [HR] 0.35, P = 0.02) persisted after 9.9 years of overall follow-up (29 vs. 53 events, HR 0.54, P < 0.01). These effects were greater in earlier-stage CKD (P = 0.04) and at lower baseline systolic blood pressure levels (P = 0.01). The effects of glucose lowering on the risks of death, cardiovascular death, or major cardiovascular events did not differ by levels of kidney function (P > 0.26). CONCLUSIONS: Intensive glucose control was associated with a long-term reduction in ESKD, without evidence of any increased risk of cardiovascular events or death. These benefits were greater with preserved kidney function and with well-controlled blood pressure.

 a1935-5548 (Electronic)
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