Determining the Reference Range of Amino Acids in Healthy Neonatal Blood Samples in Northeast Iran Using LC-MS/MS

سال انتشار: 1403
نوع سند: مقاله ژورنالی
زبان: انگلیسی
مشاهده: 277

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شناسه ملی سند علمی:

JR_RBMB-13-1_010

تاریخ نمایه سازی: 18 آبان 1403

چکیده مقاله:

Background: Amino acid analysis is an important tool for the diagnosis of metabolic disorders in newborns. Today, Liquid Chromatography tandem mass spectrometry (LC-MS/MS) has emerged as a powerful technique for amino acid analysis. We aimed to determine the local normal range of amino acids in dried blood spot (DBS) samples of neonates using LC-MS/MS. Methods: A total of ۱۰۰۵ samples from healthy neonates of northeast and east of Iran aged ۲-۷ days were utilized for normal range determination. The amino acids were extracted from dried blood spot samples using organic solvent and then analyzed using LC-MS/MS system. The ۱%, ۲.۵%, ۹۷.۵%, and ۹۹% percentiles were calculated, and the results were compared to the global cut-off values. Results: The results showed that glutamic acid has the highest concentration range among amino acids evaluated in this study (۱۷۸.۹۴ – ۴۲۱.۳۱mmol/L). Moreover, the plasma concentrations of Glycine (۱۴۲.۶۵ – ۳۹۷.۰۶ mmol/L), Alanine (۹۷.۰۰–۳۴۹.۷۲ mmol/L), Proline (۶۳.۷۷ – ۲۳۶.۵۳ mmol/L), and Tyrosine (۲۵.۷۹ – ۱۵۰.۵۸ mmol/L) were in the next ranks. Comparing the obtained results with the global values obtained in the R۴S study indicated a slight difference between the obtained local normal values and the global values. Conclusion: The calculated values were slightly different from global values obtained in the R۴S study and regional values calculated in other studies. This further emphasized the importance of the local establishment of reference values, which facilitates the correct interpretation and diagnosis in the Newborn Screening Programs.

کلیدواژه ها:

Amino acids ، Dried blood spots ، Inborn Errors of metabolism ، LC-MS/MS ، Newborn screening.

نویسندگان

Zeinab Saeed

Department of Clinical Biochemistry, Mashhad University of Medical Sciences, Mashhad, Iran.

Baratali Mashkani

Department of Clinical Biochemistry, Mashhad University of Medical Sciences, Mashhad, Iran.

Amin Alaei

Department of Medical Laboratory Science, Varastegan Institute for Medical Sciences, Mashhad, Iran & Division of Metabolic Disorder, Pardis Clinical and Genetic Laboratory, Mashhad, Iran & Research Committee, Department of Medical Laboratory Science, Vara

Abdol Reza Varasteh

Department of Medical Laboratory Science, Varastegan Institute for Medical Sciences, Mashhad, Iran & Division of Metabolic Disorder, Pardis Clinical and Genetic Laboratory, Mashhad, Iran.

Fatemeh Keyfi

Department of Medical Laboratory Science, Varastegan Institute for Medical Sciences, Mashhad, Iran & Division of Metabolic Disorder, Pardis Clinical and Genetic Laboratory, Mashhad, Iran.

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