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Nutrición Hospitalaria

versión On-line ISSN 1699-5198versión impresa ISSN 0212-1611

Nutr. Hosp. vol.28  supl.2 Madrid  2013

 

ORIGINAL

 

Other aspects of bariatric surgery: liver steatosis, ferritin and cholesterol metabolism

Otros aspectos de la cirugía bariátrica: esteatosis hepática, metabolismo de ferritina y colesterol

 

 

A. E. Pontiroli; with collaboration of A. Benetti, L. Folini, C. Merlotti, and F. Frigè

Dipartamento di Medicina, Chirurgia e Odonoiatria. Università degli Studi di Milano. Ospedale San Paolo. Milano. Italy

Correspondence

 

 


ABSTRACT

Bariatric surgery developed in the late 1970 to treat severe hyperlipidemias in overweight individuals, not necessarily obese. Several techniques have been developed, and the concept has come first of a surgery for morbid obesity, then of a cure for diabetes in morbid obesity. There are other aspects of bariatric surgery that deserve attention, beyond BMI and diabetes, such as hypertension, poor life expectancy, increased prevalence of cancer, congestive heart failure, social inadequacy. The aim of this presentation is to review some recent development in clinical research, in the fields of liver steatosis, ferritin metabolism, and cholesterol metabolism.
Liver steatosis, also called fatty liver encompasses a graduation of diseases with different clinical relevance and prognosis. NAFLD correlates with atherosclerosis, insulin resistance and diabetes mellitus. There is now evidence that weight loss, obtained through diet or restrictive surgery, reduces the prevalence (and the severity) of NAFLD.
An other issue is represented by serum ferritin concentrations, that are strongly associated with fibrosis, portal and lobular inflammation in NAFLD patients, especially in the presence of obesity. Body iron contributes to excess oxidative stress already at non iron overload concentrations. Moreover, serum ferritin is an important and independent predictor of the development of diabetes. Weight loss is accompanied by reduction of ferritin, more after restrictive than malabsorptive surgery.
Metabolic changes are greater after malabsorptive or mixed surgery than after purely restrictive surgery, and this has been ascribed to a greater weight loss. Studies comparing the two kinds of surgery indicate that, for the same amount of weight loss, decrease of cholesterol is greater with the former than with the latter techniques, and this difference is mainly due to a greater reduction of intestinal absorption of cholesterol. In the choice of surgery for the single patient, among other aspects, malabsorptive surgery seems to be more indicated in subjects with hyperlipidemia, especially with high cholesterol levels.

Key words: Bariatric surgery. Liver steatosis. Ferritin. Cholesterol metabolism.


RESUMEN

La cirugía bariátrica se desarrolló a finales de la década de los 70 para tratar la hiperlipidemia severa en personas con sobrepeso, no necesariamente obesos. A lo largo de los años se han desarrollado varias técnicas quirúrgicas que han sido utilizadas en primer lugar en la obesidad mórbida y posteriormente en el tratamiento de la diabetes. Hay otros aspectos de la cirugía bariátrica que merecen atención más allá del IMC y la diabetes, como la hipertensión, la pobre esperanza de vida, una mayor prevalencia de cáncer, insuficiencia cardíaca e inadaptación social. El objetivo de este artículo es revisar los recientes avances clínicos en campos de investigación relacionados con la esteatosis hepática, el metabolismo de ferritina y el metabolismo del colesterol.
La esteatosis hepática, también llamada hígado graso abarca una serie de las enfermedades con diferente pronóstico y relevancia clínica. El Hígado Graso No Alcohólico (NAFLD siglas en ingles) se correlaciona con la aterosclerosis, resistencia a la insulina y diabetes mellitus. Hoy en día existen evidencias de que la pérdida de peso que se obtiene a través de la dieta o cirugía restrictiva, reduce la prevalencia (y la gravedad) de la NAFLD.
Otro tema de estudio incluye las concentraciones de ferritina sérica, que están fuertemente asociadas con la fibrosis e inflamación lobular y portal en pacientes con NAFLD, especialmente en presencia de obesidad. El exceso de hierro corporal en obesos contribuye a un aumento del estrés oxidativo debido a una sobrecarga en su concentración. Por otra parte, la ferritina sérica es un indicador importante e independiente del desarrollo de la diabetes. La pérdida de peso se acompaña de una disminución de la ferritina. Esta disminución es más evidente tras una cirugía restrictiva que tras una malabsortiva.
Los cambios metabólicos son mayores después de una cirugía malabsortiva o mixta que tras una cirugía puramente restrictiva, y esto se ha atribuido a una mayor pérdida de peso. Estudios que comparan los dos tipos de cirugía indican que, para la mismo índice de pérdida de peso, la disminución de colesterol es mayor con las primeras técnicas que con las últimas, y esta diferencia se debe principalmente a una mayor reducción de la absorción intestinal del colesterol. En la elección de la cirugía para un paciente concreto, entre otros aspectos, la cirugía de malabsorción parece estar más indicada en sujetos con hiperlipemia, especialmente con altos niveles de colesterol.

