Regression of albuminuria and its association with incident cardiovascular outcomes and mortality in type 1 diabetes: the FinnDiane Study

被引:33
作者
Jansson, Fanny J. [1 ,2 ,3 ,4 ]
Forsblom, Carol [1 ,2 ,3 ,4 ]
Harjutsalo, Valma [1 ,2 ,3 ,4 ,5 ]
Thorn, Lena M. [1 ,2 ,3 ,4 ]
Waden, Johan [1 ,2 ,3 ,4 ]
Elonen, Nina [1 ,2 ,3 ,4 ]
Ahola, Aila J. [1 ,2 ,3 ,4 ]
Saraheimo, Markku [1 ,2 ,3 ,4 ]
Groop, Per-Henrik [1 ,2 ,3 ,4 ,6 ]
机构
[1] Biomedicum Helsinki, Folkhalsan Inst Genet, Folkhalsan Res Ctr, FIN-00290 Helsinki, Finland
[2] Univ Helsinki, Abdominal Ctr Nephrol, Helsinki, Finland
[3] Univ Helsinki, Cent Hosp, Helsinki, Finland
[4] Univ Helsinki, Diabet & Obes, Res Programs Unit, Helsinki, Finland
[5] Natl Inst Hlth & Welf, Chron Dis Prevent Unit, Helsinki, Finland
[6] Monash Univ, Cent Clin Sch, Dept Diabet, Melbourne, Vic, Australia
基金
芬兰科学院;
关键词
Albumin excretion rate; Albuminuria; Cardiovascular disease; Diabetic nephropathy; Mortality; Type; 1; diabetes; RENAL OUTCOMES; BLOOD-PRESSURE; FOLLOW-UP; NEPHROPATHY; REMISSION; DISEASE; RISK; MICROALBUMINURIA; EXCRETION; REDUCTION;
D O I
10.1007/s00125-018-4564-8
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims/hypothesis Our aim was to assess regression of albuminuria and its clinical consequences in type 1 diabetes. Methods The analysis included 3642 participants from the Finnish Diabetic Nephropathy (FinnDiane) Study with a 24 h urine sample and a history of albuminuria available at baseline. A total of 2729 individuals had normal AER, 438 a history of microalbuminuria and 475 a history of macroalbuminuria. Regression was defined as a change from a higher category of albuminuria pre-baseline to a lower category in two out of the three most recent urine samples at baseline. The impact of regression on cardiovascular events (myocardial infarction, stroke, coronary procedure) and mortality was analysed over a follow-up of 14.0 years (interquartile range 11.9-15.9). Results In total, 102 (23.3%) individuals with prior microalbuminuria and 111 (23.4%) with prior macroalbuminuria had regressed at baseline. For individuals with normal AER as a reference, the age-adjusted HRs (95% CI) for cardiovascular events were 1.42 (0.75, 2.68) in individuals with regression from microalbuminuria, 2.62 (1.95, 3.54) in individuals with sustained microalbuminuria, 3.15 (2.02, 4.92) in individuals with regression from macroalbuminuria and 5.49 (4.31, 7.00) in individuals with sustained macroalbuminuria. Furthermore, for all-cause and cardiovascular mortality rates, HRs in regressed individuals were comparable with those with sustained renal status at the achieved level (i.e. those who did not regress but remained at the most advanced level of albuminuria noted pre-baseline). Conclusions/interpretation Progression of diabetic nephropathy confers an increased risk for cardiovascular disease and premature death. Notably, regression reduces the risk to the same level as for those who did not progress.
引用
收藏
页码:1203 / 1211
页数:9
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