Use of the Biphasic <sup>13</sup>C-Sucrose/Glucose Breath Test to Assess Sucrose Maldigestion in Adults with Functional Bowel Disorders

Opekun, Antone R.; Balesh, Albert M.; Shelby, Harold T.

doi:https://doi.org/10.1155/2016/7952891

BioMed Research International

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Research Article | Open Access

Volume 2016 | Article ID 7952891 | https://doi.org/10.1155/2016/7952891

Use of the Biphasic ¹³C-Sucrose/Glucose Breath Test to Assess Sucrose Maldigestion in Adults with Functional Bowel Disorders

Antone R. Opekun,^1,2Albert M. Balesh,¹and Harold T. Shelby¹

Academic Editor: Louise E. Glover

Received19 Mar 2016

Accepted10 Jul 2016

Published08 Aug 2016

Abstract

Sucrase insufficiency has been observed in children with of functional bowel disorders (FBD) and symptoms of dietary carbohydrate intolerance may be indistinguishable from those of FBD. A two-phase ¹³C-sucrose/¹³C-glucose breath test (¹³C-S/GBT) was used to assess sucrase activity because disaccharidase assays are seldom performed in adults. When ¹³C-sucrose is hydrolyzed to liberate monosaccharides, oxidation to ¹³CO₂ is a proportional indicator of sucrase activity. Subsequently, ¹³C-glucose oxidation rate was determined after a secondary substrate ingestion (superdose) to adjust for individual habitus effects (Phase II). ¹³CO₂ enrichment recovery ratio from ¹³C-sucrose and secondary ¹³C-glucose loads reflect the individualized sucrase activity [Coefficient of Glucose Oxidation for Sucrose (CGO-S)]. To determine if sucrase insufficiency could be a factor in FBD, ¹³C-S/GBT was validated using subjects with known sucrase gene mutation status by comparing ¹³CO₂-breath enrichment with plasma ¹³C-glucose enrichment. ¹³C-S/GBT was used to assess sucrose digestion in FBD patients and asymptomatic controls. ¹³CO₂-breath enrichment correlated with the appearance of ¹³C-sucrose-derived glucose in plasma (). Mean, control group CGO-S-enrichment outcomes were 1.01 at 60′, 0.92 at 75′, and 0.96 at mean 60′–75′ with normal CGO-S defined as >0.85 (95% C.I.). In contrast, FBD patients demonstrated lower CGO-S values of 0.77 at 60′, 0.77 at 75′, and 0.76 at mean 60′–75′ (Chi Square: 6.55; ), which points to sucrose maldigestion as a cause of FBD.

1. Background

Functional bowel disorders (FBD) have an estimated prevalence of 10–21% of the general population for which the pathophysiology remains elusive [1]. As outlined by Rome III criteria, functional conditions include symptoms of recurrent abdominal discomfort (pain and bloating) associated with changes in bowel habits (diarrhea, constipation, or both) that persist for long periods in the absence of organic pathology [2, 3]. There is considerable overlap in the manner in which patients present with FBD and irritable bowel syndrome; often features of bloating and abdominal distension predominate without fully meeting specific criteria [4, 5]. The symptom complex appears similar to many conditions, including celiac disease, motility disorders, infectious enteritis, food allergies, inflammatory bowel disease, microscopic colitis, small bowel bacterial overgrowth syndrome, lactose intolerance, and nutrient malabsorption [6]. Some individuals seem to be disproportionally hypersensitive, and, at rare times, the discomfort may be incapacitating, having been equated to symptoms produced by someone with a bowel obstruction [7]. The diagnosis is based on exclusion of other organic disease entities [8], and without specific biomarkers, differentiating organic disease can be challenging [9, 10]. Many patients with functional symptoms report having experienced symptoms since childhood, which implies that a genetic predisposition may exist [11], but the risk-genes have not yet been validated [12]. The onset of first symptoms has often been associated with prior gastroenteritis and stressful life events [13], but the specific triggers, molecular mechanisms, and neurogut targets remain obscure such that the treatment approach largely aims to relieve symptoms in the absence of a specific etiology. The role of dietary factors in FBD appears important and understudied [7].

Up to 65% of FBD patients report symptoms exacerbated by meals with or without specific dietary intolerances [15, 16]. However, it is not clear what role food allergies may play in FBD, but it appears to be minimal [17]. A significant portion of pediatric patients evaluated for unexplained chronic abdominal pain were found to have decreased mucosal disaccharidase activity [18]. Patients with specific carbohydrate intolerance, such as lactose, frequently report symptom improvement with dietary restriction, and the reintroduction of those substrates (a so-called dietary challenge) results in symptom exacerbation, serving to confirm clinical suspicions [19, 20]. Since carbohydrates collectively provide approximately 60–70 percent of the daily dietary caloric load, one could postulate that even some degree of maldigestion could be a significant putative FBD factor [21].

Normal sucrose digestion to glucose and fructose and transporter-mediated monomer absorption that follows have been well-described [22–24]. The sequence of events that occurs in lactose intolerance is a paradigm for other malabsorptive circumstances, including starches and sucrose. Other oligosaccharides also require luminal, mucosal enzyme hydrolysis by additional gene products, and substrates include maltose, maltotriose, and maltodextrin with α-1,4- and α-1,6-glycosidic linkages [25]. Sucrase and isomaltase, chromosome 3 gene product, handle the bulk of sucrose and dextrin digestion (an incomplete, solubilized postpancreatic alpha-amylase hydrolysate) with a contribution by maltase-glucoamylase, chromosome 7-related gene product [26]. When undigested/malabsorbed nutrients pass distally to the colon where microbiota fermentation occurs, gas and short-chain fatty acids are produced which, in turn, diminish water reabsorption, induce inflammation, alter colonic motility, and theoretically bring on abdominal discomfort [27]. It is not clear if the observed gut dysbiosis is a consequence of maldigestion or is causally related to the symptoms.

The idea that disaccharide maldigestion, such as sucrose, could be causally involved in FBD is difficult to discount due to the striking similarity of symptoms [28, 29] and requires innovative approaches. The use of the breath-hydrogen test to evaluate maldigestion has only been helpful in some cases due to nonspecificity and poor sensitivity [30–32]. Breath-hydrogen production is dependent upon colonic microbiota and it is difficult to predict if the floras, in any patient, are hydrogen producers. Alternatively, when a link between carbohydrate maldigestion and GI symptomatology is suspected, specific approaches could include the use of endoscopic biopsy direct assays for sucrase, maltase, and palatinase (a surrogate for isomaltase). However, mucosal enzyme assays are onerous to perform, may not represent the confluent digestive capacity of the small intestine, and are often considered too expensive.

This study investigated the possibility of intestinal sucrase insufficiency as a contributing factor in FBD (functional bloating type) by using stable (nonradioactive) isotope tracer-labeled sucrose breath testing. Specifically, this study asked if sucrase insufficiency, as measured by an innovative two-phase ¹³C-sucrose/¹³C-glucose breath testing could, in part, explain the symptoms of FBD.

2. Methods

2.1. Study Design

This study was a prospective, open-label survey of adult patients with FBD as defined by Rome criteria and control subjects who presented to Baylor Clinic during a three-month period and subsequently underwent testing using biphasic ¹³C-S/GBT. A validation substudy was also performed to demonstrate that the biphasic breath test measures sucrose digestion. Additionally, the substudy evaluated four nondiabetic adult women with known sucrase-isomaltase genotypes to validate biphasic ¹³C-S/GBT.

