Patent Application
20240053331
The present invention relates to a combination comprising 2H2O enriched water and H218O depleted water. Further, the present invention relates to a kit for measuring energy expenditure of a subject, said kit comprises the combination comprising 2H2O enriched water and H218O depleted water. Furthermore, the present invention relates to the use of said combination or kit for measuring energy expenditure of a subject. In addition, the present invention relates to a method of measuring energy expenditure of a subject.
Various calorimetric methods are used in medicine to determine the total energy turnover of a person. The measurement of the energy turnover by means of so-called direct calorimetry is extremely complex. In clinical studies, indirect calorimetry is often performed selectively using breathing masks with carbon dioxide (CO2) and oxygen (O2) sensors. This method is very accurate, but does not provide measured values over a longer period of time, as the test persons cannot be expected to wear the masks for longer.
Therefore, indirect methods are usually used for determining energy expenditure, in which the energy expenditure is calculated from the oxygen (O2) uptake and/or the carbon dioxide (CO2) emission.
Carbon dioxide (CO2) release can also be determined by enriching the stable isotopes 18O and deuterium (2H) in body water and determining the elimination rates of both isotopes from the body by isotope ratio determination. The underlying principle is that deuterium (2H) is depleted only by water exchange with the environment, while oxygen (O2) is also equilibrated with the environment via carbon dioxide (CO2). This method—the so-called Doubly Labeled Water (DLW) method—has been known since the 1950s and has also been applied to humans since the 1980s. It is currently used in clinical studies. The method enables the determination of energy expenditure over a period of up to two weeks with little effort on the part of the test persons. The test persons must provide a total of 3 urine samples distributed over the measurement period and drink isotopically enriched water at the beginning. The application is currently still limited by the high costs of the 18O isotope tracer.
In the sport, training and lifestyle sector there are currently many applications that estimate calorie consumption via pedometer, pulse sensor etc. However, these methods are extremely imprecise.
Thus, there is an unmet need for a new (Doubly Labeled Water (DLW)) method for determining energy expenditure/consumption which is cost-effective as well as easy and broadly applicable.
The present inventors surprisingly found that H218O depleted water can be used in a method for determining (total) energy expenditure. Due to the administration of H218O depleted water to a subject, the natural concentration of H218O in body water is slightly reduced. The H218O depleted body water further equilibrates via the water ingested during food intake and CO2 exchange during respiration until it reaches the original natural H218O concentration again. From this, the elimination rate of 18O and, thus, the CO2 turnover can be determined. The CO2 turnover then allows to determine the (total) energy expenditure.
H218O depleted water is significantly cheaper to produce than H218O enriched water. It is a waste product of 18O isotope enrichment. In this way, a cost reduction of the method by an estimated factor of 10 can be achieved. This also makes the method interesting for private consumption (sport, training, nutrition, and/or lifestyle).
The method performed by the present inventors allows the determination of energy expenditure which high accuracy and precision. It can also be used to calibrate the inaccurate methods described in the prior art for each person individually.
In addition, the present inventors surprisingly found that 170 can be used as a tracer for background correction. Due to the additional use of H217O depleted or enriched water, the detection sensitivity can be improved.
In a first aspect, the present invention relates to a combination comprising 2H2O enriched water and H218O depleted water.
In a second aspect, the present invention relates to a kit for measuring energy expenditure of a subject, said kit comprises: the combination of the first aspect.
In a third aspect, the present invention relates to the use of the combination of the first aspect or the kit of the second aspect for measuring energy expenditure of a subject.
In a fourth aspect, the present invention relates to a method of measuring energy expenditure of a subject comprising the steps of:
In a fifth aspect, the present invention relates to a method of training optimization comprising the steps of:
In a sixth aspect, the present invention relates to a method of diet optimization comprising the steps of:
In a seventh aspect, the present invention relates to a method of obesity therapy optimization comprising the steps of:
This summary of the invention does not necessarily describe all features of the present invention. Other embodiments will become apparent from a review of the ensuing detailed description.
Before the present invention is described in detail below, it is to be understood that this invention is not limited to the particular methodology, protocols and reagents described herein as these may vary. It is also to be understood that the terminology used herein is for the purpose of describing particular embodiments only, and is not intended to limit the scope of the present invention which will be limited only by the appended claims. Unless defined otherwise, all technical and scientific terms used herein have the same meanings as commonly understood by one of ordinary skill in the art.
Preferably, the terms used herein are defined as described in “A multilingual glossary of biotechnological terms: (IUPAC Recommendations)”, Leuenberger, H. G. W, Nagel, B. and Kölbl, H. eds. (1995), Helvetica Chimica Acta, CH-4010 Basel, Switzerland).
