Health safety aspects of foodstuffs intented for phenylketonurics
DOI:
https://doi.org/10.5219/455Keywords:
phenylketonuria, phenylalanine, low-protein product, acid hydrolysis, chromatographyAbstract
Phenylketonuria is a rare metabolic disorder that occurs due to the lack of liver enzyme phenylalanine hydroxylase. Untreated it leads to mental retardation, delayed development of speech, microcephaly, epilepsy, behavioral problems etc. Its treatment consists of strict diet, very low in phenylalanine content. The aim of this study was to determine the health safety and suitability of 17 selected foods labeled as „low in protein" respectively „foods low in phenylalanine". Analyses were focused on their phenylalanine content and aminoacid representation. The other aim was to compare phenylalanine measured with the content declared by the producers on their label. By product origin, the largest amount of foodstuffs originated from Poland (59%), followed by Germany (23%) and equal representation (6%) had Slovakia, Hungary and Sweden. Automatic analyzer AAA 400, using ion exchange chromatography, analyzed the samples. The lowest determined phenylalanine content was 1 mg.100g-1 (in rubber candy) and the highest 299 mg.100g-1 (in paté). Powdered egg alternative was monitored as the second highest source of phenylalanine. Phenylalanine content in the monitored foods ranged from 1 to 299.6 mg. 100 g-1 respectively, and increased in the following order: Gum candies (1 mg.100g-1) < Cherry jelly (1.4 mg. 100g-1) < Flour (5.8 mg.100g-1) < Flour (5.9 mg.100g-1) < Spaghetti (8.7 mg.100g-1) < Pasta (9.9 mg.100g-1) < Waffle (14.2 mg.100g-1) < Salty sticks (23.8 mg.100g-1) < Chocolate (24.1 mg.100g-1) < Bread (26 mg.100g-1) < Breadcrumbs (27.1 mg.100g-1) < Sticks with salt (30.3 mg.100g-1) < Ice Cornets (30.8 mg.100g-1) < Walnut cookie (37.2 mg.100g-1) < Instant soup with noodles (46.1 mg.100g-1) < Powdered egg alternative (58 mg.100g-1) < Pate (299.6 mg.100g-1). Only seven products of 17 observed showed low phenylalanine content, less than 20 mg.100g-1.
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Directive 2009/39/EC of the European Parlament and of the Council of 6 May 2009 on foodstuffs intended for particular nutritional uses, OJ L 124, 20.5.2009, p. 21-29.
Buňka, F., Kříž, O., Veličková, A., Buňková, L., Kráčmar, S. 2009. Effect of acid hydrolysis time on amino acid determination in casein and processed cheeses with different fat content. Journal of Food Composition and Analysis,
vol. 22. no 3. p. 224-232. https://doi.org/10.1016/j.jfca.2008.10.023 DOI: https://doi.org/10.1016/j.jfca.2008.10.023
Burnett, J. R., Mamotte, C. D. S., Williams, R. A. 2008. Phenylketonuria: An Inborn Error of Phenylalanine Metabolism. Clin. Biochem. Review. vol. 29, no.1, p. 31-41. PMid:18566668
Commission Directive 1999/21/EC of 25 March 1999 on dietary foods for special medical purposes, OJ L 91, 7.4.1999, p. 29-36.
Dvořák, J. 2009. Fenylketonurie PKU. [cit. 2015-03-02] Available at: http://www.nspku.cz/nemoci/fenylketonurie.html
EFSA. 2014. Scientific Opinion on Aspartame. [cit. 2015-03-02] Available at: http://www.efsa.europa.eu/fr/search/doc/factsheetaspartame.pdf
Komárková, J., Pazdírková, R. 2010. Fenylketonurie a mateřství (Phenylketonuria and motherhood). 1st ed Praha: Klinika dětí a dorostu 3. lékařské fakulty UK: Fakultní nemocnice Královské Vinohrady. 53 p. ISBN 978-80-254-7368-9.
Macdonald, A., Gökmen-Ozel, H., Daly, A. 2009. Changing dietary practices in phenylketonuria. The Turkish Journal of Pediatrics, vol. 51, no. 5, p. 409-415. PMid:20112594
Mitchell, J. J. 2000. Phenylalanine Hydroxylase Deficiency. PMid:NBK1504
Poustie, V. J., Wildgoose J. 2010. Dietary interventions for phenylketonuria. Cochrane Database of Systematic Reviews. no 1. https://doi.org/10.1002/14651858.CD001304.pub2 PMid:20091517 DOI: https://doi.org/10.1002/14651858.CD001304.pub2
Strnová, J., Ürge, O. 2007. Maternálna fenylketonúria. (Maternal Phenylketonuria). In Via pract., vol. 4, no. 9, p. 417-419.
Svačina, Š., Bretšnajdrová, A., Holcátová, I. et al. 2008. Klinická dietologie (Clinical Dietetics). 1st ed. Praha: Grada Publishing a.s., 384 p. ISBN 978-80-247-2256-6.
Velíšek, J., Hajšlová, J. 2009. Chemie potravin. II. (Food Chemistry. II.) 3rd ed Havličkuv Brod: OSSIS. 644 p. ISBN 978-80-86659-16-9.
Decree of the Czech Ministry of Health on 30 January 2004 no. 54/2004 Coll. on foodstuffs intended for particular nutritional uses and how they are used.
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