Palabras clave: Cirugía bariátrica. Esteatosis hepática. Ferritina. Metabolismo colesterol.


 

Introduction

Metabolic surgery has been proposed as the new name of bariatric surgery, but was developed in the late 1978 to treat severe hyperlipidemias in above-normal body weight individuals, not necessarily obese; the Program on the Surgical Control of the Hyperlipidemias (POSCH) can be considered the beginning of the era of bariatric surgery.1 Several techniques have been developed later, and the concept has come first of a surgery for morbid obesity, then of a cure for diabetes in morbid obesity. Nevertheless, there are other aspects of bariatric surgery that deserve attention, as raised Body Mass Index BMI) and diabetes are not the only co-morbidities of obesity; think of hypertension, poor life expectancy, increased prevalence of cancer, congestive heart failure, social inadequacy. Given the strict links between obesity, chronic sub-clinical inflammation, insulin resistance, diabetes, the metabolic syndrome, and steatosis, the aim of this presentation is to review some recent development in clinical research, basic and surgical.

 

Liver steatosis

Liver steatosis, also called fatty liver encompasses a graduation of diseases with different clinical relevance and prognosis; simple NAFLD (non Alcoholic Fatty Liver Disease) is more frequent and less severe than NASH (Non Alcoholic Steato Hepatitis), as the former is a benign condition, the latter can proceed to cirrhosis and probably also to hepatocellular carcinoma.2

Prevalence of NAFLD has been defined through biopsies (that is considered the gold standard for the diagnosis, in that a differentiation between steatosis, steatosis plus fibrosis, steatohepatitis is possible), autopsy series, and non-invasive methods such as liver ultrasound, liver enzymes (ALT and AST plus GGT), magnetic resonance imaging (MRI). Though considered the gold standard, biopsies are not suitable for population studies; one would wander whether it is ethical to perform repeat liver biopsies for research purposes. Expectedly, the prevalence of NAFLD varies in different studies, that is in different populations, and using different criteria and methodologies; in summary, NAFLD (and NASH) affect a significant proportion of adults of both sexes. NAFLD is quite frequent in obesity, in diabetes, in metabolic syndrome, and is expected to increase worldwide due to the obesity epidemics, and is also increased with increasing alcohol consumption.2,3

NAFLD correlates with atherosclerosis, insulin resistance and diabetes mellitus,4,5 whatever the method of assessment of NAFLD. In the large European population (RISC Study) NAFLD, evaluated through the fatty liver index, was associated with increased CHD risk, low-density lipoprotein cholesterol, systolic blood pressure, and intima-media-thickness, and inversely associated with insulin sensitivity, high-density lipoprotein cholesterol, adiponectin, and physical activity.4 Based on liver biopsies, about three quarters of bariatric surgery patients have liver steatosis, and about a quarter have fibrosis.6 There have been attempts to predict frequency and severity of fatty liver based on liver function tests; in 200 patients, multivariate analysis identified six predictive factors for NASH: the diagnosis of HT, DM, sleep apnea, AST > 27 IU/L, ALT > 27 IU/L, and non-black race;7 however, In 139 patients undergoing bariatric surgery, NASH was found in 57 (41%): age, gender, race, BMI, DM, HT, and liver function tests and triglyceride, cholesterol, iron, and prealbumin measurements were not strong predisctors of NASH [8]. Imaging has been proposed as a surrogate of liver biopsies; ultrasound, compared with biopsy, has an accuracy 0.81%;6 a recent meta-analysis indicates that the diagnostic accuracy is greater for magnetic resonance imaging (MRI), chemical-shift MRI and for spectroscopy-MRI;9 the two latter techniques correlate, and accurately estimate the severity of steatosis.10,11 During the last 5 years we have developed a MRI chemical-shift analysis to differentiate NAFLD from other infiltrative liver disorders such as glycogenosis.12-14 This technique requires simple MRI instruments, correlates with ultrasound, and preliminary data indicate a high frequency of NAFLD in obese subjects, paralleled by frequent elevation of liver enzymes.15

