Journal of Inherited Metabolic Disease

, Volume 34, Issue 2, pp 409–414 | Cite as

Newborn screening for galactosemia by a second-tier multiplex enzyme assay using UPLC-MS/MS in dried blood spots

  • Dae-Hyun Ko
  • Sun-Hee Jun
  • Kyoung Un Park
  • Sang Hoon Song
  • Jin Q Kim
  • Junghan Song


Galactosemia is one of the most important inherited metabolic disorders detected by newborn screening tests. Abnormal results during screening should be confirmed by enzyme activity assays. Recently, we developed a multiplex enzyme assay for galactosemia in erythrocytes using ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS). In this study, we proposed a second-tier multiplex enzyme assay for galactosemia that can be directly applied to dried blood spots (DBSs). Supernatants from two rehydrated-punched 3.2-mm DBSs were incubated with a reaction mixture containing [13C6]galactose, [13C2]galactose-1-phosphate, and UDP-glucose as substrates for three galactose-metabolizing enzymes. After a 4-hour incubation, the end products from the combined reaction mixture, [13C6]galactose-1-phosphate, UDP-[13C2]galactose, and UDP-galactose, were simultaneously measured using UPLC-MS/MS. Substrates, products, and internal standards from the mixture of the three enzyme reactions were clearly separated in the UPLC-MS/MS system, with an injection cycle time of 10 min. Intra- and inter-assay imprecisions of the UPLC-MS/MS were 8.4-14.8% and 13.2-15.7% CV, respectively. Enzyme activities in DBSs from 37 normal individuals and 10 patients with enzyme deficiencies were analyzed. DBSs from galactosemia patients showed consistently lower enzyme activities as compared to those of normal individuals. In conclusion, multiplex enzyme assays using UPLC-MS/MS can be successfully applied to DBS analysis. This method allows a fast and effective second-tier test for newborns showing abnormal screening results.


Newborn Screening Galactosemia Classical Galactosemia GALT Activity Enzyme Reaction Mixture 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.



Dried blood spot




Galactose-1-phosphate uridyltransferase




High Strength Silica


Uridine diphosphate


Ultraperformance liquid chromatography-tandem mass spectrometry



This study was supported by Grant A090742 from the Korea Healthcare Technology R&D Project, Ministry for Health & Welfare, Republic of Korea.


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Copyright information

© SSIEM and Springer 2011

Authors and Affiliations

  • Dae-Hyun Ko
    • 1
  • Sun-Hee Jun
    • 2
  • Kyoung Un Park
    • 1
    • 2
  • Sang Hoon Song
    • 2
  • Jin Q Kim
    • 3
  • Junghan Song
    • 1
    • 2
  1. 1.Department of Laboratory MedicineSeoul National University College of MedicineSeoulKorea
  2. 2.Department of Laboratory MedicineSeoul National University Bundang HospitalGyeonggi-doKorea
  3. 3.Konkuk UniversitySeoulKorea

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