2.2. Ethics

This study was performed in accordance with the Declaration of Helsinki and approved by the Institutional Review Board at Baylor College of Medicine under protocol H-31197. The Institutional Review Board at Baylor College of Medicine is organized, operates, and is registered with the United States Office for Human Research Protections according to the regulations codified in the United States Code of Federal Regulations at 45 CFR 46 and 21 CFR 56. The BCM IRB operates under the BCM Federal Wide Assurance number 00000286. Written documentation of informed consent was obtained from all participants and, in addition to consent for prospective study participation, explicitly permits the use of health information obtained from health records including diagnoses, medications, laboratory data (exclusive of the whole genotype), and demographic information including age, gender, race, and ethnicity; such authorization does not have an expiration date.

2.3. Study Population

Twenty-two subjects participated in this pilot study. Subjects were either asymptomatic healthy controls or symptomatic test subjects that met inclusion criteria for clinical diagnosis of FBD-functional bloating by Rome III criteria (FBD group: ; 8 women and 3 men, 24–66 years of age) and in otherwise good health (Table 1).

Table 1

Summary of the clinical features of 11 subjects diagnosed with functional bowel disorder as per gastroenterologist (HTS). All patient subjects experienced recurrent feeling of bloating or visible distension for at least 3 days/month during the prior 3 months and did not meet criteria for a diagnosis of functional dyspepsia, irritable bowel syndrome, or other functional GI disorders. All symptomatic subjects were scored as “severely affected” in accordance with the 2011 Rome Foundation working-team report [14]. None of the asymptomatic control subjects met any criteria for functional bowel syndrome of any type (data not shown).

Affected patients reporting any alarming issues, such as gastrointestinal bleeding, were not referred for study participation. Other exclusion criteria included, pregnancy, current lactation, allergy to food coloring, other causes of abdominal pain or altered bowel habits (e.g., celiac disease, pancreatitis, malignancy, or inflammatory bowel disease), history of diabetes mellitus, gastroparesis, recent febrile illness (5 days prior to the study), ingestion of an investigational drug or placement of an investigational device 30 days prior to the study start date, and absence of the mental capacity necessary to comprehend the protocol. Symptom severity to assess FBD was determined by patient reports, behavior of symptoms, and impact on health-related quality of life [14]. Symptom severity was scored according to the following summary definitions: mild: aware of signs or symptoms but maintained a good health-related quality of life; moderate: interfered with activities of daily living; or severe: marked impairment with psychological comorbidities and requires specialty medical intervention. There was no interventional component to this pilot study, and no long-term follow-up was done.

The asymptomatic control group (; eight women and three men, 22.8–60.8 years of age) was recruited from the student body and institutional staff at Baylor College of Medicine, none of whom met any criteria for FBD; all had a long history of tolerating sucrose in generous portions without inducing symptoms. The control subjects had no prior history of functional GI disorder, congenital sucrase-isomaltase deficiency, or irritable bowel syndrome. All reported an absence of current GI signs and symptoms, and all were in a state of excellent health.

To validate the breath test, four additional nondiabetic adult women were recruited as subjects for a substudy based upon their sucrase-isomaltase (SI) genotype (mutation status) and detailed self-reported dietary sucrose tolerance. As described below, ¹³CO₂ breath test enrichment was compared with ¹³C-plasma enrichment since the only source of the tracer could be sucrose digestion with resultant monosaccharide absorption. One subject was symptomatic and homozygous for congenital sucrase-isomaltase (SI) deficiency, two subjects were heterozygous for congenital sucrase-isomaltase deficiency in the sucrase gene domain and moderately symptomatic, and one subject was sucrose tolerant (completely asymptomatic) without any of the known mutations in the sucrase-isomaltase gene (3q25.2-q26.2).

2.4. Description of Study and Breath Testing

Commercial Mylar® breath collection bags (1.3 L and 0.25 L) fitted with one-way valves (Otsuka Electronics, Tokyo, Japan) were used. Mouthpieces were fashioned from drinking straws to facilitate inflation by study participants and establish airtight connections between airway and collection bags to reduce the possibility of room air cross-contamination. Each kit contained five bags labeled for timed collections: one large bag for baseline collection for repeated reference enrichment comparisons and four test sample bags for 60-minute and 75-minute breath collections postsucrose and postglucose substrate ingestions (delta-over-baseline). Measured oxidation values typically peak between these time points in normal subjects at oral tracer dosage levels.

¹³C-tracer isotopes (Isotec, Div. of Sigma-Aldrich, Miamisburg, OH) and aqueous excipients were prepared and labeled under a clean Class 5 bench hood in 100 mL volumes [MediPak USP Sterile Water (37-6250), McKesson Medical-Surgical, Richmond, VA]. Dosed tracers and aqueous excipients composing the substrates were weighed analytically and mixed by combining 25.0 mg uniformly labeled ¹³C-sucrose and 125.0 mg uniformly labeled ¹³C-glucose with 15.0 grams unlabeled sucrose and 15 grams unlabeled glucose, respectively, as challenge loads. The unlabeled challenge-load gram-weight was selected because it approximates a threshold unlikely to induce symptoms or delay gastric emptying in most adults. To avoid confusion, substrates were color-coded using McCormick® food coloring (blue for sucrose and pink for glucose) to match the color-coordinated sample collection bags and flavored, respectively, with Adams® strawberry and coconut extracts for taste and aroma. All substrates were frozen at −20°C until needed in Nalgen® polyethylene bottles. Breath testing was performed in the clinic, home, or laboratory setting in the early morning hours before 12 p.m. after an overnight fast.

At study initiation, subjects were asked to hold their breath for a 10-second count and then inflate the reference breath sample for isotopic comparison later with timed breath samples. ¹³C-sucrose substrate solution with 15% excipient was then ingested (at time 0). At 60 minutes post-¹³C-sucrose ingestion, a breath sample was collected, followed by another breath sample at 75 minutes. Immediately after Part I sample collections related to sucrose ingestion were complete, a comparative ¹³C-glucose substrate solution was ingested (Part II of the biphasic breath test) to assess the inherent rate of metabolism for free glucose. This was used for comparison with Part I outcomes (see Section 2.5). The superdose (125 mg, 5 times the ¹³C-sucrose dose) was intended to dilute (mask) any residual ¹³CO₂ carryover effects from the sucrose and to assess inherent body oxidation capacity. As before, Part II breath samples were collected at 60 minutes and 75 minutes after ¹³C–glucose substrate ingestion and results were adjusted by a factor of 0.2x to account for superdosing and to compare, pairwise, ¹³C–sucrose oxidation data with ¹³C–glucose data. Postprocedure breath test kits were promptly returned to the laboratory for analysis.

Measurement of ¹³CO₂ sample enrichment was performed for each 60-minute and 75-minute breath collection using ¹³CO₂ mass dispersive infrared spectrometer (POCone®, Otsuka Electronics, Tokyo, Japan). Each timed sample was analytically compared with the baseline sample (common, presubstrate ingestion sample) and breath test data were expressed as a ratio of the change in ¹³CO₂ enrichment (delta) between the baseline sample and the periodically timed, postsubstrate ingested samples [delta over baseline (DOB) at 60 and 75 minutes (DOB 60′) and (DOB 75′)].

