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. Author manuscript; available in PMC: 2019 Oct 1.
Published in final edited form as: Diabetes Obes Metab. 2018 Oct;20(Suppl 3):6–13. doi: 10.1111/dom.13416

Table 1:

Progression and treatment response phenotype.

Endpoint Challenges Advantages
ESRD ● Insensitive
● Long follow-up
● Low number of events
● Gold standard
● Clinically relevant for patient
eGFR
decline 30 -
57 %
● Inter-lab assay variation
● Influenced by drugs hemodynamics
● Diet and hydration status influence
 assay
● Variation attributed to nephron loss
 only reliable in advanced DKD
● Higher precision in advanced
 DKD
● Strong association with ESRD
eGFR slope ● Laboratory issues as described
 above
● Non linearity in eGFR slopes
 complicates interpretation
● Accuracy relies on multiple values
 over time
● Cut-off value for steep or shallow
 slope is arbitrary
● Can be used as continuous
 variable or a cut-off value can
 be applied to allow
 dichotomous comparison
● Can be assessed earlier than
 40% or 57% eGFR decline
● Allow studies in patients in
 early stages DKD
UACR /
Albuminuria
/Proteinuria
increase of
30%
● Reliability differs across assays
● Large day-to-day variation
● Unclear if decreased UACR
 necessarily improve clinical
 outcomes for all interventions
● Non-invasive
● High precision in early DKD