- What causes polycythemia?
- What are the causes of primary polycythemia?
- What are the common causes of secondary polycythemia?
- Can other sources of erythropoietin (EPO) cause polycythemia?
- Patient Comments: Polycythemia (High Red Blood Cell Count) - Cause
- Patient Comments: Polycythemia - Experience
- Patient Comments: Polycythemia - Symptoms
- Patient Comments: Polycythemia - Treatment
Polycythemia (high red blood cell count) definition and facts
- Polycythemia means increased red blood cell volume.
- Polycythemia is divided into two main categories; primary and secondary.
- Polycythemia can be linked to secondary causes, such as, chronic hypoxia or tumors releasing erythropoietin.
- Abnormally increased red cell production in the bone marrow causes polycythemia vera.
- Treatment of secondary polycythemia is dependent on the underlying condition.
- Polycythemia is treated by phlebotomy (controlled blood letting) and hydroxyurea.
What is polycythemia?
Polycythemia is a condition that results in an increased level of circulating red blood cells in the bloodstream. People with polycythemia have an increase in hematocrit, hemoglobin, or red blood cell count above the normal limits.
Polycythemia is normally reported in terms of increased hematocrit (hematocrit is the ratio of the volume of red blood cells to the total volume of blood) or hemoglobin concentration (hemoglobin is a protein responsible for transporting oxygen in the blood).
- Hematocrit (HCT): Polycythemia is considered when the hematocrit is greater than 48% in women and 52% in men.
- Hemoglobin (HGB): Polycythemia is considered when there is a hemoglobin level of greater than 16.5g/dL in women or hemoglobin level greater than18.5 g/dL in men.
Polycythemia can be divided into two categories: primary and secondary.
- Primary polycythemia: In primary polycythemia the increase in red blood cells is caused by inherent problems in the process of red blood cell production.
- Secondary polycythemia: Secondary polycythemia generally occurs as a response to other factors or underlying conditions that promote red blood cell production.
Red cell production (erythropoiesis) takes place in the bone marrow through a complex sequence of tightly regulated steps. The main regulator of the red cell production is the hormone erythropoietin (EPO). This hormone is largely secreted by the kidneys, although, about 10% may be produced and secreted by the liver.
Erythropoietin secretion is up-regulated in response to low oxygen levels (hypoxia) in the blood. More oxygen can be carried to tissues when erythropoietin stimulates red blood cell production in the bone marrow to compensate for the hypoxia.
Neonatal (newborn) polycythemia can be seen in 1% to 5% of newborns. The most common causes may be related to transfusion of blood, transfer of placental blood to the infant after delivery, or chronic inadequate oxygenation of the fetus (intrauterine hypoxia) due to placental insufficiency.
What are normal ranges of hematocrit, red cell counts, and hemoglobin?
Red blood cell count ranges
- Hematocrit is the ratio of the volume of red cells to the volume of whole blood. The normal range for hematocrit varies between sexes and is approximately 45% to 52% for men and 37% to 48% for women.
- Red cell count signifies the number of red blood cells in a volume of blood. The normal range in men is approximately 4.7 to 6.1 million cells/ul (microliter). The normal range in women ranges from 4.2 to 5.4 million cells/ul, according to NIH (National Institutes of Health) data.
- Hemoglobin is a protein in the red blood cells that carries oxygen and gives blood its red color. The normal range for hemoglobin may differ between the sexes and is approximately 13 to 18 grams per deciliter for men and 12 to 16 grams per deciliter for women.
What causes polycythemia?
Causes of polycythemia are primary or secondary. In primary polycythemia, abnormalities in red blood cell production cause an increase in red cell count. In secondary polycythemia, factors external to red blood cell production (for example, hypoxia, sleep apnea, certain tumors) result in polycythemia.
What are the causes of primary polycythemia?
Primary polycythemias are due to acquired or inherited genetic mutations causing abnormally high levels of red blood cell precursors. Primary familial and congenital polycythemia (PFCP) and polycythemia vera (PV) are in this category.
Polycythemia vera is a rare condition. One study indicated that there were 65,243 patients with PV in the United States in 2003. Polycythemia vera is typically associated with an elevated white blood cell count (leukocytosis) and platelet count (thrombocytosis). An enlarged spleen (splenomegaly) and low erythropoietin levels are other clinical features of polycythemia vera.
