Development of a newborn screening tool for mucopolysaccharidosis type I based on bivariate normal limits: Using glycosaminoglycan and alpha‐L‐iduronidase determinations on dried blood spots to predict symptoms
Autor: | Kenji E. Orii, Kabir Jalal, Toshiyuki Fukao, Seiji Yamaguchi, Molly Stapleton, Hironori Kobayashi, Amy Barczykowski, Randy L. Carter, Shunji Tomatsu, Thomas J. Langan |
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Jazyk: | angličtina |
Rok vydání: | 2020 |
Předmět: |
Research Report
medicine.medical_specialty heparan lcsh:QH426-470 Endocrinology Diabetes and Metabolism sulfate Biochemistry Genetics and Molecular Biology (miscellaneous) Gastroenterology lcsh:Diseases of the endocrine glands. Clinical endocrinology Glycosaminoglycan 03 medical and health sciences Mucopolysaccharidosis type I 0302 clinical medicine Internal medicine alpha‐L‐iduronidase Internal Medicine medicine Dried blood 030304 developmental biology 0303 health sciences Newborn screening lcsh:RC648-665 business.industry newborn screening mucopolysaccharidosis type I biomarkers Research Reports medicine.disease Predictive value 3. Good health lcsh:Genetics glycosaminoglycans Krabbe disease business Iduronidase 030217 neurology & neurosurgery |
Zdroj: | JIMD Reports, Vol 52, Iss 1, Pp 35-42 (2020) JIMD Reports |
ISSN: | 2192-8312 |
Popis: | Purpose Current newborn screening (NBS) for mucopolysaccharidosis type I (MPSI) has very high false positive rates and low positive predictive values (PPVs). To improve the accuracy of presymptomatic prediction for MPSI, we propose an NBS tool based on known biomarkers, alpha‐L‐iduronidase enzyme activity (IDUA) and level of the glycosaminoglycan (GAG) heparan sulfate (HS). Methods We developed the NBS tool using measures from dried blood spots (DBS) of 5000 normal newborns from Gifu Prefecture, Japan. The tool's predictive accuracy was tested on the newborn DBS from these infants and from seven patients who were known to have early‐onset MPSI (Hurler's syndrome). Bivariate analyses of the standardized natural logarithms of IDUA and HS levels were employed to develop the tool. Results Every case of early‐onset MPSI was predicted correctly by the tool. No normal newborn was incorrectly identified as having early‐onset MPSI, whereas 12 normal newborns were so incorrectly identified by the Gifu NBS protocol. The PPV was estimated to be 99.9%. Conclusions Bivariate analysis of IDUA with HS in newborn DBS can accurately predict early MPSI symptoms, control false positive rates, and enhance presymptomatic treatment. This bivariate analysis‐based approach, which was developed for Krabbe disease, can be extended to additional screened disorders. |
Databáze: | OpenAIRE |
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