Key result
In incident hemodialysis patients with diabetes, the lowest quartile of proteinuria was associated with a greater risk of atherosclerotic cardiovascular disease compared to the third quartile.
Why the study?
The clinical implications of proteinuria levels at the start of dialysis have not been confirmed in patients with diabetic kidney disease.
Does lower proteinuria at dialysis initiation predict atherosclerotic cardiovascular disease in incident hemodialysis patients with diabetes?
Cohort (n=361)
Yes
Does lower proteinuria at dialysis initiation predict atherosclerotic cardiovascular disease in incident hemodialysis patients with diabetes?
In incident hemodialysis patients with diabetes, lower proteinuria at dialysis initiation is associated with a higher risk of atherosclerotic cardiovascular disease, reflecting more severe underlying macroangiopathy.
Answers are grounded in this paper and cite their sources.
May warrant closer ASCVD monitoring in low-proteinuria diabetic HD patients; leaves open whether it refines risk stratification.
Diabetic kidney disease (DKD) is heterogeneous in terms of proteinuria. Patients with DKD who present with low-grade proteinuria are more likely to have nephrosclerosis rather than traditional diabetic nephropathy. The amount of proteinuria might reflect the underlying pathology of renal failure and influence the prognosis after dialysis initiation. Clinical implications of proteinuria at the start of dialysis have not been confirmed, while greater proteinuria is associated with higher risk of cardiovascular disease (CVD) in the predialysis stages of chronic kidney disease. We performed a retrospective multicenter cohort study enrolling incident hemodialysis patients with diabetes. Patients were stratified using proteinuria quartiles. We examined the association of proteinuria quartiles with types of subsequent CVD. Among the enrolled 361 patients, the estimated mean glomerular filtration rate and proteinuria was 5.4 mL/min/1.73 m2 and 6.3 g/gCr, respectively. Lower quartile of proteinuria (cut-offs: 3.0, 5.4, and 8.8 g/gCr) was significantly associated with male, older age, and history of atherosclerotic CVD including coronary artery disease, peripheral arterial disease, and cerebral infarction (Ptrend<0.05). Kidney size was smaller in patients with lower levels of proteinuria. Patients with higher levels of proteinuria were more likely to have proliferative diabetic retinopathy (Ptrend<0.05). Multivariate competing risk analysis revealed that the first quartile of proteinuria was associated with a greater risk of atherosclerotic CVD than the third quartile (subhazard ratio [95% confidence interval]: 2.04 [1.00-4.14]). This association was attenuated after additional adjustments for history of atherosclerotic CVD. Furthermore, patients with lower quartiles of proteinuria were more likely to die of atherosclerotic CVD than those with non-atherosclerotic CVD (Ptrend = 0.01). Diabetic patients with lower proteinuria at dialysis initiation were characterized by severer macroangiopathy, as shown by a more atrophic kidney and higher prevalence of past atherosclerotic CVD. Hence, they are at a high risk of developing atherosclerotic CVD.
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Yamaguchi et al. (2022) conducted a cohort in Diabetic kidney disease (n=361). Lowest quartile of proteinuria (<3.0 g/gCr) vs. Third quartile of proteinuria (5.4-8.8 g/gCr) was evaluated on Fatal atherosclerotic CVD and re-hospitalization for atherosclerotic CVD (SHR 2.04, 95% CI 1.00-4.14, p=0.049). In incident hemodialysis patients with diabetes, the lowest quartile of proteinuria was associated with a greater risk of atherosclerotic cardiovascular disease compared to the third quartile.
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