Novel Mutations and Clinical Characteristics in Seven Chinese Families With Congenital Nephrogenic Diabetes Insipidus.

OBJECTIVE

Mutations in lead to rare congenital nephrogenic diabetes insipidus (NDI), which has been limitedly studied in Chinese population.

METHODS

Twenty-five subjects from seven families with NDI in a department (Beijing, PUMCH) were screened for mutations. Clinical characteristics were described and genotype-phenotype correlation analysis was performed.

RESULTS

We identified 9 mutations in 13 patients with NDI, including 3 novel mutations (p.G165D, p.Q255RfsTer72 and IVS3-3delC). Missense mutations were the most common mutation type, followed by splicing mutations, and frameshift mutations caused by small deletion or insertion. The onset-age in our patients was younger than 1 year old. Common manifestations included polydipsia, polyuria (7/7) and intermittent fever (6/7). Less common presentations included short stature (3/7) and mental impairment (1/7). High osmotic hypernatremia and low osmotic urine were the main biochemical features. Dilation of the urinary tract was a common complication of NDI (3/6). Level of serum sodium in NDI patients with compound het AQP2 mutations was higher than non-compound het mutations.

CONCLUSION

In the first and largest case series of NDI caused by mutation in Chinese population, we identified 9 mutations, including 3 novel mutations. Phenotype was found to correlate with genotypes, revealed by higher level of serum sodium in patients with compound het mutations than non-compound het mutations. This knowledge broadens genotypic and phenotypic spectrum for rare congenital NDI and provided basis for studying molecular biology of AQP2.