Several documents are cited throughout the text of this specification. Each of the documents cited herein (including all patents, patent applications, scientific publications, manufacturer's specifications, instructions, GenBank Accession Number sequence submissions etc.), whether supra or infra, is hereby incorporated by reference in its entirety. Nothing herein is to be construed as an admission that the invention is not entitled to antedate such disclosure by virtue of prior invention. In the event of a conflict between the definitions or teachings of such incorporated references and definitions or teachings recited in the present specification, the text of the present specification takes precedence.
The term “comprise” or variations such as “comprises” or “comprising” according to the present invention means the inclusion of a stated integer or group of integers but not the exclusion of any other integer or group of integers. The term “consisting essentially of” according to the present invention means the inclusion of a stated integer or group of integers, while excluding modifications or other integers which would materially affect or alter the stated integer. The term “consisting of” or variations such as “consists of” according to the present invention means the inclusion of a stated integer or group of integers and the exclusion of any other integer or group of integers.
The terms “a” and “an” and “the” and similar reference used in the context of describing the invention (especially in the context of the claims) are to be construed to cover both the singular and the plural, unless otherwise indicated herein or clearly contradicted by context.
The term “(total) energy expenditure (TEE)”, as used herein, refers to the amount of energy a subject uses to maintain essential body functions (respiration, circulation, digestion) and to be physically active. (Total) energy expenditure can be partitioned into three components, the basal metabolism, the diet-induced thermogenesis, and the muscular contraction. However, the relative contribution of each component to (total) energy expenditure is largely dependent upon the interindividual variability of each component. For example, (total) energy expenditure from physical activity is the most variable.
The term “basal metabolism”, as used herein, refers to the first and primary component of (total) energy expenditure. It comprises 60% to 70% of (total) energy expenditure. The basal metabolism is defined as the turnover of energy in a fasting and resting organism using energy solely to maintain vital cellular activity, respiration, and circulation as measured by the basal metabolic rate (BMR).
The term “diet-induced thermogenesis” as used herein, refers to the second component of (total) energy expenditure. The diet-induced thermogenesis is defined as the energy required to digest, absorb, and store food. Adaptive thermogenesis or the energy required to thermoregulate and respond to changes in the environmental temperature comprises 10% to 15% of (total) energy expenditure.
The term “muscular contraction”, as used herein, refers to the third and most variable component of (total) energy expenditure. It comprises 6% to 10% of (total) energy expenditure. The muscular contraction is defined as physical activity thermogenesis or the work derived from all forms of physical activity. This includes both physical activity due to exercise and all other types of physical activity excluding exercise (e.g. spontaneous physical activity or non-exercise activity).
The components of (total) energy expenditure and measurement approaches are summarized in
Please note that the terms “energy expenditure” and “energy consumption” are interchangeable used herein.
(Total) energy expenditure can be estimated by measuring macronutrient or oxygen consumption, or heat production or carbon dioxide production. Since measuring the heat generated during physical activity (direct calorimetry) is extremely complex, indirect methods are usually used in practice, in which energy expenditure is calculated from oxygen uptake and/or carbon dioxide release. One such method is the Doubly Labeled Water (DLW) method.
The term “Doubly Labeled Water (DLW) method”, as used herein, refers to a method allowing the determination of (total) energy expenditure of a subject. It is widely acknowledged as the criterion or “gold standard” approach to assess (total) energy expenditure. The technique is applicable in a wide range of populations including the most vulnerable such as pregnant and lactating women and infants. Importantly, the technique is suitable for use in a free-living context, is non-invasive and imposes minimal participant burden. (Total) energy expenditure is typically assessed over a 7- to 14-day period (depending on the analysis approach and age of participant). In this method, a certain amount of water, which is isotopically labelled with stable hydrogen (2H) and oxygen (18O) isotopes, is added to the organism. After adding the isotopically labeled water, the absorbed water mixes with the body water after a short time. As a result, the isotope ratios of the water in the organism change in a characteristic way. In the course of time, both isotopes (2H as well as 18O) are gradually eliminated from the body. While the stable hydrogen isotope (2H) leaves the body only in the form of water and water vapor, the oxygen isotope (18O) is also excreted in the form of carbon dioxide (CO2) during respiration. This results in a significantly higher elimination rate for the latter oxygen isotope. By periodically measuring the isotope ratios of hydrogen and oxygen in a body fluid/body water such as plasma, urine, saliva during a defined period of time, the relative difference between them can be used to determine the CO2 emission/production. The rate of carbon dioxide emission/production can then be converted to (total) energy expenditure such as average (total) energy expenditure.
