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Research Article

The Entero-Insular-Axis is retained in Patients with Alcoholic Liver Disease

Christoph Elsing1,2*,Hi Kha1,2, Wolfgang Stremmel1,2, Martin Volkmann3

1Department of Internal Medicine, Gastroenterology and Metabolic Diseases, St. Elisabeth Hospital, Dorsten, Germany
2Department of Gastroenterology, University Clinic Heidelberg, Heidelberg, Germany
3MVZ Laboratory Prof. Seelig, Karlsruhe, Germany

*Corresponding author:     Dr. Christoph Elsing, Department of Internal Medicine, Gastroenterology and Metabolic Diseases, St. Elisabeth-Hospital, Pf.-W.-Schmitz Str. 1, 46282 Dorsten, Germany,

Tel: (49)23622955202; Fax: + 49-2362-9217044; Email: dr.c.elsing@kkrn.de

Submitted: 04-17-2016  Accepted: 06-29-2016 Published:  07-05-2016

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The incretins glucose-dependent insulinotropic polypeptide (GIP) and glucagon-like peptide-1 (GLP-1) are secreted after mealsand are involved in the pathogenesis of different metabolic diseases, such as non alcoholic liver disease (NALD). GLP-1 agonists are in addition evaluated for the treatment of NALD. The role of incretins is the pathogenesis of alcoholic liver disease (ALD) is however unclear. We determined the secretion of incretins in patients with alcoholic liver disease after oral glucose administration.
In 23 patients with alcoholic liver disease in the early withdrawn state and 19 control patients serum levels of total GIP, intact GLP-1, insulin and C-peptide were determined after an oral glucose load (75g glucose after an overnight fasting).
In this function test, none of the investigated subjects showed a disturbance of glucose metabolism as indicated by the kinetic
of serum glucose. There was a slight tendency for higher insulin resistance and lower insulin sensitivity in alcoholic patients (p = 0.0064). GLP-1 and GIP secretion after the oral stimulation was not different between the two groups, despite marked differences in liver function tests.
We conclude that chronic alcohol abuse and alcoholic liver disease is not associated with a disturbed entero-insular axis, which might have influence on treatment options.
Keywords: Alcohol Dependence; Glp-1; Gip; Insulin Secretion; Oral Glucose Tolerance Test
Alcohol consumption and abuse is common [1] and in Germany it is estimated that approximately two million people are alcohol dependent [2]. Alcoholic liver disease (ALD) is a major cause of morbidity and mortality in these patients. Approximately 40%-90% of patients with cirrhosis have a history of  alcohol abuse and about one third of patients with hepatocellular  carcinoma are attributable to alcoholic liver disease [3, 4]. The mechanisms for the development of ALD are multiple. Alcohol itself acts as a potential hepatotoxin with the development of liver disease depending on host factors, such as gender, polymorphism of alcohol-metabolizing enzymes, immunological factors and concomitant diseases like chronic hepatic viral infections, obesity, diabetes and nutritional deficiencies [3].
Steatosis is one of the earliest responses of the liver to alcohol abuse. Triglycerides, phospholipids and cholesterol ester are accumulated in hepatocytes due to disruption of mitochondrial ß-oxidation of fatty acids [5]. Recent studies have also focused on the direct or indirect regulation of lipid metabolism- associated transcription factors by alcohol exposure leading to hepatic fat accumulation [6].
Non-alcoholic fatty liver disease (NAFLD) and its subgroup steatohepatitis (NASH) are also characterized by hepatic lipid accumulation due to different mechanisms including increased dietary intake, de-novo lipogenesis and influx of free fatty acids. A major risk factor for hepatic fat accumulation is Insulin resistance (IR) [7].
The incretins glucagon-like peptide-1 (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP) are gastrointestinal peptide hormones regulating postprandial insulin release and are shown to be involved in the development of non-alcoholic fatty liver disease and insulin resistance [8]. Both hormones are secreted from neuroendocrine cells (L and K cells) located in the intestinal mucosa [9]. Chronic alcohol consumption has been shown to lead to an increase of the number of Glucagon- and GIP-secreting cells in the duodenal mucosa [10]. In addition, a reduction of the activity of the metabolising enzyme dipeptidyl peptidase-IV (DPP-IV) in serum has been described [11], potentially leading to increased incretin serum levels. These morphological and metabolic changes are seen  on the basis of long term alcohol abuse and thus can be assumedto influence glucose metabolism independently of an acute drinking episode.
