Description
You should get tested for ATTR-CM (Transthyretin Amyloid Cardiomyopathy) if you suspect you might have symptoms like heart failure, especially if you are older, because it is a potentially serious heart condition that can be effectively treated if diagnosed early, and often goes undetected due to its subtle symptoms; a genetic test can also identify if you have a hereditary form of ATTR-CM which could impact your family members as well.
Key reasons to get tested for ATTR-CM:
- Early detection is crucial:
- Early diagnosis allows for prompt treatment to slow disease progression and improve quality of life.
- Non-specific symptoms:
- Symptoms like fatigue, shortness of breath, and swelling in the legs can mimic other conditions, making early diagnosis challenging.
- Family history:
- If you have a family history of heart disease or amyloidosis, genetic testing can identify if you carry the mutation for hereditary ATTR-CM.
- Risk factors:
- Age, male sex, and certain ethnicities may increase your risk for ATTR-CM.
Fasting not required. Test takes 4-6 weeks to perform.
