What is the Heart Condition, ATTR-CM? What are the Symptoms?
- Transthyretin amyloid cardiomyopathy (ATTR-CM) is a rare heart condition in which fibers of amyloid protein build up in the heart muscle making it difficult to pump blood.
- Hereditary ATTR-CM involves a mutation of the transthyretin gene, which leads to amyloid deposits in the heart and elsewhere in the body. Wild-type ATTR-CM doesn’t involve a gene mutation and typically starts to cause symptoms when someone is in their 60s or older.
- Symptoms can include shortness of breath, lighteheadedness and decreased exercise endurance.
Transthyretin amyloid cardiomyopathy (ATTR-CM) is a rare heart condition in which fibers of amyloid protein build up in the walls of the heart muscle. As a result, the heart stiffens and becomes unable to relax sufficiently to fill with blood and/or squeeze enough blood out of the heart to meet the body’s needs.
“These proteins that are sitting there do not allow the heart muscle to function as it was designed to function,” says New York cardiologist Dr. Philip Weintraub. “And in fact, they can cause scar tissue that can limit the pump function of the heart.”
He adds that the amyloid fibers can also become arrhythmogenic, meaning they can lead to various heart rhythm disturbances called arrhythmias. For some people with arrhythmias due to ATTR-CM, an implantable defibrillator is necessary to avoid cardiac arrest or other severe complications.
Because ATTR-CM is a rare condition and not especially well understood by many physicians, the actual prevalence of the disease isn’t clear. A 2021 study suggests that 10% of men and 2% of women who have heart failure have the disease because of ATTR-CM. The findings suggest that screening individuals with heart failure, especially older male adults, could identify more people with ATTR-CM who could benefit from proper treatment.
Causes and Types
The amyloid protein in the heart is made of transthyretin, which is known as a “transport protein,” as it carries substances such as thyroid hormone and vitamin A throughout the body.
“Sometimes what happens is that this protein becomes unstable or misshaped in your body,” explains Dr. Aeshita Dwivedi, a cardiologist at Lenox Hill Hospital/Northwell Health. “And when this happens, it can deposit in multiple organs of your body, like your heart, leading to the condition known as transthyretin cardiomyopathy.”
There are two types of ATTR-CM:
- Hereditary ATTR-CM involves a mutation of the transthyretin gene, which leads to amyloid deposits in the heart and elsewhere in the body. It tends to run in families and may cause symptoms to appear starting at age 20 or much later in life. According to the American Heart Association, hereditary ATTR-CM occurs more often in areas of Japan, Portugal, and Sweden, and in the U.S., this type of ATTR-CM affects African Americans at higher rates than other groups.
- Wild-type ATTR-CM doesn’t involve a gene mutation and typically starts to cause symptoms when someone is in their 60s or older. The origins of wild-type ATTR-CM aren’t well understood, and this could mean that the condition is underdiagnosed. An individual with wild-type ATTR-CM may have no symptoms or mild symptoms for a long time, while someone else with the condition may go on to develop severe heart failure.
Males are at higher risk than females for both types of ATTR-CM. And while hereditary ATTR-CM may present with symptoms at a young age, older adults are generally at higher risk for both types.
Symptoms
Because ATTR-CM is directly related to the heart’s ability to effectively pump blood throughout the body, some of the more common symptoms may include those associated with heart failure, including:
- Decreased exercise endurance
- Fluid retention and swelling
- Lightheadedness and fainting
- Shortness of breath
“You could have lightheadedness,” Dr. Weintraub adds. “You could have fatigue, but a lot of that is based upon the fact that without the necessary oxygen that needs to be in your bloodstream, it’ll compromise the body’s ability to function properly. The heart works best when it’s enriched with oxygen and nutrients, and to deprive the heart of that leads to a compromised lifestyle.”
ATTR-CM also tends to bring on problems such as an enlarged heart and arrhythmia, such as atrial fibrillation. ATTR-CM is an unusual heart condition in that some common symptoms appear to have little to do with the heart and circulation. For example, carpal tunnel syndrome is present in about half of people with ATTR-CM, according to a 2019 study in the Journal of the American College of Cardiology.
“When the protein deposits in your nervous system, patients may develop condition called neuropathy, commonly this presents with carpal tunnel syndrome or spinal stenosis,” Dr. Dwivedi says. “A lot of patients may also find that their blood pressure becomes variable.”
And because ATTR-CM can involve other organs and the nervous system, it’s not unusual to experience other symptoms, such as:
- Abdominal pain
- Balance problems
- Constipation
- Muscle impairment
- Vision problems
A 2021 study involving two focus groups with the condition noted that individuals with ATTR-CM reported 26 different and wide-ranging symptoms. They also told researchers that their symptoms had significant impacts on their quality of life. “There can be many side effects, because it is a systemic disease,” Dr. Weintraub says.
Questions to Ask Your Doctor
- If you have a relative with ATTR-CM, or who was diagnosed with heart failure, ask your doctor about genetic testing to determine whether you are at risk for hereditary ATTR-CM
- What are my treatment options for ATTR-CM?
- Am I at risk for other conditions because of my ATTR-CM?
- Should I get a second opinion?
Learn more about SurvivorNet's rigorous medical review process.
James Roland has been a health journalist since 2007, not long after his father died of non-Hodgkin’s lymphoma. Read More
What is the Heart Condition, ATTR-CM? What are the Symptoms?
