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Also known as: Dopamine; Epinephrine; Norepinephrine; Free Urine Catecholamines
Formal name: Catecholamines, Plasma and Urine
Why Get Tested?
To help diagnose or rule out a pheochromocytoma or other neuroendocrine tumor
When to Get Tested?
When you have symptoms of increased catecholamine release, such as persistent or episodic high blood pressure, severe headaches, rapid heart rate, and sweating
What is being tested?
Catecholamines are a group of similar hormones produced in the adrenal medulla, the interior portion of the adrenal glands. Adrenal glands are small, triangular organs located on top of each kidney. The primary catecholamines are dopamine, epinephrine (adrenaline), and norepinephrine. These hormones are released into the bloodstream in response to physical or emotional stress. They help transmit nerve impulses in the brain, increase glucose and fatty acid release for energy, dilate bronchioles, and dilate the pupils. Norepinephrine also constricts blood vessels, increasing blood pressure, and epinephrine increases heart rate and metabolism. After completing their actions, the hormones are metabolized to inactive compounds. Dopamine becomes homovanillic acid (HVA), norepinephrine breaks down into normetanephrine and vanillylmandelic acid (VMA), and epinephrine becomes metanephrine and VMA. Both the hormones and their metabolites are excreted in the urine.
About 90% of pheochromocytomas are located in the adrenal glands. While a few are cancerous, most are benign and they do not spread beyond their original location, although they may continue to grow. Left untreated, the symptoms may worsen as the tumor grows and, over a period of time, the hypertension that the pheochromocytoma causes may damage the kidneys and heart and raise the risk of an affected patient having a stroke or heart attack.
Urine and plasma catecholamine testing can be used to help detect the presence of pheochromocytomas. Although only about 800 cases a year are diagnosed in the U.S. according to the National Cancer Institute, it is important to diagnose and treat these rare tumors because they cause a potentially curable form of hypertension. In most cases, the tumors can be surgically removed and/or treated to significantly reduce the amount of catecholamines being produced and to reduce or eliminate their associated symptoms and complications.
Catecholamine testing measures the amounts of epinephrine, norepinephrine, and dopamine in the plasma or urine. The plasma test measures the amount of hormone present in the blood at the moment of collection, while the urine test measures the amount excreted over a 24-hour period.
How is the sample collected for testing?
For the 24-hour urine collection, all of your urine should be saved for a 24-hour period. It is important that the sample be refrigerated during this time period.
Plasma catecholamines are collected by inserting a needle into a vein in your arm. Although there is some disagreement over the specifics of how the sample should be collected, you may be asked to lie down and rest quietly for 15 – 30 minutes prior to sample collection, and your blood may be collected while you are lying down. In other circumstances, you may just be seated upright with little or no rest time before the sample collection.
What does the test result mean?Formal name: Catecholamines, Plasma and Urine
Why Get Tested?
To help diagnose or rule out a pheochromocytoma or other neuroendocrine tumor
When to Get Tested?
When you have symptoms of increased catecholamine release, such as persistent or episodic high blood pressure, severe headaches, rapid heart rate, and sweating
What is being tested?
Catecholamines are a group of similar hormones produced in the adrenal medulla, the interior portion of the adrenal glands. Adrenal glands are small, triangular organs located on top of each kidney. The primary catecholamines are dopamine, epinephrine (adrenaline), and norepinephrine. These hormones are released into the bloodstream in response to physical or emotional stress. They help transmit nerve impulses in the brain, increase glucose and fatty acid release for energy, dilate bronchioles, and dilate the pupils. Norepinephrine also constricts blood vessels, increasing blood pressure, and epinephrine increases heart rate and metabolism. After completing their actions, the hormones are metabolized to inactive compounds. Dopamine becomes homovanillic acid (HVA), norepinephrine breaks down into normetanephrine and vanillylmandelic acid (VMA), and epinephrine becomes metanephrine and VMA. Both the hormones and their metabolites are excreted in the urine.
Normally, catecholamines and their metabolites are present in the body in small, fluctuating amounts that only increase appreciably during and shortly after a bout of stress. Pheochromocytomas and other neuroendocrine tumors, however, can produce large amounts of catecholamines, resulting in greatly increased concentrations of the hormones and their metabolites in both the blood and urine. This can cause persistent or episodic bouts of hypertension, which may lead to severe headaches. Other symptoms of catecholamine release include palpitations, sweating, nausea, anxiety, and tingling in the extremities.
About 90% of pheochromocytomas are located in the adrenal glands. While a few are cancerous, most are benign and they do not spread beyond their original location, although they may continue to grow. Left untreated, the symptoms may worsen as the tumor grows and, over a period of time, the hypertension that the pheochromocytoma causes may damage the kidneys and heart and raise the risk of an affected patient having a stroke or heart attack.
Urine and plasma catecholamine testing can be used to help detect the presence of pheochromocytomas. Although only about 800 cases a year are diagnosed in the U.S. according to the National Cancer Institute, it is important to diagnose and treat these rare tumors because they cause a potentially curable form of hypertension. In most cases, the tumors can be surgically removed and/or treated to significantly reduce the amount of catecholamines being produced and to reduce or eliminate their associated symptoms and complications.
Catecholamine testing measures the amounts of epinephrine, norepinephrine, and dopamine in the plasma or urine. The plasma test measures the amount of hormone present in the blood at the moment of collection, while the urine test measures the amount excreted over a 24-hour period.
How is the sample collected for testing?
For the 24-hour urine collection, all of your urine should be saved for a 24-hour period. It is important that the sample be refrigerated during this time period.
Plasma catecholamines are collected by inserting a needle into a vein in your arm. Although there is some disagreement over the specifics of how the sample should be collected, you may be asked to lie down and rest quietly for 15 – 30 minutes prior to sample collection, and your blood may be collected while you are lying down. In other circumstances, you may just be seated upright with little or no rest time before the sample collection.
Since the catecholamine test is sensitive to many outside influences and pheochromocytomas are rare, a doctor may see more false positives with this test than true positives. If a symptomatic patient has large amounts of catecholamines in her blood and/or urine, further investigation is indicated. Serious illnesses and stresses can cause moderate to large temporary increases in catecholamine levels. Doctors must evaluate the patient as a whole - her physical condition, emotional state, medications, and diet. When interfering substances and/or conditions are found and resolved, the doctor will frequently re-test the patient to determine whether the catecholamines are still elevated. The doctor may also order blood and/or urine metanephrine testing to help confirm his findings and imaging tests, such as an MRI, to help find the tumor(s).
If levels are elevated in a patient who has had a previous pheochromocytoma, then it is likely that either treatment was not fully effective or that the tumor is recurring.
If the concentrations of catecholamines are normal in both the plasma and urine, then it is unlikely that a patient has a pheochromocytoma. Pheochromocytomas do not necessarily produce catecholamines at a constant rate, however. If the patient has not had a recent paroxysm of hypertension, their plasma and urine concentrations of catecholamines could be at normal or near normal levels even when a pheochromocytoma is present.
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