Literature DB >> 25172236

Early effect of NTBC on renal tubular dysfunction in hereditary tyrosinemia type 1.

A Maiorana1, M Malamisura2, F Emma3, S Boenzi4, V M Di Ciommo5, C Dionisi-Vici6.   

Abstract

BACKGROUND: Hereditary tyrosinemia type 1 (HT1) is characterized by severe progressive liver disease and renal tubular dysfunction. NTBC therapy has revolutionized the management of HT1 but its effect on renal tubular function has so far been poorly investigated. The aim of this study was to describe the early effect of NTBC on renal tubular disease in patients with HT1.
METHODS: Five HT1 patients (age between 5 and 53 months) with different types of presentation were evaluated before and during the first 2 weeks of therapy with NTBC in a retrospective case analysis for phosphate metabolism and renal tubular function.
RESULTS: Before starting NTBC therapy, all children manifested signs of renal dysfunction which included hypophosphatemia, acidosis, reduced phosphate reabsorption, aminoaciduria, glycosuria (Fanconi syndrome), and variable degree of proteinuria. Some patients also presented increased urinary calcium/creatinine ratio and raised fractional excretion of sodium. Starting of NTBC therapy resulted in the rapid normalization of plasma phosphate within one week from its initiation in majority of patients and in all patients during the second week of therapy. TmP/GFR normalized in 48h, while the other markers of renal dysfunction showed an improving trend over 2 weeks.
CONCLUSIONS: NTBC is an efficient treatment for renal tubular dysfunction in HT1, allowing the return to normal function within a few weeks. Its early effect on renal tubular cells appeared to be very rapid, particularly in normalizing plasma phosphate and TmP/GFR. In our series of patients, the TmP/GFR resulted as the most reliable index of tubular function.
Copyright © 2014 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Hereditary tyrosinemia type 1; NTBC; Phosphate homeostasis; Renal tubular dysfunction; Rickets; TmP/GFR

Mesh:

Substances:

Year:  2014        PMID: 25172236     DOI: 10.1016/j.ymgme.2014.07.021

Source DB:  PubMed          Journal:  Mol Genet Metab        ISSN: 1096-7192            Impact factor:   4.797


  10 in total

1.  Tyrosinemia type I and not treatment with NTBC causes slower learning and altered behavior in mice.

Authors:  Megan A Hillgartner; Sarah B Coker; Ashton E Koenig; Marissa E Moore; Elizabeth Barnby; Gordon G MacGregor
Journal:  J Inherit Metab Dis       Date:  2016-06-06       Impact factor: 4.982

2.  Unusual first presentation of a metabolic disorder.

Authors:  Claire Emma Strauss; Gayle Hann
Journal:  BMJ Case Rep       Date:  2019-03-22

3.  Assessment of Proximal Tubular Function by Tubular Maximum Phosphate Reabsorption Capacity in Heart Failure.

Authors:  Johanna E Emmens; Martin H de Borst; Eva M Boorsma; Kevin Damman; Gerjan Navis; Dirk J van Veldhuisen; Kenneth Dickstein; Stefan D Anker; Chim C Lang; Gerasimos Filippatos; Marco Metra; Nilesh J Samani; Piotr Ponikowski; Leong L Ng; Adriaan A Voors; Jozine M Ter Maaten
Journal:  Clin J Am Soc Nephrol       Date:  2022-02       Impact factor: 8.237

4.  Hereditary tyrosinemia type Ⅰ: newborn screening, diagnosis and treatment.

Authors:  Yue Tang; Yuanyuan Kong
Journal:  Zhejiang Da Xue Xue Bao Yi Xue Ban       Date:  2021-08-25

5.  Type 1 tyrosinemia in Finland: a nationwide study.

Authors:  Linnea Äärelä; Pauliina Hiltunen; Tea Soini; Nina Vuorela; Heini Huhtala; Pasi I Nevalainen; Markku Heikinheimo; Laura Kivelä; Kalle Kurppa
Journal:  Orphanet J Rare Dis       Date:  2020-10-12       Impact factor: 4.123

6.  Phenotype, genotype, and outcome of 25 Palestinian patients with hereditary tyrosinemia type 1.

Authors:  Imad Dweikat; Nada Qawasmi; Aysha Najeeb; Mohammad Radwan
Journal:  Metabol Open       Date:  2021-01-28

Review 7.  Fumarylacetoacetate hydrolase gene as a knockout target for hepatic chimerism and donor liver production.

Authors:  Ellen L Larson; Dong Jin Joo; Erek D Nelson; Bruce P Amiot; Rajagopal N Aravalli; Scott L Nyberg
Journal:  Stem Cell Reports       Date:  2021-10-21       Impact factor: 7.765

8.  A case report of two siblings with hypertyrosinemia type 1 presenting with hepatic disease with different onset time and severity.

Authors:  Kazuo Kawabata; Jun Kido; Takanobu Yoshida; Shirou Matsumoto; Kimitoshi Nakamura
Journal:  Mol Genet Metab Rep       Date:  2022-07-01

9.  In vivo quantitative photoacoustic evaluation of the liver and kidney pathology in tyrosinemia.

Authors:  Guojia Huang; Jing Lv; Yong He; Jian Yang; Lvming Zeng; Liming Nie
Journal:  Photoacoustics       Date:  2022-09-28

Review 10.  Diagnosis and treatment of tyrosinemia type I: a US and Canadian consensus group review and recommendations.

Authors:  Jeffrey M Chinsky; Rani Singh; Can Ficicioglu; Clara D M van Karnebeek; Markus Grompe; Grant Mitchell; Susan E Waisbren; Muge Gucsavas-Calikoglu; Melissa P Wasserstein; Katie Coakley; C Ronald Scott
Journal:  Genet Med       Date:  2017-08-03       Impact factor: 8.822

  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.