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[Measurement of angiotensin-I-converting enzyme in the blood: help for method validation]
Bruno Baudin1, Mustapha Zendjabil2, Stéphane Allouche3
1Service de biochimie, Hôpital Armand Trousseau, DMU BioGem, AP-HP-Sorbonne Université, Paris, France.
Annales De Biologie Clinique
|July 4, 2020
Summary
The blood angiotensin-converting enzyme (ACE) assay using synthetic substrate FAPGG is reliable for serum and plasma. This method is adaptable to automated analyzers and provides accurate results for clinical diagnostics.
Area of Science:
- Clinical Biochemistry
- Enzymology
Background:
- Blood angiotensin-converting enzyme (ACE) activity is typically measured using synthetic substrates like FAPGG.
- Current assays are optimized for serum or plasma and may not be suitable for other biological fluids like cerebrospinal fluid due to lower ACE activity.
Purpose of the Study:
- To describe the adaptation and validation of a blood ACE assay for automated biochemistry analyzers.
- To outline sample handling, storage, and assay performance characteristics.
Main Methods:
- Enzyme activity determination using the synthetic substrate furylacryloyl-phenylalanyl-L-glycyl-L-glycine (FAPGG).
- Adaptation of the assay to various automated biochemistry analyzers.
- Evaluation of sample stability and storage conditions (+4°C for one week, -20°C without refreezing).
Main Results:
- The assay demonstrates linearity from 10 to 200 UI/L with excellent fidelity after calibration.
- Analytical uncertainty ranges from 2% to 5%, depending on serum ACE levels.
- ACE activity may be higher in adolescent males, with further studies on age and sex expected.
Conclusions:
- The described blood ACE assay is robust, accurate, and adaptable to automated platforms for clinical use.
- Understanding ACE activity variations is crucial for diagnosing conditions like sarcoidosis and monitoring ACE inhibitor therapy.
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