Objectives: In the last decade gut microbial diversity was associated with the pathogenesis of obesity in humans. Plasma citrulline was a simple and accurate biomarker for the severity of intestinal failure and was associated with short bowel syndrome and alteration of gut permeability, being developed as an alternative to D-xylose tolerance test for the diagnosis of an abnormal small intestinal absorption of nutrients. This study was performed to ascertain whether obesity might be associated with dysregulation of epithelial gut function. Methods: Fifteen obese individuals (5 M/10 F; BMI 37.4 ± 6.1 Kg/m2; 42 ± 6 yrs) and 15 healthy gender- and age-matched controls (6 M/9 F BMI: 22.7 ± 2.1 Kg/m2; 39 ± 7 yrs) underwent D-xylose load (25 g) and plasma citrulline, plasma insulin, glucose and lipid profile testing. Results: Plasma citrulline was significantly lower in the obese group (p = 0.045) with respect to controls, whilst total cholesterol, LDL and trygliceri- des concentration, insulin level and HOMA-IR were significantly higher in obese patients. In contrast, after D-xylose load no difference in serum xylose was found between the two groups (p = ns). Conclusions: Obese patients show a decreased citrulline concentration with respect to lean subjects. Since citrulline is a known marker of intestinal health, alterations in the gut epithelium are likely to be associated with the obesity syndrome. We propose to measure citrulline level in obese patients on a routine basis.
Overweight and obesity are major risk factors for a number of chronic-degenerative diseases. In the last decade gut microbial diversity was associated to the pathogenesis of obesity in humans [
Fifteen obese patients without diabetes mellitus, dyslipidemia and in stable condition were recruited in the population of over 600 patients at the Nutrition/Metabolism Unit of San Raffaele Hospital. A BMI of ≥30 kg/m2 was used for obesity classification. Fifteen healthy volunteers, matched for anthropometric parameters, served as a control group. All the subjects were recruited between July 2007 and January 2008.
All subjects involved in this protocol were studied on two separate days. The subjects assumed an isocaloric diet in the 4 weeks preceding the study. On day 1, they were admitted to the Metabolic Unit of the Department of Medicine of San Rafael Scientific Institute after an overnight fast. At 08.00 of day 1, a polyethylene catheter was inserted in the antecubital vein of one forearm. At 08.30, a basal blood sample for the measurement of hormones and metabolites was drawn and the urinary cortisol concentration was measured in the total urine specimen collected over the preceding 24 hours. Then the patients were discharged. On day 2, all subjects were re- admitted to the San Raffaele Hospital and underwent a D-xylose load (25 g) as well a blood sample for measurement of plasma citrulline concentration.
Aliquots of blood for the measurement of metabolites (glucose, triglycerides, total cholesterol, HDL cholesterol, LDL cholesterol, TSH) level were placed in heparinized tubes. Plasma glucose was measured utilizing the glucose oxidase methodology. Blood aliquots for insulin and TSH were collected in tubes for serum separation. Urine collection (24 h) was performed to quantify cortisol excretion. All blood samples were placed in ice until the plasma/serum was prepared by centrifugation at 4˚C (within 1.5 h of sampling). All plasma and serum aliquots were frozen at −60˚C until later analysis.
All subjects ingested an oral solution composed by 25 g of D-xylose in 250 ml of water. Blood samples were drawn and measured for D-xylose concentration at baseline and at 120 minutes after xylose ingestion.
| Subject characteristics | Obese patients | Controls |
|---|---|---|
| Sex (M/F) | 5/10 | 6/9 |
| Age (y) | 42 ± 6 | 39 ± 7 |
| Weight (kg) | 97 ± 22* | 69 ± 15 |
| Height (cm) | 160 ± 8 | 165 ± 9 |
| BMI (kg/m2) | 37.4 ± 6.1* | 22.7 ± 2.1 |
*p < 0.001 vs. CON.
Plasma levels of the amino acid were obtained using an adaptation of an HPLC procedure based on pre-column derivatization with o-phthaldialdehyde (OPA) and carried out on reversed-phase C18 column [
All data are expressed as means ± SD. Comparisons between obese and control groups were performed with the Student’s t-test for unpaired data (a value of less than 0.05 was considered statistically significant). We used non parametric methods (Mann-Whitney test) to compare HOMA-IR in the groups because the distribution of these dependent variable were not normal.
