Total body skeletal muscle mass: estimation by creatine (<i>methyl</i>-d₃) dilution in humans

Current methods for clinical estimation of total body skeletal muscle mass have significant limitations. We tested the hypothesis that creatine ( methyl-d 3 ) dilution (D 3 -creatine) measured by enrichment of urine D 3 -creatinine reveals total body creatine pool size, providing an accurate estimate of total body skeletal muscle mass. Healthy subjects with different muscle masses [ n = 35: 20 men (19–30 yr, 70–84 yr), 15 postmenopausal women (51–62 yr, 70–84 yr)] were housed for 5 days. Optimal tracer dose was explored with single oral doses of 30, 60, or 100 mg D 3 -creatine given on day 1. Serial plasma samples were collected for D 3 -creatine pharmacokinetics. All urine was collected through day 5. Creatine and creatinine (deuterated and unlabeled) were measured by liquid chromatography mass spectrometry. Total body creatine pool size and muscle mass were calculated from D 3 -creatinine enrichment in urine. Muscle mass was also measured by magnetic resonance imaging (MRI), dual-energy x-ray absorptiometry (DXA), and traditional 24-h urine creatinine. D 3 -creatine was rapidly absorbed and cleared with variable urinary excretion. Isotopic steady-state of D 3 -creatinine enrichment in the urine was achieved by 30.7 ± 11.2 h. Mean steady-state enrichment in urine provided muscle mass estimates that correlated well with MRI estimates for all subjects ( r = 0.868, P &lt; 0.0001), with less bias compared with lean body mass assessment by DXA, which overestimated muscle mass compared with MRI. The dilution of an oral D 3 -creatine dose determined by urine D 3 -creatinine enrichment provides an estimate of total body muscle mass strongly correlated with estimates from serial MRI with less bias than total lean body mass assessment by DXA.