Fasting substrates predict chronic kidney disease progression in CREDENCE trial patients with type 2 diabetes


Here are the Fasting substrates predict chronic kidney disease progression in CREDENCE trial patients with type 2 diabetes journals presenting the latest research across various disciplines. From social sciences to technology, each article is expected to provide valuable insights to our readers.

Fasting substrates predict meaning, fasting substrates predict chronic inflammatory, fasting substrates predict chronic kidney disease, fasting substrates predict chronic cough, fasting substrates predictem, fasting substrates of cellular, fasting substrates synonym, fasting substrates predictive index, fasting substrates and enzymes.

Fasting substrates predict chronic kidney disease progression in CREDENCE trial patients with type 2 diabetes

BACKGROUND. Sodium-glucose cotransporter 2 inhibitors slow down progression of chronic kidney disease (CKD). We tested whether the circulating substrate mix is related to CKD progression and cardiovascular outcomes in patients with type 2 diabetes (T2D) and albuminuric CKD in the CREDENCE trial. METHODS. We measured fasting substrates in 2,543 plasma samples at baseline and 1 year after randomization to either 100 mg canagliflozin or placebo and used multivariate Cox models to explore their association with CKD progression, heart failure hospitalization/cardiovascular death (hHF/CVD), and mortality. RESULTS. Higher baseline lactate and free fatty acids (FFAs) were independently associated with a lower risk of CKD progression (HR = 0.73 [95% CI: 0.54–0.98] and HR = 0.67 [95% CI: 0.48–0.95], respectively) and hHF/CVD HR = 0.70 [95% CI: 0.50–0.99] and HR = 0.63 [95% CI: 0.42–0.94]). Canagliflozin led to a rise in plasma FFAs, glycerol, β-hydroxybutyrate, and acetoacetat e. Changes in substrate between baseline and year 1 predicted an approximately 30% reduction in relative risk of both CKD progression and hHF/CVD independently of treatment. More patients who did not respond to canagliflozin treatment in terms of CKD progression belonged to the bottom lactate and FFA distribution tertiles. CONCLUSION. In T2D patients with albuminuric CKD, basic energy substrates selectively influenced major long-term endpoints; canagliflozin treatment amplified their effects by chronically raising their circulating levels. © 2024, Ferrannini et al.

Authors : Ferrannini E.; Baldi S.; Scozzaro M.T.; Ferrannini G.; Hansen M.K.

Source : American Society for Clinical Investigation

Article Information

Year 2024
Type Article
DOI 10.1172/jci.insight.180637
ISSN 23793708
Volume 9

You can download the article here


If You have any problem, contact us here


Support Us:

Download Now Buy me a coffee Request Paper Here