Until recently, the exact mechanism of polycythemia vera was not well understood. In 2005, genetic mutations of the JAK2 gene were found to be responsible for most cases of polycythemia vera. These mutations are thought to possibly increase the sensitivity of the red blood cell precursors to erythropoietin, thereby, increasing red blood cell production.
Primary familial and congenital polycythemia (PFCP)
Primary familial and congenital polycythemia (PFCP) is also thought to be caused by genetic mutations resulting in increased responsiveness to normal levels of erythropoietin. Most cases are caused by different mutations to the EPOR gene.
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What are the common causes of secondary polycythemia?
Secondary polycythemia is usually caused by increased erythropoietin (EPO) production either in response to chronic hypoxia (low blood oxygen level) or from an erythropoietin secreting tumor.
Common conditions causing chronic hypoxia are chronic lung diseases such as:
- emphysema and chronic bronchitis which are collectively known as chronic obstructive pulmonary disease (COPD) or hypoventilation syndrome,
- chronic heart diseases (congestive heart failure, or abnormal flow of blood from the right side to the left side of the heart),
- sleep apnea, and
- pulmonary hypertension.
Abnormal blood flow to the kidneys can be perceived by the kidneys as decreased oxygenation (renal hypoxia), even though, other tissues may have normal oxygenation. Renal hypoxia may promote an increase in erythropoietin production. This condition can occur after kidney transplantation or narrowing of renal arteries (blood vessels supplying the kidneys).
People living in high altitudes can develop polycythemia. In high altitudes, increased red blood cell production occurs in order to compensate for the low ambient oxygen levels and inadequate tissue oxygenation.
Rare congenital defects in the hemoglobin molecule, such as 2, 3-BPG deficiency, can result in a higher oxygen affinity by hemoglobin. In these conditions, oxygen is held on tightly by hemoglobin and is less readily released from hemoglobin to the tissues. The resulting tissue hypoxia from poor oxygen delivery may lead to polycythemia.
Erythropoietin secreting tumors
Certain tumors can release an increased amount of erythropoietin. The most common erythropoietin secreting tumors are:
- liver cancer (hepatocellular carcinoma),
- kidney cancer (renal cell carcinoma),
- adrenal adenoma (adenocarcinomas), and
- uterine (womb) tumors.
A rare genetic condition, called Chuvash polycythemia, causes increased activity of the gene that produces erythropoietin. The overproduction of erythropoietin causes polycythemia.
Can other sources of erythropoietin (EPO) cause polycythemia?
Erythropoietin (EPO) has been made synthetically for clinical treatment of certain types of anemia. Some professional athletes have used this type of injectable EPO (blood doping) to improve their performance in competitions by producing more hemoglobin and, therefore, improving the delivery of oxygen to their tissues, mainly muscles. This type of doping practice is banned by many professional sport committees.
What is relative polycythemia?
In some forms of secondary polycythemia, the hemoglobin or red blood cell count is perceived to be abnormally high due to an increased concentration of blood. This can happen as a result of plasma volume loss from dehydration, severe vomiting or diarrhea, or excessive sweating. Polycythemia in these situations may be called relative polycythemia, because the actual numbers of red blood cells are not abnormal.
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What are the risk factors for polycythemia?
Polycythemia risk factors
- Hypoxia from long standing (chronic) lung disease and smoking are common causes of polycythemia. Therefore, smoking can be a significant risk factor for polycythemia.
- Chronic carbon monoxide (CO) exposure can also be a risk factor for polycythemia. Hemoglobin has a higher affinity for CO than for oxygen; therefore, as it replaces oxygen in favor of CO, polycythemia may ensue to compensate for the low oxygen carried by hemoglobin.
- Chronic carbon monoxide exposure is a risk factor for people working in underground tunnels or parking garages, cab drivers in highly polluted and congested cities, or workers in factories with exposure to engine exhaust.
- People living at high altitudes may also be at risk of developing polycythemia due to low environmental oxygen levels.
- People with genetic mutations and familial types of polycythemia and certain hemoglobin abnormalities also carry risk factors for this condition as mentioned in earlier sections.