The next question is: what is the effect of weight loss on NAFLD? There is now abundant evidence that weight loss, obtained through diet or restrictive surgery, reduces the prevalence (and the degree) of NAFLD; this applies to biopsies, to ultrasound studies, to MRI studies, as well as to liver function tests, and the different criteria seem to yield the same kind of information; also NASH seems to regress to simple NAFLD.15-20 The drop of AST and ALT correlates with loss of visceral fat.21 Interestingly, the effect of malabsorptive surgery (biliointestinal bypass) is less clear (liver enzymes),22 but there is no recent data showing worsening of NAFLD or NASH after bariatric surgery.

 

Ferritin

Serum ferritin concentrations and BMI are strongly associated with fibrosis, portal and lobular inflammation in NAFLD patients.23 Diabetes and metabolic syndrome are the main contributors to high ferritin levels in obesity.24 Growing evidence has shown that even moderately increased iron stores, represented by high-normal ferritin concentrations, are associated with diabetes.25-28 More recently the results from prospective studies from Caucasian populations suggested that iron overload could predict the development of abnormal glucose metabolism.29

It is unclear whether elevated ferritin may simply be another marker of insulin resistance or whether elevated ferritin concentrations identify iron stores that may contribute to the pathogenesis of altered metabolic states. A recent study has suggested that body iron contributes to excess oxidative stress already at non iron overload concentrations.30 Moreover, serum ferritin has been identified as an important and independent predictor of the development of diabetes31 and high concentrations of ferritin, together with low oral glucose insulin sensitivity, have been identified as independent markers of fibrosis in NASH.32

It has been hypothesized that iron could be an important cofactor in the pathogenesis and progression of some cases of NASH31 since NAFLD subjects have increased hepatic fatty acid oxidation, and increased production of ROS.30-32 In a large cohort of NASH patients, 21.1% had hyper-ferritinemia while only 7.4% had signs of peripheral iron overload and 9% had signs of hepatic iron overload.31

Among other things, weight loss is accompanied by reduction of inflammation, and ferritin is both a storage protein for iron and a marker of inflammation; ferritin decreases after surgery, more after restrictive than malabsorptive surgery.33-36 Considering the close relationship between obesity, insulin resistance and development of NAFLD, we studied their association with hepatic profile and ferritin concentrations.34 Since bariatric surgery-weight loss is associated with reduced insulin resistance, restored glucose tolerance, reduced hepatic steatosis, and improved liver enzymes, we repeated the analyses after laparoscopic gastric banding surgery to evaluate the impact of weight loss on the association between hepatic profile, ferritin concentrations, and insulin resistance. In our group of 169 obese subjects (89 with normal liver enzymes, 70 with raised liver enzymes), before bariatric surgery, ferritin concentrations were increased proportionally to ALT concentrations, although, in general, within normal ranges and similar in NGT, IGT, and T2DM. A positive correlation was observed between ferritin plasma concentrations and insulin resistance. After surgery, however, we did not observe a significant decrease in plasma ferritin concentrations despite the improvement in hepatic function and insulin resistance. However, the correlations between ferritin, ALT, and insulin resistance remained suggesting that ferritin may simply identify a new phenotype of insulin resistance.34

 