The readers are encouraged to access a number of recent International Atomic Energy Agency (IAEA) publications for a detailed overview of the DLW technique for the assessment of TEE and other isotopic techniques in nutrition and also recent papers in the area, see, for example Speakman J. R. “The history and theory of the doubly labeled water technique”, Am J Clin Nutr (1998) 68(4): 932S-8S. An overview of the DLW method can be taken from
Physically, stable isotopes are atoms which take the same position in the table of elements, but have a different number of neutrons and, therefore, mass. The most relevant isotopes for the determination of (total) energy expenditure are 18O for oxygen (corresponding to the most abundant isotope 16O), and 2H for hydrogen (corresponding to the most abundant isotope 1H). The isotope 17O for oxygen is further known. The isotope 17O is less abundant in normal water than 18O.
The term “2H2O enriched water”, as used herein, refers to a form of water that contains more 2H (also designated as deuterium or D, also known as heavy hydrogen) than usually present therein. Generally, common 1H isotope (also designated as hydrogen-1 isotope or H, also known as protium) makes up most of the hydrogen in normal water. The presence of the heavier hydrogen isotope gives the water an increased molecular mass with nearly the same physical and chemical properties when compared to normal water. In a preferred embodiment, 2H2O enriched water contains between 0.02% and 100% 2H2O (specified as 2H fraction). For comparison, in the isotopic reference standard VSMOW (Vienna Standard Mean Ocean Water) only about 0.0156% of the hydrogen atoms are of the heavy type.
The term “deuterium”, as used herein, refers to a hydrogen isotope with a nucleus containing a neutron and a proton; the nucleus of a protium (normal hydrogen) atom consists of just a proton. The additional neutron makes a deuterium atom roughly twice as heavy as a protium atom. A molecule of heavy water has two deuterium atoms in place of the two protium atoms of ordinary “light” water. The weight of a heavy water molecule, however, is not substantially different from that of a normal water molecule, because about 89% of the molecular weight of water comes from the single oxygen atom rather than the two hydrogen atoms.
The term “H218O depleted water”, as used herein, refers to a form of water that contains less 18O than usually present therein. Generally, common 16O isotope makes up most of the oxygen in normal water. In a preferred embodiment, H218O depleted water contains between 0% and <0.2% H218O (specified as 18O fraction). For comparison, in the isotopic reference standard VSMOW≥0.2% of the oxygen atoms are of the 18O type.
The term “H217O enriched water”, as used herein, refers to a form of water that contains more 17O than usually present therein. H217O enriched water contains between 0.037% and 100% H217O (specified as 17O fraction). Generally, common 16O isotope makes up most of the oxygen in normal water.
The term “H217O depleted water”, as used herein, refers to a form of water that contains less 17O than usually present therein. Generally, common 16O isotope makes up most of the oxygen in normal water. H217O depleted water contains between 0% and <0.037% H217O (specified as 17O fraction). For comparison, in the isotopic reference standard VSMOW about 0.0379% of the oxygen atoms are of the 17O type.
The isotope 17O is preferably used herein as a new, additional tracer for the determination of (total) energy expenditure. There is a strong autocorrelation between all isotope ratios in natural water (2H/1H, 17O/16O 18O/16O). This autocorrelation can be used to correct for natural isotope ratio fluctuations. Ideally, the tracer used for the DLW-method should have nearly the natural abundance of 17O. Therefore, the measured 17O/16O ratio can be used to correct natural 2H/1H and 18O/16O ratio fluctuation to improve the accuracy of the DLW method. The 17O/16O ratio can be determined from the parallel measurement of all three oxygen isotopes (16O, 17O, and 18O). This was made possible by a new generation of laser spectrometers, which have a significantly improved spectral resolution and sensitivity.
The term “18O/16O ratio”, as used herein, refers to the relation of the isotopes 18O and 16O which are present/comprised in a body water sample obtained from a subject.
The term “2H/1H ratio”, as used herein, refers to the relation of the isotopes 2H and 1H which are present/comprised in a body water sample obtained from a subject.
The term “17O/16O ratio”, as used herein, refers to the relation of the isotopes 17O and 16O which are present/comprised in a body water sample obtained from a subject.
The term “17O-excess”, as used herein, refers to the deviation of the 17O/16O ratio of a body fluid sample compared to the reference relationship between δ18O and δ17O of the “Global Meteoric Water Line”.
The term “subject”, as used herein, refers to any individual whose (total) energy expenditure is to be determined/measured. In particular, the subject is a hobby or professional athlete, an obese person, or a person suffering from a metabolic disorder such as diabetes or cardiovascular disease.
In one preferred embodiment, the subject is a human being or an animal. The animal may be selected from the group consisting of a dog, cat, sheep, goat, cow, horse, and pig. In one more preferred embodiment, the subject is a human being.
The terms “subject”, “individual”, “person”, or “patient” are used interchangeably herein.
