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An UPLC-MSMS method to measure plasma homocysteine concentration
Caroline Vayne1, Luc Deroche1, Nicolas Drillaud1
1Laboratoire de biochimie et biologie moléculaire, CHRU Tours, France.
A new mass spectrometry method offers a rapid and reliable way to measure plasma homocysteine (Hcy) concentrations. This validated technique provides excellent performance and establishes new normal value ranges for routine clinical practice.
Area of Science:
- Clinical Chemistry
- Analytical Chemistry
- Biomedical Science
Background:
- Homocysteine (Hcy) monitoring is increasingly important for various diseases.
- Existing methods for Hcy measurement may lack the speed or reliability required for routine clinical practice.
- Accurate and efficient Hcy quantification is essential for patient diagnosis and management.
Purpose of the Study:
- To validate a novel mass spectrometry (MS) method for quantifying plasma homocysteine (Hcy).
- To establish targeted Hcy concentration ranges aligned with COFRAC recommendations.
- To assess the method's suitability for routine laboratory use.
Main Methods:
- Validation of a new mass spectrometry assay for plasma Hcy.
- Data collection of Hcy concentrations from 2014-2015.
- Comparison of Hcy values across different clinical groups.
- Evaluation of method performance characteristics including reproducibility and sensitivity.
Main Results:
- The mass spectrometry method demonstrated excellent reproducibility and sensitivity (CV <10%).
- New reference ranges for normal plasma Hcy concentrations were determined: 12.4 [11.8-13.0] μmol/L.
- The method proved robust and suitable for high-throughput clinical laboratory analysis.
Conclusions:
- The validated mass spectrometry method is rapid, robust, and reliable for routine plasma Hcy measurement.
- This new assay addresses the growing demand for Hcy testing in clinical settings.
- The established normal value ranges support accurate interpretation of Hcy levels.
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