03/24/2015 11:30 PM EDT
Source: National Library of Medicine
Related MedlinePlus Page: Pulmonary Hypertension
Related MedlinePlus Page: Pulmonary Hypertension
Pulmonary veno-occlusive disease
What is pulmonary veno-occlusive disease?
Pulmonary veno-occlusive disease (PVOD) is characterized by the blockage (occlusion) of the blood vessels that carry oxygen-rich (oxygenated) blood from the lungs to the heart (the pulmonary veins). The occlusion is caused by a buildup of abnormal fibrous tissue in the small veins in the lungs, which narrows the vessels and impairs blood flow. Because blood flow through the lungs is difficult, pressure rises in the vessels that carry blood that needs to be oxygenated to the lungs from the heart (the pulmonary arteries). Increased pressure in these vessels is known as pulmonary arterial hypertension.
The problems with blood flow in PVOD also impair the delivery of oxygenated blood to the rest of the body, which leads to the signs and symptoms of the condition. Shortness of breath (dyspnea) and tiredness (fatigue) during exertion are the most common symptoms of this condition. Other common features include dizziness, a lack of energy (lethargy), difficulty breathing when lying down, and a cough that does not go away. As the condition worsens, affected individuals can develop a bluish tint to the skin (cyanosis), chest pains, fainting spells, and an accumulation of fluid in the lungs (pulmonary edema).
Certain features commonly seen in people with PVOD can be identified using a test called a CT scan. One of these features, which is seen in the lungs of affected individuals, is an abnormality described as centrilobular ground-glass opacities. Affected individuals also have abnormal thickening of certain tissues in the lungs, which is described as septal lines. In addition, lymph nodes in the chest (mediastinal lymph nodes) are abnormally enlarged in people with PVOD.
PVOD can begin at any age, and the blood flow problems worsen over time. Because of the increased blood pressure in the pulmonary arteries, the heart must work harder than normal to pump blood to the lungs, which can eventually lead to fatal heart failure. Most people with this severe disorder do not live more than 2 years after diagnosis.
Read more about pulmonary arterial hypertension.
How common is pulmonary veno-occlusive disease?
The exact prevalence of PVOD is unknown. Many cases are likely misdiagnosed as idiopathic pulmonary arterial hypertension, which is increased blood pressure in the pulmonary arteries without a known cause. Research suggests that 5 to 25 percent of people diagnosed with idiopathic pulmonary arterial hypertension have PVOD. Based on these numbers, PVOD is thought to affect an estimated 1 to 2 per 10 million people.
What genes are related to pulmonary veno-occlusive disease?
The primary genetic cause of PVOD is mutations in the EIF2AK4 gene. Mutations in other genes may cause a small percentage of cases. Other suspected causes of PVOD include viral infection and exposure to toxic chemicals, including certain chemotherapy drugs.
The protein produced from the EIF2AK4 gene helps cells respond appropriately to changes that could damage the cell. For example, when the level of protein building blocks (amino acids) in a cell falls too low, the activity of the EIF2AK4 protein helps reduce the production of other proteins, which conserves amino acids. The EIF2AK4 gene mutations involved in PVOD likely eliminate functional EIF2AK4 protein; however, it is unknown how absence of this protein's function leads to the pulmonary vessel abnormalities that underlie PVOD.
Read more about the EIF2AK4 gene.
See a list of genes associated with pulmonary veno-occlusive disease.
How do people inherit pulmonary veno-occlusive disease?
When caused by mutations in the EIF2AK4 gene, PVOD is inherited in an autosomal recessive pattern, which means both copies of the gene in each cell have mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene, but they typically do not show signs and symptoms of the condition.
In contrast, when caused by mutations in the BMPR2 gene, PVOD has an autosomal dominant pattern of inheritance, which means one copy of the altered gene in each cell is sufficient to cause the disorder. Affected individuals typically have one parent with increased blood pressure in the vessels of the lungs.
Where can I find information about diagnosis or management of pulmonary veno-occlusive disease?
These resources address the diagnosis or management of pulmonary veno-occlusive disease and may include treatment providers.
You might also find information on the diagnosis or management of pulmonary veno-occlusive disease in Educational resources and Patient support.
General information about the diagnosis and management of genetic conditions is available in the Handbook. Read more about genetic testing, particularly the difference between clinical tests and research tests.
To locate a healthcare provider, see How can I find a genetics professional in my area? in the Handbook.
Where can I find additional information about pulmonary veno-occlusive disease?
You may find the following resources about pulmonary veno-occlusive disease helpful. These materials are written for the general public.
- MedlinePlus - Health information (3 links)
- Additional NIH Resources - National Institutes of Health
- Educational resources - Information pages (3 links)
- Patient support - For patients and families (5 links)
You may also be interested in these resources, which are designed for healthcare professionals and researchers.
- Genetic Testing Registry - Repository of genetic test information (1 link)
ClinicalTrials.gov- Linking patients to medical research PubMed- Recent literature
- OMIM - Genetic disorder catalog (2 links)
What other names do people use for pulmonary veno-occlusive disease?
- isolated pulmonary venous sclerosis
- obstructive disease of the pulmonary veins
- pulmonary venoocclusive disease
- venous form of primary pulmonary hypertension
For more information about naming genetic conditions, see the Genetics Home Reference Condition Naming Guidelines and How are genetic conditions and genes named? in the Handbook.
What if I still have specific questions about pulmonary veno-occlusive disease?
Where can I find general information about genetic conditions?
The Handbook provides basic information about genetics in clear language.
- What does it mean if a disorder seems to run in my family?
- What are the different ways in which a genetic condition can be inherited?
- If a genetic disorder runs in my family, what are the chances that my children will have the condition?
- Why are some genetic conditions more common in particular ethnic groups?
These links provide additional genetics resources that may be useful.
What glossary definitions help with understanding pulmonary veno-occlusive disease?
acids ; arteries ; autosomal ; autosomal dominant ; autosomal recessive ; cell ; chemotherapy ;CT scan ; cyanosis ; diagnosis ; dyspnea ; edema ; fainting ; gene ; heart failure ; hypertension ;idiopathic ; infection ; inheritance ; inherited ; lethargy ; lymph ; obstructive ; occlusion ; oxygen ;pattern of inheritance ; prevalence ; protein ; pulmonary ; recessive ; sclerosis ; stress ; tissue ; toxic ;veins ; venoocclusive disease ; veno-occlusive disease
You may find definitions for these and many other terms in the Genetics Home Reference Glossary.
See also Understanding Medical Terminology.
References (4 links)
The resources on this site should not be used as a substitute for professional medical care or advice. Users seeking information about a personal genetic disease, syndrome, or condition should consult with a qualified healthcare professional. See How can I find a genetics professional in my area? in the Handbook
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