- Transthyretin amyloid cardiomyopathy (ATTR-CM) is a rare heart condition in which fibers of amyloid protein build up in the heart muscle making it difficult to pump blood.
- Hereditary ATTR-CM involves a mutation of the transthyretin gene, which leads to amyloid deposits in the heart and elsewhere in the body. Wild-type ATTR-CM doesn’t involve a gene mutation and typically starts to cause symptoms when someone is in their 60s or older.
- Symptoms can include shortness of breath, lighteheadedness and decreased exercise endurance.
Transthyretin amyloid cardiomyopathy (ATTR-CM) is a rare heart condition in which fibers of amyloid protein build up in the walls of the heart muscle. As a result, the heart stiffens and becomes unable to relax sufficiently to fill with blood and/or squeeze enough blood out of the heart to meet the body’s needs.
“These proteins that are sitting there do not allow the heart muscle to function as it was designed to function,” says New York cardiologist Dr. Philip Weintraub. “And in fact, they can cause scar tissue that can limit the pump function of the heart.”
Read More He adds that the amyloid fibers can also become arrhythmogenic, meaning they can lead to various heart rhythm disturbances called arrhythmias. For some people with arrhythmias due to ATTR-CM, an implantable defibrillator is necessary to avoid cardiac arrest or other severe complications.
Because ATTR-CM is a rare condition and not especially well understood by many physicians, the actual prevalence of the disease isn’t clear. A 2021 study suggests that 10% of men and 2% of women who have heart failure have the disease because of ATTR-CM. The findings suggest that screening individuals with heart failure, especially older male adults, could identify more people with ATTR-CM who could benefit from proper treatment.
Causes and Types
The amyloid protein in the heart is made of transthyretin, which is known as a “transport protein,” as it carries substances such as thyroid hormone and vitamin A throughout the body.
“Sometimes what happens is that this protein becomes unstable or misshaped in your body,” explains Dr. Aeshita Dwivedi, a cardiologist at Lenox Hill Hospital/Northwell Health. “And when this happens, it can deposit in multiple organs of your body, like your heart, leading to the condition known as transthyretin cardiomyopathy.”
There are two types of ATTR-CM:
- Hereditary ATTR-CM involves a mutation of the transthyretin gene, which leads to amyloid deposits in the heart and elsewhere in the body. It tends to run in families and may cause symptoms to appear starting at age 20 or much later in life. According to the American Heart Association, hereditary ATTR-CM occurs more often in areas of Japan, Portugal, and Sweden, and in the U.S., this type of ATTR-CM affects African Americans at higher rates than other groups.
- Wild-type ATTR-CM doesn’t involve a gene mutation and typically starts to cause symptoms when someone is in their 60s or older. The origins of wild-type ATTR-CM aren’t well understood, and this could mean that the condition is underdiagnosed. An individual with wild-type ATTR-CM may have no symptoms or mild symptoms for a long time, while someone else with the condition may go on to develop severe heart failure.
Males are at higher risk than females for both types of ATTR-CM. And while hereditary ATTR-CM may present with symptoms at a young age, older adults are generally at higher risk for both types.
Symptoms
Because ATTR-CM is directly related to the heart’s ability to effectively pump blood throughout the body, some of the more common symptoms may include those associated with heart failure, including:
- Decreased exercise endurance
- Fluid retention and swelling
- Lightheadedness and fainting
- Shortness of breath
“You could have lightheadedness,” Dr. Weintraub adds. “You could have fatigue, but a lot of that is based upon the fact that without the necessary oxygen that needs to be in your bloodstream, it’ll compromise the body’s ability to function properly. The heart works best when it’s enriched with oxygen and nutrients, and to deprive the heart of that leads to a compromised lifestyle.”
ATTR-CM also tends to bring on problems such as an enlarged heart and arrhythmia, such as atrial fibrillation. ATTR-CM is an unusual heart condition in that some common symptoms appear to have little to do with the heart and circulation. For example, carpal tunnel syndrome is present in about half of people with ATTR-CM, according to a 2019 study in the Journal of the American College of Cardiology.
“When the protein deposits in your nervous system, patients may develop condition called neuropathy, commonly this presents with carpal tunnel syndrome or spinal stenosis,” Dr. Dwivedi says. “A lot of patients may also find that their blood pressure becomes variable.”
And because ATTR-CM can involve other organs and the nervous system, it’s not unusual to experience other symptoms, such as:
- Abdominal pain
- Balance problems
- Constipation
- Muscle impairment
- Vision problems
A 2021 study involving two focus groups with the condition noted that individuals with ATTR-CM reported 26 different and wide-ranging symptoms. They also told researchers that their symptoms had significant impacts on their quality of life. “There can be many side effects, because it is a systemic disease,” Dr. Weintraub says.
Questions to Ask Your Doctor
- If you have a relative with ATTR-CM, or who was diagnosed with heart failure, ask your doctor about genetic testing to determine whether you are at risk for hereditary ATTR-CM
- What are my treatment options for ATTR-CM?
- Am I at risk for other conditions because of my ATTR-CM?
- Should I get a second opinion?
Learn more about SurvivorNet's rigorous medical review process.
James Roland has been a health journalist since 2007, not long after his father died of non-Hodgkin’s lymphoma. Read More