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Status: Bibliographieeintrag

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Verfasst von:Shibata, Naoaki [VerfasserIn]   i
 Hasegawa, Yuki [VerfasserIn]   i
 Yamada, Kenji [VerfasserIn]   i
 Kobayashi, Hironori [VerfasserIn]   i
 Purevsuren, Jamiyan [VerfasserIn]   i
 Yang, Yanling [VerfasserIn]   i
 Dung, Vu Chi [VerfasserIn]   i
 Khanh, Nguyen Ngoc [VerfasserIn]   i
 Verma, Ishwar C. [VerfasserIn]   i
 Bijarnia-Mahay, Sunita [VerfasserIn]   i
 Lee, Dong Hwan [VerfasserIn]   i
 Niu, Dau-Ming [VerfasserIn]   i
 Hoffmann, Georg Friedrich [VerfasserIn]   i
 Shigematsu, Yosuke [VerfasserIn]   i
 Fukao, Toshiyuki [VerfasserIn]   i
 Fukuda, Seiji [VerfasserIn]   i
 Taketani, Takeshi [VerfasserIn]   i
 Yamaguchi, Seiji [VerfasserIn]   i
Titel:Diversity in the incidence and spectrum of organic acidemias, fatty acid oxidation disorders, and amino acid disorders in Asian countries
Titelzusatz:Selective screening vs. expanded newborn screening
Verf.angabe:Naoaki Shibata, Yuki Hasegawa, Kenji Yamada, Hironori Kobayashi, Jamiyan Purevsuren, Yanling Yang, Vu Chi Dung, Nguyen Ngoc Khanh, Ishwar C. Verma, Sunita Bijarnia-Mahay, Dong Hwan Lee, Dau-Ming Niu, Georg F. Hoffmann, Yosuke Shigematsu, Toshiyuki Fukao, Seiji Fukuda, Takeshi Taketani, Seiji Yamaguchi
E-Jahr:2018
Jahr:21 May 2018
Umfang:6 S.
Fussnoten:Gesehen am 01.10.2019
Titel Quelle:Enthalten in: Molecular genetics and metabolism reports
Ort Quelle:Amsterdam [u.a.] : Elsevier, 2014
Jahr Quelle:2018
Band/Heft Quelle:16(2018), Seite 5-10
ISSN Quelle:2214-4269
Abstract:Background - Expanded newborn screening (ENBS) utilizing tandem mass spectrometry (MS/MS) for inborn metabolic diseases (IMDs), such as organic acidemias (OAs), fatty acid oxidation disorders, (FAODs), and amino acid disorders (AAs), is increasingly popular but has not yet been introduced in many Asian countries. This study aimed to determine the incidence rates of OAs, FAODs, and AAs in Asian countries and Germany using selective screening and ENBS records. - Materials and methods - Selective screening for IMDs using gas chromatography-mass spectrometry and MS/MS was performed among patients suspected to be afflicted in Asian countries (including Japan, Vietnam, China, and India) between 2000 and 2015, and the results from different countries were compared. Similarly, ENBS results from Japan, South Korea, Taiwan, and Germany were compared. Additionally, the results of selective screening and ENBS in Japan were compared. - Results - Among 39,270 patients who underwent selective screening, IMDs were detected in 1170. Methylmalonic acidemia was frequently identified in several countries, including Japan (81/377 diagnosed IMDs), China (94/216 IMDs), and India (72/293 IMDs). In Vietnam, however, β-ketothiolase deficiency was particularly frequent (33/250 IMDs). ENBS yielded differences in overall IMD rates by country: 1:8557 in Japan, 1:7030 in Taiwan, 1:13,205 in South Korea, and 1:2200 in Germany. Frequently discovered diseases included propionic acidemia (PPA) and phenylketonuria (PKU) in Japan, 3-methylcrotonyl-CoA carboxylase deficiency (MCCD) and PKU in Taiwan, MCCD and citrullinemia type I in South Korea, and PKU and medium-chain acyl-CoA dehydrogenase deficiency in Germany. Furthermore, in Japan, selective screening and ENBS yielded respective PPA frequencies of 14.7% and 49.4% among all organic acidemias. - Conclusion - The incidence rates of IMDs vary by country. Moreover, the disease spectra of IMDs detected via selective screening differ from those detected via ENBS.
DOI:doi:10.1016/j.ymgmr.2018.05.003f per
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext: https://doi.org/10.1016/j.ymgmr.2018.05.003
 Verlag: http://www.sciencedirect.com/science/article/pii/S221442691830034X
 DOI: https://doi.org/10.1016/j.ymgmr.2018.05.003f per
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:Amino acid disorder
 Expanded newborn screening
 Fatty acid oxidation disorder
 Incidence rate
 Inherited metabolic disease
 Organic acidemia
K10plus-PPN:1677996943
Verknüpfungen:→ Zeitschrift

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