Yonsei Med J.  2016 Jan;57(1):146-152. 10.3349/ymj.2016.57.1.146.

Irritable Bowel Syndrome May Be Associated with Elevated Alanine Aminotransferase and Metabolic Syndrome

Affiliations
  • 1Department of Family Medicine, Seo-Hae Hospital, Seocheon, Korea.
  • 2Department of Family Practice and Community Health, Ajou University School of Medicine, Suwon, Korea. ktwonm@hanmail.net

Abstract

PURPOSE
Recent studies have revealed close relationships between hepatic injury, metabolic pathways, and gut microbiota. The microorganisms in the intestine also cause irritable bowel syndrome (IBS). The aim of this study was to examine whether IBS was associated with elevated hepatic enzyme [alanine aminotransferase (ALT) and aspartate aminotransferase (AST)], gamma-glutamyl transferase (gamma-GT) levels, and metabolic syndrome (MS).
MATERIALS AND METHODS
This was a retrospective, cross-sectional, case-control study. The case and control groups comprised subjects who visited our health promotion center for general check-ups from June 2010 to December 2010. Of the 1127 initially screened subjects, 83 had IBS according to the Rome III criteria. The control group consisted of 260 age- and sex-matched subjects without IBS who visited our health promotion center during the same period.
RESULTS
Compared to control subjects, patients with IBS showed significantly higher values of anthropometric parameters (body mass index, waist circumference), liver enzymes, gamma-GT, and lipid levels. The prevalences of elevated ALT (16.9% vs. 7.7%; p=0.015) and gamma-GT (24.1% vs. 11.5%; p=0.037) levels were significantly higher in patients with IBS than in control subjects. A statistically significant difference was observed in the prevalence of MS between controls and IBS patients (12.7% vs. 32.5%; p<0.001). The relationships between elevated ALT levels, MS, and IBS remained statistically significant after controlling for potential confounding factors.
CONCLUSION
On the basis of our study results, IBS may be an important condition in certain patients with elevated ALT levels and MS.

Keyword

Irritable bowel syndrome; liver enzymes; metabolic syndrome

MeSH Terms

Adult
Alanine Transaminase/analysis/*metabolism
Aspartate Aminotransferases/analysis/*metabolism
Body Mass Index
Case-Control Studies
Cross-Sectional Studies
Female
Humans
Irritable Bowel Syndrome/diagnosis/*enzymology/epidemiology
Liver/metabolism
Male
Metabolic Syndrome X/complications/diagnosis/*enzymology/epidemiology
Middle Aged
Obesity/epidemiology
Prevalence
Retrospective Studies
Waist Circumference
gamma-Glutamyltransferase/analysis/*metabolism
Alanine Transaminase
Aspartate Aminotransferases
gamma-Glutamyltransferase

Figure

  • Fig. 1 Prevalences of elevated ALT and γ-GT levels and metabolic syndrome in IBS patients and control subjects. Elevated ALT and γ-GT were defined as >41 IU/L for males and >31 IU/L for females for ALT and >66 IU/L for males and >39 IU/L for females for γ-GT. Metabolic syndrome (MS) was defined as the presence of three or more of the guidelines of the American Heart Association/National Heart, Lung, and Blood Institute (AHA/NHLBI) Scientific Statement published in 2005. A significant difference was observed between the two groups with respect to ALT (16.9% vs. 7.7%; p=0.015), γ-GT (24.1% vs. 11.5%; p=0.037), and MS (32.5% vs. 12.7%; p<0.001). IBS, irritable bowel syndrome; ALT, alanine aminotransferase; γ-GT, gamma-glutamyl transferase.


Cited by  1 articles

Dose-Response Relationship between Alanine Aminotransferase Levels within the Reference Interval and Metabolic Syndrome in Chinese Adults
Peipei Wu, Qicai Chen, Lili Chen, Pengpeng Zhang, Juan Xiao, Xiaoxiao Chen, Meng Liu, Shumei Wang
Yonsei Med J. 2017;58(1):158-164.    doi: 10.3349/ymj.2017.58.1.158.


