Experiences during newborn screening for glutaric aciduria type 1: Diagnosis, treatment, genotype, phenotype, and outcomes
- PMID: 28302372
- DOI: 10.1016/j.jcma.2016.07.006
Experiences during newborn screening for glutaric aciduria type 1: Diagnosis, treatment, genotype, phenotype, and outcomes
Abstract
Background: Glutaric aciduria type 1 (GA-1) is an organic acidemia with potentially severe neurological sequelae. In Taiwan, newborn screening (NBS) for GA-1 began in 2001, but large-scale reporting is lacking. This study describes Taiwan's largest newborn screening population to date.
Methods: Between 2001 and 2015, 1,490,636 newborns were screened for GA-1. Confirmatory examinations included the carnitine loading test. Confirmed patients were treated with a low lysine diet, carnitine, and high-energy intake during illness. Clinical, laboratory, and neuroimaging data were analyzed.
Results: Fourteen newborns were diagnosed with GA-1 (incidence: 1/106,474). C5DC concentration was clearly increased after carnitine loading in the affected newborns, but not in false-positive newborns (p = 0.004), indicating that this test is useful as an adjuvant diagnostic method. Eleven patients followed in our hospital were enrolled, namely nine NBS patients and two patients diagnosed clinically. IVS10-2A>C was the most common mutation. Two novel mutations (T36fs and N291K) were identified. Pendular nystagmus was found in two pediatric GA-1 patients. The corresponding pathology was optic atrophy in one patient, but remained undetermined in the other patient. The frequency of encephalopathic crisis decreased substantially following NBS. Among patients diagnosed by NBS, cognitive functioning was better among patients with good compliance than patients with poor compliance (p = 0.03). Abnormalities were detected by brain MRI including diffusion-weighted imaging and apparent diffusion coefficient maps; these affected various brain regions at different stages of the disease. Basal ganglion injuries occurred after an encephalopathic crisis. White matter disease was prevalent among older patients, either with or without an encephalopathic crisis.
Conclusion: Early diagnosis by newborn screening followed by full compliance with treatment guidelines is important to a good outcome.
Keywords: Taiwan; glutaric aciduria type 1; newborn screening; nystagmus; optic atrophy.
Copyright © 2017. Published by Elsevier Taiwan LLC.
Similar articles
-
Renal insufficiency mimicking glutaric acidemia type 1 on newborn screening.Pediatr Int. 2018 Jan;60(1):67-69. doi: 10.1111/ped.13438. Epub 2017 Dec 14. Pediatr Int. 2018. PMID: 29059480
-
Promising outcomes in glutaric aciduria type I patients detected by newborn screening.Metab Brain Dis. 2013 Mar;28(1):61-7. doi: 10.1007/s11011-012-9349-z. Epub 2012 Oct 27. Metab Brain Dis. 2013. PMID: 23104440
-
Biochemical, molecular, and clinical features of patients with glutaric acidemia type 1 identified through large-scale newborn screening in Zhejiang Province, China.Clin Chim Acta. 2022 May 1;530:113-118. doi: 10.1016/j.cca.2022.03.026. Epub 2022 Apr 1. Clin Chim Acta. 2022. PMID: 35367405
-
Diagnosis and management of glutaric aciduria type I--revised recommendations.J Inherit Metab Dis. 2011 Jun;34(3):677-94. doi: 10.1007/s10545-011-9289-5. Epub 2011 Mar 23. J Inherit Metab Dis. 2011. PMID: 21431622 Free PMC article. Review.
-
[Complex heterogeneity phenotypes and genotypes of glutaric aciduria type 1].Zhongguo Dang Dai Er Ke Za Zhi. 2016 May;18(5):460-5. doi: 10.7499/j.issn.1008-8830.2016.05.016. Zhongguo Dang Dai Er Ke Za Zhi. 2016. PMID: 27165598 Free PMC article. Review. Chinese.
Cited by
-
Enlargement of the Optic Chiasm: A Novel Imaging Finding in Glutaric Aciduria Type 1.AJNR Am J Neuroradiol. 2021 Sep;42(9):1722-1726. doi: 10.3174/ajnr.A7199. Epub 2021 Jul 8. AJNR Am J Neuroradiol. 2021. PMID: 34244130 Free PMC article.
-
Audiological and otologic manifestations of glutaric aciduria type I.Orphanet J Rare Dis. 2020 Dec 1;15(1):337. doi: 10.1186/s13023-020-01571-w. Orphanet J Rare Dis. 2020. PMID: 33256818 Free PMC article.
-
Long-term prognosis of 35 patients with methionine adenosyltransferase deficiency based on newborn screening in China.Front Cell Dev Biol. 2023 Jan 10;10:1059680. doi: 10.3389/fcell.2022.1059680. eCollection 2022. Front Cell Dev Biol. 2023. PMID: 36704196 Free PMC article.
-
What are the information needs of parents caring for a child with Glutaric aciduria type 1?BMC Pediatr. 2019 Oct 13;19(1):349. doi: 10.1186/s12887-019-1742-x. BMC Pediatr. 2019. PMID: 31607269 Free PMC article.
-
The biochemical subtype is a predictor for cognitive function in glutaric aciduria type 1: a national prospective follow-up study.Sci Rep. 2021 Sep 29;11(1):19300. doi: 10.1038/s41598-021-98809-9. Sci Rep. 2021. PMID: 34588557 Free PMC article.
MeSH terms
Substances
Supplementary concepts
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Research Materials
Miscellaneous