No difference was observed in the xylosemia between the two study groups. In particular the obese group had a value of xylosemia slightly lower compared to controls.
The HOMA-IR was higher in obese group with respect to controls (p < 0.03).
Plasma citrulline concentration was lower in obese patients with respect to controls (p = 0.045), indicating a reduction of production of this amino-acid by small bowel epithelium.
Plasma lipid profile was normal in obese patients and in control group. The total cholesterol was higher in obese group (p < 0.01). Also triglyceride concentrations were higher in obese group (p < 0.01).
Plasma insulin was higher in the obese group with respect to controls (p < 0.01). The free urinary cortisol was normal in obese patients but within the upper 50% of the normal range (p = 0.07).
| Obese patients | Controls | |
|---|---|---|
| Plasma glucose (mmol/l) | 4.7 ± 0.6 | 5 ± 0.3 |
| Free insulin (pmol/l) | 49.8* ± 15.06 | 30.5 ± 10.1 |
| Total cholesterol (mmol/l) | 5.2* ± 0.4 | 4.4 ± 0.3 |
| Cholesterol HDL | 1.3 ± 0.3 | 1.4 ± 0.2 |
| Cholesterol LDL (calculated) | 3.4* ± 1.4 | 2.6 ± 1.1 |
| Triglycerides (mmol/l) | 1.3* ± 0.9 | 0.7 ± 0.4 |
| HOMA-IR | 1.75* ± 0.93 | 0.98 ± 0.44 |
| Blood D-xylose (mmol/L) | 2.82 ± 0.76 | 3.21 ± 0.89 |
| Plasma citrulline (mmol/L) | 22.3* ± 6.2 | 26.3 ± 3.9 |
| Free urinary cortisol (nmol/24 h) | 342 ± 74 | 296 ± 63 |
| TSH (mU/l) | 1.72 ± 0.90 | 1.92 ± 1.03 |
*p < 0.05 vs. CON.
The current study presents a new observation regarding the possibility that obesity may be associated with dysregulation of epithelial gut function.
It is well known that intestinal microflora and diet influence both body weight and insulin-resistance, notably through an action on adipose cells [
The gut epithelium is not only involved in the absorption of nutrients, but must also provide a barrier between the gastrointestinal lumen and the rest of the body.
In our study, all obese subjects were insulin resistant and with alteration of gut epithelium, possibly of inflammatory origin.
In patients with intestinal transplantation low value of blood citrulline is now considered a marker of graft dysfunction (acute rejection) [
In animal model citrulline supplementation improved gut function by decreasing intestinal permeability and positively affecting immune function [
In the same fashion the alterations present in obese patients seem to be similar to patients with early stage of graft rejection.
One possible explanation of our results in the obese subjects may be the presence of chronic inflammation in the epithelium of gut.
Therapies of obesity have focused on reducing caloric intake, decreasing nutrient absorption, or increasing physical activity. Future treatments for obesity may attempt to modulate the intestinal microbiota through the use of antibiotics, probiotics, and prebiotics [
In conclusion, our results indicate that there is a strict correlation between the characteristic metabolic picture present in obesity and low value of citrulline (a marker of integrity of gut epithelium). In accordance with other authors [
There are some possible limitations to consider in the present study. First, the number of obesity in the sample is somewhat small. Second, this is a case-control study and we cannot draw a cause-effect conclusion about gastrointestinal alteration and obesity.
Further studies are needed to elucidate the potential role of citrulline as useful biomarker to label patients affected by obesity as patients with dysregulation of epithelial gut absorption.
This study was fully supported by a grant kindly provided by BRACCO, SpA.
StefanoBenedini,IsabellaFermo,AndreaCaumo,IleanaTerruzzi,LivioLuzi,11, (2015) Plasma Citrulline: A New Marker of Gut Epithelium Alteration in Obese Patients?. Journal of Diabetes Mellitus,05,233-237. doi: 10.4236/jdm.2015.54028