BACKGROUND: Current methods to measure skeletal muscle mass are not practical in a clinical setting. Liquid chromatography-tandem mass spectrometry (LC-MS/MS) methods that measure the amount of urinary d3-creatinine enrichment after a single tracer dose of d3-creatine was developed. RESULTS: The biomarkers d3-creatinine and creatinine were detected in human urine using LC-MS/MS. In this assay a surrogate analyte, d3-creatinine, was used to quantify endogenous creatinine. However, since endogenous concentrations of creatinine were orders of magnitude higher than d3-creatinine, the peak area of a less intense isotope of creatinine was acquired. A response factor is used to correct for using a less intense isotope multiple reaction monitoring transition. CONCLUSION: Novel LC-MS/MS assays were developed that quantify the biomarkers d3-creatinine, creatinine and d3-creatine in urine. This method allows the estimation of total body creatine pool size and subsequent calculation of muscle mass. This assay was originally validated as fit-for-purpose and was followed by full validation.
BACKGROUND: Current methods to measure skeletal muscle mass are not practical in a clinical setting. Liquid chromatography-tandem mass spectrometry (LC-MS/MS) methods that measure the amount of urinary d3-creatinine enrichment after a single tracer dose of d3-creatine was developed. RESULTS: The biomarkers d3-creatinine and creatinine were detected in human urine using LC-MS/MS. In this assay a surrogate analyte, d3-creatinine, was used to quantify endogenous creatinine. However, since endogenous concentrations of creatinine were orders of magnitude higher than d3-creatinine, the peak area of a less intense isotope of creatinine was acquired. A response factor is used to correct for using a less intense isotope multiple reaction monitoring transition. CONCLUSION: Novel LC-MS/MS assays were developed that quantify the biomarkers d3-creatinine, creatinine and d3-creatine in urine. This method allows the estimation of total body creatine pool size and subsequent calculation of muscle mass. This assay was originally validated as fit-for-purpose and was followed by full validation.
Authors: Richard V Clark; Ann C Walker; Robin L O'Connor-Semmes; Michael S Leonard; Ram R Miller; Stephen A Stimpson; Scott M Turner; Eric Ravussin; William T Cefalu; Marc K Hellerstein; William J Evans Journal: J Appl Physiol (1985) Date: 2014-04-24
Authors: Richard V Clark; Ann C Walker; Ram R Miller; Robin L O'Connor-Semmes; Eric Ravussin; William T Cefalu Journal: J Appl Physiol (1985) Date: 2017-08-31