2.5. Calculations

Because of body habitus and age-related variations in carbon dioxide production [33], ¹³CO₂ oxidation value for ¹³C-glucose (Part II) was used to adjust for different intersubject ¹³C-sucrose (Part I) oxidation rates. Oxidized components derived from ¹³C-sucrose (fructose and glucose) were compared to oxidized enrichment values and expressed components derived from the secondary ¹³C-glucose superdose ( glucose enrichment). After mathematical adjustment for the superdosing of glucose, the enrichment ratio of ¹³CO₂ was attributed to sucrose digestion, absorption, and metabolism. (Note: glucose requires no further digestion.) All glucose oxidation-related values were universally adjusted by a standard factor (1.12x) to account for minor inherent increased rate of fructose metabolism as compared with glucose (no isomerization needed) and the 17% proportionally greater atomic weight of sucrose. The ratio of two ¹³CO₂ enrichment values was stated as the Coefficient of Glucose for Sucrose (CGO-S).

2.6. Validation

Considering the tremendous resources that would be required to conventionally validate the ¹³C-sucrose breath test using duodenal/jejunal biopsies obtained from adult patients coincidentally undergoing gastroduodenal endoscopy, an alternative validation substudy approach was undertaken in four genetically distinct subjects. The subjects were identified based upon their sucrase-isomaltase (SI) genotype and tolerance to dietary sucrose and, in two cases, mucosal biopsy results were available which demonstrated diminished sucrase activity by Dahlqvist-assay. The substudy was performed by comparison of ¹³CO₂ appearance in the breath with the timed appearance of ¹³C-monosaccharides in the plasma, the primary products of sucrose digestion.

Successful sucrose digestion results in absorption of ¹³C-fructose and ¹³C-glucose, for which ¹³C-fructose is mostly taken up by the liver on first-pass portal circulation while most resultant ¹³C-glucose passes to the systemic circulation for immediate use by vital organs [34]. Blood sugar samples were then obtained, and comparisons were made to indirectly assess sucrose digestion independent of mucosal biopsies. Concurrently, plasma samples were obtained with timed biphasic ¹³C-sucrose breath test sampling at 30, 60, and 75 minutes after substrate ingestion and assayed. The breath samples were analyzed for ¹³CO₂ enrichment by infrared mass dispersive spectrophotometry. The appearance of ¹³C-plasma glucose was determined by yeast fermentation of plasma and expression of ¹³CO₂ with comparison against a reference substrate standard fermentation [35, 36]. Resultant gas samples were quantitatively eluted from reaction vessels and similarly analyzed for ¹³CO₂ enrichment, and both outcomes were compared.

Subject-A was a healthy, asymptomatic 45.9-year-old woman that routinely ingested dietary sucrose without adverse reactions; her SI genotype (WT/WT) revealed no genetic aberrations (ABI PRISM SNaPshot Assay Life Technologies, performed by LabCorp test 511570 SI, RTP, North Carolina). Subject-D was a profoundly symptomatic 46.7-year-old woman that avoided dietary sucrose and required sacrosidase supplementation with most meals to avoid typical symptoms of maldigestion; her SI genotype revealed homozygous aberrations [c.3218G>A (p.G1073D)]. A recent mucosal biopsy revealed no sucrase activity (only one sample obtained). Subject-B was a moderately symptomatic 23.3-year-old woman that restricted dietary sucrose to avoid typical symptoms. She was the biologic daughter of Subject-D and her sucrase-isomaltase genotype revealed heterozygous aberrations [c.3218G>A; (p.G1073D)/WT]. She has not required sacrosidase supplementation and she manages her symptoms by dietary sucrose restriction. Subject-C was a moderately symptomatic 43.9-year-old woman with a different SI mutation [c.5234T>G; (p.P1745C)] that also restricted dietary sucrose to avoid typical symptoms and periodically required sacrosidase supplementation. A sucrase assay of mucosal biopsy performed 13 years earlier demonstrated diminished sucrase activity (25 μm/min/gm protein: exactly at the diagnostic threshold, 5th percentile).

The plasma samples were processed in a closed reaction system where aliquots of plasma (1.00 mL) were incubated (37°C) overnight with a 20 mL culture of baker’s yeast (Red Star, Cedar Rapids, IA). Each test tube was fitted to a standard 250 mL Mylar breath collection bag and each system was primed with 20.0 mL oxygen (100%). After 24 hours of elapsed time, the system was purged with 100.0 mL of carrier gas containing 3% unlabeled (¹²C) carbon dioxide. Samples were analyzed for ¹³CO₂ enrichment by comparison with a reference standard using mass dispersive spectrophotometry, adjusted for individual plasma volume (DOB PV), and results were stratified according to genotype.

2.7. Statistical Analysis

Deidentified clinical data were abstracted from the Baylor Clinic EPIC health care software (Epic Systems; Verona, Wisconsin). Clinical and experiment data were collected and transcribed to spreadsheets (Excel, Microsoft, Redmond, WA). Statistical analyses utilized an online statistical application [VassarStats (http://vassarstats.net/)]. Graphs and figures were prepared using DeltaGraph 6 (Red Rock Software, Inc., Salt Lake City, UT).

2.8. Generation of Diagnostic Cut-Off Value

We were unable to directly validate the adult control group using comparative enzyme assays on biopsy sample; therefore, a diagnostic cut-off point for the breath test was determined by calculating the lower 95% confidence interval of ¹³CO₂ enrichment data obtained for the asymptomatic control group (CGO-S cut-off ~ 85%). For the purpose of estimating a reference diagnostic cut-off point from normal subjects, a single sample -test was used to determine the difference between the observed mean of the asymptomatic, historically sucrose-tolerant control sample, and the theoretically normal value (CGO-S = 1.00). The CGO-S values of the control group at 60-minute, 75-minute, and mean 60–75-minute time points were tested against the hypothetical CGO mean (60′: ; 75′: ; 60–75′: ), and the data point to 75′ time point was the most telling. The lower limit of the 95% confidence interval (CGO-S) was determined for each time point.

3. Results

The four genetically SI-characterized subjects undertook ¹³C-S/GBT with simultaneous breath and blood sampling to validate breath test outcomes. High enrichment values, derived from effective sucrase activity, resulted in the appearance of high ¹³CO₂ tracer from the plasma and vice versa. Results are shown in Figure 1. Panel (a) (Subject-A: genotype WT/WT) breath enrichment was compared with blood test enrichment. The data closely paralleled each other and were markedly higher than the results obtained from Subject-D (SI homozygous mutation genotype c.3218G>A), whose results for the sucrase portion of the test approached zero. As predicted, the results for the heterozygous subjects (B & C) were depressed as compared to Subject-A and were markedly improved over the data obtained for the SI-affected Subject-D. The intermediate results (B & C) were consistent with those to be expected for the heterozygous subjects.

(a)

(b)

(c)

(d)

Figure 1

The four genetically SI-characterized (chromosome 3-NC_000003.12) subjects undertook ¹³C-S/GBT with simultaneous breath and blood sampling for plasma fermentation to release ¹³CO₂ to validate breath sample enrichment outcomes; Phase I ¹³C-sucrose oxidation data and plasma fermentation data are shown. (a) 45.9 y/o healthy, asymptomatic woman without suspected SI gene mutation and normal CGO for ¹³C-sucrose (>80%); (Chr. 3q25.2-26.2) WT/WT. (b) 23.3 y/o symptomatic woman with heterozygous SI gene mutation and abnormal mean CGO for ¹³C-sucrose (<80%); Chr. 3q25.2-26.2 [c.3218G>A (p.G1073D)/WT]. (c) 53.9 y/o symptomatic woman with heterozygous SI gene mutation and abnormal mean CGO for ¹³C-sucrose (<80%); Chr. 3q25.2-26.2 [c.5234T>G (p.P1745C)/WT]. (d) 46.7-year-old symptomatic woman with homozygous SI gene mutation and abnormal (very low) mean CGO for ¹³C-sucrose (c/o < 80%); Chr. 3q25.2-26.2 [c.3218G>A (p.G1073D)/c.3218G>A (p.G1073D)]. B: ¹³CO₂ breath sample enrichment (delta per mil); P: plasma sample ¹³CO₂ enrichment (delta per mil); C: theoretical target ¹³CO₂ plasma enrichment derived from in vitro reference substrate (¹³C-glucose 3 mg/L).

