The edition · Diabetes & Endocrinology
Empagliflozin's benefit holds across every subgroup Medicare could slice
A real-world analysis finds no sociodemographic group left behind by SGLT2 inhibition, a Swedish register quantifies what early-onset type 1 diabetes costs over a lifetime, and the risks of stopping an incretin come into focus.
The edition in brief
Today's diabetology edition leads with EMPRISE, a propensity-matched Medicare analysis of adults aged 65 and over with type 2 diabetes. Empagliflozin was associated with lower major adverse cardiovascular events (HR 0.77), heart failure hospitalisation (HR 0.72) and all-cause mortality (HR 0.66) than DPP-4 inhibitors, and lower heart failure hospitalisation than GLP-1 receptor agonists (HR 0.88). No effect heterogeneity appeared by age, sex, race, ethnicity or socioeconomic factors; absolute benefit was largest in those with established cardiovascular disease. A Swedish national register study of 34,155 adults with type 1 diabetes found each additional year of age at diagnosis associated with 1.7% lower all-cause mortality, and a more than threefold excess mortality where diagnosis fell between birth and age 10. A meta-analysis of ten longitudinal studies associated higher pancreatic fat with incident type 2 diabetes, though the pooled estimate was unstable and driven substantially by one ultrasound-based study. A controlled feeding trial of the DASH4D diet in 101 adults showed small but consistent falls in fructosamine, fasting glucose and HbA1c. The edition closes on a review of what happens when GLP-1 receptor agonists and tirzepatide are stopped: weight regain, deteriorating cardiometabolic risk factors, and the possibility that repeated cycles of starting and stopping do their own harm. The practical thread through the edition is that persistence, not initiation, is where much of the benefit is won or lost.
Empagliflozin's cardiovascular benefit did not vary by who the patient was
In older adults with type 2 diabetes and cardiovascular disease, empagliflozin's advantage over a DPP-4 inhibitor is large and does not depend on the patient's demographics.
Each year later that type 1 diabetes starts, the long-term risk falls
Treat childhood-onset type 1 diabetes in an adult as a higher-risk phenotype and bring forward cardiovascular surveillance accordingly.
Pancreatic fat tracks with future diabetes, but the pooled estimate is fragile
Interesting as a marker, not usable in clinic — keep screening for dysglycaemia the way you already do.
A DASH diet adapted for diabetes moves glycaemia a little, reliably
Recommend a DASH-style diet for its blood pressure benefit and count the small glycaemic gain as extra.
Ask what the patient will do when the injection runs out
Counsel on nausea, cost and the stopping plan at the first prescription — that conversation is where persistence is won.
Stopping and restarting an incretin may be worse than either steady state
Before starting an incretin, ask whether the patient can stay on it for years — intermittent use may cost more than it gives.
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