The aim of the present study was therefore to evaluate incretin and insulin secretion and insulin resistance in patients with alcoholic liver disease by the use of a standardized oral glucose tolerance test.
Materials and Methods
Forty-two subjects participated in this study. Twenty three subjects were alcohol dependent and nineteen abstinent  participants served as controls. The alcohol dependent patients were hospitalized in the Medical Department of the St. Elisabeth Hospital, Dorsten, Germany. They participated in the structured withdrawal program of the department. As from admission into the hospital the alcohol dependent patients received Tiapride and Carbamazepine which was tapered of during a 1-week period. There was no evidence of pancreatic dysfunction (clinical, ultrasound, laboratory values) in any of the alcoholic patients, all alcoholic patients in this study had elevated liver enzymes more than twice the normal range (Alanin aminotransferase (ALT), Aspartate aminotransferase (AST) and Gamma glutamyl transpeptidase (yGT)).
All patients received ultrasound examination of the liver with a 3.75 Mhz convex transducer (Elegra, Siemens Medical Systems, Erlangen, Germany). Classification of steatosis was based on the criteria of Saadeh et al. [12]. The severity of echogenicity was graded as follows: grade 0, normal echogenicity; grade 1, slight, diffuse increase in fine echoes in liver parenchyma with normal visualization of diaphragm and intrahepatic vessel borders; grade 2, moderate, diffuse increase in fine echoes with slightly impaired visualization of intrahepatic vessels and diaphragm; grade 3, marked increase in fine echoes with poor or nonvisualization of the intrahepatic vessel borders, diaphragm, and posterior right lobe of the liver [12].
Exclusion criteria for controls were alcohol intake, any liver disease with elevated liver function tests and intake of any drug with known influence on glucose homeostasis. All controls had Grade 0 steatosis on ultrasound examination.
The study design was approved by the local ethical committee, and all participants gave informed consent.
Oral Glucose Tolerance Test
The study was performed three to five days after admission and patients had received a norm caloric diet for at least three days. The same conditions were applied to the control group. After overnight fasting patients were provided with an  antecubital vein catheter and given 75g glucose as a 300 ml liquid (Roche, Mannhein, Germany). Blood samples were taken 0, 15, 30, 45, 60, 90 and 120 minutes following oral glucose administration. Samples were collected in chilled tubes containing K-EDTA (Sarstedt, Nümbrecht, Germany) and for GLP-1 determination 50 μL DPP-IV inhibitor (DRG Instruments, Marburg; Germany). After centrifugation at 4° all samples were stored at – 20° C for subsequent assessment of GLP-1, GIP, insulin and c-peptide. Glucose, Hba1c, and baseline liver function tests (Alanine aminotransferase (ALT), Aspartate aminotransferase (AST) and Gamma glutamyl transpeptidase (yGT)) were determined within four hours.
Hormones, Glucose, HbA1c and Liver Function Test
Insulin and C-peptide serum levels were analysed by ECLIA technique on a Modular E Analyzer (Roche Diagnostics, Mannheim, Germany). Intact GLP-1 was measured using GLP-1 ELISA (DRG Instruments, Marburg, Germany), according to the instructions of the manufacturer (intra-assay coefficient of variation was below 9%, inter-assay coefficient of variation was below 13%, and the sensitivity was typically 2 pmmol/l). Total GIP serum levels were measured using human GIP ELISA (DRG Instruments, Marburg, Germany), according to the instructions of the manufacturer (intra-assay coefficient of variation was below 8.8%, inter-assay coefficient of variation was below 6.1%, and the sensitivity was typically less than 8.2 pg/ mL). Routine laboratory values including blood glucose levels, Hba1c and liver enzymes were measured on an automated clinical chemistry analyser using standard IFCC approved methods (Dimension EXL, Siemens Diagnostics Healthcare, Erlangen, Germany).
Insulin resistance
IR was assessed calculating the homeostasis model assessment HOMA2-IR, HOMA-%%B2 and HOMA-%S2 were derived using the HOMA calculator [13].
Mean ± SD or SE are shown throughout. Statistical analysis was calculated by the appropriate test as stated in the text. P < 0.05 was considered to indicate statistically significance. Values were compared by the Mann-Whitney U-Test. A P value less than 0.05 were considered significant. XLSTAT (Addinosoft SARL, Paris, France) was used to perform the statistical analyses.