Reference

1. Caricilli AM, Saad MJ. The role of gut microbiota on insulin resistance. Nutrients. 2013; 5:829–851.
Article
2. D'Aversa F, Tortora A, Ianiro G, Ponziani FR, Annicchiarico BE, Gasbarrini A. Gut microbiota and metabolic syndrome. Intern Emerg Med. 2013; 8:Suppl 1. S11–S15.
3. Le Roy T, Llopis M, Lepage P, Bruneau A, Rabot S, Bevilacqua C, et al. Intestinal microbiota determines development of non-alcoholic fatty liver disease in mice. Gut. 2013; 62:1787–1794.
Article
4. Gerritsen J, Smidt H, Rijkers GT, de Vos WM. Intestinal microbiota in human health and disease: the impact of probiotics. Genes Nutr. 2011; 6:209–240.
Article
5. Cholongitas E, Pipili C, Dasenaki M. Gastro-oesophageal reflux disease and irritable bowel syndrome significantly associated with metabolic syndrome. Scand J Gastroenterol. 2008; 43:1405–1406.
Article
6. Collins SM. Translating symptoms into mechanisms: functional GI disorders. Adv Physiol Educ. 2007; 31:329–331.
Article
7. Agrawal A, Whorwell PJ. Irritable bowel syndrome: diagnosis and management. BMJ. 2006; 332:280–283.
Article
8. Han SH, Lee OY, Bae SC, Lee SH, Chang YK, Yang SY, et al. Prevalence of irritable bowel syndrome in Korea: population-based survey using the Rome II criteria. J Gastroenterol Hepatol. 2006; 21:1687–1692.
Article
9. Song SW, Park SJ, Kim SH, Kang SG. Relationship between irritable bowel syndrome, worry and stress in adolescent girls. J Korean Med Sci. 2012; 27:1398–1404.
Article
10. Drossman DA, Li Z, Andruzzi E, Temple RD, Talley NJ, Thompson WG, et al. U.S. householder survey of functional gastrointestinal disorders. Prevalence, sociodemography, and health impact. Dig Dis Sci. 1993; 38:1569–1580.
11. Saito YA, Locke GR, Talley NJ, Zinsmeister AR, Fett SL, Melton LJ 3rd. A comparison of the Rome and Manning criteria for case identification in epidemiological investigations of irritable bowel syndrome. Am J Gastroenterol. 2000; 95:2816–2824.
Article
12. American gastroenterological association medical position statement: irritable bowel syndrome. Gastroenterology. 1997; 112:2118–2119.
13. Parkes GC, Brostoff J, Whelan K, Sanderson JD. Gastrointestinal microbiota in irritable bowel syndrome: their role in its pathogenesis and treatment. Am J Gastroenterol. 2008; 103:1557–1567.
Article
14. Ohman L, Simrén M. New insights into the pathogenesis and pathophysiology of irritable bowel syndrome. Dig Liver Dis. 2007; 39:201–215.
Article
15. Di Stefano M, Corazza GR. Treatment of small intestine bacterial overgrowth and related symptoms by rifaximin. Chemotherapy. 2005; 51:Suppl 1. 103–109.
Article
16. Singh VV, Toskes PP. Small bowel bacterial overgrowth: presentation, diagnosis, and treatment. Curr Treat Options Gastroenterol. 2004; 7:19–28.
Article
17. Walters B, Vanner SJ. Detection of bacterial overgrowth in IBS using the lactulose H2 breath test: comparison with 14C-D-xylose and healthy controls. Am J Gastroenterol. 2005; 100:1566–1570.
Article
18. Pimentel M, Chow EJ, Lin HC. Eradication of small intestinal bacterial overgrowth reduces symptoms of irritable bowel syndrome. Am J Gastroenterol. 2000; 95:3503–3506.
Article
19. Szabo G, Bala S, Petrasek J, Gattu A. Gut-liver axis and sensing microbes. Dig Dis. 2010; 28:737–744.