The term “body water sample”, as used herein, refers to any watery/aqueous sample taken from a subject, e.g. human being. In other words, the body water (also designated as body fluid or bodily fluid) is any liquid within the body of a subject, e.g. human being. A body water sample can be obtained, for example, by collection of any of urine, blood, saliva and exhaled breath from a subject. Preferably, the body water sample is selected from the group consisting of blood, saliva, urine, tissue fluids, and exhaled breath. The blood sample may be whole blood or a blood fraction. The blood fraction may be, in turn, serum or plasma.
In the context of the present invention, the term “kit of parts (in short: kit)” is understood to be any combination of at least some of the components identified herein, which are combined, coexisting spatially, to a functional unit, and which can contain further components.
The present invention will now be further described. In the following passages, different aspects of the invention are defined in more detail. Each aspect so defined may be combined with any other aspect or aspects unless clearly indicated to the contrary. In particular, any feature indicated as being preferred or advantageous may be combined with any other feature or features indicated as being preferred or advantageous, unless clearly indicated to the contrary.
The present inventors surprisingly found that H218O depleted water can be used in a method for determining (total) energy expenditure. Due to the administration of H218O depleted water to a subject, the natural concentration of H218O in body water is slightly reduced. The H218O depleted body water further equilibrates via the water ingested during food intake and CO2 exchange during respiration until it reaches the original natural H218O concentration again. From this, the elimination rate of 18O and, thus, the CO2 turnover can be determined. The CO2 turnover then allows to determine the (total) energy expenditure.
H218O depleted water is significantly cheaper to produce than H218O enriched water. It is a waste product of 18O isotope enrichment. In this way, a cost reduction of the method by an estimated factor of 10 can be achieved. This also makes the method interesting for private consumption (sport, training, nutrition, and/or lifestyle).
The method performed by the present inventors allows the determination of energy expenditure with high accuracy and precision. It can also be used to calibrate the inaccurate methods described in the prior art for each person individually.
In addition, the present inventors surprisingly found that 17O can be used as a tracer for background correction. Due to the additional use of H217O depleted or enriched water, the detection sensitivity can be improved.
Thus, in a first aspect, the present invention relates to a combination comprising, consisting of, or consisting essentially of 2H2O enriched water and H218O depleted water.
In one embodiment, the 2H2O enriched water comprises between 0.02% and 100% 2H2O (specified as 2H fraction). Particularly, the 2H2O enriched water comprises between 10% and 1000% 2H2O.
In one (alternative or additional) embodiment, the H218O depleted water comprises between 0% and <0.2% H218O (specified as 18O fraction). Particularly, the H218O depleted water comprises between 0% and <0.18%.
For example, the combination comprises 2H2O enriched water and H218O depleted water, wherein the 2H2O enriched water comprises between 0.02% and 100% 2H2O and wherein the H218O depleted water comprises between 0% and <0.2% H218O.
In one preferred embodiment, the combination further comprises H217O enriched water and H217O depleted water.
Such a combination comprises 2H2O and H217O enriched water and H218O and H217O depleted water. For example, the combination comprises 2H2O and H217O enriched water and H218O and H217O depleted water, wherein the 2H2O enriched water comprises between 0.02% and 100% 2H2O and wherein the H218O depleted water comprises between 0% and <0.2% H218O.
In one more preferred embodiment,
Particularly, the present invention relates to a combination comprising
Thus, the combination may consist of/represent a (first) composition comprising 2H2O enriched water and a (second/different) composition comprising H218O depleted water or a (single) composition comprising (a mixture of)2H2O enriched water and H218O depleted water.
More particularly, the present invention relates to a combination comprising
In one even more preferred embodiment, the (first/second/single) composition (further) comprises H217O enriched water and H217O depleted water.
Particularly, the combination comprises
In this respect, it should be noted that in the (single) composition comprising (a mixture of) 2H2O enriched water and H218O depleted water, the H217O content (nearly) approaches the natural 17O content.
More particularly, the combination comprises
In this respect, it should be noted that in the (single) composition comprising (a mixture of) 2H2O enriched water and H218O depleted water, the H217O content (nearly) approaches the natural 17O content.
The combination, more specifically the first composition, the second composition, and/or the single composition, of the first aspect, is (are) are preferably sterilized. The sterilization may be performed by distillation or filtration through a filtering system, e.g. through a 0.22-μm filtering system.
Further, the combination, more specifically the first composition, the second composition, and/or the single composition, of the first aspect, is (are) are preferably provided as liquid/in liquid form, e.g. as solution(s) such as drinking solution(s).
Furthermore, the combination, more specifically the first composition, the second composition, and/or the single composition, of the first aspect, is (are) preferably administered to a subject for measuring/determining (total) energy expenditure of the subject. Particularly, the subject is a human being or an animal. More particularly, the subject is a human being. The administration may take place by oral ingestion or injection. Preferably, the administration takes place by oral ingestion.
