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Published on: 2/7/2026
There are several factors to consider: after 65, amyloidosis becomes more common and often involves the heart, where protein deposits can stiffen the muscle and cause symptoms like shortness of breath, leg swelling, fatigue, dizziness, and irregular heartbeat. Because diagnosis requires specialized blood, urine, imaging, and sometimes biopsy tests and treatments differ for AL vs ATTR, early recognition can improve outcomes and some symptoms need urgent care. See below for key red flags, testing and treatment options, and heart health steps that could influence your next decisions.
Amyloidosis is a rare but serious condition that becomes more common with age, particularly after 65. It happens when abnormal proteins—called amyloid—build up in organs and tissues. Over time, these deposits can interfere with how organs work. The heart is one of the most commonly affected organs in older adults, which is why understanding Amyloidosis and heart health is especially important.
This guide explains what Amyloidosis is, why age matters, how it can affect the heart, and what steps you can take to protect your health—without unnecessary alarm, but with clear, honest information.
Amyloidosis is not a single disease. It's a group of conditions caused by misfolded proteins that clump together and deposit in tissues. These deposits are not easily cleared by the body.
Over time, amyloid buildup can damage organs such as the:
There are several types of Amyloidosis, but in people over 65, two types are most relevant to heart health:
Credible medical organizations like national heart and aging institutes recognize age as a key risk factor, especially for ATTR Amyloidosis.
As we age, our bodies become less efficient at maintaining protein quality. This increases the chance that proteins may misfold and form amyloid deposits.
Key age-related risk factors include:
Importantly, many people over 65 live for years with Amyloidosis before it is recognized. Awareness can make a meaningful difference.
When amyloid builds up in the heart, it is called cardiac Amyloidosis. The deposits make the heart muscle stiff, limiting its ability to fill and pump properly.
This can lead to a form of heart failure called restrictive cardiomyopathy.
Symptoms often develop slowly and may include:
Because these symptoms are common in other heart conditions, Amyloidosis is often overlooked at first.
While heart symptoms are critical, Amyloidosis often affects more than one system. Additional signs may include:
Digestive symptoms like chronic diarrhea or abdominal pain can sometimes be confused with inflammatory bowel conditions such as Crohn's Disease—though the causes and treatments differ significantly, so accurate assessment is essential.
Diagnosing Amyloidosis requires careful testing. There is no single "yes or no" blood test.
Doctors may use:
Early and accurate diagnosis is critical because treatment depends on the specific type of Amyloidosis.
There is no one-size-fits-all treatment for Amyloidosis, but medical advances have significantly improved outcomes—especially when the condition is caught early.
Depending on the type, treatments may involve:
Your care team may include cardiologists, hematologists, and other specialists experienced in Amyloidosis.
Whether or not you have Amyloidosis, heart health becomes increasingly important with age. If you are at risk or already diagnosed, these steps matter even more.
These actions won't cure Amyloidosis, but they can help slow complications and improve daily life.
A diagnosis of Amyloidosis can feel overwhelming. It is normal to feel uncertain or concerned, especially when heart health is involved. At the same time, many people live meaningful lives with proper treatment and monitoring.
Helpful strategies include:
Being informed is empowering, not alarming.
Some symptoms should never be ignored. Speak to a doctor immediately or seek urgent care if you experience:
These can be life-threatening, whether related to Amyloidosis or another heart condition.
Amyloidosis over 65 is more common than many people realize, particularly when it affects the heart. While it is a serious condition, earlier recognition, better testing, and improved treatments are changing what it means to live with this diagnosis.
If you or a loved one have unexplained heart symptoms, nerve changes, or ongoing digestive issues, trust your instincts and speak to a doctor. Ask whether Amyloidosis could be part of the picture and what steps make sense next. Clear information and timely care can make a real difference in both safety and quality of life.
(References)
* Maurer MS, Sultan MB, Gottlieb SS, et al. Transthyretin Amyloid Cardiomyopathy: JACC State-of-the-Art Review. *J Am Coll Cardiol*. 2023;81(11):1087-1110. doi:10.1016/j.jacc.2023.01.036
* Manrique J, Perricone J, Hanna M. Cardiac Amyloidosis in the Elderly: A Clinical Review. *Am J Med*. 2021;134(11):1347-1355. doi:10.1016/j.amjmed.2021.05.021
* Li Y, Deng C, Li W, et al. ATTR Amyloidosis: Diagnosis and Treatment in Older Patients. *J Geriatr Cardiol*. 2022;19(1):79-90. doi:10.11909/j.issn.1671-5411.2022.01.006
* Basha TA, Manolis AS, Katsanos S, et al. Update on Cardiac Amyloidosis: Novel Therapeutic Approaches for ATTR Amyloid Cardiomyopathy. *Cardiol Rev*. 2023;31(1):1-8. doi:10.1097/CRD.0000000000000431
* Siddiqi OK, Solomon SD. Understanding and Managing Transthyretin Cardiac Amyloidosis in the Elderly. *Curr Cardiol Rep*. 2020;22(2):7. doi:10.1007/s11886-020-1256-4
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