Collectively, the results obtained from the blood assay (fermentation products of digestion) closely correlated () with ¹³CO₂ breath enrichment (Figure 2).

Eleven patients with FBD and 11 paired control subjects were enrolled and underwent the ¹³C-S/GBT (Figure 3). The primary data sets, on which the conclusions presented herein rely, are appended (see Supplemental Table in Supplementary Material available online at http://dx.doi.org/10.1155/2016/7952891). There were no adverse reactions observed or reported during the study. Seven patients (64%) showed decreased sucrose digestion with CGO-S cut-off values below 87% at the 60-minute time point (mean CGO-S = 0.80; 95% CI = 64–96%) and seven FBD patients (73%) showed decreased sucrose digestion with values below 85% at the 75-minute time point (mean CGO-S = 0.82; 95% CI = 62–98%) and eight patients showed decreased sucrose digestion with values below 85% at the mean 60–75-minute time point (mean CGO-S = 0.85; 95% CI = 85–100%).

Three subjects experienced typical, mild abdominal bloating and abdominal discomfort during the test. In sharp contrast, only one control subject (9%) demonstrated diminished sucrose digestive capacity at the 60-minute, 75-minute, and 60–75-minute time points but did not report any adverse symptoms. Using the derived breath test diagnostic CGO-S cut-off value of 0.85 at the 60–75-minute time points, a Fisher Exact Probability Test of proportions discriminated between the groups (Chi Statistic: 6.55; ).

¹³CO₂ Enrichment Coefficient of Glucose Oxidation for ¹³C-Sucrose (CGO-S) data values obtained at 60-minute, 75-minute, and the mean 60–75-minute values are shown in Supplemental Table .

4. Discussion

Free sucrose is a relatively modern component to the human diet. Sucrose is pervasive in commercially prepared foods, is frequently added to drinks and recipes, and is, therefore, difficult to avoid in the habitual diet. The specific association between sucrose intolerance and FBD-like symptoms has been previously observed [37] but has not been well evaluated. Like lactose, the opportunity for dietary sucrose to be included among the causes of abdominal discomforts is present, and testing is a key component to the therapeutic approach. This small pilot study indicates that sucrose maldigestion could be a factor in some cases of FBD, especially with more difficult cases. This finding was exemplified by eight of the eleven patients with FBD who demonstrated diminished sucrase activity by breath testing. Due to cost constraints, the affected patients could not be assessed by genotyping or mucosal biopsy assays. However, the parallel blood testing for ¹³C-labeled products of sucrose digestion in the four patients with SI gene mutations, used as a surrogate for assay of random intestinal biopsies, successfully validated use of ¹³C-S/GBT.

Approximately two-thirds of the glucose and one-quarter of the fructose (or half of the total stable isotopic-tracer load) were expected to appear in the systemic circulation and to be available as a proportional indicator of normal digestion since very little free sucrose is passively absorbed by the intestines. After fasting, most absorbed fructose is converted to trioses in the liver over time, and trioses are subsequently released into the systemic circulation as lactate for oxidation in extrahepatic tissues or stored as glycogen. Plasma content of ¹³C-labeled monosaccharides closely paralleled breath sample enrichment as the appearance of ¹³CO₂ in either breath or plasma and are both dependent upon mucosal sucrase activity. As such, ¹³CO₂ breath sample enrichment is a valid measure of sucrase activity.

We note that reference values for mucosal disaccharidase assay activities are also determined by mathematical analysis of the distribution of the means of thousands of samples (all comers) assayed over a long period and were not by stratified comparison with symptoms [38]. Furthermore, random biopsies of proximal duodenum may not be representative of true digestive capacity, which occurs distally just beyond the Ligament of Treitz. Therefore, validity would be difficult to ascribe using an endoscopic approach. Sucrose maldigestion may be qualitatively tested by dietary challenge-load testing and assay or breath testing for bacterial-derived, expired methane and hydrogen [39, 40]. Elimination diets and food records are tedious, but they appear to be somewhat helpful in the evaluation of sucrose maldigestion [41]. At the time of this writing, it is difficult to precisely correlate symptoms with CGO-S values in patients since the cohort sample size was small.

A monophasic ¹³C-sucrose breath test was previously applied to a rat model with chemotherapy-induced gastrointestinal mucositis and varying degrees of sucrose activity [42], but that test is not directly applicable for human use because it did not correct for individual differences in metabolic activity and the carbon dioxide production rate. A biphasic ¹³C-sucrose/glucose breath test (¹³C-S/GBT) was successfully used to stratify homozygous, heterozygous, and compound heterozygous cases of congenital sucrase-isomaltase insufficiency [43]. That test had been validated in children and adolescents by comparison with sucrase assay of endoscopic mucosal biopsies. It was also observed that cachectic patients, with cancer and FBD-like symptoms, have markedly diminished ¹³C-S/GBT oxidation scores that worsen with chemotherapy (unpublished). As such, the new test reported on herein has greater utility, particularly since improvements have been made beyond the currently marketed test [44]. In a way similar to the breath-hydrogen test, it is unlikely that the biphasic ¹³C-S/GBT could be fully validated since gastroenterologists that treat adults are reluctant to perform small bowel biopsies for disaccharidase activity. Nevertheless, the implication of this study is large and points to the need for a stronger study with comparative ¹³C-blood-sugar assays using gas chromatographic mass spectrometry, which might be superior to invasive approaches.

The findings of this study also point to the need for clinicians to carefully obtain a dietary history during the evaluation, admittedly a time-consuming task that in this day and age could be initially approached using a handheld device application if a dietician is not readily available [45]. Rao et al. noted that in recent years sucrose consumption had significantly increased and that the source of sweetener had changed from cane sugar (i.e., sucrose, a disaccharide of glucose, and fructose) to corn sweetener (primarily equimolar quantities of sucrose and fructose) [46]. Levels of fructose consumption have increased by more than 1000% between 1970 and 1990 and this suggests that a relatively limited distal absorptive capacity and overindulgence might be a factor in the FBD constellation [47]. Rao et al. also observed a distinct improvement in FBD symptoms when the fructose dose was decreased to less than 25 grams [46]. This finding suggests that recognition of dietary fructose intolerance might be clinically useful, but it remains unclear if digestion, absorption, or both mechanisms could be at fault. Of note, there has been one recent report of symptomatic relief with the use of empiric pancreatic enzymes, which proposes to potentiate residual, downstream mucosal disaccharidase activity and might point to the need for further diagnostic testing [42].

As predicted, the sucrose load used in this study was well tolerated but does not eliminate the possibility of fructose intolerance that could be confirmed by additional ¹³C-fructose testing [48]. An abnormal ¹³C-S/GBT should also prompt evaluation for fructose malabsorption. The sucrose load might be increased for subsequent studies, but responding to this criticism is at the risk of delaying gastric emptying by increasing caloric load.

