# Clinical outcomes among children with primary nephrogenic diabetes insipidus

**Authors:** 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

PMC · DOI: 10.1093/ckj/sfaf303 · 2025-10-01

## 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.

## Key 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 lower than that at birth. Weight and weight-for-height Z-scores initially declined and then improved, with slope changes at 0.5 and 0.7 years. By the age of 18, 38.9% were overweight or obese. eGFR increased rapidly before 1.4 years (slope 25.61 ml/min/1.73 m2/year), and slowly thereafter (slope 0.58), reaching eGFR ≥90 ml/min/1.73 m2 at a median age of 5.1 years. The proportion of patients with eGFR <90 ml/min/1.73 m2 decreased to 34.6% at 14 years, then rose to 43.8% by the age of 18. Treatment-associated complications included hypokalemia (64.5%), alkalosis (61.1%), and hyperuricemia (60.7%).

Patients with primary NDI exhibit a dynamic growth trajectory, delayed achievement of normal GFR with subsequent risk of chronic kidney disease, and frequent treatment-associated complications. These findings underscore the need for timely and individualized long-term management.

Graphical Abstract

## Linked entities

- **Genes:** AVPR2 (arginine vasopressin receptor 2) [NCBI Gene 554], AQP2 (aquaporin 2) [NCBI Gene 359]
- **Diseases:** nephrogenic diabetes insipidus (MONDO:0016383)

## Full-text entities

- **Genes:** AQP2 (aquaporin 2) [NCBI Gene 359] {aka AQP-2, AQP-CD, NDI2, WCH-CD}, AVPR2 (arginine vasopressin receptor 2) [NCBI Gene 554] {aka ADHR, DI1, DIR, DIR3, NDI, NDI1}
- **Diseases:** obese (MESH:D009765), chronic kidney disease (MESH:D051436), primary (MESH:D010538), hyperuricemia (MESH:D033461), inherited disorder (MESH:D030342), hypokalemia (MESH:D007008), NDI (MESH:D018500), short stature (MESH:D006130), overweight (MESH:D050177), alkalosis (MESH:D000471)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12585523/full.md

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Source: https://tomesphere.com/paper/PMC12585523