Dominican heritage may raise risk of hereditary ATTR-CM variant
A genetic variant linked to ATTR-CM was more common in Hispanic individuals with more African ancestry, especially Dominican descent.
A genetic variant linked to ATTR-CM was more common in Hispanic individuals with more African ancestry, especially Dominican descent.
Patients with ATTR-CM who took both GLP-1RA and SGLT2i had lower death rates and fewer heart events than those on SGLT2i alone.
Cardiac transthyretin amyloidosis (ATTR-CM) was found in 12% of patients with Alzheimer’s disease and heart enlargement after death.
Tailored exercise programs can reduce symptoms and improve quality of life in patients with HFpEF, including those with ATTR-CM.
Patients with amyloidosis, including ATTR-CM, value longevity, affordability and symptom relief above all.
One-third of patients diagnosed with ATTR-CM had normal heart wall thickness, suggesting current screening may miss early-stage cases.
RNAi therapies may reduce heart-related complications in patients with transthyretin amyloid cardiomyopathy (ATTR-CM).
Tafamidis and acoramidis reduce mortality and improve quality of life for many patients living with ATTR-CM.
Sixteen percent of patients developed transthyretin amyloid cardiomyopathy (ATTR-CM) within six years of surgery for lumbar spinal stenosis.
Barriers to care in ATTR-CM include disparities in diagnosis, treatment access, and awareness among medical professionals.