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Updated: Aug 5, 2026

Modeling and Evaluation of Murine Diabetic Cardiomyopathy Model
Published on: November 29, 2024
Racial outcomes in patients with diabetic cardiomyopathy treated with an aldose reductase inhibitor: the ARISE-HF
Jose L Batista1, Yuxi Liu2, Javed Butler3,4
1Section of Clinical Cardiac Electrophysiology, University of Michigan Samuel and Jean Frankel Cardiovascular Center, Ann Arbor, Michigan, USA josebati@med.umich.edu.
Insights
Black and Hispanic individuals with diabetic cardiomyopathy (DbCM) show faster disease progression. AT-001 did not significantly alter peak oxygen uptake (peak VO2) changes across racial groups.
Area of Science:
- Cardiology
- Diabetology
- Pharmacology
Background:
- Racial and ethnic disparities exist in diabetic cardiomyopathy (DbCM), with Black and Hispanic individuals experiencing poorer health outcomes.
- The impact of these disparities on the natural progression of DbCM remains under investigation.
- Understanding these differences is crucial for developing targeted therapeutic strategies.
Purpose of the Study:
- To evaluate disease progression in individuals diagnosed with diabetic cardiomyopathy (DbCM).
- To assess potential racial differences in the response to the investigational drug AT-001.
- To analyze the impact of race and ethnicity on key clinical outcomes in DbCM.
Main Methods:
- A randomized controlled trial involving 625 participants with DbCM.
- Participants were assigned to receive either placebo or AT-001 for 15 months.
- Primary outcome: change in peak oxygen uptake (peak VO2); Secondary outcomes: Kansas City Cardiomyopathy Questionnaire (KCCQ) and Physical Activity Scale for the Elderly scores. Analyses were stratified by race (Black, Hispanic, White).
Main Results:
- Placebo recipients: Black and Hispanic participants showed significantly greater declines in peak VO2 compared to White participants.
- AT-001 treatment: A trend towards slower peak VO2 decline was observed in Black and Hispanic participants, though not statistically significant.
- Quality of Life: Black participants receiving placebo experienced the most substantial declines in Kansas City Cardiomyopathy Questionnaire (KCCQ) scores.
Conclusions:
- Black and Hispanic individuals with DbCM exhibit accelerated disease progression, marked by pronounced functional and quality-of-life impairments.
- The investigational drug AT-001 did not demonstrate statistically significant effects on peak VO2 changes, with similar trends observed across racial and ethnic groups.
- Further research is warranted to explore effective interventions for mitigating racial disparities in diabetic cardiomyopathy progression.
Background:
Racial and ethnic differences in diabetic cardiomyopathy (DbCM) exist, with black and Hispanic participants showing poorer health status. It remains unclear whether these differences affect the natural progression of the disease. We aimed to evaluate disease progression in individuals with DbCM, as well as racial differences in the response to AT-001.
Methods:
A total of 625 participants with DbCM were randomised to either placebo or AT-001 and followed for 15 months. The primary outcome was change in peak oxygen uptake (peak VO2) and secondary outcomes included Kansas City Cardiomyopathy Questionnaire (KCCQ) and Physical Activity Scale for the Elderly scores. Analyses were stratified by race and ethnicity (black, Hispanic, white).
Results:
Black and Hispanic participants who received placebo experienced greater declines in peak VO2 (-0.74 and -1.67 mL/kg/min, respectively) compared with white participants (-0.23 mL/kg/min, p=0.005). AT-001 demonstrated a non-statistically significant trend towards slower declines in peak VO2 in black and Hispanic participants (-0.31 and -0.62 mL/kg/min, p=0.29, respectively). Black participants who received placebo had the largest declines in most KCCQ scores.
Conclusion:
Black and Hispanic participants with DbCM experienced faster disease progression, with black participants showing the most pronounced functional and quality of life declines. The effect of AT-001 on peak VO2 changes was not statistically significant with similar effects between racial and ethnic groups (NCT04083339).
Trial Registration Number:
NCT04083339.
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