Literature DB >> 24206934

Dietary practices in pyridoxine non-responsive homocystinuria: a European survey.

S Adam1, M F Almeida, E Carbasius Weber, H Champion, H Chan, A Daly, M Dixon, K Dokoupil, D Egli, S Evans, F Eyskens, A Faria, C Ferguson, P Hallam, M Heddrich-Ellerbrok, J Jacobs, C Jankowski, R Lachmann, R Lilje, R Link, S Lowry, K Luyten, A MacDonald, C Maritz, E Martins, U Meyer, E Müller, E Murphy, L V Robertson, J C Rocha, I Saruggia, P Schick, J Stafford, L Stoelen, A Terry, R Thom, T van den Hurk, M van Rijn, A van Teefelen-Heithoff, D Webster, F J White, J Wildgoose, H Zweers.   

Abstract

BACKGROUND: Within Europe, the management of pyridoxine (B6) non-responsive homocystinuria (HCU) may vary but there is limited knowledge about treatment practice. AIM: A comparison of dietetic management practices of patients with B6 non-responsive HCU in European centres.
METHODS: A cross-sectional audit by questionnaire was completed by 29 inherited metabolic disorder (IMD) centres: (14 UK, 5 Germany, 3 Netherlands, 2 Switzerland, 2 Portugal, 1 France, 1 Norway, 1 Belgium).
RESULTS: 181 patients (73% >16 years of age) with HCU were identified. The majority (66%; n=119) were on dietary treatment (1-10 years, 90%; 11-16 years, 82%; and >16 years, 58%) with or without betaine and 34% (n=62) were on betaine alone. The median natural protein intake (g/day) on diet only was, by age: 1-10 years, 12 g; 11-16 years, 11 g; and >16 years, 45 g. With diet and betaine, median natural protein intake (g/day) by age was: 1-10 years, 13 g; 11-16 years, 20 g; and >16 years, 38 g. Fifty-two percent (n=15) of centres allocated natural protein by calculating methionine rather than a protein exchange system. A methionine-free l-amino acid supplement was prescribed for 86% of diet treated patients. Fifty-two percent of centres recommended cystine supplements for low plasma concentrations. Target treatment concentrations for homocystine/homocysteine (free/total) and frequency of biochemical monitoring varied.
CONCLUSION: In B6 non-responsive HCU the prescription of dietary restriction by IMD centres declined with age, potentially associated with poor adherence in older patients. Inconsistencies in biochemical monitoring and treatment indicate the need for international consensus guidelines.
© 2013.

Entities:  

Keywords:  Betaine; Homocysteine; Homocystinuria; Methionine; Protein restricted diet

Mesh:

Substances:

Year:  2013        PMID: 24206934     DOI: 10.1016/j.ymgme.2013.10.003

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


  7 in total

1.  Low bone mineral density is a common finding in patients with homocystinuria.

Authors:  David R Weber; Curtis Coughlin; Jill L Brodsky; Kristin Lindstrom; Can Ficicioglu; Paige Kaplan; Cynthia L Freehauf; Michael A Levine
Journal:  Mol Genet Metab       Date:  2015-12-10       Impact factor: 4.797

2.  Altered hepatic sulfur metabolism in cystathionine β-synthase-deficient homocystinuria: regulatory role of taurine on competing cysteine oxidation pathways.

Authors:  Hua Jiang; Sally P Stabler; Robert H Allen; Steven H Abman; Kenneth N Maclean
Journal:  FASEB J       Date:  2014-06-02       Impact factor: 5.191

Review 3.  Guidelines for the diagnosis and management of cystathionine beta-synthase deficiency.

Authors:  Andrew A M Morris; Viktor Kožich; Saikat Santra; Generoso Andria; Tawfeg I M Ben-Omran; Anupam B Chakrapani; Ellen Crushell; Mick J Henderson; Michel Hochuli; Martina Huemer; Miriam C H Janssen; Francois Maillot; Philip D Mayne; Jenny McNulty; Tara M Morrison; Helene Ogier; Siobhan O'Sullivan; Markéta Pavlíková; Isabel Tavares de Almeida; Allyson Terry; Sufin Yap; Henk J Blom; Kimberly A Chapman
Journal:  J Inherit Metab Dis       Date:  2016-10-24       Impact factor: 4.982

4.  Growth Patterns in the Irish Pyridoxine Nonresponsive Homocystinuria Population and the Influence of Metabolic Control and Protein Intake.

Authors:  Orla Purcell; Aoife Coughlan; Tim Grant; Jenny McNulty; Anne Clark; Deirdre Deverell; Philip Mayne; Joanne Hughes; Ahmad Monavari; Ina Knerr; Ellen Crushell
Journal:  J Nutr Metab       Date:  2017-11-15

5.  Homocysteine aggravates ROS-induced depression of transmitter release from motor nerve terminals: potential mechanism of peripheral impairment in motor neuron diseases associated with hyperhomocysteinemia.

Authors:  Ellya Bukharaeva; Anastasia Shakirzyanova; Venera Khuzakhmetova; Guzel Sitdikova; Rashid Giniatullin
Journal:  Front Cell Neurosci       Date:  2015-10-06       Impact factor: 5.505

Review 6.  Newborn screening for homocystinurias and methylation disorders: systematic review and proposed guidelines.

Authors:  Martina Huemer; Viktor Kožich; Piero Rinaldo; Matthias R Baumgartner; Begoña Merinero; Elisabetta Pasquini; Antonia Ribes; Henk J Blom
Journal:  J Inherit Metab Dis       Date:  2015-03-12       Impact factor: 4.982

7.  Cystathionine beta synthase deficiency and brain edema associated with methionine excess under betaine supplementation: Four new cases and a review of the evidence.

Authors:  Bernd C Schwahn; Thomas Scheffner; Hedwig Stepman; Peter Verloo; Anibh M Das; Janice Fletcher; Henk J Blom; Jean-Francois Benoist; Bruce A Barshop; Jaime J Barea; Annette Feigenbaum
Journal:  JIMD Rep       Date:  2020-01-08
  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.