In addition, the combination, more specifically the first composition, the second composition, and/or the single composition, of the first aspect, is (are) preferably comprised in an administration container. This administration container should be easy to drink from. Said administration container should be washed with water after the dose is consumed and the washing water should also be consumed. This ensures that the entire dose is received (most containers will not deliver the total dose without washing). For children and the elderly, a straw can be used in order to prevent water loss during administration.
In a second aspect, the present invention relates to a kit for (in vitro) measuring (total) energy expenditure of a subject, said kit comprises:
Preferably, the kit further comprises additional means for measuring (total) energy expenditure of a subject.
More preferably, the additional means encompass:
Even more preferably, the kit further comprises
The administration container(s) is (are) preferably sterilized. The administration container(s) should be easy to drink from.
The label or packaging insert may further comprise information/instructions for sample collection and/or for taking the combination, more specifically the first composition, second composition and/or single composition, of the first aspect. For example, the label or packaging insert may comprise the information that the (administration) container(s) should be emptied completely and washed with water after the dose is consumed by the subject. The washing water should also be consumed. This ensures that the entire dose is received (most containers will not deliver the total dose without washing). Particularly, the subject is a human being or an animal. More particularly, the subject is a human being.
In a third aspect, the present invention relates to the (in vitro) use of the combination of the first aspect or the kit of the second aspect for measuring energy expenditure of a subject. In particular, the energy expenditure is the total energy expenditure (TEE). Preferably, the subject is a human being or an animal. More preferably, the subject is a human being.
The present inventors surprisingly found that H218O depleted water can be used in a method for determining (total) energy expenditure. Due to the administration of H218O depleted water to a subject, the natural concentration of H218O in body water is slightly reduced. The H218O depleted body water further equilibrates via the water ingested during food intake and CO2 exchange during respiration until it reaches the original natural H218O concentration again. From this, the elimination rate of 18O and, thus, the CO2 turnover can be determined. The CO2 turnover then allows to determine the (total) energy expenditure.
H218O depleted water is significantly cheaper to produce than H218O enriched water. It is a waste product of 18O isotope enrichment. In this way, a cost reduction of the method by an estimated factor of 10 can be achieved. This also makes the method interesting for private consumption (sport, training, nutrition, and/or lifestyle).
The method performed by the present inventors allows the determination of energy expenditure which high accuracy and precision. It can also be used to calibrate the inaccurate methods described in the prior art for each person individually.
Thus, in a fourth aspect, the present invention relates to a (an in vitro) method of measuring (total) energy expenditure of a subject comprising the steps of:
There are two approaches for carrying out the above method: the two-point approach and the multi-point (more than two-point) approach. The two-point approach in its minimal form requires three body water samples, a pre-dose baseline body water sample (before the administration of the combination comprising 2H2O enriched water and H218O depleted water), a post-dose body water sample (preferably at the day of dosing after the isotopes have equilibrated throughout the body of the subject) and a final body water sample taken at the end of the analysis (that is, for example, between day 10 to 14). The multi-point (more than two-point) approach in its most extreme form generally involves taking a pre-dose baseline body water sample (before the administration of the combination comprising 2H2O enriched water and H218O depleted water) and body water samples every day after intake of the dose until the end of the sampling period.
An advantage of the two-point approach is that it requires fewer samples and provides the more exact estimate of (total) energy expenditure. The disadvantage of this approach is that it is prone to analytical or sampling disadvantages of the protocol and provides little data for assessing variance and internal consistency. In contrast, the multi-point approach has the advantage of data averaging and, thus, minimizes analytical errors. The disadvantage of this approach is that it requires more samples and, thus, places a greater burden on the subject tested.
In this respect, it should be noted that the pre-dose ratio is measured before the administration of the combination comprising 2H2O enriched water and H218O depleted water, the post-dose ratio is measured after 2H2O and H218O has equilibrated throughout the body of the subject, and the final ratio is measured at the end of the study.
In one embodiment, the 2H2O enriched water comprises between 0.02% and 100% 2H2O (specified as 2H fraction). Particularly, the 2H2O enriched water comprises between 10% and 1000% 2H2O.
In one (alternative or additional) embodiment, the H218O depleted water comprises between 0% and <0.2% H218O (specified as 18O fraction). Particularly, the H218O depleted water comprises between 0% and <0.18% H218O.
In one example, the combination comprises 2H2O enriched water and H218O depleted water, wherein the 2H2O enriched water comprises between 0.02% and 100% 2H2O and wherein the H218O depleted water comprises between 0% and <0.2% H218O.
In one preferred embodiment, the combination comprising 2H2O enriched water and H218O depleted water had been administered to the subject after the first point in time. More specifically, the combination comprising 2H2O enriched water and H218O depleted water had been administered to the subject after the first point in time and before the second point in time. The first point in time may be immediately, e.g. 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10 minutes or within 1 or 2 hours, before the administration of a combination comprising 2H2O enriched water and H218O depleted water to the subject.
