Development of a Universal Second-Tier Newborn Screening LC-MS/MS Method for Amino Acids, Lysophosphatidylcholines, and Organic Acids

被引:19
作者
Kilgore, Matthew B. [1 ]
Platis, Dimitrios [2 ]
Lim, Timothy [1 ]
Isenberg, Samantha [1 ]
Pickens, C. Austin [1 ]
Cuthbert, Carla [1 ]
Petritis, Konstantinos [1 ]
机构
[1] US Ctr Dis Control & Prevent, Newborn Screening & Mol Biol Branch, Atlanta, GA 30341 USA
[2] Inst Child Hlth, Dept Newborn Screening, Athens 11526, Greece
关键词
DRIED-BLOOD SPOTS; TANDEM MASS-SPECTROMETRY; SYRUP-URINE-DISEASE; RAPID DIAGNOSIS; QUANTIFICATION; ACYLCARNITINES; MARKERS;
D O I
10.1021/acs.analchem.2c03098
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
First-tier MS-based newborn screening by flow injection analysis can have high presumptive positive rates, often due to isomeric/isobaric compounds or poor biomarker specificity. These presumptive positive samples can be analyzed by second-tier screening assays employing separations such as liquid chromatography-mass spectrometry (LC-MS/MS), which increases test specificity and drastically reduces false positive referrals. The ability to screen for multiple disorders in a single multiplexed test simplifies workflows and maximizes public health laboratories' resources. In this study, we developed and validated a highly multiplexed second-tier method for dried blood spots using a hydrophilic interaction liquid chromatography (HILIC) column coupled to an MS/MS system. The LC-MS/MS method was capable of simultaneously detecting second-tier biomarkers for maple syrup urine disease, homocystinuria, methylmalonic acidemia, propionic acidemia, glutaric acidemia type 1, glutaric acidemia type 2, guanidinoacetate methyltransferase deficiency, short-chain acyl-CoA dehydrogenase deficiency, adrenoleukodystrophy, and Pompe disease.
引用
收藏
页码:3187 / 3194
页数:8
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