Literature DB >> 28101774

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

Gwendolyn Gramer1, Ghassan Abdoh2, Tawfeg Ben-Omran2, Noora Shahbeck2, Rehab Ali2, Laila Mahmoud2, Junmin Fang-Hoffmann3, Georg F Hoffmann3, Hilal Al Rifai2, Jürgen G Okun3.   

Abstract

BACKGROUND: Newborn screening is a precondition for early diagnosis and successful treatment of remethylation disorders and classical homocystinuria (cystathionine-ß-synthase deficiency). Newborn screening for classical homocystinuria using total homocysteine measurement in dried blood spots has been very successfully performed for many years for newborns from Qatar.
METHODS: A new optimized newborn screening strategy for remethylation disorders and homocystinuria was developed and evaluated for newborns from Qatar using total homocysteine measurement as first-tier and methionine, methionine-phenylalanine-ratio and propionylcarnitine as second-tiers. Proposed cut-offs were also retrospectively evaluated in newborn screening samples of 12 patients with remethylation disorders and vitamin B12 deficiency from Qatar and Germany.
RESULTS: Over a 12 months period, the proposed strategy led to a decrease in the recall rate in homocysteine screening for Qatar from 1.09% to 0.68%, while allowing for additional systematic inclusion of remethylation disorders and vitamin B12 deficiency into the screening panel for Qatar. In the evaluated period the applied strategy would have detected all patients with classical homocystinuria identified by the previous strategy and in addition 5 children with maternal nutritional vitamin B12 deficiency and one patient with an isolated remethylation disorder. Additional retrospective evaluation of newborn screening samples of 12 patients from Germany and Qatar with remethlyation disorders or vitamin B12 deficiency showed that all of these patients would have been detected by the cut-offs used in the proposed new strategy. In addition, an adapted strategy for Germany using methionine, methionine-phenylalanine-ratio and propionylcarnitine as first-tier, and homocysteine as a second-tier test was also positively evaluated retrospectively.
CONCLUSIONS: The proposed strategy for samples from Qatar allows inclusion of remethylation disorders and vitamin B12 deficiency in the screening panel, while lowering the recall rate. An adapted second-tier strategy is presented for screening in Germany and will be prospectively evaluated over the next years in a pilot project named "Newborn Screening 2020".

Entities:  

Keywords:  classical homocystinuria; newborn screening; remethylation disorders; second-tier; vitamin B12 deficiency

Mesh:

Year:  2017        PMID: 28101774     DOI: 10.1007/s12519-017-0003-z

Source DB:  PubMed          Journal:  World J Pediatr            Impact factor:   2.764


  17 in total

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

Authors:  Jürgen G Okun; Hongying Gan-Schreier; Tawfeq Ben-Omran; Kathrin V Schmidt; Junmin Fang-Hoffmann; Gwendolyn Gramer; Ghassan Abdoh; Noora Shahbeck; Hilal Al Rifai; Abdul Latif Al Khal; Gisela Haege; Chuan-Chi Chiang; David C Kasper; Bridget Wilcken; Peter Burgard; Georg F Hoffmann
Journal:  JIMD Rep       Date:  2016-06-21

2.  Two-tier approach to the newborn screening of methylenetetrahydrofolate reductase deficiency and other remethylation disorders with tandem mass spectrometry.

Authors:  Silvia Tortorelli; Coleman T Turgeon; James S Lim; Steve Baumgart; Debra-Lynn Day-Salvatore; Jose Abdenur; Jonathan A Bernstein; Fred Lorey; Uta Lichter-Konecki; Devin Oglesbee; Kimiyo Raymond; Dietrich Matern; Lisa Schimmenti; Piero Rinaldo; Dimitar K Gavrilov
Journal:  J Pediatr       Date:  2010-04-14       Impact factor: 4.406

3.  Clinical onset and course, response to treatment and outcome in 24 patients with the cblE or cblG remethylation defect complemented by genetic and in vitro enzyme study data.

