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Clinical Chemistry 53: 717-722, 2007. First published February 1, 2007; 10.1373/clinchem.2006.076679
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(Clinical Chemistry. 2007;53:717-722.)
© 2007 American Association for Clinical Chemistry, Inc.


Endocrinology and Metabolism

Long-Term Stability of Amino Acids and Acylcarnitines in Dried Blood Spots

Kristina Anna Strnadová1,2, Margareta Holub2, Adolf Mühl2, Georg Heinze3, Rene Ratschmann2, Hermann Mascher4, Sylvia Stöckler-Ipsiroglu5, Franz Waldhauser2, Felix Votava1, Jan Lebl1 and Olaf A. Bodamer2,a

1 Department of Paediatrics, 3rd Faculty of Medicine, Charles University, Prague, Czech Republic.
2 Department of General Pediatrics, University Children’s Hospital Vienna, Vienna, Austria.
3 Section of Clinical Biometrics, Core Unit for Medical Statistics and Informatics, Medical, University of Vienna, Vienna, Austria.
4 Pharm-analyt Laboratory GmbH, Baden, Germany.
5 Children’s Hospital British Columbia University, Vancouver, British Columbia, Canada.

aAddress correspondence to this author at: Department of General Pediatrics, Division of Biochemical and Pediatric Genetics, University Children’s Hospital Vienna, Währinger Gürtel 18-20, A-1090 Vienna, Austria. Fax 43-1-406-3484; e-mail olaf.bodamer{at}meduniwien.ac.at.

Background: Dried blood filter cards, collected for newborn screening, are often stored for long periods of time. They may be suitable for the retrospective diagnosis of inborn errors of metabolism, but no data are currently available on the long-term stability of amino acids and acylcarnitine species.

Methods: We analyzed amino acids and acylcarnitines by tandem mass spectrometry in 660 anonymous, randomly selected filter cards from 1989 through 2004. We assessed long-term stability of metabolites by linear regression and estimated annual decrease of concentration for each metabolite.

Results: Concentrations of free carnitine increased by 7.6% per year during the first 5 years of storage and decreased by 1.4% per year thereafter. Alanine, arginine, leucine, methionine, and phenylalanine decreased by 6.5%, 3.3%, 3.1%, 7.3%, and 5.7% per year, respectively. Acetylcarnitine, propionylcarnitine, citrulline, glycine, and ornithine decreased by 18.5%, 27.4%, 8.1%, 14.7%, and 16.3% per year during the first 5 years, respectively; thereafter the decline was more gradual. Tyrosine decreased by 1.7% per year during the first 5 years and 7.9% per year thereafter. We could not analyze medium- and long-chain acylcarnitine species because of low physiological concentrations.

Conclusions: Estimation of the annual decrease of metabolites may allow for the retrospective diagnosis of inborn errors of metabolism in filter cards that have been stored for long periods of time.




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Clin. Chem.Home page
D. Oglesbee, K. A. Sanders, J. M. Lacey, M. J. Magera, B. Casetta, K. A. Strauss, S. Tortorelli, P. Rinaldo, and D. Matern
Second-Tier Test for Quantification of Alloisoleucine and Branched-Chain Amino Acids in Dried Blood Spots to Improve Newborn Screening for Maple Syrup Urine Disease (MSUD)
Clin. Chem., March 1, 2008; 54(3): 542 - 549.
[Abstract] [Full Text] [PDF]




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