The concern over excessive amounts of maldigested sucrose contributing to the FBD condition has been the subject of some debate [49]. The role of sucrase insufficiency has not been adequately tested in adult FBD patients whose gastrointestinal evaluations have seldom included direct-biopsy disaccharidase assays. Clinicians might consider dietary sucrose restriction and assess symptom response as a means of evaluation and, if sucrase insufficiency is suspected, obtain a consultation with a dietician to help minimize sucrose exposure. Our finding of sucrase insufficiency in FBD by ¹³C-sucrose breath testing was not surprising since the patients that were recruited for participation had resistant symptoms, and we had observed these epiphenomena before in children. However, our expectation was that the diagnostic yield would be lower. Our group’s earlier pediatric experience involved the use endoscopic biopsy assays and demonstrated that sucrase deficiency occurs in 28% of children presenting with unexplained subacute or chronic abdominal pain that encompassed FBD-like symptoms [50]. This study’s outcome is higher than the frequency of known sucrase mutations, and our findings suggest that the sucrose intolerance may be acquired or that epigenetic factors may be in play. This present study was not designed to investigate the cause of sucrase insufficiency, which could be genetic [51, 52], acquired due to inflammation, cachexia, and anticancer therapy [53] or specifically related to the fructose component or the GLUT-5 transporter that might be involved [54].

Since the 1980s, various sucrose-load breath tests have been used as a means to estimate intestinal absorptive function and sucrase activity in humans, rodents, and swine [55], and this approach falls into the realm of metabolomics, a field that is still expanding. This study demonstrated the feasibility to apply the test clinically. Earlier tests assessed changes in carbon isotopic enrichment as a metabolic indicator but were of limited value because they solely relied upon naturally enriched substrates and the use of cumbersome mass spectrometry [56, 57]. Further refinements to ¹³C-breath test technologies incorporate highly enriched stable isotope tracers and are based on the principle that intake of ¹³C-labeled substrates is expected to be predictably metabolized to ¹³CO₂ and that the measured increase of ¹³CO₂ above baseline proportionally reflects the targeted metabolic functions [58–60]. The use of stable isotope tracers with mass dispersion spectrophotometry also provides convenient point-of-care functionality to the breath test in a typical outpatient scenario, an advancement that has made ¹³C-breath testing affordable and convenient at the bedside [61]. Furthermore, infrared spectrophotometric breath testing can be performed safely in an outpatient center with minimal personnel training necessary to conduct analyses [62].

The modus of the biphasic ¹³C-S/GBT exploits the principle that the constituents of sucrose (glucose and fructose) should be promptly oxidized after ingestion and undergo glycosidic hydrolysis, portal absorption, and systemic oxidation such that the timed appearance and magnitude of ¹³CO₂ recovery from breath sampling provide a good assessment of the digestive process. Modified Scofield equations have been used in the past to adjust ¹³C-urea breath test outcomes in children [63], but that application appears to best relate to bacterial urease in the stomach lumen. However, significant technical differences exist such that onerous mathematical models would be needed to apply that approach here [64]. In this study, the digested components of sucrose were oxidized and the resultant, exhaled carbon dioxide (¹³CO₂) was used as a quantifiable correlate of hydrolysis. However, an innovative adjustment approach, using superdosed ¹³C-glucose, was also used to correct for individual variations in habitus known to affect metabolic rate. (e.g., individuals, with normal digestive activity and increased body mass index would be expected to yield proportionally low tracer signals as compared to lean individuals). This advancement was implemented because ¹³CO₂ enrichment derived from sucrose directly provides no information on retained tracer in body enrichment pools and fluxes [65]. Considering that normal substrate-oxidation peaks early and begins to diminish slowly in concentration, the relatively stable isotopic flux condition, after 75 minutes, provided the opportunity to piggyback a secondary, superdosed ¹³C-glucose breath test, using the same stable isotope tracer; proportional adjustments were then made. The use of ¹³C-glucose provided for a direct and practical adjustment approach that was not dependent on mucosal disaccharidase, and when paired with oxidation results of the target ¹³C-sucrose substrate, individualized mucosal enzyme activity was measured.

The application of a secondary, superdosed ¹³C-glucose breath test also addressed the issue of variable habitus, leaving only mucosal sucrase activity as the isolated physiological difference. In theory, ¹³C-glucose undergoes the same metabolic fate as the hydrolyzed sucrose-derived glucose and fructose monomers but requires no further digestion before oxidation [66, 67]. Therefore, oxidation results were expressed as a proportional change in ¹³CO₂ enrichment ratio between the target ¹³C-sucrose substrate and the change in ¹³CO₂ enrichment associated with the ¹³C-glucose substrate and reported as the Coefficient of Glucose Oxidation for Sucrose (CGO-S) with 100% (1.00) being theoretically ideal. Since the second phase test was applied under the same conditions, it effectively removed the need to consider confounders, such as intercurrent illness, activity changes, fasting status, and metabolic flux, because such effects are conceptually negated (cancelled out). In the sucrase-insufficient condition, delayed digestion would result in a diminished primary sucrose-related oxidation value and isotopic-carryover into the subsequent ¹³C-glucose test period and increase the divisor value. This is a subtle, but important consideration, since initial ¹³CO₂ recovery is attributed to proximal small bowel sucrose digestion and oxidation.

Delayed digestion is expected to contribute to distal fermentation and symptoms related to the production of small molecule effectors, such as N-acyl-3-hydroxypalmitoyl-glycine (commendamide) [68]. In the cases of sucrase insufficiency and delayed digestion, aberrant enrichment carryover would be expected to accentuate the resultant glucose oxidation data (divisor) and theoretically increase the sensitivity of the test and possibly decrease the test specificity. However, the carryover effect is substantially diminished after mathematical adjustment for the superdosing (x/5). As such, any significant ratio discrepancy from unity could be attributed to faulty sucrose digestion at the mucosal level in the absence of other pathologies, such as gastroparesis.

The diagnostic cut-off value used in this study (<0.85) was derived indirectly by determining 95% confidence intervals bracketing the breath test outcomes of the symptom-free control group. However, this diagnostic cut-off point should be considered tenuous at this time, and the issue should be revisited by a larger, direct comparative study of nonmutants with endoscopic mucosal sucrase assays and/or blood enrichment assays.

5. Conclusions

Sucrase deficiency appears to be a factor in the FBD condition. ¹³C-S/GBT was successfully used to assess sucrose digestion and the results reported herein support the need for a larger study. Sucrose maldigestion may also be an indicator of a larger issue, starch maldigestion. This is considered since isomaltase is concurrently expressed with sucrase (same gene product 3q25.2-q26.2) and because starch is the major dietary staple that is difficult to limit. A careful history identifying a link between GI symptoms and starchy food intake, in addition to sucrose intake, should be helpful in predicting the contribution of dietary intolerances to recurrent GI symptomatology [69]. Like sucrose, for adults suffering from carbohydrate malabsorption, a low fermentable diet might be considered in therapeutic planning since maldigestion may promote colonic proliferation of saccharolytic taxa [70]. It raises the possibility that sacrosidase [43], amyloglucosidase [71, 72], or other enzyme supplementation [73] might benefit some patients with FBD or cachexia-induced maldigestion [74], for which further studies are also needed.

Abbreviations

BT:	Breath test
¹³C-S/GBT:	¹³Carbon-sucrose/¹³C-glucose breath test
CGO-S:	Coefficient of Glucose Oxidation for Sucrose
DOB:	Delta over baseline
FBD:	Functional bowel disorder
GI:	Gastrointestinal
IBS:	Irritable bowel syndrome
NSD:	Not significantly different
PV:	Plasma volume in liters
SI:	Sucrase-isomaltase
WT:	Wild type.

Disclosure

Albert M. Balesh and Harold T. Shelby are coauthors.

Competing Interests

Antone R. Opekun’s laboratory, through Baylor College of Medicine, has a standing service-for-fee contract for research breath testing with QOL Medical, LLC, makers of a sacrosidase product. Authors Albert M. Balesh and Harold T. Shelby declare that they have no competing interests.