The area under the concentration curves (AUC) for glucose, insulin and c-peptide were calculated with the trapezium method. Hepatic insulin extraction (HIE) represents the proportion of insulin secreted from the ß-cells which is removed by the liver prior to entering the systemic circulation. The equitation used is [1-(AUCinsulin/AUCc-Peptide)].
Baseline characteristics
Baseline characteristics are shown in Table 1. While gender distribution, BMI and Hba1c levels were comparable, the patient group was older. Liver enzymes were all significantly elevated in the alcoholic patients.
Degree of hepatic steatosis and liver enzymes in patients with alcoholic liver disease
We diagnosed in 14 patients with alcoholic liver disease hepatic steatosis by ultrasound. Regarding degrees, 8 patients had grade 1, 4 patients’ grade 2 and 2 patients grade 3, while in 9 patients steatosis of the liver was absent using ultra sound technique.
Mean ALT levels showed significant variation in the degree of hepatic steatosis (P < 0.05), as shown in Table 2. AST and y-GT showed no significant variation with the severity of steatosis (Kruskal-Wallis-Test).
Fasting plasma glucose, insulin and c-peptide concentrations
No difference was seen between the patients with alcoholic liver disease and the control group regarding fasting levels of  glucose, insulin and C-peptide. Moreover, all baseline parameters for glucose metabolism were within the physiological ranges (Table 1). 
Homeostatic model assessment of insulin sensitivity (HOMA2-% S) and insulin resistance (HOMA2-IR) and hepatic insulin extraction
There was a slight tendency for higher insulin resistance in patients with alcoholic liver disease, the difference was however not significant (12.9±6.3 vs. 9.2±5.0 p = 0.064). The same was shown for insulin sensitivity with lower values in patients with alcoholic liver disease (9.9±5.5 vs. 15.5±10.3 p= 0.064). There was no difference in hepatic insulin extraction between patients with alcoholic liver disease and controls (0.986±0.003 vs. 0.987±0.004 n.s.).
Fasting levels of incretin hormones
For both incretin hormones (GLP-1 and GIP) there was no statistical difference observed during the fasting state in alcoholics and the control group (Table 1).
inmed fig 20.1
Figure 1. Glucose (A), Insulin (B) and C-peptide (C) serum levels during the oral glucose tolerance test (oGTT) (75 g glucose). Means ± SDs are given.
Glucose, Insulin and C-Peptide levels during the OGTT (Figure 1)
After the ingestion of 75 grams of glucose there was an increase of circulating glucose, insulin and C-peptide, in both groups. The mean 2-h glucose level was similar in both groups (5.0±1.7 mmol/L in the study group vs. 5.3±1.5 mmol/L in controls n.s.) as were the AUC´s (0-120 min) (866±193 mmol x min/L (alcoholic) vs. 829±182mmol x min/L (control)). In addition, the kinetic behaviours of the tested serum levels were equal. Glucose levels peaked after 45 minutes, while insulin and C-peptide peaked after 60 minutes in both groups. Thereafter, glucose values returned to baseline values in both groups, while insulin and c-peptide levels did not return to baseline values during the 120 minutes observation period. Two patients from the alcoholic liver disease group showed glucose level above 7.8 mmol/L after 2 hours but below 11.0 mmol/l, thus being diagnosed as impaired glucose tolerance. In those subjects, AUC´s (0-120 min) for insulin and c-peptide were both in the upper and in the lower normal range.
Figure 2. Glucose-dependent insulinotropic polypeptide (GIP) (A) and Glucagon-like peptide-1 (GLP-1) (B) secretion during the  oralglucose tolerance test (oGTT). GLP-1 and GIP secretion in responseto oGTT is not different between patients with alcoholic liver disease and controls. Means ± SDs are given.
GLP-1 and GIP (Figure 2)
After oral glucose ingestion, intact GLP-1 and total GIP increased promptly to reach maximum levels after 30 minutes for GLP-1 and 60 minutes for GIP. Thereafter, GLP-1 and GIP gradually declined during the 120 minutes observation period, but did not reach baseline values.
The AUC´s (0-120 min) for GLP-1 were in patients with alcoholic liver disease 785.5±277.7 vs. 713.3 ±338.3 pmol x min/L (n.s.) in controls. The corresponding values for GIP were 33853.2±13365.6 vs. 31267.2±11179.7 pg x min/mL (n.s.) respectively.
