Heuser Alexander, Frings-Meuthen Petra, Rittweger Jörn, Galer Stephen J G
Steinmann-Institut für Geologie, Mineralogie und Paläontologie, Universität Bonn, Bonn, Germany.
Institute of Aerospace Medicine, German Aerospace Center (DLR), Cologne, Germany.
Front Physiol. 2019 Jan 25;10:12. doi: 10.3389/fphys.2019.00012. eCollection 2019.
The calcium (Ca) isotopic composition in urine during bed rest has been demonstrated to be systematically light, indicating a negative bone mineral balance (i.e., bone loss). Here we present new Ca isotope data on urine during the "nutritional countermeasures" (NUC) bed rest study. We analyzed the Ca isotopic composition of 24 h pooled urine samples from seven healthy male subjects during baseline data collection (BDC), head-down-tilt bed rest and recovery. Additionally, we analyzed urine from two follow-up examinations after the regeneration phase. We observed a change in Ca isotopic composition during the bed rest phase, indicative of bone loss with a time delay of 10 to 21 days. We also observe that the Ca isotopic composition of urine is strongly dependent on the individual Ca metabolism and varies between subjects. We relate this individuality in Ca metabolism to differences in the amounts of Ca being recycled in the kidneys. Previous studies have shown that the more Ca is reabsorbed in the kidneys the more enriched the urine becomes in heavy isotopes of calcium. The Ca isotopic composition of urine is thus modified by more than one process and cannot be used in a straightforward manner to monitor net bone mineral balance. To overcome this problem, we propose a new baseline approach for using Ca isotopes, which effectively cancels out the effects of individual renal Ca reabsorption. This allows us to detect bone loss in patients without ambiguity by combining measurements of the Ca isotopic composition of urine and daily Ca excretion rate and comparing these to data collected on healthy individuals with a normal steady-state bone balance.
卧床休息期间尿液中的钙(Ca)同位素组成已被证明系统地偏轻,表明骨矿物质平衡为负(即骨质流失)。在此,我们展示了“营养对策”(NUC)卧床休息研究期间尿液的新钙同位素数据。我们分析了7名健康男性受试者在基线数据收集(BDC)、头低位卧床休息和恢复期间24小时混合尿液样本的钙同位素组成。此外,我们还分析了再生期后两次随访检查的尿液。我们观察到卧床休息阶段钙同位素组成发生了变化,这表明骨质流失存在10至21天的时间延迟。我们还观察到尿液的钙同位素组成强烈依赖于个体的钙代谢,且在不同受试者之间存在差异。我们将这种钙代谢的个体差异与肾脏中钙再循环量的差异联系起来。先前的研究表明,肾脏中重吸收的钙越多,尿液中钙的重同位素就越富集。因此,尿液的钙同位素组成受到不止一个过程的影响,不能直接用于监测净骨矿物质平衡。为克服这一问题,我们提出了一种使用钙同位素的新基线方法,该方法有效地消除了个体肾脏钙重吸收的影响。通过结合尿液钙同位素组成测量和每日钙排泄率,并将这些数据与具有正常稳态骨平衡的健康个体收集的数据进行比较,我们能够明确检测出患者的骨质流失情况。