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August 25, 2016Diabetes CareOpen Access

Dapagliflozin Enhances Fat Oxidation and Ketone Production in Patients With Type 2 Diabetes

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Why the study?

Does dapagliflozin alter mitochondrial ATP synthesis, substrate oxidation rates, and ketone production in individuals with type 2 diabetes mellitus?

Population

18 individuals with type 2 diabetes mellitus (T2DM)

Comparison

Dapagliflozin for 2 weeks vs Placebo for 2 weeks

Design

RCT, randomized

Follow-up

2 weeks

Authors

GDGiuseppe DanieleUniversity of PisaJXJuan XiongShanxi Agricultural UniversityCSCarolina Solis‐HerreraThe University of Texas Health Science Center at San Antonio

Discussion

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Implication

Dapagliflozin improves insulin sensitivity via substrate shift without altering mitochondrial ATP synthesis; extends mechanistic insights into SGLT2i effects.

Structured PICO

Does dapagliflozin alter mitochondrial ATP synthesis, substrate oxidation rates, and ketone production in individuals with type 2 diabetes mellitus?

P
Population
18 individuals with type 2 diabetes mellitus (T2DM)
I
Intervention
Dapagliflozin for 2 weeks
C
Comparator
Placebo for 2 weeks
O
Outcome
Mitochondrial ATP synthesis, substrate oxidation rates, and ketone productionsurrogate

Dapagliflozin improves insulin sensitivity but shifts metabolism from glucose to lipid oxidation, providing a mechanistic explanation for increased ketone production and potential ketoacidosis risk in T2DM.

Cite This Study

Daniele et al. (2016) studied this question.

synapsesocial.com/papers/6a708cf031a3df824328ce28https://doi.org/10.2337/dc15-2688

Topics

SGLT2 inhibitors in heart failure
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