Literature DB >> 28649554

Comments on 'Newborn screening in southeastern Europe' published in Molecular Genetics and Metabolism, 2014 Sept-Oct;113(1-2):42-45 by U. Groselj, M. ZerjavTansek, A. Smon, N. Angelkova, D. Anton, I. Baric, M. Djordjevic, L. Grimci, M. Ivanova, A. Kadam, V. Mulliqi Kotori, H. Maksic, O. Marginean, O. Margineanu, O. Milijanovic, F. Moldovanu, M. Muresan, S. Murko, M. Nanu, B. Repic Lampert, M. Samardzic, V. Sarnavka, A. Savov, M. Stojiljkovic, B. Suzic, R. Tincheva, H. Tahirovic, A. Toromanovic, N. Usurela, T. Battelino.

Mirjana Kocova1, Violeta Anastasovska2.   

Abstract

Entities:  

Keywords:  Newborn screening; Southeastern Europe; Survey

Year:  2015        PMID: 28649554      PMCID: PMC5471394          DOI: 10.1016/j.ymgmr.2015.11.003

Source DB:  PubMed          Journal:  Mol Genet Metab Rep        ISSN: 2214-4269


× No keyword cloud information.
One year ago, a study for assessment of the current state of newborn screening (NBS) in the region of southeastern Europe, focusing also on the future plans, was published [1]. We would like to correct data for the NBS program, future plans, and also GDP per capita in Macedonia. Methodology of data collection is questionable since ISNS (International Society for Neonatal Screening) has not been included as a data resource. The authors claimed that PKU newborn screening was not introduced in 4 of 11 countries: Albania, Kosovo, Macedonia, and Montenegro, and that in the Macedonia there aren't plans to expand NBS in the next 5 years [1]. However, in Macedonia a selective newborn screening for inborn errors of metabolism, including PKU, by tandem mass spectrometry, has been implemented. In 2012, a total of 4072 newborns from six bigger nurseries, were screened (17.14%) and two newborns with inborn errors of metabolism (phenylketonuria and hypermethioninemia) were detected. Metabolic newborn screening is performed under an external independent quality control by CDC (Centers for Disease Control and Prevention, www.cdc.gov) Atlanta, USA. On the other side, the experience with the newborn screening for congenital hypothyroidism in Macedonia has been reported previously [2]. In the paper of Groselj et al. [1], the economic backgrounds responses from participating countries showed that Macedonia had GDP 11,834 USD per capita for 2012. These data correspond to GDP in International dollars (Int$) and are significantly higher than GDP in USD. However, all given GDP values in the paper are in International dollars but are discussed as USD. Macedonian GDP per capita for 2012 was 3680 EUR (4127 USD) [3]. In conclusion, in Macedonia, as a country with the low GDP per capita, selective neonatal screening has been introduced for more than 30 inherited metabolic disorders, by tandem mass spectrometry, since 2011. Activities to cover all newborns are underway.

Conflict of interest

The authors do not have any conflict of interest.
  2 in total

1.  Newborn screening in southeastern Europe.

Authors:  Urh Groselj; Mojca Zerjav Tansek; Andraz Smon; Natalija Angelkova; Dana Anton; Ivo Baric; Maja Djordjevic; Lindita Grimci; Maria Ivanova; Adil Kadam; Vjosa Mulliqi Kotori; Hajrija Maksic; Oana Marginean; Otilia Margineanu; Olivera Milijanovic; Florentina Moldovanu; Mariana Muresan; Simona Murko; Michaela Nanu; Barbka Repic Lampret; Mira Samardzic; Vladimir Sarnavka; Aleksei Savov; Maja Stojiljkovic; Biljana Suzic; Radka Tincheva; Husref Tahirovic; Alma Toromanovic; Natalia Usurelu; Tadej Battelino
Journal:  Mol Genet Metab       Date:  2014-08-01       Impact factor: 4.797

2.  Clinical practice: experience with newborn screening for congenital hypothyroidism in the Republic of Macedonia - a multiethnic country.

Authors:  Mirjana Kocova; Violeta Anastasovska; Elena Sukarova-Angelovska; Milica Tanaskoska; Elizabeta Taseva
Journal:  Eur J Pediatr       Date:  2014-09-07       Impact factor: 3.183

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.