2017
DOI: 10.2174/1573399812666161207123007
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Distinct Biomarkers for Early Diagnosis of Diabetic Nephropathy

Abstract: Optimization of biomarkers for a clinical situation requires a prospective validation in large numbers of patients with diabetic nephropathy and needs to be performed in different critically ill populations.

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Cited by 36 publications
(35 citation statements)
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“…The large number of patients with T2DM who developed DN within the first year may be explained by the design of the ACCORD study, which was intended to investigate whether intensive vs. standard therapies that normalize a patient's HbA1c would have an impact on the incidence of cardiovascular events . Presence of DN in the first 6 months may only represent transient changes in kidney perfusion or function . Yet, given the fact that none of these patients developed micro‐albuminuria by that time, they are likely predominantly in stage 2 of DN, where hyperfiltration is observed .…”
Section: Discussionmentioning
confidence: 99%
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“…The large number of patients with T2DM who developed DN within the first year may be explained by the design of the ACCORD study, which was intended to investigate whether intensive vs. standard therapies that normalize a patient's HbA1c would have an impact on the incidence of cardiovascular events . Presence of DN in the first 6 months may only represent transient changes in kidney perfusion or function . Yet, given the fact that none of these patients developed micro‐albuminuria by that time, they are likely predominantly in stage 2 of DN, where hyperfiltration is observed .…”
Section: Discussionmentioning
confidence: 99%
“…The ACCORD data set did not include more novel biomarkers of DN; it only contains routinely measured clinical factors, such as eGFR, SCr, HbA1c, etc. Testing of other predictive biomarkers, such as tumor necrosis factor‐α, transforming growth factor‐β, vascular endothelial growth factor, or interleukin‐1β, that may be more closely related to mechanisms of DN pathogenesis was not possible. However, studies focusing on the pathophysiologic mechanism of diabetic kidney disease have been performed showing that tumor necrosis factor receptor‐1, tumor necrosis factor receptor‐2, and plasma kidney injury molecule‐1 are associated with higher risk of eGFR decline in persons with T2DM with early and advanced diabetic kidney disease …”
Section: Discussionmentioning
confidence: 99%
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