Lung symptoms in pseudohypoaldosteronism type 1 are associated with deficiency of the α-subunit of the epithelial sodium channel

• Published in: The Journal of pediatrics 1999-12, Vol.135 (6), p.739-745
• Main Authors: Schaedel, Charlotta, Marthinsen, Lars, Kristoffersson, Ann-Charlotte, Kornfält, Ragnhild, Nilsson, Karl Olof, Orlenius, Bo, Holmberg, Lars
• Format: Article
• Language: English
• Subjects: Adrenals. Adrenal axis. Renin-angiotensin system (diseases); Biological and medical sciences; Child, Preschool; Endocrinopathies; Epithelium; Female; Humans; Lung Diseases - etiology; Lung Diseases - genetics; Medical sciences; Mutation; Non tumoral diseases. Target tissue resistance. Benign neoplasms; Polymorphism, Single-Stranded Conformational; Pseudohypoaldosteronism - complications; Pseudohypoaldosteronism - genetics; Sequence Analysis, DNA; Sodium Channels - deficiency; Sodium Channels - genetics
• ISSN: 0022-3476; 1097-6833
• DOI: 10.1016/S0022-3476(99)70094-6

Objective: To study patients with autosomal recessive pseudohypoaldosteronism type 1 and to relate pulmonary disease to gene mutations of the epithelial sodium channel (ENaC). Study design: Clinical and laboratory data were collected from 4 Swedish patients with pseudohypoaldosteronism type 1. The genes for ENaC and cystic fibrosis transmembrane conductance regulator were analyzed for mutations with methods including DNA sequencing. Results: Three novel mutations were found in the α-gene of ENaC, 2 frameshifts (1449delC and 729delA) and 1 missense mutation resulting in the substitution of leucine for serine 562 in the α-chain (S562L). The 1449delC mutation was found in all patients in either homozygous or heterozygous form and seems to be the predominant cause of pseudohypoaldosteronism in Sweden. The allele coding for S562L also contained a transition converting tryptophan 493 to arginine (W493R), which seems to be a rare polymorphism. All patients had pulmonary symptoms to various degrees. The bacterial findings resembled, to some extent, those in cystic fibrosis, but development of chronic lung disease and progressive decline in lung function were not observed. Conclusions: Genetic deficiencies of the α subunit of the ENaC are associated with prominent lung symptoms, which are, however, clearly different from those in cystic fibrosis. (J Pediatr 1999;135:739-45)