Literature DB >> 27325427

Newborn Screening for Vitamin B6 Non-responsive Classical Homocystinuria: Systematical Evaluation of a Two-Tier Strategy.

Jürgen G Okun1, Hongying Gan-Schreier2, Tawfeq Ben-Omran3, Kathrin V Schmidt2, Junmin Fang-Hoffmann2, Gwendolyn Gramer2, Ghassan Abdoh3, Noora Shahbeck3, Hilal Al Rifai3, Abdul Latif Al Khal3, Gisela Haege2, Chuan-Chi Chiang4, David C Kasper5, Bridget Wilcken6, Peter Burgard2, Georg F Hoffmann2.   

Abstract

BACKGROUND: In classical homocystinuria (HCU, MIM# 236200) due to the deficiency of cystathionine β-synthase (EC 4.2.1.22) there is a clear evidence for the success of early treatment. The aim of this study was to develop and evaluate a two-tier strategy for HCU newborn screening.
METHODS: We reevaluated data from our newborn screening programme for Qatar in a total number of 125,047 neonates including 30 confirmed HCU patients. Our hitherto existing screening strategy includes homocysteine (Hcy) measurements in every child, resulting in a unique dataset for evaluation of two-tier strategies. Reevaluation included methionine (Met) levels, Met to phenylalanine (Phe) ratio, and Hcy. Four HCU cases identified after database closure were also included in the evaluation. In addition, dried blood spot samples selected by Met values >P97 in the newborn screening programs in Austria, Australia, the Netherlands, and Taiwan were analyzed for Hcy.
RESULTS: Met to Phe ratio was found to be more effective for first sieve than Met, sorting out nearly 90% of normal samples. Only 10% of the samples would have to be processed by second-tier measurement of Hcy in dried blood spots. As no patient with HCU was found neither in the samples investigated for HCU, nor by clinical diagnosis in the other countries, the generalization of our two-tier strategy could only be tested indirectly.
CONCLUSION: The finally derived two-tier algorithm using Met to Phe ratio as first- and Hcy as second-tier requires 10% first-tier positives to be transferred to Hcy measurement, resulting in 100% sensitivity and specificity in HCU newborn screening.

Entities:  

Keywords:  Classical homocystinuria; Cystathionine β-synthase; Dried blood spots; Homocysteine; Newborn screening; Two-tier strategy

Year:  2016        PMID: 27325427      PMCID: PMC5362558          DOI: 10.1007/8904_2016_556

Source DB:  PubMed          Journal:  JIMD Rep        ISSN: 2192-8304


  22 in total

1.  Rapid determination of total homocysteine in blood spots by liquid chromatography-electrospray ionization-tandem mass spectrometry.

Authors:  K Gempel; K D Gerbitz; B Casetta; M F Bauer
Journal:  Clin Chem       Date:  2000-01       Impact factor: 8.327

2.  Newborn screening: toward a uniform screening panel and system--executive summary.

Authors: 
Journal:  Pediatrics       Date:  2006-05       Impact factor: 7.124

3.  Homocysteine measurement in dried blood spot for neonatal detection of homocystinurias.

Authors:  Ahmad N Alodaib; Kevin Carpenter; Veronica Wiley; Tiffany Wotton; John Christodoulou; Bridget Wilcken
Journal:  JIMD Rep       Date:  2011-12-13

4.  Determination of total homocysteine, methylmalonic acid, and 2-methylcitric acid in dried blood spots by tandem mass spectrometry.

Authors:  Coleman T Turgeon; Mark J Magera; Carla D Cuthbert; Perry R Loken; Dimitar K Gavrilov; Silvia Tortorelli; Kimiyo M Raymond; Devin Oglesbee; Piero Rinaldo; Dietrich Matern
Journal:  Clin Chem       Date:  2010-08-31       Impact factor: 8.327

5.  Screening newborns for inborn errors of metabolism by tandem mass spectrometry.

Authors:  Bridget Wilcken; Veronica Wiley; Judith Hammond; Kevin Carpenter
Journal:  N Engl J Med       Date:  2003-06-05       Impact factor: 91.245

Review 6.  A revisit to the natural history of homocystinuria due to cystathionine beta-synthase deficiency.

