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Do different assays for human acylated ghrelin concentrations provide comparable results?
Günes Kadas1, Markus Klotz2, Karl-Herbert Schäfer2
1Saarland University, Department of Neurology, Homburg, Germany.
Two common methods for measuring human ghrelin blood concentrations, ELISA and Luminex, show acceptable agreement and reliability. This cross-validation is crucial in the absence of a gold standard assay for ghrelin.
Area of Science:
- Biochemistry
- Analytical Chemistry
Background:
- Human ghrelin blood concentrations vary significantly across studies.
- Discrepancies may stem from patient factors, sample processing, analytical methods, and assay manufacturers.
- Limited data exist on the comparability and external validity of ghrelin assays.
Purpose of the Study:
- To compare acylated ghrelin concentrations measured by ELISA and Luminex technology.
- To assess the agreement and reliability of these two common analytical methods for ghrelin measurement.
Main Methods:
- Analyzed 256 human plasma samples for acylated ghrelin.
- Utilized a commercially available enzyme-linked immunoassay (ELISA).
- Employed a multiplex analysis kit with Luminex® technology.
Main Results:
- Both ELISA and Luminex yielded ghrelin concentrations within a similar range.
- ELISA measurements were systematically higher (median 1.4-fold).
- High correlation (Pearson's r=0.753, p<0.01) and good agreement observed via Bland-Altman plots.
Conclusions:
- The two investigated techniques (ELISA and Luminex) demonstrate acceptable agreement for ghrelin measurement.
- The concordance suggests good external consistency and reliability for both analytical methods.
- This study provides a cross-validation for both assays in the absence of a definitive gold standard.
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