Further, the second point in time may be between 1 and 5 hours, such as between 2 to 4 hours, e.g. 1, 2, 3, 4, or 5 hours, after the administration of a combination comprising 2H2O enriched water and H218O depleted water to the subject. After this time period, it is assumed that the isotopes have equilibrated throughout the body of the subject.
Furthermore, the time period between the second point in time and the later point in time may be between 1 and 14 days (2 weeks), e.g. 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, or 14 days (2 weeks).
In one more preferred embodiment,
Particularly, the combination comprises
Thus, the combination may consist of/represent a composition comprising 2H2O enriched water and a (another/different) composition comprising H218O depleted water or a (single) composition comprising (a mixture of)2H2O enriched water and H218O depleted water.
More particularly,
Thus, the compositions can be administered concurrently or consecutively.
The isotope 17O is preferably used herein as a new, additional tracer for the determination of the (total) energy expenditure. In contrast to the investigation of the absolute oxygen isotope ratios, which are subject to mass-dependent dilution and fractionation processes in the body, the Δ17O signal behaves conservatively and can, therefore, be used as an additional, source-specific tracer to correct disturbing influences in the determination of (total) energy consumption. The 17O excess can be determined from the parallel measurement of all three oxygen isotopes (16O, 17O, and 18O). In addition, the 17O/16O ratio can be determined.
Thus, in one even more preferred embodiment, the subject is a subject to whom a combination further comprising H217O enriched water and H217O depleted water had been administered. Such a combination comprises, consists essentially of, or consists of 2H2O and H217O enriched water and H218O and H217O depleted water. For example, the combination comprises 2H2O and H217O enriched water and H218O and H217O depleted water, wherein the 2H2O enriched water comprises between 0.02% and 100% 2H2O and wherein the H218O depleted water comprises between 0% and <0.2% H218O.
Particularly, the 17O/16O ratio and/or the 17O-excess is further measured (in step (i)) in a body water sample obtained from a subject at a first point in time (baseline ratio).
More particularly, the 17O/16O ratio and/or the 17O-excess is further measured (in step (ii)) in a body water sample obtained from the subject at a second point in time (plateau ratio) and in at least one further body water sample obtained from said subject at a later point in time.
Even more particularly, a reference value of isotopic background fluctuation is further determined (in step (iii)) from a change in measured 17O/16O ratios and/or the 17O-excess over time.
Still even more particularly, the reference value of isotopic background fluctuation is used to adjust the change in measured 18O/16O ratio and/or 2H/1H ratio over time. In this way, natural fluctuations of the isotopes 18O and 2H, which may influence the measuring accuracy, can be compensated.
In one still even more preferred embodiment, the combination comprising 2H2O and H217O enriched water and H218O and H217O depleted water had been administered to the subject after the first point in time. More specifically, the combination comprising 2H2O and H217O enriched water and H218O and H217O depleted water had been administered to the subject after the first point in time and before the second point in time.
The first point in time may be immediately, e.g. 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10 minutes or within 1 or 2 hours, before the administration of a combination comprising 2H2O and H217O enriched water and H218O and H217O depleted water to the subject.
Further, the second point in time may be between 1 and 5 hours, such as between 2 to 4 hours, e.g. 1, 2, 3, 4, or 5 hours, after the administration of a combination comprising 2H2O and H217O enriched water and H218O and H217O depleted water to the subject. After this time period, the isotopes have equilibrated throughout the body of the subject.
Furthermore, the time period between the second point in time and the later point in time may be between 1 and 14 days (2 weeks), e.g. 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, or 14 days (2 weeks).
In one most preferred embodiment,
Particularly, the combination comprises
In this respect, it should be noted that in the (single) composition comprising (a mixture of) 2H2O enriched water and H218O depleted water, the H217O content (nearly) approaches the natural 17O content.
More particularly,
In this respect, it should be noted that in the (single) composition comprising (a mixture of) 2H2O enriched water and H218O depleted water, the H217O content (nearly) approaches the natural 17O content.
In one preferred example of the method of the fourth aspect, a base line sample of urine is analysed within one hour before administration of the 2H-enriched water and 18O-depleted water. After 2 to 4 hours, a second urine sample is measured (plateau sample). On days 1, 2, 4, 7, 8 and 9 further urine samples are analysed (or at least on days 1 and 9).
The skilled person is aware of techniques which allow the calculation of the (total) energy expenditure on the basis of the exhaled/released CO2 over time calculated from the combined values determined in step (iii). In this respect, it is referred to IAEA Protocoll “Assessment of Body Composition and Total Energy Expenditure in Humans Using Stable Isotope Techniques” (© IAEA, 2009, ISBN 978-92-0-111708-3).
