Understanding Amyloidosis: Causes, Risk Factors, and Symptoms

July. 16,2025

Amyloidosis is a rare condition involving abnormal protein deposits in organs, which can cause severe health issues including organ failure. Risk factors include age, genetics, and chronic diseases. Symptoms vary based on affected tissues and include heart irregularities, neurological symptoms, and organ dysfunction. While incurable, treatments focus on managing symptoms and preventing progression. Early diagnosis is crucial for better management. This overview covers the causes, risk factors, and symptoms associated with amyloidosis, emphasizing the importance of medical consultation.

Understanding Amyloidosis: Causes, Risk Factors, and Symptoms

Understanding Amyloidosis: Causes, Risk Factors, and Symptoms

Amyloidosis is a rare disorder characterized by the accumulation of abnormal protein deposits called amyloid in various organs. This protein is produced in the bone marrow and can build up in tissues such as the heart, liver, spleen, nervous system, and digestive tract. The severity depends on the extent of organ involvement, potentially leading to organ failure, which can be life-threatening.

The condition can develop in anyone, with symptoms varying based on affected organs. It primarily impacts kidney function—causing protein leakage—and impairs cardiac health, leading to breathing difficulties. Nervous system symptoms include numbness and tingling in extremities. Certain factors, like age and underlying health conditions, increase risk.

Amyloidosis Causes and Symptoms
Older adults, especially those aged 60-70 years, are more prone to AL amyloidosis, caused by abnormal immune proteins from the bone marrow. Genetic factors may also play a role. People with chronic infections or inflammatory diseases are at higher risk of AA amyloidosis. Men are more frequently affected, and dialysis patients may develop amyloidosis due to protein buildup. Specific types include:

AL Amyloidosis: The most common form, affecting organs like kidneys, heart, skin, and nerves, resulting from abnormal antibody production in the bone marrow.

Hereditary Amyloidosis: An inherited form linked to genetic mutations, affecting organs similarly but with variable progression depending on genetic factors.

Dialysis-Related Amyloidosis: Occurs after prolonged dialysis, caused by protein deposits in tendons and joints, leading to stiffness and conditions like carpal tunnel syndrome.

AA Amyloidosis: Often secondary to chronic inflammatory diseases like rheumatoid arthritis, impacting multiple organs such as the kidneys and liver.

Symptoms may initially be silent but become apparent as the disease progresses. Common signs include irregular heartbeat, unexplained weight loss, skin changes, numbness, weakness, tongue enlargement, digestive issues, breathing difficulties, and joint swelling. While there is no cure, treatments aim to control symptoms and reduce amyloid production.