Literature DB >> 34176718

Prospective diagnosis of MT-ATP6-related mitochondrial disease by newborn screening.

Ryan H Peretz1, Nicholas Ah Mew2, Hilary J Vernon3, Rebecca D Ganetzky4.   

Abstract

Elevated citrulline and C5-OH levels are reported as part of the newborn screening of core and secondary disorders on the Recommended Uniform Screening Panel (RUSP). Additionally, some state laboratory newborn screening programs report low citrulline levels, which may be observed in proximal urea cycle disorders. We report six patients who were found on newborn screening to have low citrulline and/or elevated C5-OH levels in whom confirmatory testing showed the combination of these two abnormal analytes. Mitochondrial sequencing revealed known pathogenic variants in MT-ATP6 at high heteroplasmy levels in all cases. MT-ATP6 at these heteroplasmy levels is associated with Leigh syndrome, a progressive neurodegenerative disease. Patients were treated with supplemental citrulline and, in some cases, mitochondrial cofactor therapy. These six patients have not experienced metabolic crises or developmental regression, and early diagnosis and management may help prevent the neurological sequelae of Leigh syndrome. The affected mothers and siblings are asymptomatic or paucisymptomatic (e.g. intellectual disability, depression, migraines, obsessive-compulsive disorder, and poor balance) despite high heteroplasmy or apparent homoplasmy of the familial variant, thus expanding the clinical spectrum seen in pathogenic variants of MT-ATP6. Confirmatory plasma amino acid analysis and acylcarnitine profiling should be ordered in a patient with either low citrulline and/or elevated C5-OH, as this combination appears specific for pathogenic variants in MT-ATP6.
Copyright © 2021 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Acylcarnitine; Amino acids; Citrulline; Leigh syndrome; Mitochondrial disease; Newborn screening

Mesh:

Substances:

Year:  2021        PMID: 34176718      PMCID: PMC8578202          DOI: 10.1016/j.ymgme.2021.06.007

Source DB:  PubMed          Journal:  Mol Genet Metab        ISSN: 1096-7192            Impact factor:   4.204


  9 in total

1.  Biochemical signatures mimicking multiple carboxylase deficiency in children with mutations in MT-ATP6.

Authors:  Austin A Larson; Shanti Balasubramaniam; John Christodoulou; Lindsay C Burrage; Ronit Marom; Brett H Graham; George A Diaz; Emma Glamuzina; Natalie Hauser; Bryce Heese; Gabriella Horvath; Andre Mattman; Clara van Karnebeek; S Lane Rutledge; Amy Williamson; Lissette Estrella; Johan K L Van Hove; James D Weisfeld-Adams
Journal:  Mitochondrion       Date:  2018-01-04       Impact factor: 4.160

2.  Metabolism of citrulline in man.

Authors:  D Rabier; P Kamoun
Journal:  Amino Acids       Date:  1995-12       Impact factor: 3.520

Review 3.  MT-ATP6 mitochondrial disease variants: Phenotypic and biochemical features analysis in 218 published cases and cohort of 14 new cases.

Authors:  Rebecca D Ganetzky; Claudia Stendel; Elizabeth M McCormick; Zarazuela Zolkipli-Cunningham; Amy C Goldstein; Thomas Klopstock; Marni J Falk
Journal:  Hum Mutat       Date:  2019-03-04       Impact factor: 4.878

4.  Leigh-Like Syndrome Due to Homoplasmic m.8993T>G Variant with Hypocitrullinemia and Unusual Biochemical Features Suggestive of Multiple Carboxylase Deficiency (MCD).

Authors:  Shanti Balasubramaniam; B Lewis; D M Mock; H M Said; M Tarailo-Graovac; A Mattman; C D van Karnebeek; D R Thorburn; R J Rodenburg; J Christodoulou
Journal:  JIMD Rep       Date:  2016-07-22

5.  m.8993T>G-Associated Leigh Syndrome with Hypocitrullinemia on Newborn Screening.

Authors:  Mari Mori; John R Mytinger; Lisa C Martin; Dennis Bartholomew; Scott Hickey
Journal:  JIMD Rep       Date:  2014-09-21

Review 6.  Diagnosis and management of mitochondrial disease: a consensus statement from the Mitochondrial Medicine Society.

Authors:  Sumit Parikh; Amy Goldstein; Mary Kay Koenig; Fernando Scaglia; Gregory M Enns; Russell Saneto; Irina Anselm; Bruce H Cohen; Marni J Falk; Carol Greene; Andrea L Gropman; Richard Haas; Michio Hirano; Phil Morgan; Katherine Sims; Mark Tarnopolsky; Johan L K Van Hove; Lynne Wolfe; Salvatore DiMauro
Journal:  Genet Med       Date:  2014-12-11       Impact factor: 8.822

7.  The ability of human nuclear DNA to cause false positive low-abundance heteroplasmy calls varies across the mitochondrial genome.

Authors:  Levent Albayrak; Kamil Khanipov; Maria Pimenova; George Golovko; Mark Rojas; Ioannis Pavlidis; Sergei Chumakov; Gerardo Aguilar; Arturo Chávez; William R Widger; Yuriy Fofanov
Journal:  BMC Genomics       Date:  2016-12-12       Impact factor: 3.969

8.  LEIGH SYNDROME: A CASE REPORT WITH A MITOCHONDRIAL DNA MUTATION.

Authors:  Tânia Lopes; Margarida Coelho; Diana Bordalo; António Bandeira; Anabela Bandeira; Laura Vilarinho; Paula Fonseca; Sónia Carvalho; Cecília Martins; José Gonçalves Oliveira
Journal:  Rev Paul Pediatr       Date:  2018-10-29

9.  Reducing False-Positive Results in Newborn Screening Using Machine Learning.

Authors:  Gang Peng; Yishuo Tang; Tina M Cowan; Gregory M Enns; Hongyu Zhao; Curt Scharfe
Journal:  Int J Neonatal Screen       Date:  2020-03-03
  9 in total

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