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Low frequency of BMPR2 mutations in a German cohort of patients with sporadic idiopathic pulmonary arterial hypertension
- Source :
- Journal of Medical Genetics. 41:e127-e127
- Publication Year :
- 2004
- Publisher :
- BMJ, 2004.
-
Abstract
- Idiopathic pulmonary arterial hypertension (IPAH; formerly known as primary pulmonary hypertension, PPH) is a rare disorder characterised by pulmonary vascular proliferation and remodelling resulting in loss of patency of the pulmonary arteries. This leads to sustained elevation of pulmonary artery pressures with subsequent progressive right heart failure and often death.1–3 While the majority of cases (>90%) have no known family history of the disease, ∼6% of the cases are known to be familial and are inherited in an autosomal dominant manner with markedly reduced penetrance.4 In previous studies, linkage analysis identified a familial IPAH locus on chromosome 2q33.5,6 Subsequent heterozygous germline mutations in the bone morphogenetic protein receptor, type II (BMPR II) gene ( BMPR2 ) were identified in at least 50% of familial cases.7–9 BMPR-II is a member of the transforming growth factor-β (TGF-β) receptor superfamily signalling pathway, which is critical in both cell differentiation and cell growth mediated through transcriptional regulation.10,11 Interestingly, germline mutations were also identified in 26–40% of sporadic cases.12,13 This study was performed to establish the frequency of BMPR2 mutations in a different population of patients with sporadic IPAH. ### Patients Between March 2002 and January 2004, 99 consecutive non-related patients >20 years of age with IPAH and negative family history were evaluated. In all cases, diagnosis of IPAH was made by experienced and specialised cardiologists or pulmonologists according to WHO criteria.1,14 Other causes of pulmonary hypertension such as illicit drug abuse or anorectic drug use were excluded by careful medical history evaluation. Underlying heart and lung diseases (recurrent pulmonary embolism, connective tissue disease, obstructive or restrictive lung disease) and HIV infection were excluded by a cascade of clinical examinations including laboratory tests, arterial blood gas analysis, chest x ray, pulmonary function tests, echocardiography, ventilation perfusion …
- Subjects :
- Adult
medicine.medical_specialty
Hypertension, Pulmonary
DNA Mutational Analysis
Molecular Sequence Data
Population
Protein Serine-Threonine Kinases
Bone Morphogenetic Protein Receptors, Type II
Pulmonary function testing
Cohort Studies
Gene Frequency
Germany
Internal medicine
medicine.artery
Genetics
medicine
Animals
Humans
Restrictive lung disease
Amino Acid Sequence
education
Genetics (clinical)
education.field_of_study
Lung
Reverse Transcriptase Polymerase Chain Reaction
business.industry
medicine.disease
Connective tissue disease
Pulmonary hypertension
BMPR2
medicine.anatomical_structure
Mutation
Immunology
Pulmonary artery
Cardiology
Online Mutation Report
business
Sequence Alignment
Subjects
Details
- ISSN :
- 14686244
- Volume :
- 41
- Database :
- OpenAIRE
- Journal :
- Journal of Medical Genetics
- Accession number :
- edsair.doi.dedup.....33c0776d61044a25066604fe069489ed
- Full Text :
- https://doi.org/10.1136/jmg.2004.023101