Association between caffeine and the eGFR dip after initiation of SGLT2 inhibitors in adult patients
Zach Kisley, Amanda J. Kalishman, Aliza A. Memon, Sandeep S. Dhindsa, John C. Edwards, Amy Mosman, Krista L. Lentine, Paul Kunnath, Emily Wood, Kana N. Miyata

TL;DR
High caffeine intake may reduce the initial kidney function decline seen when starting a specific heart and kidney medication.
Contribution
This study is the first to show a link between caffeine consumption and a smaller eGFR dip after SGLT2 inhibitor initiation.
Findings
Caffeine intake was negatively correlated with eGFR dip at 1 month (r = -0.31, p = 0.02).
Caffeine and baseline creatinine were independently associated with the eGFR dip in multivariable regression.
High caffeine consumption may help reduce early kidney function decline with SGLT2 inhibitors.
Abstract
Sodium‐glucose cotransporter‐2 inhibitors (SGLT2i) are cornerstone therapies for heart failure and chronic kidney disease. Clinical trials have demonstrated that the estimated glomerular filtration rate (eGFR) typically declines within the first few weeks after SGLT2i initiation. One proposed mechanism of the acute eGFR dip is the reduced intraglomerular pressure through tubuloglomerular feedback (TGF). Adenosine is a key mediator in TGF signaling, and caffeine, a nonselective adenosine receptor antagonist, may influence this process. We conducted a retrospective cohort study at SSM Health Saint Louis University Hospital to examine whether caffeine intake influences the initial eGFR dip following SGLT2i initiation. Eligible patients completed a caffeine consumption survey, and chart reviews assessed creatinine and proteinuria at baseline and 1 month post‐initiation. Data from 62…
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Taxonomy
TopicsDiabetes Treatment and Management · Chronic Kidney Disease and Diabetes · Coffee research and impacts
