Analysis of glucocerebrosidase activity in dry blood spots using tandem mass spectrometry

详细信息    查看全文

• 作者：Elisa Legini ; Joseph J. Orsini ; Christina Hung ; Monica Martin ; Am ; a Showers ; Maurizio Scarpa ; X Kate Zhang ; Joan Keutzer ; Adolf Mü ; hl ; Olaf A. Bodamer
• 关键词：Dry blood spot ; Enzyme ; Filter card ; Lysosomal ; Mass spectrometry
• 刊名：Clinica Chimica Acta
• 出版年：2011
• 出版时间：30 January 2011
• 年：2011
• 卷：412
• 期：3-4
• 页码：343-346
• 全文大小：304 K

文摘

Background

Gaucher disease (GD) is due to deficiency of acid-β-glucosidase (ABG) and comprises a clinical spectrum with variable age of onset and severity. We evaluated a tandem mass spectrometry (MS/MS) method to measure ABG activity for high through-put screening.

Methods

ABG activity was measured in 3.2 mm punches from dry blood spots (DBS). Each punch was incubated for 21 h with the substrate D-Glucosyl-β1-1′-N-dodecanoyl-D-erythro-sphingosine [C12-glucocerebroside (C₃₆H₆₉NO₈)] and internal standard N-myristoyl-D-erythro-sphingosine [C14-ceramide (C₃₂H₆₃NO₃)]. The product and internal standard were quantified using MS/MS.

Results

ABG activities in anonymized newborn screening samples from NY State were (mean) 22.0 μmol/h/L ± (SD) 13.8 μmol/h/L (n = 2088, median 19.9 μmol/h/L, 95 % CI 22.59–21.41 μmol/h/L). The enzymatic activity in DBS from 10 treatment naïve adult Gaucher patients was less than 4.2 μmol/h/L. ABG activity was stable for 3 months at room temperature a 20 % activity reduction was observed. Inter- and intra-run imprecisions were 8 % and 13.7 % , respectively. The limit of detection was 0.75 μmol/h/L and limit of quantification was 1.25 μmol/h/L.

Conclusions

The measurement of ABG activities in DBS using MS/MS is suitable for high-throughput analysis of at-risk individuals and potentially for newborn screening for GD.