Clinical outcomes among children with primary nephrogenic diabetes insipidus
Seon Hee Lim, Jin-Soon Suh, Ji Hyun Kim, Seung Jae Lee, Naye Choi, Ji Yeon Song, Eujin Park, Hee Sun Baek, Hyun Kyung Lee, Se Jin Park, Min Ji Park, Min Hyun Cho, Eun Mi Yang, Hee Gyung Kang, Yo Han Ahn

TL;DR
Children with primary nephrogenic diabetes insipidus experience growth delays and kidney function changes, highlighting the need for long-term care.
Contribution
This study provides longitudinal clinical data on growth and kidney function in children with primary nephrogenic diabetes insipidus.
Findings
Height Z-scores declined early but improved after 1.5 years, with final heights below average.
eGFR increased rapidly until age 1.4, then slowed, with many patients still below normal GFR at 14 years.
Treatment complications like hypokalemia and hyperuricemia were common among patients.
Abstract
Primary nephrogenic diabetes insipidus (NDI) is a rare inherited disorder with limited data on long-term outcomes. This study assessed longitudinal outcomes with primary NDI. This multicenter retrospective study included 63 patients with primary NDI. Growth rates and estimated glomerular filtration (eGFR) were analyzed via a piecewise linear mixed-effects model during the pediatric period. AVPR2 and AQP2 mutations were identified in 74.6% and 9.5% of patients, respectively. The median ages at diagnosis and last follow up were 0.41 and 12.37 years, respectively. Height Z-scores declined from birth to 1.5 years and improved thereafter, with slopes of −2.626, −0.563, 0.102, and 0.031 per year across breakpoints at 0.5, 1.5, and 7 years. Although none of the patients met the criteria for short stature by age 18, the mean final height Z-score remained below average and was significantly…
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Taxonomy
TopicsQuantum optics and atomic interactions · Lanthanide and Transition Metal Complexes