Cholesterol metabolism

Metabolic changes are greater after malabsorptive or mixed surgery (biliopancreatic diversion, gastric bypass) than after purely restrictive surgery (vertical banded gastroplasty, gastric banding, intra-gastric balloon), and this has been ascribed to a greater weight loss; no surprise that disappearance of comorbidities like diabetes mellitus happens more frequently after the former than after the latter interventions.37 Even though improvement of hyperlipidemia was present in a fair proportion of subjects undergoing gastric banding (triglycerides 78%, 94%, 87%; cholesterol 77%, 91%, 100% with gastric banding, gastric bypass, and biliopancreatic diversion, respectively, the degree of reduction of cholesterol levels was clearly different (-0.30, 0.96, 1.97 mmol, respectively). We reported decreased cholesterol levels after bilio-intestinal by-pass (an other malabsorptive surgery)22 or after biliopancreatic diversion,38 but not after gastric banding. The cholesterol reduction that we and others have reported after after bilio-intestinal by-pass, biliopancreatic diversion, or gastric by-pass is a quite dramatic phenomenon and is likely due to the major reduction in bile acid re-absorption in the intestine, and possibly to altered regulation of the feedback mechanisms controlled by nuclear protein such as LXR, FXR and PPAR; these transcriptional factors are involved in bile acid and cholesterol metabolism, occurring in patients undergoing after bilio-intestinal by-pass, biliopancreatic diversion or gastric by-pass (which cause malabsorption and also reduced bile re-absorption), but not gastric banding (a purely restrictive bariatric procedure).39 It is also possible that reduced gastric volume and reduced production of gastric lipase, as well as reduced secretion of cholecystokinin (that physiologically stimulates digestive enzyme secretion such as lipases and proteases) might result in a marked decrease in the hydrolysis of triacylglycerols, with a reduction of the absorption of free fatty acids.40 Both biliopancreatic diversion and gastric by-pass include partial gastric resection, or functional gastric disconnection; therefore, gastric by-pass and biliopancreatic diversion can not be regarded as purely restrictive or purely malabsorptive surgical techniques. we hypothesized that, aside from greater weight loss, a specific effect of malabsorptive surgery on cholesterol metabolism might exist, probably mediated by intestinal milieu.41,42 We also observed that, at six months, weight loss was similar with gastric banding and with bilio-intestinal by-pass.22 Therefore we performed a comparison of gastric banding, intra-gastric balloon, and bilio-inte-stinal by-pass, and hypocaloric diet (1,200 kcal/day), on glucose and cholesterol levels in morbid obesity. We could confirm that, at 6 months, weight loss is similar with the three surgical techniques, greater than with diet, and that glucose metabolism was also similarly affected; however, serum cholesterol and LDL-cholesterol levels were affected in a significant way only by bilio-intestinal by-pass.43 Then we evaluated intestinal cholesterol absorption, endogenous cholesterol synthesis, and cholesterol catabolism through the bile acids pathway, and we found that after bilio-intestinal by-pass, together with decreased cholesterol levels, intestinal cholesterol absorption is reduced, associated with enhanced cholesterol synthesis and enhanced cholesterol catabolism; in contrast, after gastric banding there is no change in cholesterol levels, in cholesterol absorption, synthesis, and only a marginal increase in cholesterol catabolism.44

 

Conclusion

Decision on which surgical procedure to choose for the individual obese patients is a complex matter, that has to take into consideration expectations, invasiveness and reversibility, surgical mortality, drawbacks of each surgical procedure;45,46 among other aspects, malabsorptive surgery seems to be more indicated in subjects with hyperlipidemia, especially with high cholesterol levels.

 

Declaration

The authors have no conflict of interests with the contents of this paper.

 

References

1. Buchwald H. Metabolic surgery: a brief history and perspective. Surg Obes RelatDis 2010; 6 (2): 221-222.         [ Links ]

2. Vernon G, Baranova A, Younossi ZM. Systematic review: the epidemiology and natural history of non-alcoholic fatty liver disease and non-alcoholic steatohepatitis in adults. Aliment Pharmacol Ther 2011; 34: 274-285.         [ Links ]

3. Ruhl CE, Everhart JE. Joint effects of body weight and alcohol on elevated serum alanine aminotransferase in the United States population. Clin Gastroenterol Hepatol 2005; 3 :1260-1268.         [ Links ]

4. Gastaldelli A, Kozakova M, H0jlund K, Flyvbjerg A, Favuzzi A, Mitrakou A, Balkau B; RISC Investigators. Fatty liver is associated with insulin resistance, risk of coronary heart disease, and early atherosclerosis in a large European population. Hepatology 2009; 49: 1537-1544.         [ Links ]

5. Williamson RM, Price JF, Glancy S, Perry E, Nee LD, Hayes PC, Frier BM, Van Look LA, Johnston GI, Reynolds RM, Strachan MW; Edinburgh Type 2 Diabetes Study Investigators. Prevalence of and risk factors for hepatic steatosis and nonalcoholic Fatty liver disease in people with type 2 diabetes: the Edinburgh Type 2 Diabetes Study. Diabetes Care 2011; 34: 1139-1144.         [ Links ]

6. Wu J, You J, Yerian L, Shiba A, Schauer PR, Sessler DI. Prevalence of Liver Steatosis and Fibrosis and the Diagnostic Accuracy of Ultrasound in Bariatric Surgery Patients. Obes Surg 2011 (Epub ahead of print).         [ Links ]

