Key result
GDF-15, NTproBNP, and hs-TnT link to renal events, while NTproBNP predicts ~245% higher cardiovascular risk.
Why the study?
Patients with type 2 diabetes and nephropathy are at high risk for renal and cardiovascular complications, but relevant predictive biomarkers have been poorly identified and may be confounded by renal impairment.
Do baseline levels of GDF-15, NTproBNP, and hs-TnT predict renal and cardiovascular events in patients with type 2 diabetes and nephropathy?
Cohort (n=861)
Do baseline levels of GDF-15, NTproBNP, and hs-TnT predict renal and cardiovascular events in patients with type 2 diabetes and nephropathy?
Hazard Ratio: 3.45
p-value: p=<0.001
In patients with type 2 diabetes and nephropathy, baseline NTproBNP independently predicts cardiovascular risk and improves risk stratification beyond standard clinical variables.
GDF-15, NTproBNP, and hs-TnT may refine renal risk assessment in T2D nephropathy; extends prior biomarker data but leaves open need for prospective validation.
OBJECTIVE Although patients with type 2 diabetes (T2D) with nephropathy are at high risk for renal and cardiovascular complications, relevant biomarkers have been poorly identified. Because renal impairment may increase biomarker levels, this potentially confounds associations between biomarker levels and risk. To investigate the predictive value of a biomarker in such a setting, we examined baseline levels of growth differentiation factor-15 (GDF-15), N-terminal prohormone of B-type natriuretic peptide (NTproBNP), and high-sensitivity troponin T (hs-TnT) in relation to renal and cardiovascular risk in T2D patients with nephropathy. RESEARCH DESIGN AND METHODS Eight hundred sixty-one T2D patients from the sulodexide macroalbuminuria (Sun-MACRO) trial were included in our post hoc analysis. Prospective associations of baseline serum GDF-15, NTproBNP, and hs-TnT with renal and cardiovascular events were determined by Cox multiple regression and C-statistic analysis. Renal base models included albumin-to-creatinine ratio (ACR), serum creatinine, hemoglobin, age, and sex. Cardiovascular base models included diastolic blood pressure, ACR, cholesterol, age, and sex. RESULTS The mean (±SD) estimated glomerular filtration rate was 33 ± 9 mL/min/1.73 m2, and the median serum concentration for GDF-15 was 3,228 pg/mL (interquartile range 2,345–4,310 pg/mL), for NTproBNP was 380 ng/L (155–989 ng/L), and for hs-TnT was 30 ng/L (20–47 ng/L). In multiple regression analysis, GDF-15 (hazard ratio [HR] 1.83, P = 0.04), NTproBNP (HR 2.34, P = 0.004), and hs-TnT (HR 2.09, P = 0.014) were associated with renal events, whereas NTproBNP (HR 3.45, P < 0.001) was associated with cardiovascular events. The C-statistic was improved by adding NTproBNP and hs-TNT to the renal model (0.793 vs. 0.741, P = 0.04). For cardiovascular events, the C-statistic was improved by adding NTproBNP alone (0.722 vs. 0.658, P = 0.018). CONCLUSIONS Biomarkers GDF-15, NTproBNP, and hs-TnT associate independently with renal risk, whereas NTproBNP independently predicts cardiovascular risk.
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Bidadkosh et al. (2017) conducted a cohort in Type 2 diabetes with nephropathy (n=861). Baseline serum GDF-15, NTproBNP, and hs-TnT was evaluated on Renal and cardiovascular events (HR 3.45, p=<0.001). Baseline GDF-15, NTproBNP, and hs-TnT were independently associated with renal events, while NTproBNP independently predicted cardiovascular events (HR 3.45, P<0.001).
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