We examined the responses kinetics of incretins and insulin after oral glucose tolerance test in alcohol dependent patients with alcoholic liver disease in the early withdrawal state and abstinent control subjects. Despite long term and high daily alcohol abuse, no alterations in incretin and insulin secretion could be observed. There was a tendency towards decreased insulin sensitivity and increased insulin resistance in patients  with alcoholic liver disease, but the response curves to an oralglucose tolerance test were similar in both groups, as were the levels of GLP-1 and GIP. Alcoholic liver disease seems therefore not to be associated with disturbances in the entero-insular  axis.
Chronic alcohol consumption is associated with alterations in the peptidergic nerve system and endocrine cells involved in peptide secretion in the duodenal mucosa [10]. The observed alterations are however mild and functional data are rare. In one study it was demonstrated that in chronic alcohol consumers insulin and c-peptide secretion was diminished while the incretin effect was unaltered, which might indicate an early  beta-cell dysfunction but an intact entero-pancreatic axis [14].Our data from direct determinations of incretin hormone levels after an oral glucose tolerance test are in accordance with these observations; however we were unable to find a significant  alteration in glucose and insulin homeostasis in our patients. A reason might be that carbohydrate intolerance in alcoholics is largely dependent on caloric malnutrition [15-17]. Our patients were however at least for three days on a normocaloric  diet with prophylactic thiamine substitution and hada normal BMI indicating absence of significant malnutrition.
A direct effect of the medication of our study patients with Tiapride and Carbamazepine on the investigated parameters cannot completely be ruled out. Incretin hormones are metabolized by the enzyme Dipeptidyl peptidase-IV (DPP-IV). We did not measure DPP-IV activity in our study, but in studies performed with patients suffering from major depression and or schizophrenia, no effect of neuroleptics and or antidepressants on serum DPP-IV activity were detected [18-20], therefore  disturbances in incretin metabolism appears unlikely. Furthermore, the incretin kinetics after the oral glucose tolerance test were similar in alcoholic and non-alcoholic subjects, which does not indicates lower serum peptidase activity in our alcohol-dependent patients [11].
Ultrasound is widely used as the first-line diagnostic test in patients with abnormal liver enzymes. In our patients with alcoholic liver disease only ALT showed a significant variation with the degree of hepatic steatosis, however no correlation was found for GGT, AST or HOMA-IR. This is in contrast to findings observed in patients with non-alcoholic steatosis [21] and may underline the different mechanisms involved in the development of hepatic steatosis in alcoholic and non-alcoholic fatty liver disease.
A limitation of our study is, that we did not determine the degree of alcoholic liver disease by histological examination. However, studies performed in alcoholic patients with hepatic  istology found alterations in insulin resistance, even in the  presence of normal liver histology [22], therefore, we could also expect alterations in glucose metabolism in our patients.
In contrast to alcoholic liver disease, non-alcoholic fatty liver disease is accompanied by several alterations in glucose  tolerance, ß-cell function and also in the secretion of the incretin hormone GLP-1 [8]. These pathophysiological findings have led to the evaluation of GLP-1 agonists for the treatment of NAFLD [23]. The GLP-1 related mechanisms (enhanced hepatic fatty acid oxidation, lipid export and insulin sensitivity) decrease liver inflammation and apoptotic liver injuries [24, 25]. And in deed, in a phase 2 randomized controlled trial, GLP-1agonists resolved NASH in a higher (39% of patients) proportion of patients than those given placebo (9% of patients) [26]. There are also data showing that GLP-1 agonists might be useful in the treatment of alcohol related disorders, since they are able to reduce alcohol intake [27]. Whether GLP-1 agonists can also be used for the treatment of alcoholic liver disease can not be concluded from our study, since we detected no alterations in the entero-insular axis in our patients with alcoholic liver disease in the early withdrawal state.
We thank Ms. A. Fink and Ms. A. Weber for expert technical assistance with the determination of GIP and GLP-1 serum levels. The technical support and help of Ms I. Kunz and Ms. C. Schallwich is also gratefully acknowledged.
The authors report no conflicts of interest.



