SGLT2 Inhibitors and Cognitive Function in Adults With Type 2 Diabetes (SaveMinD)

Detailed Description

Type 2 diabetes mellitus (T2D) is associated with an increased risk of cognitive impairment, particularly affecting executive function and processing speed. Multiple mechanisms, including chronic hyperglycaemia, glycaemic variability, vascular dysfunction, systemic inflammation, oxidative stress, and neurodegenerative processes, are thought to contribute to cognitive decline in individuals with T2D.

Sodium-glucose cotransporter-2 (SGLT2) inhibitors have demonstrated cardiovascular and renal benefits and may also exert neuroprotective effects through improvements in metabolic control and modulation of inflammatory and vascular pathways. However, prospective randomized evidence regarding their effects on cognition remains limited.

The SaveMinD study is a prospective, randomized, open-label trial with blinded outcome assessment (PROBE design) evaluating whether the addition of an SGLT2 inhibitor to standard diabetes care influences cognitive outcomes in adults with T2D over 12 months. The primary endpoint is change in executive cognitive function, assessed using a composite score derived from standardized neuropsychological tests. Secondary outcomes include global cognitive function, glycaemic control and variability, circulating biomarkers of neurodegeneration and inflammation, physical activity, functional status, sleep quality, psychological well-being, and safety.

The study also incorporates baseline structural brain magnetic resonance imaging (MRI), APOE genotyping, frailty assessment, continuous glucose monitoring, and objective physical activity monitoring to explore biological and behavioural factors associated with cognitive change. These assessments will be used to investigate potential mechanisms underlying cognitive decline and to identify factors that may modify the response to SGLT2 inhibitor therapy.

The findings are expected to improve understanding of the relationship between metabolic health and cognitive function in T2D and may contribute to the development of strategies for the prevention of diabetes-associated cognitive decline.

Inclusion criteria

• adults aged 50 years or older.
• diagnosis of type 2 diabetes mellitus according to current American Diabetes - - association (ADA) diagnostic criteria.
• duration of type 2 diabetes mellitus of at least 5 years.
• glycated haemoglobin (HbA1c) ≤8.5% (≤69 mmol/mol) at screening.
• estimated glomerular filtration rate (eGFR) ≥45 mL/min/1.73 m².
• stable glucose-lowering therapy for at least 3 months before enrolment.
• able to complete neuropsychological assessments and all study procedures.
• willing and able to wear a continuous glucose monitoring (CGM) sensor and a physical activity monitor.
• able to provide written informed consent.

Exclusion criteria

• previous or current treatment with a sodium-glucose cotransporter-2 (SGLT2) inhibitor.
• Montreal Cognitive Assessment (MoCA) score <20 at screening.
• diagnosis of dementia or another major neurocognitive disorder.
• history of stroke or transient ischaemic attack within the previous 6 months.
• Parkinson's disease, multiple sclerosis, epilepsy, or another major neurological disorder affecting cognitive function.
• severe psychiatric illness likely to interfere with study participation or cognitive assessment.
• estimated glomerular filtration rate (eGFR) <45 mL/min/1.73 m².
• history of diabetic ketoacidosis.
• recurrent urinary tract infections (≥3 episodes during the previous year).
• contraindication to magnetic resonance imaging (MRI).
• pregnancy, breastfeeding, or planned pregnancy during the study period.
• active malignancy requiring systemic treatment (except adequately treated non-melanoma skin cancer).
• moderate or severe hepatic impairment (Child-Pugh Class B or C).
• alcohol or substance abuse likely to interfere with study participation.
• presence of an established indication for mandatory SGLT2 inhibitor therapy according to current international clinical practice guidelines (e.g., symptomatic heart failure or chronic kidney disease).
• participation in another interventional clinical trial within the previous 30 days.
• any medical condition that, in the opinion of the investigator, could compromise participant safety, adherence to the protocol, or interpretation of study results.