Aldosterone signaling defect in young infants: single-center report and review

• Published in: BMC endocrine disorders Vol. 21; no. 1; p. 149
• Main Authors: Wijaya, Melati, Ma, Huamei, Zhang, Jun, Du, Minlian, Li, Yanhong, Chen, Qiuli, Guo, Song
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 09.07.2021; BioMed Central; BMC
• Subjects: Acidosis; Adrenal disease; Adrenal Hyperplasia, Congenital - etiology; Adrenal Hyperplasia, Congenital - metabolism; Adrenal Hyperplasia, Congenital - pathology; Aldosterone; Aldosterone - metabolism; Aldosterone synthase; Aldosterone synthase deficiency; Biomarkers - blood; Birth weight; Cardiac patients; Case studies; Child, Preschool; Corticosteroids; Cytochrome P-450; Cytochrome P-450 CYP11B2 - genetics; Development and progression; Disease; DNA sequencing; Electrolytes; Etiology; Female; Follow-Up Studies; Gene mutations; Genetic disorders; Homeostasis; Hospitals; Humans; Hydroxylase; Hyperkalemia; Hyperplasia; Hypoaldosteronism; Hyponatremia; Hypoplasia; Infant; Infant, Newborn; Infants; Infants (Newborn); Male; Metabolism; Mutation; Neonates; Nucleotide sequencing; Parents & parenting; Patients; Pedigree; Plasma; Point mutation; Potassium; Primary adrenal insufficiency; Prognosis; Pseudohypoaldosteronism; Questions and answers; Retrospective Studies; Salt wasting; Sodium; Syndrome; Vomiting; Primary adrenal insufficiency; Infant; Adrenal disease; Aldosterone synthase deficiency; Pseudohypoaldosteronism; Salt wasting
• ISSN: 1472-6823; 1472-6823
• DOI: 10.1186/s12902-021-00811-9

Aldosterone (Ald) is a crucial factor in maintaining electrolyte and water homeostasis. Defect in either its synthesis or function causes salt wasting (SW) manifestation. This disease group is rare, while most reported cases are sporadic. This study aimed to obtain an overview of the etiology and clinical picture of patients with the above condition and report our rare cases. A combination of retrospective review and case studies was conducted at the Pediatric Endocrine unit of The First Affiliated Hospital Sun Yat Sen University from September 1989 to June 2020. A total of 187 patients with SW were enrolled, of which 90.4% (n = 169) were diagnosed with congenital adrenal hyperplasia (CAH). SW type 21-hydroxylase deficiency accounted for 98.8% (n = 167) of CAH diagnosis, while 1.2% (n = 2) was of lipoid CAH. Non-CAH comprised 9.6% (n = 18) of the total patients whose etiologies included SF-1 gene mutation (n = 1), X-linked adrenal hypoplasia congenita (n = 9), aldosterone synthase deficiency (ASD, n = 4), and pseudo-hypoaldosteronism type 1 (PHA1, n = 1). Etiologies were not identified in three patients. All of patients with ASD and PHA1 exhibited SW syndrome in their early neonatal period. DNA sequencing showed mutations of CYP11B2 for P1-P4 and NR3C2 for P5. P1 and P2 were sibling brothers affected by compound heterozygous mutations of c.1121G > A (p.R374Q) and c.1486delC p.(L496fs); likewise, P4 was identified with compound heterozygous mutations of c.1200 + 1G > A and c.240-1 G > T; meanwhile P3 demonstrated c.1303G > A p.(G435S) homozygous mutation in CYP11B2 gene. Lastly, P5 showed c.1768 C > T p.(R590*) heterozygous mutation in the NR3C2 gene. Etiology of infant with aldosterone defect was mostly congenital. Renal and adrenal imaging are recommended to exclude renal causes. If clinical picture is suggestive, normal plasma Ald in early infancy cannot rule out aldosterone insufficiency.