1. Rehm J, Mathers C, Popova S, Thavorncharoensap M, Teerawattananon Y et al. Global burden of disease and injury and economic cost attributable to alcohol use and alcohol-use disorders. Lancet. 2009, 373(9682): 2223-2233.

2. Robert Koch-Institut (Eds.) Alkoholkonsum und alkoholbezogene Störungen. Gesundheitsberichterstattung des Bundes. 2008, Heft 40. RKI, Berlin.

3. Barve A1, Khan R, Marsano L, Ravindra KV, McClain C. Treatment of alcoholic liver disease. Ann Hepatol. 2008, 7(1): 5-15.

4. Hassan MM, Hwang LY, Hatten CJ, Swaim M, Li D et al. Risk factors for hepatocellular carcinoma: synergism of alcohol with viral hepatitis and diabetes mellitus. Hepatology. 2002, 36(5): 1206-1213.

5. Baraona E, Lieber CS. Alcohol and lipids. Recent Dev Alcohol. 1998, 14: 97-134.

6. Gao B, Bataller R. Alcoholic liver disease: pathogenesis and new therapeutic targets. Gastroenterology. 2011, 141(5): 1572-1585.

7. Chai SY, Pan XY, Song KX, Huang YY, Li F et al. Differential patterns of insulin secretion and sensitivity in patients with type 2 diabetes mellitus and nonalcoholic fatty liver disease versus patients with type 2 diabetes mellitus alone. Lipids Health Dis. 2014, 13: 7.

8. Bernsmeier C, Meyer-Gerspach AC, Blaser LS, Jeker L, Steinert RE et al. Glucose-induced glucagon-like Peptide 1 secretion is deficient in patients with non-alcoholic fatty liver disease. PLoS One. 2014, 9(1).

9. Deacon CF. What do we know about the secretion and degradation of incretine hormones. Regul Pept. 2005, 128(2): 117-124.

10. Hauge T, Persson J, Sjölund K. Neuropeptides in the duodenal mucosa of chronic alcoholic heavy drinkers. Alcohol Alcohol. 2001, 36(3): 213-218.

11. Maes M, Lin A, Bonaccorso S, Vandoolaeghe E, Song C et al. Lower activity of serum peptidases in abstinent alcohol- dependent patients. Alcohol. 1999, 17(1): 1-6.

12. Saadeh S, Younossi ZM, Remer EM, Gramlich T, Ong JP et al. The utility of radiological imaging in nonalcoholic fatty liver disease. Gastroenterology. 2002, 123(3): 745-750.

