A New Approach to Measuring Energy Expenditure in Humans

The high prevalence of obesity in the US (17) is a major public health concern, as overweight and obese individuals are at increased risk for many chronic diseases (5, 7, 15, 18). Obesity stems from an imbalance between total caloric consumption and total energy expenditure (TEE), although the causes of this imbalance remain debated (29). Accurate and precise measurements of TEE therefore play a pivotal role in understanding and ultimately reversing this epidemic. TEE can be measured using direct (measurement of heat production) or indirect (measurement of respiratory gas exchange) calorimetry (4), but neither of these approaches are practical for measuring TEE in free living subjects. The gold standard for measuring TEE in free-living individuals is the doubly labeled water (DLW) method, which is based on the principle that the oxygen in body water is in complete isotopic equilibrium with the oxygen in dissolved respiratory carbon dioxide due to the action of carbonic anhydrase. The consequence of this exchange is that an isotopic label of oxygen introduced into body water is eliminated by the combined flux of body water and the exhaled carbon dioxide. Lifson and colleagues reasoned that, since hydrogen is found only in water and not in carbon dioxide, the elimination of a hydrogen isotope would be affected solely by the flux of body water (11). Thus the difference in the rates of isotope elimination of simultaneously administered oxygen and hydrogen labels is a measure of CO2 production. However, despite its widespread use (6, 9, 10, 20, 25, 29), the DLW method has some major limitations. Individual measurements are only precise to ± 7 % at best (23), so the method is currently most suitable for studies of groups rather than individual variation. A second problem is that the test is expensive to perform due to the need for relatively large sample sizes to achieve sufficient statistical power, the large quantities of H218O needed for dosing (23), and IRMS analysis. High levels of 18O are required to distinguish the dose from background isotope levels after 10 - 21 days of elimination. It currently costs $500 - $750 for the 18O required to perform a DLW measurement on an adult subject (50 - 75 kg fat free mass) and the cost is unpredictable due to fluctuations in demand from the medical diagnostic PET scan. The need for high 18O enrichments is caused by fluctuations in the background isotope levels over time (8). This uncertainty in the background levels increases the isotope dose that must be administered and contributes to the uncertainty in the DLW measurements as compared to the reference calorimetry measurements of TEE in validation studies. Finally, IRMS analysis presents its own set of challenges, including the need for sophisticated, expensive instrumentation with dedicated, highly trained operators, and, in general, measurement of only one isotope ratio at a time, reducing analytical throughput. Because of these challenges, most researchers conducting DLW tests do not maintain in-house IRMS facilities, relying instead on expensive and slow analyses by outside measurement laboratories. The proposed work will address these problems by developing a new triple-isotope method for DLW analysis, significantly improving the individual accuracy of the measurements and reducing the cost of the DLW method, leading to more widespread use of the DLW method in both clinical and research applications. The overall goal of this Small Business Innovation Research (SBIR) Phase II grant is to develop and validate a new instrument to measure and correct for the background isotope levels of 18O and 2H during DLW analysis by measuring the 17O stable isotope of oxygen in body water. This approach will address the two major limitations addressed above. First, by using 17O measurements to correct for background fluctuations in 18O and 2H, this approach will reduce the amount of 18O, and thus cost, of performing DLW studies. Results from our Phase I studies (see Preliminary Data below) show that background fluctuations in 18O and 17O in body water are correlated with an R2 of 0.96, background fluctuations in 2H and 17O are correlated with an R2 of 0.89, and background fluctuations in 2H and 18O are correlated with an R2 of 0.92. Based on these correlations, using 17O measurements to estimate the background fluctuations of the 2H and 18O will provide an estimated forty percent decrease in the uncertainty of the DLW method due to background fluctuation. Second, The proposed instrument will be utilized in the new, triple-isotope method for DLW which will reduce existing barriers to widespread use of the DLW method by improving precision, reducing costs, reducing the technical expertise required to perform the analysis, and increasing throughput. Development of the new instrument will be performed by our business partners, Los Gatos Research, and validation studies will be performed at the University of Colorado Anschutz Medical campus. In this work, we will apply Los Gatos Research's ultrasensitive absorption spectroscopy technology, Off-Axis Integrated Cavity Output Spectroscopy (Off-Axis ICOS), to simultaneously and inexpensively (\< $50 per sample) measure 2H, 18O, and 17O in liquid water samples. Briefly, in Off-Axis ICOS, laser light is coupled to an optical cavity in an off-axis fashion and is continuously measured similar to a standard absorption experiment (Figure 1) (1). The cavity provides an extraordinarily long effective optical pathlength (e.g. typically 5 - 10 km) allowing for the accurate quantification of weakly absorbing molecules. Moreover, since the off-axis beam path is not unique, the system is extremely insensitive to changes in alignment, making it robust. This robustness combined with the long effective optical pathlength makes it possible to measure water isotopomers with very high precision. Since its development, Los Gatos Research (LGR) and its commercial customers have performed many experiments to validate the sensitivity and robustness of Off-Axis ICOS to measure a variety of trace gases including water isotopomers H2O, 1H2HO, and H218O (2, 12, 14, 19, 26, 27) and most recently water isotopomers in undistilled human urine (3).