Transthyretin-targeting therapies are effective for managing ATTR-CM
Drugs that target the transthyretin protein have life-extending potential for patients with ATTR-CM and are safe to use.
Drugs that target the transthyretin protein have life-extending potential for patients with ATTR-CM and are safe to use.
Tafamidis and acoramidis reduce mortality and improve quality of life for many patients living with ATTR-CM.
Arrhythmias appear to be a common complication in patients with ATTR-CM and may contribute to an increased risk of mortality.
In a recent study, left atrial dilation and advanced age were identified as predictors of atrial fibrillation in patients with ATTR-CM.
Abnormalities in the function of arteries and small blood vessels represent a key component of ATTR-CM pathology and a therapeutic target.
A recent case report showed that transthyretin amyloid cardiomyopathy (ATTR-CM) may not always follow the same rules in every patient.
A recent case study describes the dual occurrence of Alzheimer’s disease and ATTRwt, the most common form of ATTR-CM.
In the last decade, better awareness, improved diagnostic tools and new treatments have helped doctors diagnose ATTR-CM earlier on.
Sixteen percent of patients developed transthyretin amyloid cardiomyopathy (ATTR-CM) within six years of surgery for lumbar spinal stenosis.
A recently published review summarized the advances in ATTR-CM screening, diagnosis and treatment and analyzed future perspectives.