Literature DB >> 18584216

Long-term growth of children with nephrogenic diabetes insipidus.

Horacio Lejarraga1, Maria Gracia Caletti, Silvia Caino, Alejandra Jiménez.   

Abstract

Primary nephrogenic diabetes insipidus (NDI) is a genetic, chronic disease characterised by lack of distal renal tubule to antidiuretic hormone. The condition produces polyuria, polydipsia, and consequently, reduced caloric intake and growth failure. There is very scarce information on physical growth of affected children. The objective of the paper is to describe long-term growth of 14 patients from 11 families, studied retrospectively and followed for 3-16 years (median 11.6 years). Diagnosis was made on the basis of clinical and laboratory data and concentration test under pitressin. Patients were treated with indomethacin, thiazides, and amiloride. Weight and standing height was measured periodically at the Laboratory of Anthropometry, following standardised techniques. Information was obtained from clinical notes. The majority of children grew below the third centile of local standards, and many showed improvement of weight, height, and body mass index (BMI) over time. Mean height, weight, and BMI gain during follow-up was 1.72, 1.06, and 1.46 standard deviations (SDs), respectively. Three children who did not adhere to treatment showed growth delay. Height gain during the first 2 years of follow-up was inversely associated with height deficit at diagnosis. Further studies on growth at adolescence and in different mutations are recommended.

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Year:  2008        PMID: 18584216     DOI: 10.1007/s00467-008-0844-8

Source DB:  PubMed          Journal:  Pediatr Nephrol        ISSN: 0931-041X            Impact factor:   3.714


  17 in total

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Journal:  Nephrol Dial Transplant       Date:  2004-03-05       Impact factor: 5.992

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Journal:  Klin Padiatr       Date:  1989 Nov-Dec       Impact factor: 1.349

Review 5.  Molecular and cellular defects in nephrogenic diabetes insipidus.

Authors:  N V Knoers; P M Deen
Journal:  Pediatr Nephrol       Date:  2001-12       Impact factor: 3.714

Review 6.  Molecular mechanisms and drug development in aquaporin water channel diseases: molecular mechanism of water channel aquaporin-2 trafficking.

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Journal:  Clin Sci (Lond)       Date:  1984-06       Impact factor: 6.124

Review 9.  Nephrogenic diabetes insipidus: clinical symptoms, pathogenesis, genetics and treatment.

Authors:  N Knoers; L A Monnens
Journal:  Pediatr Nephrol       Date:  1992-09       Impact factor: 3.714

10.  Congenital nephrogenic diabetes insipidus-vasopressin and prostaglandins in response to treatment with hydrochlorothiazide and indomethacin.

Authors:  W Rascher; W Rosendahl; I A Henrichs; R Maier; H W Seyberth
Journal:  Pediatr Nephrol       Date:  1987-07       Impact factor: 3.714

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  8 in total

1.  Pre- and post-treatment urinary tract findings in children with nephrogenic diabetes insipidus.

Authors:  María Gracia Caletti; Alejandro Balestracci; Diana Di Pinto
Journal:  Pediatr Nephrol       Date:  2013-12-14       Impact factor: 3.714

Review 2.  Nephrogenic diabetes insipidus in children (Review).

Authors:  Carmen Duicu; Ana Maria Pitea; Oana Maria Săsăran; Iulia Cozea; Lidia Man; Claudia Bănescu
Journal:  Exp Ther Med       Date:  2021-05-11       Impact factor: 2.447

3.  Congenital nephrogenic diabetes insipidus with a novel mutation in the aquaporin 2 gene.

Authors:  Youn Jong Park; Haing Woon Baik; Hae Il Cheong; Ju Hyung Kang
Journal:  Biomed Rep       Date:  2014-05-19

4.  Novel de novo AVPR2 Variant in a Patient with Congenital Nephrogenic Diabetes Insipidus.

Authors:  Shivani Joshi; Per Brandstrom; Niels Gregersen; Søren Rittig; Jane Hvarregaard Christensen
Journal:  Case Rep Nephrol Dial       Date:  2017-09-27

5.  Diagnosis, Treatment, and Outcomes in Children With Congenital Nephrogenic Diabetes Insipidus: A Pediatric Nephrology Research Consortium Study.

Authors:  Cynthia D'Alessandri-Silva; Melinda Carpenter; Rose Ayoob; John Barcia; Aftab Chishti; Alex Constantinescu; Katherine M Dell; Julie Goodwin; Shireen Hashmat; Sandra Iragorri; Cristin Kaspar; Sherene Mason; Jason M Misurac; Melissa Muff-Luett; Christine Sethna; Shweta Shah; Patricia Weng; Larry A Greenbaum; John D Mahan
Journal:  Front Pediatr       Date:  2020-01-21       Impact factor: 3.418

6.  Nephrogenic diabetes insipidus (NDI): clinical, laboratory and genetic characterization of five Brazilian patients.

Authors:  Maria Helena Vaisbich; Juliana Carneiro; Wolfanga Bóson; Bruna Resende; Luiz De Marco; Rachel S Honjo; Chong Ae Kim; Vera H Koch
Journal:  Clinics (Sao Paulo)       Date:  2009-05       Impact factor: 2.365

7.  Valine-279 Deletion-Mutation on Arginine Vasopressin Receptor 2 Causes Obstruction in G-Protein Binding Site: A Clinical Nephrogenic Diabetes Insipidus Case and Its Sub-Molecular Pathogenic Analysis.

Authors:  Ming-Chun Chen; Yu-Chao Hsiao; Chun-Chun Chang; Sheng-Feng Pan; Chih-Wen Peng; Ya-Tzu Li; Cheng-Der Liu; Je-Wen Liou; Hao-Jen Hsu
Journal:  Biomedicines       Date:  2021-03-15

8.  Clinical and Functional Characterization of a Novel Mutation in AVPR2 Causing Nephrogenic Diabetes Insipidus in a Four-Generation Chinese Family.

Authors:  Shusen Guo; Shimin Wu; Zhuxi Li; Lianjing Huang; Di Zhan; Cai Zhang; Xiaoping Luo
Journal:  Front Pediatr       Date:  2021-12-09       Impact factor: 3.418

  8 in total

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