Authors’ Contributions

Antone R. Opekun, as principal investigator, conceived the study idea, supervised execution of the studies, interpreted literature, data analyses, paper writing, and revisions. Albert M. Balesh performed clinical testing, reviewed and interpreted cited literature, and drafted aspects of the preliminary paper under the close supervision of the principal investigator. Harold T. Shelby provided interpretation of cited literature and recruited study subjects.

Acknowledgments

The authors thank Ms. Susan A. Kennedy who provided editorial review and Karol M. Hernandez for stable isotope substrate preparation and spectrophotometer analysis of samples. They also thank students Christina Lecea-Plaisance, B. S., and Katie Fracoli, PA-SIII, for assistance with some breath sample collections associated with this project. QOL Medical, LLC graciously supported the genetic testing. This work was supported, in part by, NIH Digestive Disease Center Grant P30 DK56338 which funds the Texas Medical Center Digestive Disease Center and by a generous contribution from D.R. and G.P. Laws to the BCM G.I. Research Laboratory Fund.

Supplementary Materials

The primary data are tabulated in Supplemental Table 1 and stratified according to clinical condition. Data include coded identifiers, age, BMI, 60 minute CGO-S values, 75 minute CGO-S values, and mean 60-75 minute CGO-S values. Descriptive statistics are provided.

