Abstract
Background: It has long been debated whether patients with atrial septal defect (ASD) Eisenmenger syndrome have idiopathic pulmonary arterial hypertension with an incidental ASD or severe pulmonary hypertension on the basis of their ASD shunt magnitude alone. Hyphothesis: It was hypothesized that if ASD Eisenmenger patients had idiopathic pulmonary arterial hypertension with an incidental ASD, a mutation in the bone morphogenetic protein receptor-2 (BMPR2) would be found in some of these patients. Patients and methods: All adult patients with ASD Eisenmenger syndrome were identified from the databases of two adult congenital cardiac units, and were matched to a control group with similar types of ASDs and no pulmonary hypertension. Gene coding for BMPR2 was examined for mutation using denaturing high-performance liquid chromatography of the entire coding sequence. Results: Eighteen adult patients with ASD Eisenmenger syndrome and 18 control patients were identified. ASD Eisenmenger patients had significantly larger ASDs than the control patients (3.7±1.2 cm versus 1.9±0.7 cm, P
| Original language | English |
|---|---|
| Pages (from-to) | 1133-1136 |
| Number of pages | 3 |
| Journal | The Canadian journal of cardiology |
| Volume | 22 |
| Issue number | 13 |
| Publication status | Published - Nov 2006 |
Keywords
- Atrial septal defect
- Genetics
- Pulmonary hypertension