7. Campos GM, Bambha K, Vittinghoff E, Rabl C, Posselt AM, Ciovica R, Tiwari U, Ferrel L, Pabst M, Bass NM, Merriman RB. A clinical scoring system for predicting nonalcoholic stea-tohepatitis in morbidly obese patients. Hepatology 2008; 47: 1916-1923.         [ Links ]

8. Helling TS, Helzberg JH, Nachnani JS, Gurram K. Predictors of nonalcoholic steatohepatitis in patients undergoing bariatric surgery: when is liver biopsy indicated? Surg Obes Relat Dis 2008; 4: 612-617.         [ Links ]

9. Bohte AE, van Werven JR, Bipat S, Stoker J. The diagnostic accuracy of US, CT, MRI and 1H-MRS for the evaluation of hepatic steatosis compared with liver biopsy: a meta-analysis. Eur Radiol 2011; 21: 87-97.         [ Links ]

10. Meisamy S, Hines CD, Hamilton G, Sirlin CB, McKenzie CA, Yu H, Brittain JH, Reeder SB. Quantification of hepatic steatosis with T1-independent, T2-corrected MR imaging with spectral modeling of fat: blinded comparison with MR spectroscopy. Radiology 2011; 258: 767-775.         [ Links ]

11. McPherson S, Jonsson JR, Cowin GJ, O'Rourke P, Clouston AD, Volp A, Horsfall L, Jothimani D, Fawcett J, Galloway GJ, Benson M, Powell EE. Magnetic resonance imaging and spectroscopy accurately estimate the severity of steatosis provided the stage of fibrosis is considered. J Hepatol 2009; 51: 389-397.         [ Links ]

12. Fishbein MH, Gardner KG, Potter CJ, Schmalbrock P, Smith MA. Introduction of fast MR imaging in the assessment of hepatic steatosis. Magn Reson Imaging 1997; 15: 287-293.         [ Links ]

13. Pozzato C, Dall'asta C, Radaelli G, Torcoletti M, Formenti A, Riva E, Cornalba G, Pontiroli AE. Usefulness of chemical-shift MRI in discriminating increased liver echogenicity in glycogenosis. Dig Liver Dis 2007; 39: 1018-1023.         [ Links ]

14. Pozzato C, Radaelli G, Dall'Asta C, Verduci E, Villa A, Villa C, Scaglioni S, Riva E, Pontiroli AE, Cornalba G, Giovannini M. MRI in identifying hepatic steatosis in obese children and relation to ultrasonography and metabolic findings. J Pediatr Gastroenterol Nutr 2008; 47: 493-499.         [ Links ]

15. Benetti A, Folini L, Pozzato C, Veronelli A, Masci E, Micheletto G, Pontiroli AE. Liver steatosis evaluated through chemical-shift magnetic resonance imaging and liver enzymes; effect of weight loss obtained with intragastric balloon and gastric banding. Diabetes 2011; 60 (Suppl. 1): A33 (abstract).         [ Links ]

16. Dixon JB, Bhathal PS, O'Brien PE. Weight loss and non-alcoholic fatty liver disease: falls in gamma-glutamyl transferase concentrations are associated with histologic improvement. Obes Surg 2006; 16: 1278-1286.         [ Links ]

17. Furuya CK Jr, de Oliveira CP, de Mello ES, Faintuch J, Raskovski A, Matsuda M, Vezozzo DC, Halpern A, Garrido AB Jr, Alves VA, Carrilho FJ. Effects of bariatric surgery on nonalcoholic fatty liver disease: preliminary findings after 2 years. J Gastroenterol Hepatol 2007; 22: 510-514.         [ Links ]

18. Weiner RA. Surgical treatment of non-alcoholic steatohepatitis and non-alcoholic fatty liver disease. Dig Dis 2010; 28: 274-279.         [ Links ]

19. Forlano R, Ippolito AM, Iacobellis A, Merla A, Valvano MR, Niro G, Annese V, Andriulli A. Effect of the BioEnterics intra-gastric balloon on weight, insulin resistance, and liver steatosis in obese patients. Gastrointest Endose 2010; 71: 927-933.         [ Links ]

20. van Werven JR, Schreuder TC, Aarts EO, Nederveen AJ, Meijer JW, Berends FJ, Janssen IM, Mulder CJ, Jansen PL, Stoker J. Hepatic steatosis in morbidly obese patients undergoing gastric bypass surgery: assessment with open-system 1H-MR spectroscopy. AJR Am J Roentgenol 2011; 196: W736-742.         [ Links ]