13.Niemczyk S, Szamotulska K, Giers K, Jasik M, Bartoszewicz Z et al. Homeostatic model assessment indices in evaluation of insulin resistance and secretion in hemodialysis patients. Med Sci Monit. 2013, 19: 592-598.

14. Patto RJ, Russo EK, Borges DR, Neves MM. The enteroinsular axis and endocrine pancreatic function in chronic alcohol consumers: evidence for early beta-cell hypofunction. Mt Sinai J Med. 1993, 60(4): 317-320.

15. Pezzarossa A, Cervigni C, Ghinelli F, Molina E, Gnudi A. Glucose tolerance in chronic alcoholics after alcohol withdrawal: effect of accompanying diet. Metabolism. 1986, 35(11): 984-988.

16. Adner N, Nygren A. Insulin secretion in alcoholics in a withdrawal state. Acta Med Scand. 1986,219(2): 201-207.

17. Iturriaga H, Kelly M, Bunout D, Pino ME, Pereda T et al. Glucose tolerance and the insulin response in recently drinking alcoholic patients: possible effects of withdrawal. Metabolism. 1986, 35(3): 238-243.

18. Maes M, Goossens F, Scharpé S, Calabrese J, Desnyder R et al. Alterations in plasma prolyl endopeptidase activity in depression, mania, and schizophrenia: effects of antidepressants, mood stabilizers, and antipsychotic drugs. Psychiatry Res. 1995, 58(3): 217-225.

19. Maes M, De Meester I, Scharpe S, Desnyder R, Ranjan R et al. Alterations in plasma dipeptidyl peptidase IV enzyme activity in depression and schizophrenia: effects of antidepressants and antipsychotic drugs. Acta Psychiatr Scand. 1996, 93(1): 1-8.

20. Maes M, Goossens F, Scharpé S, Meltzer HY, D’Hondt P, Cosyns P. Lower serum prolyl endopeptidase enzyme activity in major depression: further evidence that peptidases play a role in the pathophysiology of depression. Biol Psychiatry. 1994, 35(8): 545-552.

21. Ferreiraa Cruz MA, Ferreira Cruz J, Baracho Macena L, Silva de Santana D, Costa da Cunha Oliveira C et al. Association of  the Nonalcoholic Hepatic Steatosis and its degrees with the values of liver enzymes and homeostasis model assessment-insulin resistance Index. Gastroenterol Res. 2015, 8(5): 260-264.

22. Andersen BN, Hagen C, Faber OK, Lindholm J, Boisen P et al. Glucose tolerance and B cell function in chronic alcoholism: Its relation to hepatic histology and exocrine pancreatic function. Metabolism. 1983, 32(11): 1029-1032.

23. Wang XC, Gusdon AM, Liu H, Qu S. Effects of glucagon-like peptide-1 receptor agonists on non-alcoholic fatty liver disease and inflammation. World J Gastroenterol. 2014, 20(40): 14821-14830.

24. Kim YO, Schuppan D. When GLP-1 hits the liver: a novel approach for insulin resistance and NASH. Am J Physiol Gastrointest Liver Physiol. 2012, 302(8): G759–G761.

25.Armstrong MJ, Hull D, Guo K. Glucagon-like peptide 1 decreases lipotoxicity in non-alcoholic steatohepatitis. J Hepatol. 2016, 64(2): 399–408.

26.Armstrong MJ, Gaunt P, Aithal GP. Liraglutide safety and efficacy in patients with non-alcoholic steatohepatitis (LEAN):a  multicentre, double-blind, randomised, placebo-controlled phase 2 study. Lancet. 2016, 387: 679–690.

27.Shirazi RH, Dickson SL, Skibicka KP. Gut peptide GLP-1 and its analogue, Exendin-4, decrease alcohol intake and reward. Plos One. 2013, 8(4): e61965.

Cite this article: Christoph Elsing. The Entero-Insular-Axis is retained in Patients with Alcoholic Liver Disease. J J Intern Medicine. 2016, 2(2): 020.

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