What is stress polycythemia?
Stress polycythemia is a term applied to a chronic (long-standing) state of low plasma volume, which is seen commonly in active, hard-working, anxious, middle-aged men. In these people, the red blood cell volume is normal, but the plasma volume is low. This condition is also known as Gaisbock's disease, stress erythrocytosis, or pseudopolycythemia.
Smoker's polycythemia is a similar condition in which increased levels of deoxygenated hemoglobin (hemoglobin that does not carry oxygen, instead carrying carbon dioxide) causes an increase in red blood cell counts.
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What are the symptoms of polycythemia?
Symptoms of polycythemia can be none to minimal in many people. Some general and non-specific polycythemia symptoms include:
In patients with polycythemia vera, other blood disorders are also very common. Thus, bleeding problems or clotting events may occur in these patients. Itching after showers or baths (post-bath pruritus) can also occur in patients with polycythemia vera for unclear reasons. Joint pains also are common in patients with polycythemia vera. Tender redness of the palms and soles is called erythromelalgia.
Symptoms of secondary polycythemia may be more closely attributed to the underlying condition, such as, chronic lung disease, than to polycythemia itself. Therefore, shortness of breath, chronic cough, sleep disturbance (sleep apnea), dizziness, poor exercise tolerance, or fatigue may be common in patients with polycythemia.
If polycythemia is related to kidney cancer, liver cancer, or other erythropoietin secreting tumors, the symptoms of these conditions -- such as, weight loss, abdominal pain or fullness, or jaundice -- may be predominant.
When should I see a doctor about polycythemia?
In cases of unstoppable bleeding (hemorrhage), severe breathing difficulty, shortness of breath, or symptoms suggestive of a stroke (weakness on one side or difficulty speaking, for example), seek a prompt evaluation by a physician or make an immediate visit to the emergency room.
People with polycythemia are seen routinely based on the recommendation of the treating doctor. Commonly these patients are seen by their primary care physicians, internists, lung doctors (pulmonologists), or blood specialists (hematology oncology).
How do doctors diagnose the condition?
Polycythemia may be diagnosed incidentally on routine blood work. Hemoglobin, hematocrit, and red blood cell concentration are typically found on a complete blood count (CBC). Repeating the laboratory tests (blood work) to confirm the diagnosis is usually advised to rule out possible laboratory or drawing errors.
More importantly, the cause of polycythemia needs to be determined. Medical history and physical examination are important components of the evaluation of polycythemia. The history usually includes questions about smoking history, living at high altitudes for extended periods, breathing difficulties, sleep disturbances, or chronic cough. Other parts of the history may focus on a prior diagnosis of lung disease, heart disease, kidney or liver cancer, bleeding or clotting problems.
A complete physical examination -- including the assessment of body habitus (stature), vital signs, oxygen saturation, heart and lung exams, and evaluating for an enlarged spleen (splenomegaly) -- is essential in the evaluation of people with polycythemia.
Evidence of a long-standing low body oxygen level (chronic hypoxia) is an important clue in patients with polycythemia. Signs of long-standing hypoxia may include cyanosis (blue or purple appearing finger, nail, earlobes, or lips), clubbing of the fingers (elevation of the nail beds outward), or pursed lip breathing. Redness of the palms and soles may be another sign of polycythemia.
A chest X-ray, electrocardiogram (EKG), and echocardiogram may be performed to screen for lung disease or heart disease. Hemoglobin analysis may be necessary if conditions with high affinity for oxygen or 2, 3-BPG deficiency are suspected. If carbon monoxide poisoning is in question, a blood test can detect its level.
Erythropoietin (EPO) blood levels may also be helpful, although the results need to be interpreted carefully, as the level may be high in response to chronic hypoxia. In polycythemia vera, the EPO levels are low as a response to an increased production of red blood cells. In tumors secreting erythropoietin, the EPO levels may be abnormally high.
Polycythemia vera diagnosis
The diagnosis of polycythemia vera requires special attention. There have been traditional diagnostic criteria for this condition. However, in 2008, the World Health Organization (WHO) established the most recent guidelines. The guidelines include major and minor criteria.
- The major criteria for polycythemia vera include a hemoglobin level of greater than 18.5 gram / deciliter in men or 16.5 gram / deciliter in women (or similar numbers based on the hematocrit) and the presence of JAK2 mutation.