Further, the combination/composition(s) administered to the subject was (were) preferably sterilized, e.g. by distillation or filtration through a filtering system such as a 0.22-μm filtering system.
Furthermore, the combination/composition(s) administered to the subject was (were) preferably provided as liquid/in liquid form, e.g. as solution(s) such as drinking solution(s). Preferably, the administration had been taken place by oral ingestion or injection. More preferably, the administration had been taken place by oral ingestion.
In addition, the combination/composition(s) administered to the subject was (were) preferably comprised in an administration container.
The subject tested in the method of the fourth aspect may be any individual whose (total) energy expenditure is to be determined/measured. In particular, the subject is a hobby or professional athlete, an obese person, or a person suffering from a metabolic disorder such as diabetes. Preferably, the subject tested in the fourth aspect of the present invention is a human being or an animal. The animal may be selected from the group consisting of a dog, cat, sheep, goat, cow, horse, and pig. More preferably, the subject is a human being.
The ratios in the method of the fourth aspect are preferably determined using optical spectroscopy, laser spectroscopy, or mass spectroscopy such as isotope ratio mass spectroscopy. In particular, the optical spectroscopy comprises cavity ring-down spectroscopy (CRDS) and off-axis integrated cavity output spectroscopy (OA-ICOS).
The body water sample analysed in the method of the fourth aspect refers to any watery/aqueous sample taken from a subject, e.g. human being. In other words, the body water (also designated as body fluid or bodily fluid) is any liquid within the body of a subject, e.g. human being. A body water sample can be obtained, for example, by collection of any of urine, blood, saliva and exhaled breath from a subject. Preferably, the body water sample is selected from the group consisting of blood, saliva, urine, tissue fluids, and exhaled breath. The blood sample may be whole blood or a blood fraction. The blood fraction may be, in turn, serum or plasma. More preferably, the body water sample is urine.
It is specifically preferred that the combination of the first aspect had been administered to the subject tested in the method of the fourth aspect.
Dietary intake of athletes (in particular of professional athletes) must match training volume to fuel physiological demands. Inadequate energy is detrimental to bone health, immune health, cognitive performance, as well as exercise performance in physically active populations. In particular, adequate dietary intake is important for promoting adaptation and prevention of musculoskeletal injury in response to large volumes of physical training.
Not only power or endurance training is important. It is often important to include strength, power, endurance, and functional training.
Usually, athletes (in particular professional athletes) have unique fueling needs due to the large variety in training intensity and duration. Strength and power athletes have, for example, higher protein needs than endurance athletes and endurance athletes have, for example, higher carbohydrate and fat intake needs than strength and power athletes. Clearly understanding training volume and nutrition intakes of athletes (in particular professional athletes) is, thus, critical in ensuring training success.
Accordingly, in a fifth aspect, the present invention relates to a method of training optimization comprising the steps of:
The world is currently experiencing a nutrition transition in which energy undernutrition coexists with energy overnutrition as a consequence of significant lifestyle changes. Both industrialized and developing societies are suffering the burden of obesity related to inactivity and excess of energy consumption and co-morbid conditions including hyperlipidaemias, insulin resistance, type 2 diabetes, cardiovascular diseases and cancer. There is also increasing evidence of the link between undernutrition in utero and obesity and chronic disease in later life. In either under- or overnutrition, there is an increasing need for nutritional status methodologies that provide reliable results for risk assessment and for the evaluation of nutrition and physical activity intervention programmers. Such measures require assessment of (total) energy expenditure.
Thus, in a sixth aspect, the present invention relates to a method of diet optimization comprising the steps of:
Thus, in a seventh aspect, the present invention relates to a method of obesity therapy optimization comprising the steps of:
The present invention is further summarized as follows:
Various modifications and variations of the invention will be apparent to those skilled in the art without departing from the scope of invention. Although the invention has been described in connection with specific preferred embodiments, it should be understood that the invention as claimed should not be unduly limited to such specific embodiments. Indeed, various modifications of the described modes for carrying out the invention which are obvious to those skilled in the art in the relevant fields are intended to be covered by the present invention.
The present invention is further illustrated by the following examples and Figures, however, without being restricted thereto.
Testing protocol for the determination of total energy expenditure (TTE) by the DLW method using 2H-enriched water and 18O-depleted water:
A base line sample of urine is analysed within one hour before administration of the 2H-enriched water and 18O-depleted water (body weight of the test person 70 kg). According to the IAEA protocol, the test person gets 0.12 g/kg body weight of 99 at. % 2H enriched water (=8.4 g). Additionally, the test person gets a dose of 800 ml of to 0.1 at. % 18O-depleted water. The 2H-enriched water and the 18O-depleted water has to be drunken within 20 min. After 2-4 hours, a second urine sample is measured (plateau sample). On day 1, 2, 4, 7, 8 and 9 further urine samples are analysed (or at least on day one and on day 9). 18O/16O and 2H/1H ratios can optionally be adjusted by 17O excess analysis. The isotope elimination rates (kO and kD) can be calculated from the slope of the natural logarithm of the ppm excess values vs. time after isotope administration. Isotope dilution space at time of dosing is calculated from the intercept of the 2H-plot. For 18O, the natural logarithm of the negative ppm excess value has to be used (see
Sample preparation: Before analysis the samples have to be prepared for instrument analysis. Urine and plasma samples should be centrifuged and ultrafiltrated.
