Literature DB >> 20136525

DNA carrier testing and newborn screening for maple syrup urine disease in Old Order Mennonite communities.

Stephanie M Carleton1, Dawn S Peck, Julie Grasela, Kristin L Dietiker, Charlotte L Phillips.   

Abstract

Maple syrup urine disease (MSUD) is an inherited metabolic disorder caused by mutations in the branched chain alpha-keto acid dehydrogenase complex. Worldwide incidence of MSUD is 1:225,000 live births. However, within Old Order Mennonite communities, the incidence is 1:150 live births and results from a common tyrosine to asparagine substitution (Y438N) in the E1alpha subunit of branched chain alpha-keto acid dehydrogenase. We developed a new DNA diagnostic assay utilizing TaqMan technology and compared its efficacy, sensitivity, and duration with an existing polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) assay. Carrier testing was performed by both TaqMan technology and PCR-RFLP on DNA isolated from buccal swabs of 160 individuals as well as from buccal swabs and blood spots of nine at-risk newborns; assay time, sensitivity, and reliability were also evaluated. The TaqMan assay, like the PCR-RFLP assay, accurately determined Y438N E1alpha allele status. However, the TaqMan assay appeared (1) more sensitive than the PCR-RFLP assay, requiring 10-fold less DNA (10 ng) to reliably determine genotype status and (2) faster, reducing the assay time required for diagnosis from approximately 12 to 5 h. TaqMan technology allowed more rapid DNA diagnoses of MSUD in the neonate, thereby reducing the likelihood of neurological impairment while enhancing health and prognosis for affected infants.

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Year:  2010        PMID: 20136525      PMCID: PMC5586154          DOI: 10.1089/gtmb.2009.0107

Source DB:  PubMed          Journal:  Genet Test Mol Biomarkers        ISSN: 1945-0257


  10 in total

1.  Allelic discrimination using fluorogenic probes and the 5' nuclease assay.

Authors:  K J Livak
Journal:  Genet Anal       Date:  1999-02

2.  Maple syrup urine disease: favourable effect of early diagnosis by newborn screening on the neonatal course of the disease.

Authors:  E Simon; R Fingerhut; J Baumkötter; V Konstantopoulou; R Ratschmann; U Wendel
Journal:  J Inherit Metab Dis       Date:  2006-08       Impact factor: 4.982

3.  Evidence of common ancestry for the maple syrup urine disease (MSUD) Y438N allele in non-Mennonite MSUD patients.

Authors:  Latisha D Love-Gregory; Julia Grasela; Richard E Hillman; Charlotte L Phillips
Journal:  Mol Genet Metab       Date:  2002-01       Impact factor: 4.797

Review 4.  Human mutations affecting branched chain alpha-ketoacid dehydrogenase.

Authors:  D J Danner; C B Doering
Journal:  Front Biosci       Date:  1998-06-03

Review 5.  Markers associated with inborn errors of metabolism of branched-chain amino acids and their relevance to upper levels of intake in healthy people: an implication from clinical and molecular investigations on maple syrup urine disease.

Authors:  Hiroshi Mitsubuchi; Misao Owada; Fumio Endo
Journal:  J Nutr       Date:  2005-06       Impact factor: 4.798

6.  Carrier detection and rapid newborn diagnostic test for the common Y393N maple syrup urine disease allele by PCR-RFLP: culturally permissible testing in the Mennonite community.

Authors:  L D Love-Gregory; J A Dyer; J Grasela; R E Hillman; C L Phillips
Journal:  J Inherit Metab Dis       Date:  2001-06       Impact factor: 4.982

7.  Maple syrup urine disease: identification and carrier-frequency determination of a novel founder mutation in the Ashkenazi Jewish population.

Authors:  L Edelmann; M P Wasserstein; R Kornreich; C Sansaricq; S E Snyderman; G A Diaz
Journal:  Am J Hum Genet       Date:  2001-08-16       Impact factor: 11.025

Review 8.  Maple syrup urine disease: it has come a long way.

Authors:  D T Chuang
Journal:  J Pediatr       Date:  1998-03       Impact factor: 4.406

9.  Relationship of causative genetic mutations in maple syrup urine disease with their clinical expression.

Authors:  Mary M Nellis; Andrea Kasinski; Martha Carlson; Richard Allen; Anna Marie Schaefer; Edward M Schwartz; Dean J Danner
Journal:  Mol Genet Metab       Date:  2003 Sep-Oct       Impact factor: 4.797

10.  Psychosocial issues in families affected by maple syrup urine disease.

Authors:  Wendy Packman; Shelly L Henderson; Indira Mehta; Rama Ronen; Dean Danner; Beth Chesterman; Seymour Packman
Journal:  J Genet Couns       Date:  2007-08-17       Impact factor: 2.537

  10 in total
  3 in total

1.  A founder AGL mutation causing glycogen storage disease type IIIa in Inuit identified through whole-exome sequencing: a case series.

Authors:  Isabelle Rousseau-Nepton; Minoru Okubo; Rosemarie Grabs; John Mitchell; Constantin Polychronakos; Celia Rodd
Journal:  CMAJ       Date:  2015-01-19       Impact factor: 8.262

2.  Predictors of acute metabolic decompensation in children with maple syrup urine disease at the emergency department.

Authors:  Yılmaz Yıldız; Leman Akcan Yıldız; Ali Dursun; Ayşegül Tokatlı; Turgay Coşkun; Özlem Tekşam; Hatice Serap Sivri
Journal:  Eur J Pediatr       Date:  2020-02-11       Impact factor: 3.183

3.  High proportion of transient neonatal zinc deficiency causing alleles in the general population.

Authors:  Yarden Golan; Adrian Lehvy; Guy Horev; Yehuda G Assaraf
Journal:  J Cell Mol Med       Date:  2018-11-18       Impact factor: 5.310

  3 in total

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