Heart failure & cardiomyopathies

Meta-Analysis of SGLT2 Inhibitors in Transthyretin Cardiac Amyloidosis: Insights by Disease-Modifying Therapy

JACC AdvPublished Meta-Analysis

Authors' conclusion

In observational studies, SGLT2i therapy in ATTR-CM is associated with lower all-cause mortality and HF hospitalizations. These findings are clinically encouraging, particularly for patients not receiving DMT, in whom therapeutic options remain limited. Prospective randomized trials are warranted to confirm these findings and better define SGLT2i benefit according to DMT.

Study context

Population
Patients with transthyretin cardiac amyloidosis (ATTR-CM)Fourteen observational studies, 5.453 patients received SGLT2i
Participants
10.852 patients
Comparison
SGLT2i in ATTR-CM, stratified by disease-modifying therapy (DMT)
  • SGLT2in = 5.453
Outcome
All-cause mortality and HF hospitalization
Methodological detailsobservational studies
  • Observational studies

Pooled result

As reported in the abstract

Risk ratio

0.44

P < 0.001

all-cause mortality; lower risk; k = 6; n = 5.135; I2 = 53.9%; 2 studies reported zero events (k = 4; n = 5.038)

Hazard ratio

0.62

P < 0.001

Heart failure (HF) hospitalization; reduced; k = 2; n = 1.438; I2 = 0%

Further pooled results

Study characteristics

Had diabetes
43.6%
Of 7.708 patients (k = 12) with known DMT status, received DMT
34.6%
Follow-up
3 months to 5.5 years

Subgroup analyses by DMT and diabetes status

Consistent direction of association
  • Findings require further validation

Safety

Pooled prevalence of adverse events

Pooled prevalence (k = 7; n = 535)
7.28%
  • I2 = 76.6%

Original publication

Meta-Analysis of SGLT2 Inhibitors in Transthyretin Cardiac Amyloidosis: Insights by Disease-Modifying Therapy. JACC Adv. Published 9 July 2026. doi:10.1016/j.jacadv.2026.102972

Composed by AI from the published abstract and checked against it. How Briefs are made →

Get them every week

New studies on this topic in My Week and in your Monday e-mail.

We e-mail you a sign-in link and a code. No password, no spam.