Isotope measurement: Isotope measurements are performed using a commercially available laser spectrometer (L2140-i Liquid Water Isotope Analyzer, Picarro Inc.). The instrument allows high-precision determination of hydrogen isotopes ratio (S2H) as well as oxygen isotope ratios (δ18O and δ17O) in water and body fluid samples. Samples are injected from a liquid autosampler into a vaporizer module and the water vapor formed is transferred to the laser spectrometer. Dry nitrogen is used as carrier gas. Isotope measurements can be performed in either normal mode or 17O-excess mode. In normal mode, only δ2H and δ18O are determined, while 17O-excess mode allows simultaneous measurement of δ2H, δ18O, δ17O, and 17O-excess respectively. The normalization of the isotopic measurements to the VSMOW-SLAP scale are performed using internal working standards previously calibrated against the international reference materials VSMOW and SLAP. The ppm values are calculated form the normalized isotope delta values according to the IAEA protocol.
Testing protocol for the determination of total energy expenditure (TTE) by the DLW method using 2H-enriched water and 18O-depleted water:
A base line sample of urine is analysed within one hour before administration of the 2H-enriched water and 18O-depleted water (body weight of the test person 70 kg). According to the IAEA protocol, the test person gets 0.12 g/kg body water of 99 at. % 2H enriched water (=4.2 g). Additionally, the test person gets a dose of 2000 ml of to 0.1 at. % 18O-depleted water. The 2H-enriched water and the 18O-depleted water has to be drunken within 60 min. After 5 hours, a second urine sample is measured (plateau sample). On day 1, 2, 4, 7, 8 and 9 further urine samples are analysed (or at least on day one and on day 9). 18O/16O and 2H/1H ratios can optionally be adjusted by 17O excess analysis. The isotope elimination rates (kO and kD) can be calculated from the slope of the natural logarithm of the ppm excess values vs. time after isotope administration. Isotope dilution space at time of dosing is calculated from the intercept of the 2H-plot. For 180, the natural logarithm of the negative ppm excess value has to be used (see
Isotope measurement: Isotope measurements are performed using a commercially available laser spectrometer (L2140-i Liquid Water Isotope Analyzer, Picarro Inc.). The instrument allows high-precision determination of hydrogen isotopes ratio (δ2H) as well as oxygen isotope ratios (δ18O and δ17O) in water and body fluid samples. Samples are injected from a liquid autosampler into a vaporizer module and the water vapor formed is transferred to the laser spectrometer. Dry nitrogen is used as carrier gas. Isotope measurements can be performed in either normal mode or 17O-excess mode. In normal mode, only δ2H and δ18O are determined, while 17O-excess mode allows simultaneous measurement of δ2H, δ18O, δ17O, and 17O-excess respectively. The normalization of the isotopic measurements to the VSMOW-SLAP scale are performed using internal working standards previously calibrated against the international reference materials VSMOW and SLAP. The ppm values are calculated form the normalized isotope delta values according to the IAEA protocol.
Feasibility Study:
A base line sample of urine was analyzed within one hour before administration of the 2H-enriched water and 18O-depleted water (body weight of the test person 70 kg). According to the IAEA protocol, the test person got 0.12 g/kg body water of 99 at. % 2H enriched water (=4.3 g). Additionally, the test person got a dose of 2000 ml of to 0.074 at. % 18O-depleted water. The 2H-enriched water and the 18O-depleted water were drunken within 60 min. After 5 hours, a second urine sample was measured (plateau sample). On day(s) 1, 2, 3, 4, 5, 6 and 7, further urine samples were analyzed according to the described method by laser spectrometry. FIG. 4, Tables 1 and 2 show the results of these measurements. The results confirm that the exact course of 18O enrichment after administration of 18O-depleted water can be measured by laser spectrometry within at least 7 days after administration. This is prerequisite for the determination of the total energy expenditure. The total energy expenditure (TEE) can be calculated with these data. Calculation of TEE can be performed according to Example 2.
18O depleted water Dose
18O abundance Dose
18O abundance Basline
2H enriched water Dose (99%
2H abundance Baseline
18O [ppm]
2H
| Number | Date | Country | Kind |
|---|---|---|---|
| 20216104.8 | Dec 2020 | EP | regional |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/EP21/86840 | 12/20/2021 | WO |