Supplementary Material

References

W. D. Chey, J. Kurlander, and S. Eswaran, “Irritable bowel syndrome: a clinical review,” The Journal of the American Medical Association, vol. 313, no. 9, pp. 949–958, 2015.
View at: Publisher Site | Google Scholar
Rome III diagnostic criteria for functional gastrointestinal disorders, May 2016, http://www.romecriteria.org/assets/pdf/19_RomeIII_apA_885-898.pdf.
A. L. Engsbro, L. M. Begtrup, J. Kjeldsen et al., “Patients suspected of irritable bowel syndrome—cross-sectional study exploring the sensitivity of rome III criteria in primary care,” The American Journal of Gastroenterology, vol. 108, no. 6, pp. 972–980, 2013.
View at: Publisher Site | Google Scholar
N. J. Talley, G. Holtmann, and M. M. Walker, “Therapeutic strategies for functional dyspepsia and irritable bowel syndrome based on pathophysiology,” Journal of Gastroenterology, vol. 50, no. 6, pp. 601–613, 2015.
View at: Publisher Site | Google Scholar
G. F. Longstreth, W. G. Thompson, W. D. Chey, L. A. Houghton, F. Mearin, and R. C. Spiller, “Functional bowel disorders,” Gastroenterology, vol. 130, no. 5, pp. 1480–1491, 2006.
View at: Publisher Site | Google Scholar
E. Rey and N. J. Talley, “Irritable bowel syndrome: novel views on the epidemiology and potential risk factors,” Digestive and Liver Disease, vol. 41, no. 11, pp. 772–780, 2009.
View at: Publisher Site | Google Scholar
E. A. Mayer, T. Savidge, and R. J. Shulman, “Brain-gut microbiome interactions and functional bowel disorders,” Gastroenterology, vol. 146, no. 6, pp. 1500–1512, 2014.
View at: Publisher Site | Google Scholar
R. Sood, G. R. Law, and A. C. Ford, “Diagnosis of IBS: Symptoms, symptom-based criteria, biomarkers or ‘psychomarkers’?” Nature Reviews Gastroenterology and Hepatology, vol. 11, no. 11, pp. 683–691, 2014.
View at: Publisher Site | Google Scholar
J. A. Tibble, G. Sigthorsson, R. Foster, I. Forgacs, and I. Bjarnason, “Use of surrogate markers of inflammation and Rome criteria to distinguish organic from nonorganic intestinal disease,” Gastroenterology, vol. 123, no. 2, pp. 450–460, 2002.
View at: Publisher Site | Google Scholar
B. M. R. Spiegel, M. Farid, E. Esrailian, J. Talley, and L. Chang, “Is irritable bowel syndrome a diagnosis of exclusion?: a survey of primary care providers, gastroenterologists, and IBS experts,” American Journal of Gastroenterology, vol. 105, no. 4, pp. 848–858, 2010.
View at: Publisher Site | Google Scholar
R. L. Levy, K. R. Jones, W. E. Whitehead, S. I. Feld, N. J. Talley, and L. A. Corey, “Irritable bowel syndrome in twins: heredity and social learning both contribute to etiology,” Gastroenterology, vol. 121, no. 4, pp. 799–804, 2001.
View at: Publisher Site | Google Scholar
M. El-Salhy, “Recent advances in the diagnosis of irritable bowel syndrome,” Expert Review of Gastroenterology and Hepatology, vol. 9, no. 9, pp. 1161–1174, 2015.
View at: Publisher Site | Google Scholar
M. Camilleri, “Peripheral mechanisms in irritable bowel syndrome,” The New England Journal of Medicine, vol. 367, no. 17, pp. 1626–1635, 2012.
View at: Publisher Site | Google Scholar
D. A. Drossman, L. Chang, N. Bellamy et al., “Severity in irritable bowel syndrome: a rome foundation working team report,” American Journal of Gastroenterology, vol. 106, no. 10, pp. 1749–1759, 2011.
View at: Publisher Site | Google Scholar
E. P. Halmos, V. A. Power, S. J. Shepherd, P. R. Gibson, and J. G. Muir, “A diet low in FODMAPs reduces symptoms of irritable bowel syndrome,” Gastroenterology, vol. 146, no. 1, pp. 67–75.e5, 2014.
View at: Publisher Site | Google Scholar
L. Böhn, S. Störsrud, T. Liljebo, P. Lindfors, H. Törnblom, and M. Simrén, “A randomized, controlled trial comparing a diet low in FODMAPs with traditional dietary advice in patients with IBS,” Gastroenterology, vol. 148, no. 4, p. S-654, 2015.
View at: Google Scholar
M.-I. Park and M. Camilleri, “Is there a role of food allergy in irritable bowel syndrome and functional dyspepsia? A systematic review,” Neurogastroenterology and Motility, vol. 18, no. 8, pp. 595–607, 2006.
View at: Publisher Site | Google Scholar
K. El-Chammas, S. E. Williams, and A. Miranda, “Disaccharidase deficiencies in children with chronic abdominal pain,” Journal of Parenteral and Enteral Nutrition, 2015.
View at: Publisher Site | Google Scholar
M. Corlew-Roath and J. A. Di Palma, “Clinical impact of identifying lactose maldigestion or fructose malabsorption in irritable bowel syndrome or other conditions,” Southern Medical Journal, vol. 102, no. 10, pp. 1010–1012, 2009.
View at: Publisher Site | Google Scholar
S. J. Shepherd and P. R. Gibson, “Fructose malabsorption and symptoms of irritable bowel syndrome: guidelines for effective dietary management,” Journal of the American Dietetic Association, vol. 106, no. 10, pp. 1631–1639, 2006.
View at: Publisher Site | Google Scholar
E. Gudmand-Høøyer and H. Skovbjerg, “Disaccharide digestion and maldigestion,” Scandinavian Journal of Gastroenterology. Supplement, vol. 216, pp. 111–121, 1996.
View at: Google Scholar
G. Neale, M. Clark, and B. Levin, “Intestinal sucrase deficiency presenting as sucrose intolerance in adult life,” The British Medical Journal, vol. 2, pp. 1223–1225, 1965.
View at: Publisher Site | Google Scholar
J. J. Rumessen and E. Gudmand-Hoyer, “Absorption capacity of fructose in healthy adults: comparison with sucrose and its constituent monosaccharides,” Gut, vol. 27, no. 10, pp. 1161–1168, 1986.
View at: Publisher Site | Google Scholar
S. Auricchio, F. Ciccimarra, L. Moauro, F. Rey, J. Jos, and J. Rey, “Intraluminal and mucosal starch digestion in congenital deficiency of intestinal sucrase and isomaltase activities,” Pediatric Research, vol. 6, no. 11, pp. 832–839, 1972.
View at: Publisher Site | Google Scholar
T. S. King, M. Elia, and J. O. Hunter, “Abnormal colonic fermentation in irritable bowel syndrome,” The Lancet, vol. 352, no. 9135, pp. 1187–1189, 1998.
View at: Publisher Site | Google Scholar
E. E. Sterchi, M. J. Lentze, and H. Y. Naim, “Molecular aspects of disaccharidase deficiencies,” Bailliere's Clinical Gastroenterology, vol. 4, no. 1, pp. 79–96, 1990.
View at: Publisher Site | Google Scholar
L. Ohman and M. Simrén, “Intestinal microbiota and its role in irritable bowel syndrome (IBS),” Current Gastroenterology Reports, vol. 15, article 323, 2013.
View at: Publisher Site | Google Scholar
T. M. Bayless, B. Rothfeld, C. Massa, L. Wise, D. Paige, and M. S. Bedine, “Lactose and milk intolerance: clinical implications,” The New England Journal of Medicine, vol. 292, no. 22, pp. 1156–1159, 1975.
View at: Publisher Site | Google Scholar
P. Born, M. Sekatcheva, T. Rösch, and M. Classen, “Carbohydrate malabsorption in clinical routine: a prospective observational study,” Hepato-Gastroenterology, vol. 53, no. 71, pp. 673–677, 2006.
View at: Google Scholar
D. Rating and C. D. Langhans, “Breath tests: concepts, applications and limitations,” European Journal of Pediatrics, vol. 156, supplement 1, pp. S18–S23, 1997.
View at: Publisher Site | Google Scholar
G. Nucera, M. Gabrielli, A. Lupascu et al., “Abnormal breath tests to lactose, fructose and sorbitol in irritable bowel syndrome may be explained by small intestinal bacterial overgrowth,” Alimentary Pharmacology and Therapeutics, vol. 21, no. 11, pp. 1391–1395, 2005.
View at: Publisher Site | Google Scholar
M. Simrén and P.-O. Stotzer, “Use and abuse of hydrogen breath tests,” Gut, vol. 55, no. 3, pp. 297–303, 2006.
View at: Publisher Site | Google Scholar
C. S. Irving, W. W. Wong, R. J. Shulman, E. O. Smith, and P. D. Klein, “[13C]bicarbonate kinetics in humans: intra—vs. interindividual variations,” The American Journal of Physiology, vol. 245, no. 2, pp. R190–R202, 1983.
View at: Google Scholar
R. Steele, C. Bjerknes, I. Rathgeb, and N. Altszuler, “Glucose uptake and production during the oral glucose tolerance test,” Diabetes, vol. 17, no. 7, pp. 415–421, 1968.
View at: Publisher Site | Google Scholar
R. C. A. Schellekens, G. G. Olsder, S. M. C. H. Langenberg et al., “Proof-of-concept study on the suitability of ¹³C-urea as a marker substance for assessment of in vivo behaviour of oral colon-targeted dosage forms,” British Journal of Pharmacology, vol. 158, no. 2, pp. 532–540, 2009.
View at: Publisher Site | Google Scholar
C. W. Swart, K. Dithebe, C. H. Pohl et al., “Gas bubble formation in the cytoplasm of a fermenting yeast,” FEMS Yeast Research, vol. 12, no. 7, pp. 867–869, 2012.
View at: Publisher Site | Google Scholar
F. Fernandez-Banares, M. Esteve-Pardo, R. de Leon et al., “Sugar malabsorption in functional bowel disease: clinical implications,” American Journal of Gastroenterology, vol. 88, no. 12, pp. 2044–2050, 1993.
View at: Google Scholar
B. L. Nichols Jr., B. Adams, C. M. Roach, C.-X. Ma, and S. S. Baker, “Frequency of sucrase deficiency in mucosal biopsies,” Journal of Pediatric Gastroenterology and Nutrition, vol. 55, supplement 2, pp. S28–S30, 2012.
View at: Publisher Site | Google Scholar
G. Metz, D. J. Jenkins, A. Newman, and L. M. Blendis, “Breath hydrogen in hyposucrasia,” The Lancet, vol. 307, no. 7951, pp. 119–120, 1976.
