Pulmonary hypertension panel
Also known as: Pulmonary veno-occlusive disease, hereditary haemorrhagic telangiectasia« Back to test list
Pulmonary hypertension can be caused by abnormalities of cardiac structure or function, of lung parenchyma, or of the pulmonary vasculature. Within these groups of disorders, there are some autosomal dominant and autosomal recessive conditions which can be caused by heritable mutations in a single gene. Mutations in such genes may cause multi-system disease, allowing a clinical diagnosis to be made. In some patients, the same mutations can cause isolated pulmonary hypertension without any clinical or radiological evidence to indicate which gene is involved. Familial disorders which can cause isolated pulmonary hypertension include primary pulmonary arterial hypertension, pulmonary veno-occlusive disease, and hereditary haemorrhagic telangiectasia. The diagnosis of pulmonary hypertension is made on the basis of clinical history and electrocardiographic findings. Genetic testing is not necessary to make this diagnosis. This test result has implications regarding the aetiology and inheritance of pulmonary hypertension in an individual, and the risk of pulmonary hypertension syndrome and related disorders in a patient’s relatives.
This is an assay for heritable mutations. It may raise issues of ethics or consent that are different from most other investigations ordered in the routine care of a patient.
This test can assist in making a diagnosis in an affected patient. It may also provide useful risk information for unaffected relatives. Testing unaffected people to provide risk information may require that the clinician comply with guidelines provided by professional and regulatory authorities regarding pre-test counselling and consent. In particular, national regulations stipulate that carrier testing of an unaffected child requires the laboratory to have evidence of pre-test counselling by a genetics professional and written consent. For advice or assistance, please contact us on 1800 010 447.
A pathogenic mutation can be found in approximately 80-90% of patients with familial pulmonary arterial hypertension, pulmonary veno-occlusive disease, or hereditary haemorrhagic telangiectasia.
In an affected person, the presence of a pathogenic mutation confirms the diagnosis and may provide additional information regarding the risk of cardiac and non-cardiac manifestations in relatives. However, the absence of a pathogenic mutation in such a patient does not exclude the diagnosis of familial pulmonary hypertension.
In an unaffected person from a family with confirmed genetic diagnosis of familial pulmonary hypertension, the presence of the family’s mutation may indicate an increased risk of developing pulmonary hypertension, and close clinical follow-up may be warranted. The interpretation of such results depends on the particular gene and mutations. Pre-test genetic counselling is strongly recommended.
This test involves analysis of a number of genes. Details of this gene panel and potential incidental findings are summarized here.
Analysis of a gene panel for sequence abnormalities and deletions/duplications.
This test is provided by Bioscientia, a Sonic Healthcare laboratory in Germany. Bioscientia is accredited within Germany and by the College of American Pathology for the provision of medical genetic tests.
This test is usually requested by a cardiologist with experience in the genetic management of cardiac disease or a clinical geneticist.
2-5 mL blood in EDTA. Specimens may be collected by the requesting practitioner or at any Sonic Healthcare pathology collection centre.
To help ensure the quality of the test, a genetic test should be done with a dedicated sample whenever possible i.e. a sample collected specifically for that test rather than a sample that is used for multiple tests.
We also recommend that the patient or another adult check the labelling of request forms and sample tubes.
Please include a statement about family history (or absence of family history) of the disease in clinical details on referral form. If family history is present, please state relationship to patient.