Article
20. Miele L, Valenza V, La Torre G, Montalto M, Cammarota G, Ricci R, et al. Increased intestinal permeability and tight junction alterations in nonalcoholic fatty liver disease. Hepatology. 2009; 49:1877–1887.
Article
21. Miele L, Beale G, Patman G, Nobili V, Leathart J, Grieco A, et al. The Kruppel-like factor 6 genotype is associated with fibrosis in nonalcoholic fatty liver disease. Gastroenterology. 2008; 135:282–291.
Article
22. Harte AL, da Silva NF, Creely SJ, McGee KC, Billyard T, Youssef-Elabd EM, et al. Elevated endotoxin levels in non-alcoholic fatty liver disease. J Inflamm (Lond). 2010; 7:15.
Article
23. Creely SJ, McTernan PG, Kusminski CM, Fisher fM, Da Silva NF, Khanolkar M, et al. Lipopolysaccharide activates an innate immune system response in human adipose tissue in obesity and type 2 diabetes. Am J Physiol Endocrinol Metab. 2007; 292:E740–E747.
Article
24. Schnabl B, Brenner DA. Interactions between the intestinal microbiome and liver diseases. Gastroenterology. 2014; 146:1513–1524.
Article
25. Reid AE. Nonalcoholic steatohepatitis. Gastroenterology. 2001; 121:710–723.
Article
26. Liu Z, Que S, Ning H, Wang L, Peng T. Elevated alanine aminotransferase is strongly associated with incident metabolic syndrome: a meta-analysis of prospective studies. PLoS One. 2013; 8:e80596.
Article
27. Guillemin F, Bombardier C, Beaton D. Cross-cultural adaptation of health-related quality of life measures: literature review and proposed guidelines. J Clin Epidemiol. 1993; 46:1417–1432.
Article
28. Greenfield TK. Ways of measuring drinking patterns and the difference they make: experience with graduated frequencies. J Subst Abuse. 2000; 12:33–49.
Article
29. Kim DM, Ahn CW. Definition and epidemiology of obesity. J Korean Med Assoc. 2004; 47:289–297.
Article
30. Grundy SM, Cleeman JI, Daniels SR, Donato KA, Eckel RH, Franklin BA, et al. Diagnosis and management of the metabolic syndrome: an American heart association/national heart, lung, and blood institute scientific statement. Circulation. 2005; 112:2735–2752.
31. Clinical and laboratory standards institute. Defining, establishing, and verifying reference intervals in the clinical laboratory: approved guideline. 3rd ed. Wayne, PA: Clinical and Laboratory Standards Institute;2008.
32. Clark JM, Brancati FL, Diehl AM. The prevalence and etiology of elevated aminotransferase levels in the United States. Am J Gastroenterol. 2003; 98:960–967.
Article
33. Suh YJ, Park SK, Choi JM, Ryoo JH. The clinical importance of serum γ-glutamyltransferase level as an early predictor of obesity development in Korean men. Atherosclerosis. 2013; 227:437–441.
Article
34. Pimentel M, Chow EJ, Lin HC. Normalization of lactulose breath testing correlates with symptom improvement in irritable bowel syndrome. a double-blind, randomized, placebo-controlled study. Am J Gastroenterol. 2003; 98:412–419.
Article
35. Lupascu A, Gabrielli M, Lauritano EC, Scarpellini E, Santoliquido A, Cammarota G, et al. Hydrogen glucose breath test to detect small intestinal bacterial overgrowth: a prevalence case-control study in irritable bowel syndrome. Aliment Pharmacol Ther. 2005; 22:1157–1160.
Article
