Combining newborn metabolic and DNA analysis for second-tier testing of methylmalonic acidemia
| العنوان: | Combining newborn metabolic and DNA analysis for second-tier testing of methylmalonic acidemia |
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| المؤلفون: | Peidong Shen, Curt Scharfe, Hongyu Zhao, Neeru Gandotra, Gang Peng, Gregory M. Enns, Tina M. Cowan, Laura L. Jelliffe-Pawlowski, Eula Fung, Anthony Le, Ronald W. Davis |
| المصدر: | Genetics in medicine : official journal of the American College of Medical Genetics |
| سنة النشر: | 2018 |
| مصطلحات موضوعية: | 0301 basic medicine, Newborn screening, Male, medicine.medical_specialty, Methylmalonic acidemia, 030105 genetics & heredity, DNA sequencing, Article, Machine Learning, 03 medical and health sciences, chemistry.chemical_compound, Unknown Significance, Neonatal Screening, Internal medicine, False positive paradox, Medicine, Humans, Multiplex, Dried blood, Amino Acid Metabolism, Inborn Errors, Genetics (clinical), business.industry, Infant, Newborn, nutritional and metabolic diseases, food and beverages, Genetic Variation, medicine.disease, 3. Good health, 030104 developmental biology, chemistry, inborn metabolic disorders, DNA diagnostics, next-generation sequencing, Female, Dried Blood Spot Testing, business, DNA, Metabolism, Inborn Errors |
| الوصف: | Purpose: Improved second-tier tools are needed to reduce false-positive outcomes in newborn screening (NBS) for inborn metabolic disorders on the Recommended Universal Screening Panel (RUSP). Methods: We designed an assay for multiplex sequencing of 72 metabolic genes (RUSPseq) from newborn dried blood spots. Analytical and clinical performance was evaluated in 60 screen-positive newborns for methylmalonic acidemia (MMA) reported by the California Department of Public Health NBS program. Additionally, we trained a Random Forest machine learning classifier on NBS data to improve prediction of true- and false-positive MMA cases. Results: Of 28 MMA patients sequenced, we found two pathogenic or likely pathogenic (P/LP) variants in a MMA-related gene in 24 patients, and one pathogenic variant and a variant of unknown significance (VUS) in one patient. No such variant combinations were detected in MMA false-positives and healthy controls. Random Forest-based analysis of the entire NBS metabolic profile correctly identified the MMA patients and reduced MMA false-positive cases by 51%. MMA screen-positive newborns were more likely of Hispanic ethnicity. Conclusions: Our two-pronged approach reduced false-positives by half and provided a reportable molecular finding for 89% of MMA patients. Challenges remain in newborn metabolic screening and DNA variant interpretation in diverse multiethnic populations. |
| اللغة: | English |
| تدمد: | 1530-0366 1098-3600 |
| URL الوصول: | https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ddb9b15bd1ded2f245a99233c02f621e http://europepmc.org/articles/PMC6416784 |
| حقوق: | OPEN |
| رقم الأكسشن: | edsair.doi.dedup.....ddb9b15bd1ded2f245a99233c02f621e |
| قاعدة البيانات: | OpenAIRE |
Find this article in full text from Springer Verlag. | تدمد: | 15300366 10983600 |
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