ESPE Abstracts (2019) 92 P2-222

ESPE2019 Poster Category 2 Pituitary, Neuroendocrinology and Puberty (27 abstracts)

Case Report of Syndrome of Inappropriate Antidiuretic Hormone Secretion (SIADH) Caused by Rare AVPR2 Gene Active Mutation

wenjing li 1 , jiajia chen 1 , jiapeng sun 2 & chunxiu gong 1

1Department of Endocrinology, Genetics and Metabolism, Beijing Children's Hospital, Capital Medical University, beijing, China. 2Department of nephrology, Beijing Children's Hospital, Capital Medical University, beijing, China

Objective: The AVPR2 gene mutation usually cause nephrogenic diabetes insipidus. We report a patient who carried an active gene mutation of AVPR2 presenting persistent hyponatremia, which resembled to the syndrome of inappropriate antidiuretic hormone secretion (SIADH)

Method: We describe a patient whose clinical and laboratory evaluation were consistent with hyponatremia, which hardly to be corrected to normal. After the AVPR2 gene mutation identified, the level of serum sodium was increased with furosemide orally.

Result: The patient was 5 years old boy with several times generalized seizures caused by hyponatremia in 2 years. His sister was in good health. There was no family history of hyponatremia. He showed apathy with otherwise normal physical examinations. His blood pressure was normal, his height and weight were in normal range. Initial laboratory evaluations demonstrated hyponatremia of 120 mmol/L with inappropriately elevated urinary sodium levels of 181.7 mmol/L, and the serum levels of potassium and bicarbonate were normal. The serum osmolality was lower to 252 mOsm/L, He had normal blood urea nitrogen and low serum creatinine levels. Adrenal hormone and thyroid- function tests were all normal. Imaging studies of the head and chest were unremarkable. Despite clinical and laboratory presentations consistent with the presence of SIADH, we cannot find any pathogenic reasons. The hyponatremia was hardly to be corrected by high doses of sodium supplementation.

DNA sequencing of the patient's AVPR2 gene identified missense mutations of nucleotide 770 mutated from cytosine to thymine, which changed codon 137 from arginine to cysteine. This mutation was reported as constitutive activation of AVP receptor by other researchers.

The patient was initially treated with fluid restriction and high doses of sodium supplementation, but both were useless. He was treated with furosemide, resulting in increased urinary output and normalization of the serum sodium level.

Conclusion: The gene mutation can cause nephrogenic diabetes insipidus and SIADH, depending on the kinds of mutations. The administration of furosemide normalized the serum sodium level and increased the urinary output. The AVP antagonist of Tolvaptan could suppress AVP receptor activity, which could prescribe to SIADH, but is more expensive than furosemide.

Volume 92

58th Annual ESPE

Vienna, Austria
19 Sep 2019 - 21 Sep 2019

European Society for Paediatric Endocrinology 

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