Evidence map›Paper›PMID 42366424›Full record

ArticleCardiovascular diabetology. Endocrinology reports2026

Safety of SGLT2 inhibitors versus DPP-4 inhibitors in super-elderly patients (≥ 80 years) with type 2 diabetes: a propensity score-matched cohort study.

Shankar Biswas, Yashasvi Srivastava, Ahmed Wahba, Bushra Amer, Ayman Hamadttu

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Article in Cardiovascular diabetology. Endocrinology reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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5 authors.

Shankar BiswasDepartment of Internal Medicine, Ivano-Frankivsk National Medical University, Ivano-Frankivsk, Ukraine. Sb740927@gmail.com.ORCID https://orcid.org/0009-0005-2421-3953
Yashasvi SrivastavaDepartment of Internal Medicine, Ivano-Frankivsk National Medical University, Ivano-Frankivsk, Ukraine.
Ahmed WahbaFaculty of Medicine, Port Said University, Port Said, Egypt.
Bushra AmerDepartment of Internal Medicine, Berkshire Medical Center, Pittsfield, USA.
Ayman HamadttuSudan University of Science and Technology, Khartoum, Sudan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSodium-glucose cotransporter-2 inhibitors (SGLT2i) provide cardiovascular and renal benefits in type 2 diabetes, yet safety data in super-elderly patients (≥ 80 years) remain limited. We compared the safety of SGLT2i versus dipeptidyl peptidase-4 inhibitors (DPP-4i) in this vulnerable population.

methodsWe conducted a retrospective, new-user, active-comparator cohort study using the TriNetX Global Collaborative Network (176 healthcare organizations). Patients aged ≥ 80 years at treatment initiation with type 2 diabetes newly prescribed SGLT2i or DPP-4i were matched 1:1 using propensity scores incorporating demographics, comorbidities, frailty proxies, and concomitant medications. Primary safety outcomes included falls, hip fracture, acute kidney injury, urinary tract infection, genital candidiasis, hypoglycemia, volume depletion, hypotension, and syncope. Secondary outcomes included stroke, myocardial infarction, heart failure hospitalization, and all-cause mortality. Subgroup analyses assessed falls risk among insulin, benzodiazepine, and loop diuretic users.

resultsAfter matching, 65,119 patients remained in each cohort (mean age 82.2 ± 2.3 years; 48.7% female). Over a mean follow-up of 269 days, SGLT2i was associated with significantly lower risks of falls (HR 0.90; 95% CI 0.85-0.95), hip fracture (HR 0.78; 0.69-0.89), acute kidney injury (HR 0.82; 0.78-0.85), urinary tract infection (HR 0.79; 0.75-0.83), hypoglycemia (HR 0.74; 0.67-0.82), volume depletion (HR 0.91; 0.86-0.97), stroke (HR 0.88; 0.82-0.95), and all-cause mortality (HR 0.73; 0.70-0.76; all p < 0.05). Genital candidiasis risk was higher with SGLT2i (HR 1.70; 1.50-1.93; p < 0.001), as was heart failure hospitalization (HR 1.07; 1.02-1.12; p = 0.007). Hypotension, syncope, and myocardial infarction did not differ significantly. The falls reduction was consistent across subgroups using insulin, benzodiazepines, and loop diuretics. Sensitivity analysis with fixed 250-day follow-up confirmed all primary findings.

conclusionsIn super-elderly patients with type 2 diabetes, SGLT2i demonstrated a favorable safety profile compared to DPP-4i, with significantly lower risks of falls (10%), hip fracture (22%), acute kidney injury (18%), hypoglycemia (26%), and mortality (27%). Safety concerns included increased genital candidiasis (70%) and modestly higher heart failure hospitalization (7%). These findings support SGLT2i use in appropriately selected super-elderly patients. CLINICAL TRIAL NUMBER: Not applicable.

Indexed as

DPP-4 inhibitorsDrug safetyElderlyFallsFracturesMortalitySGLT2 inhibitorsType 2 diabetes

Identifiers

PMID42366424
PMCPMC13312745

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