Authors:  M Huemer; C Bürer; P Ješina; V Kožich; M A Landolt; T Suormala; B Fowler; P Augoustides-Savvopoulou; E Blair; K Brennerova; A Broomfield; L De Meirleir; G Gökcay; J Hennermann; P Jardine; J Koch; S Lorenzl; A S Lotz-Havla; J Noss; R Parini; H Peters; B Plecko; F J Ramos; A Schlune; K Tsiakas; M Zerjav Tansek; M R Baumgartner
Journal:  J Inherit Metab Dis       Date:  2014-12-20       Impact factor: 4.982

4.  Neurodevelopmental and Cognitive Outcomes of Classical Homocystinuria: Experience from Qatar.

Authors:  Haitham El Bashir; Lubna Dekair; Yasmeen Mahmoud; Tawfeg Ben-Omran
Journal:  JIMD Rep       Date:  2015-02-25

Review 5.  Survival and psychomotor development with early betaine treatment in patients with severe methylenetetrahydrofolate reductase deficiency.

Authors:  Eugene F Diekman; Tom J de Koning; Nanda M Verhoeven-Duif; Maroeska M Rovers; Peter M van Hasselt
Journal:  JAMA Neurol       Date:  2014-02       Impact factor: 18.302

6.  Expanded newborn screening for inborn errors of metabolism by electrospray ionization-tandem mass spectrometry: results, outcome, and implications.

Authors:  Andreas Schulze; Martin Lindner; Dirk Kohlmüller; Katharina Olgemöller; Ertan Mayatepek; Georg F Hoffmann
Journal:  Pediatrics       Date:  2003-06       Impact factor: 7.124

7.  Heptadecanoylcarnitine (C17) a novel candidate biomarker for newborn screening of propionic and methylmalonic acidemias.

Authors:  Sabrina Malvagia; Christopher A Haynes; Laura Grisotto; Daniela Ombrone; Silvia Funghini; Elisa Moretti; Kathleen S McGreevy; Annibale Biggeri; Renzo Guerrini; Raquel Yahyaoui; Uttam Garg; Mary Seeterlin; Donald Chace; Victor R De Jesus; Giancarlo la Marca
Journal:  Clin Chim Acta       Date:  2015-09-11       Impact factor: 3.786

8.  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 9.  Three new cases of late-onset cblC defect and review of the literature illustrating when to consider inborn errors of metabolism beyond infancy.

Authors:  Martina Huemer; Sabine Scholl-Bürgi; Karine Hadaya; Ilse Kern; Ronny Beer; Klaus Seppi; Brian Fowler; Matthias R Baumgartner; Daniela Karall
Journal:  Orphanet J Rare Dis       Date:  2014-11-15       Impact factor: 4.123

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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  5 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

Review 2.  Versatile enzymology and heterogeneous phenotypes in cobalamin complementation type C disease.

Authors:  Anna J Esser; Srijan Mukherjee; Ilia A Dereven'kov; Sergei V Makarov; Donald W Jacobsen; Ute Spiekerkoetter; Luciana Hannibal
Journal:  iScience       Date:  2022-08-18

3.  Clinical genetics and genomic medicine in Qatar.

Authors:  Nader Al-Dewik; Mariam Al-Mureikhi; Noora Shahbeck; Rehab Ali; Fatma Al-Mesaifri; Laila Mahmoud; Amna Othman; Mariam AlMulla; Reem Al Sulaiman; Sara Musa; Ghassan Abdoh; Karen El-Akouri; Benjamin D Solomon; Tawfeg Ben-Omran
Journal:  Mol Genet Genomic Med       Date:  2018-09       Impact factor: 2.183

4.  Incidence of maple syrup urine disease, propionic acidemia, and methylmalonic aciduria from newborn screening data.

Authors:  Kimberly A Chapman; Gwendolyn Gramer; Sarah Viall; Marshall L Summar
Journal:  Mol Genet Metab Rep       Date:  2018-04-05

5.  High incidence of low vitamin B12 levels in Estonian newborns.

Authors:  Karit Reinson; Kadi Künnapas; Annika Kriisa; Mari-Anne Vals; Kai Muru; Katrin Õunap
Journal:  Mol Genet Metab Rep       Date:  2018-01-11
  5 in total

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