Authors:  Flemming Skovby; Mette Gaustadnes; S Harvey Mudd
Journal:  Mol Genet Metab       Date:  2010-01       Impact factor: 4.797

7.  Implementation of extended neonatal screening and a metabolic unit in the State of Qatar: developing and optimizing strategies in cooperation with the Neonatal Screening Center in Heidelberg.

Authors:  M Lindner; G Abdoh; J Fang-Hoffmann; N Shabeck; M Al-Sayrafi; M Al-Janahi; S Ho; M O Abdelrahman; T Ben-Omran; A Bener; A Schulze; H Al-Rifai; G Al-Thani; G F Hoffmann
Journal:  J Inherit Metab Dis       Date:  2007-05-12       Impact factor: 4.982

8.  Homocystinuria due to cystathionine beta-synthase deficiency in Ireland: 25 years' experience of a newborn screened and treated population with reference to clinical outcome and biochemical control.

Authors:  S Yap; E Naughten
Journal:  J Inherit Metab Dis       Date:  1998-10       Impact factor: 4.982

9.  Newborn population screening for classic homocystinuria by determination of total homocysteine from Guthrie cards.

Authors:  Hongying Gan-Schreier; Moustafa Kebbewar; Junmin Fang-Hoffmann; Julia Wilrich; Ghassan Abdoh; Tawfeg Ben-Omran; Noora Shahbek; Abdulbari Bener; Hilal Al Rifai; Abdul Latif Al Khal; Martin Lindner; Johannes Zschocke; Georg F Hoffmann
Journal:  J Pediatr       Date:  2009-11-14       Impact factor: 4.406

Review 10.  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

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  4 in total

1.  High incidence of maternal vitamin B12 deficiency detected by newborn screening: first results from a study for the evaluation of 26 additional target disorders for the German newborn screening panel.

Authors:  Gwendolyn Gramer; Junmin Fang-Hoffmann; Patrik Feyh; Glynis Klinke; Peter Monostori; Jürgen G Okun; Georg F Hoffmann
Journal:  World J Pediatr       Date:  2018-06-15       Impact factor: 2.764

2.  Newborn screening for remethylation disorders and vitamin B12 deficiency-evaluation of new strategies in cohorts from Qatar and Germany.

Authors:  Gwendolyn Gramer; Ghassan Abdoh; Tawfeg Ben-Omran; Noora Shahbeck; Rehab Ali; Laila Mahmoud; Junmin Fang-Hoffmann; Georg F Hoffmann; Hilal Al Rifai; Jürgen G Okun
Journal:  World J Pediatr       Date:  2017-01-15       Impact factor: 2.764

3.  Eight novel mutations of CBS gene in nine Chinese patients with classical homocystinuria.

Authors:  Dong-Xiao Li; Xi-Yuan Li; Hui Dong; Yu-Peng Liu; Yuan Ding; Jin-Qing Song; Ying Jin; Yao Zhang; Qiao Wang; Yan-Ling Yang
Journal:  World J Pediatr       Date:  2018-03-05       Impact factor: 2.764

4.  Cystathionine β-synthase deficiency in the E-HOD registry-part I: pyridoxine responsiveness as a determinant of biochemical and clinical phenotype at diagnosis.

Authors:  Viktor Kožich; Jitka Sokolová; Andrew A M Morris; Markéta Pavlíková; Florian Gleich; Stefan Kölker; Jakub Krijt; Carlo Dionisi-Vici; Matthias R Baumgartner; Henk J Blom; Martina Huemer
Journal:  J Inherit Metab Dis       Date:  2020-12-28       Impact factor: 4.982

  4 in total

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