- The minor criteria include bone marrow evidence of increased red blood cell production and decreased EPO levels.
What is the treatment for polycythemia?
The treatment for polycythemia is generally dependent on the cause.
In polycythemia vera or other primary polycythemia syndromes, the treatment options are more specific. Phlebotomy (drawing blood or blood letting) is the most essential part of the treatment. The recommended hematocrit of less than 45 in men and less than 42 in women is the goal of phlebotomy.
Several medications have been considered in conjunction with phlebotomy to suppress the abnormal production of red blood cells. Most of these chemotherapeutic drugs have been linked with side effects and their use has been controversial and limited.
The medication hydroxyurea (Hydrea) has been recommended for some patients with primary polycythemia and higher risk of blood clot formation due to high blood viscosity. The factors favoring treatment with hydroxyurea are age greater than 70, platelet count greater than 1.5 million, and general cardiovascular risk factors.
Aspirin and other anti-platelet agents (dipyridamole [Persantine]) may also be beneficial in patients with polycythemia by reducing clotting complications, unless the patient has a history of bleeding problems.
In patients with secondary polycythemia, the goal is to treat the underlying condition. For example, in patients with lung or heart disease with hypoxia, appropriate management of these conditions along with oxygen supplementation is generally advised.
What are the complications of polycythemia?
Potential complications of polycythemia vera are increased levels of circulating red blood cells, which increase the thickness or viscosity of the blood. This can be associated with higher risk of thrombus or clot formation leading to strokes, heart attacks, pulmonary embolism, and possibly death.
Another complication of polycythemia vera is the potential transformation into a blood cancer (leukemia), excessive bleeding (hemorrhage), or clotting problems.
Because of high turnover of blood cells in polycythemia, the excretion of the byproducts of red blood cell degradation may overburden the kidneys and result in kidney dysfunction, kidney stones, and gout.
Complications of secondary polycythemia are typically related to those of the underlying disease. For example, chronic hypoxia from severe lung disease may be complicated by right-sided heart failure and pulmonary hypertension. Chronic heart failure can lead to generalized swelling or edema (anasarca), low blood pressure, kidney dysfunction, and poor functional status.
In neonatal (infant) polycythemia, increased blood thickness or viscosity can affect several organs due to poor blood flow. As a result, kidney dysfunction, intestinal problems, increased blood pressure in the lungs, and hypoxia may ensue.
Is it possible to prevent polycythemia?
- Polycythemia due to a secondary cause such as long-standing smoking or exposure to carbon monoxide can be prevented by omitting these risks.
- Reducing risk factors for heart failure -- such as, controlling high blood pressure and diabetes mellitus -- can potentially reduce the risk of polycythemia.
- Congenital and primary polycythemia disorders, however, are not preventable.
What is the outlook (prognosis) for polycythemia?
Polycythemia life expectancy
The outlook on polycythemia depends on the underlying cause. Overall, the general outlook is favorable for people with this condition, especially those with secondary causes. The outlook for primary polycythemia is fair. While it is typically incurable and long standing, for many people, it is controllable and treatable. For example, untreated, polycythemia vera (PV) was initially thought to have a poor prognosis with a life expectancy of one to two years from the time of diagnosis. However, polycythemia vera prognosis is now greatly improved to 10 to 15 years survival after diagnosis with treatment by phlebotomy alone. The addition of medications, such as, hydroxyurea or aspirin may improve survival even more.
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Ma X, Vanasse G, Cartmel B, Wang Y, Selinger HA. Prevalence of polycythemia vera and essential thrombocythemia.Am J Hematol. 2008 May;83(5):359-62. doi: 10.1002/ajh.21129. Yale University School of Medicine, New Haven, Connecticut, USA.
Nagalla, S. "Polycythemia Vera." Medscape. Updated: June 1, 2018.
Nagalla, S. "Secondary Polycythemia." Medscape. Updated: Dec. 20, 2018.
Spivak, JL, Silver, RT, The revised World Health Organization diagnostic criteria for polycythemia vera, essential thrombocytosis, and primary myelofibrosis: an alternative proposal. (2008) 112:231-239.
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