View at: Publisher Site | Google Scholar
S. V. Rana and A. Malik, “Breath tests and irritable bowel syndrome,” World Journal of Gastroenterology, vol. 28, pp. 7587–7601, 2014.
View at: Google Scholar
R. Goldstein, D. Braverman, and H. Stankiewicz, “Carbohydrate malabsorption and the effect of dietary restriction on symptoms of irritable bowel syndrome and functional bowel complaints,” Israel Medical Association Journal, vol. 2, no. 8, pp. 583–587, 2000.
View at: Google Scholar
K. L. Tooley, G. S. Howarth, K. A. Lymn, and R. N. Butler, “Optimization of the non-invasive 13C-sucrose breath test in a rat model of methotrexate-induced mucositis,” Cancer Chemotherapy and Pharmacology, vol. 65, no. 5, pp. 913–921, 2010.
View at: Publisher Site | Google Scholar
C. C. Robayo-Torres, A. R. Opekun, R. Quezada-Calvillo et al., “13C-breath tests for sucrose digestion in congenital sucrase isomaltase-deficient and sacrosidase-supplemented patients,” Journal of Pediatric Gastroenterology and Nutrition, vol. 48, no. 4, pp. 412–418, 2009.
View at: Publisher Site | Google Scholar
F. Zhu, M. Bosch, I. Woo et al., “The use of mobile devices in aiding dietary assessment and evaluation,” IEEE Journal on Selected Topics in Signal Processing, vol. 4, no. 4, pp. 756–766, 2010.
View at: Publisher Site | Google Scholar
Metabolic Solutions, “Sucrose Breath Test,” http://www.metsol.com/assets/sites/3/Sucrose-Breath-Test.pdf.
View at: Google Scholar
S. S. C. Rao, A. Attaluri, L. Anderson, and P. Stumbo, “Ability of the normal human small intestine to absorb fructose: evaluation by breath testing,” Clinical Gastroenterology and Hepatology, vol. 5, no. 8, pp. 959–963, 2007.
View at: Publisher Site | Google Scholar
M. E. Latulippe and S. M. Skoog, “Fructose malabsorption and intolerance: effects of fructose with and without simultaneous glucose ingestion,” Critical Reviews in Food Science and Nutrition, vol. 51, no. 7, pp. 583–592, 2011.
View at: Publisher Site | Google Scholar
C. H. Wilder-Smith, A. Materna, C. Wermelinger, and J. Schuler, “Fructose and lactose intolerance and malabsorption testing: the relationship with symptoms in functional gastrointestinal disorders,” Alimentary Pharmacology and Therapeutics, vol. 37, no. 11, pp. 1074–1083, 2013.
View at: Publisher Site | Google Scholar
F. Fernández-Bañares, M. Rosinach, M. Esteve, M. Forné, J. C. Espinós, and J. Maria Viver, “Sugar malabsorption in functional abdominal bloating: a pilot study on the long-term effect of dietary treatment,” Clinical Nutrition, vol. 25, no. 5, pp. 824–831, 2006.
View at: Publisher Site | Google Scholar
W. Karnsakul, U. Luginbuehl, D. Hahn et al., “Disaccharidase activities in dyspeptic children: biochemical and molecular investigations of maltase-glucoamylase activity,” Journal of Pediatric Gastroenterology and Nutrition, vol. 35, no. 4, pp. 551–556, 2002.
View at: Publisher Site | Google Scholar
S. Uhrich, Z. Wu, J.-Y. Huang, and C. R. Scott, “Four mutations in the SI gene are responsible for the majority of clinical symptoms of CSID,” Journal of Pediatric Gastroenterology and Nutrition, vol. 55, supplement 2, pp. S34–S35, 2012.
View at: Publisher Site | Google Scholar
H. Y. Naim, M. Heine, and K.-P. Zimmer, “Congenital sucrase-isomaltase deficiency: heterogeneity of inheritance, trafficking, and function of an intestinal enzyme complex,” Journal of Pediatric Gastroenterology and Nutrition, vol. 55, supplement 2, pp. S13–S20, 2012.
View at: Publisher Site | Google Scholar
G. Richardson and R. Dobish, “Chemotherapy induced diarrhea,” Journal of Oncology Pharmacy Practice, vol. 13, no. 4, pp. 181–198, 2007.
View at: Publisher Site | Google Scholar
C. H. Wilder-Smith, X. Li, S. S. Ho et al., “Fructose transporters GLUT5 and GLUT2 expression in adult patients with fructose intolerance,” United European Gastroenterology Journal, vol. 2, no. 1, pp. 14–21, 2014.
View at: Publisher Site | Google Scholar
R. Terry, W. H. van Wettere, A. L. Whittaker, P. J. Herde, and G. S. Howarth, “Using the noninvasive ¹³C-sucrose breath test to measure intestinal sucrase activity in swine,” Comparative Medicine, vol. 62, no. 6, pp. 504–507, 2012.
View at: Google Scholar
M. Hiele, Y. Ghoos, P. Rutgeerts, G. Vantrappen, and K. De Buyser, “13CO2 breath test to measure the hydrolysis of various starch formulations in healthy subjects,” Gut, vol. 31, no. 2, pp. 175–178, 1990.
View at: Publisher Site | Google Scholar
B. K. Ritchie, D. R. Brewster, G. P. Davidson et al., “¹³C-sucrose breath test: novel use of a noninvasive biomarker of environmental gut health,” Pediatrics, vol. 124, no. 2, pp. 620–626, 2009.
View at: Publisher Site | Google Scholar
P. D. Klein and E. R. Klein, “Stable isotopes: origins and safety,” Journal of Clinical Pharmacology, vol. 26, no. 6, pp. 378–382, 1986.
View at: Publisher Site | Google Scholar
B. Braden, B. Lembcke, W. Kuker, and W. F. Caspary, “13C-breath tests: current state of the art and future directions,” Digestive and Liver Disease, vol. 39, no. 9, pp. 795–805, 2007.
View at: Publisher Site | Google Scholar
D. Graham, D. Evans Jr., L. Alpert et al., “Campylobacter pylori detected noninvasively by the 13C-urea breath test,” The Lancet, vol. 329, no. 8543, pp. 1174–1177, 1987.
View at: Publisher Site | Google Scholar
A. R. Opekun, A. B. Gotschall, N. Abdalla et al., “Improved infrared spectrophotometer for point-of-care patient 13C-urea breath testing in the primary care setting,” Clinical Biochemistry, vol. 38, no. 8, pp. 731–734, 2005.
View at: Publisher Site | Google Scholar
Y. Deng, “Fuzzy analytical hierarchy process based on canonical representation on fuzzy numbers,” Journal of Computational Analysis and Applications, vol. 22, no. 2, pp. 201–228, 2017.
View at: Google Scholar
W. N. Schofield, “Predicting basal metabolic rate, new standards and review of previous work,” Human Nutrition. Clinical Nutrition, vol. 39, supplement 1, pp. 5–41, 1985.
View at: Google Scholar
P. D. Klein, H. M. Malaty, S. J. Czinn, S. C. Emmons, R. F. Martin, and D. Y. Graham, “Normalizing results of 13C-urea breath testing for CO₂ production rates in children,” Journal of Pediatric Gastroenterology and Nutrition, vol. 29, no. 3, pp. 297–301, 1999.
View at: Publisher Site | Google Scholar
C. S. Irving, W. W. Wong, R. J. Shulman, E. O. Smith, and P. D. Klein, “[13C]bicarbonate kinetics in humans: intra- vs. interindividual variations,” The American Journal of Physiology, vol. 245, no. 2, pp. R190–R202, 1983.
View at: Google Scholar
J. J. Robert, J. Koziet, D. Chauvet, D. Darmaun, J. F. Desjeux, and V. R. Young, “Use of 13C-labeled glucose for estimating glucose oxidation: some design considerations,” Journal of Applied Physiology, vol. 63, no. 5, pp. 1725–1732, 1987.
View at: Google Scholar
B. Koletzko, H. Demmelmair, W. Hartl et al., “The use of stable isotope techniques for nutritional and metabolic research in paediatrics,” Early Human Development, vol. 53, supplement, pp. S77–S97, 1998.
View at: Publisher Site | Google Scholar
L. J. Cohen, H.-S. Kang, J. Chu et al., “Functional metagenomic discovery of bacterial effectors in the human microbiome and isolation of commendamide, a GPCR G2A/132 agonist,” Proceedings of the National Academy of Sciences of the United States of America, vol. 112, no. 35, pp. E4825–E4834, 2015.
View at: Publisher Site | Google Scholar
M. Spencer, W. D. Chey, and S. Eswaran, “Dietary renaissance in IBS: has food replaced medications as a primary treatment strategy?” Current Treatment Options in Gastroenterology, vol. 12, no. 4, pp. 424–440, 2014.
View at: Publisher Site | Google Scholar
B. P. Chumpitazi, J. L. Cope, E. B. Hollister et al., “Randomized clinical trial: gut microbiome biomarkers are associated with clinical response to a low FODMAP diet in children with the irritable bowel syndrome,” Alimentary Pharmacology and Therapeutics, vol. 42, no. 4, pp. 418–427, 2015.
View at: Publisher Site | Google Scholar
US Patent & Trademark Web site: United States Patent Application Notice: Enzyme formulation for use as food supplement, 2016, http://appft.uspto.gov/netacgi/nph-Parser?Sect1=PTO1&Sect2=HITOFF&d=PG01&p=1&u=%2Fnetahtml%2FPTO%2Fsrchnum.html&r=1&f=G&l=50&s1=%2220160114012%22.PGNR.&OS=DN/20160114012&RS=DN/2016011401.
S. Karani, M. S. Kataria, and A. E. Barber, “A double-blind clinical trial with a digestive enzyme product,” British Journal of Clinical Practice, vol. 25, no. 8, pp. 375–377, 1971.
View at: Google Scholar
M. Di Stefano, E. Miceli, S. Gotti, A. Missanelli, S. Mazzocchi, and G. R. Corazza, “The effect of oral α-galactosidase on intestinal gas production and gas-related symptoms,” Digestive Diseases and Sciences, vol. 52, no. 1, pp. 78–83, 2007.
View at: Publisher Site | Google Scholar
M. Simadibrata, R. J. A. Wanders, G. Jan et al., “Examination of small bowel enzymes in chronic diarrhea,” Journal of Gastroenterology and Hepatology, vol. 18, no. 1, pp. 53–56, 2003.
View at: Publisher Site | Google Scholar

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Copyright © 2016 Antone R. Opekun et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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