36. Collins SM, Denou E, Verdu EF, Bercik P. The putative role of the intestinal microbiota in the irritable bowel syndrome. Dig Liver Dis. 2009; 41:850–853.
Article
37. Ilan Y. Leaky gut and the liver: a role for bacterial translocation in nonalcoholic steatohepatitis. World J Gastroenterol. 2012; 18:2609–2618.
Article
38. Pande C, Kumar A, Sarin SK. Small-intestinal bacterial overgrowth in cirrhosis is related to the severity of liver disease. Aliment Pharmacol Ther. 2009; 29:1273–1281.
Article
39. Park JH, Park DI, Kim HJ, Cho YK, Sohn CI, Jeon WK, et al. The relationship between small-intestinal bacterial overgrowth and intestinal permeability in patients with irritable bowel syndrome. Gut Liver. 2009; 3:174–179.
Article
40. Cortez-Pinto H, de Moura MC, Day CP. Non-alcoholic steatohepatitis: from cell biology to clinical practice. J Hepatol. 2006; 44:197–208.
Article
41. Portincasa P, Grattagliano I, Palmieri VO, Palasciano G. Nonalcoholic steatohepatitis: recent advances from experimental models to clinical management. Clin Biochem. 2005; 38:203–217.
Article
42. Schaafsma G, Meuling WJ, van Dokkum W, Bouley C. Effects of a milk product, fermented by Lactobacillus acidophilus and with fructo-oligosaccharides added, on blood lipids in male volunteers. Eur J Clin Nutr. 1998; 52:436–440.
Article
43. Noh DO, Kim SH, Gilliland SE. Incorporation of cholesterol into the cellular membrane of Lactobacillus acidophilus ATCC 43121. J Dairy Sci. 1997; 80:3107–3113.
Article
44. Sherman KE. Alanine aminotransferase in clinical practice. A review. Arch Intern Med. 1991; 151:260–265.
Article
45. Guo Y, Niu K, Momma H, Kobayashi Y, Chujo M, Otomo A, et al. Irritable bowel syndrome is positively related to metabolic syndrome: a population-based cross-sectional study. PLoS One. 2014; 9:e112289.
Article
46. Cani PD, Amar J, Iglesias MA, Poggi M, Knauf C, Bastelica D, et al. Metabolic endotoxemia initiates obesity and insulin resistance. Diabetes. 2007; 56:1761–1772.
Article
47. Pappo I, Becovier H, Berry EM, Freund HR. Polymyxin B reduces cecal flora, TNF production and hepatic steatosis during total parenteral nutrition in the rat. J Surg Res. 1991; 51:106–112.
Article
48. Sabaté JM, Jouët P, Harnois F, Mechler C, Msika S, Grossin M, et al. High prevalence of small intestinal bacterial overgrowth in patients with morbid obesity: a contributor to severe hepatic steatosis. Obes Surg. 2008; 18:371–377.
Article
49. Million M, Lagier JC, Yahav D, Paul M. Gut bacterial microbiota and obesity. Clin Microbiol Infect. 2013; 19:305–313.
Article
50. Kang HW, Lee CG, Kim JH, Lim YJ, Lee JK, Koh MS, et al. Visceral abdominal obesity as a risk factor for irritable bowel syndrome: a case-control study. Gastroenterology. 2014; 146:5 Suppl 1. S-178.
51. Singh SP, Kar SK, Panigrahi MK, Misra B, Pattnaik K, Bhuyan P, et al. Profile of patients with incidentally detected nonalcoholic fatty liver disease (IDNAFLD) in coastal eastern India. Trop Gastroenterol. 2013; 34:144–152.
Article
52. Nam SY, Kim BC, Ryu KH, Park BJ. Prevalence and risk factors of irritable bowel syndrome in healthy screenee undergoing colonoscopy and laboratory tests. J Neurogastroenterol Motil. 2010; 16:47–51.
Article
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