21. Pontiroli AE, Frigè F, Paganelli M, Folli F. In morbid obesity, metabolic abnormalities and adhesion molecules correlate with visceral fat, not with subcutaneous fat: effect of weight loss through surgery. Obes Surg 2009; 19: 745-750.         [ Links ]

22. Frige' F, Laneri M, Veronelli A, Folli F, Paganelli M, Vedani P, Marchi M, Noe' D, Ventura P, Opocher E, Pontiroli AE. Bariatric surgery in obesity: changes of glucose and lipid metabolism correlate with changes of fat mass. Nutr Metab CardiovaseDis 2009; 19: 198-204.         [ Links ]

23. Manousou P, Kalambokis G, Grillo F, Watkins J, Xirouchakis E, Pleguezuelo M, Leandro G, Arvaniti V, Germani G, Patch D, Calvaruso V, Mikhailidis DP, Dhillon AP, Burroughs AK. Serum ferritin is a discriminant marker for both fibrosis and inflammation in histologically proven non-alcoholic fatty liver disease patients. Liver Int 2011; 31 (5): 730-739.         [ Links ]

24. Lecube A, Hernández C, Pelegrí D, Simó R. Factors accounting for high ferritin levels in obesity. Int J Obes (Lond) 2008; 32: 1665-1669.         [ Links ]

25. Tuomainen TP, Nyyssonen K, Salonen R, Tervahauta A, Korpela H, Lakka T, Kaplan GA, Salonen JT. Body iron stores are associated with serum insulin and blood glucose levels. Population study in 1,013 eastern Finnish men. Diabetes Care 1997; 20: 426-428.         [ Links ]

26. Salonen JT, Tuomainen TP, Nyyssonen K, Lakka HM, Punnonen K. Relation between iron stores and non-insulin dependent diabetes in men: case control study. BMJ 1998; 317: 727.         [ Links ]

27. Jiang R, Manson JE, Meigs JB, Ma J, Rifai N, Hu FB Body iron stores in relation to risk of type 2 diabetes in apparently healthy women. JAMA 2004; 291: 711-717.         [ Links ]

28. Forouhi NG, Harding AH, Allison M, Sandhu MS, Welch A, Luben R, Bingham S, Khaw KT, Wareham NJ. Elevated serum ferritin levels predict new-onset type 2 diabetes: results from the EPIC-Norfolk prospective study. Diabetologia 2007; 50:949-956.         [ Links ]

29. Fumeron F, Pean F, Driss F, Balkau B, Tichet J, Marre M, Grandchamp B. Insulin Resistance Syndrome (DESIR) Study Group Ferritin and transferrin are both predictive of the onset of hyperglycemia in men and women over 3 years: the data from an epidemiological study on the Insulin Resistance Syndrome (DESIR) study. Diabetes Care 2006; 29: 2090-2094.         [ Links ]

30. Tuomainen TP, Loft S, Nyyssonen K, et al. Body iron is a contributor to oxidative damage of DNA. Free Radic Res 2007; 41: 324-328.         [ Links ]

31. Bugianesi E, Manzini P, D'Antico S, et al. Relative contribution of iron burden, HFE mutations, and insulin resistance to fibrosis in non alcoholic fatty liver. Hepatology 2004; 39: 179-187.         [ Links ]

32. Machado M, Cortez-Pinto H. NASH, insulin resistance and iron. Liver Int 2006; 26: 1159-1162.         [ Links ]

33. Ramalho R, Guimaräes C, Gil C, Neves C, Guimaräes JT, Delgado L. Morbid obesity and inflammation: a prospective study after adjustable gastric banding surgery. Obes Surg 2009; 19: 915-920.         [ Links ]

34. Gastaldelli A, Perego L, Paganelli M, Sesti G, Hribal M, Chavez AO, Defronzo RA, Pontiroli AE, Folli F. Elevated concentrations of liver enzymes and ferritin identify a new phenotype of insulin resistance: effect of weight loss after gastric banding. Obes Surg 2009; 19: 80-86.         [ Links ]

35. von Drygalski A, Andris DA, Nuttleman PR, Jackson S, Klein J, Wallace JR. Anemia after bariatric surgery cannot be explained by iron deficiency alone: results of a large cohort study. Surg Obes Relat Dis 2011; 7: 151-156.         [ Links ]

36. Poyck PP, Polat F, Gouma DJ, Hesp WL. Is biliopancreatic diversion with duodenal switch a solution for patients after laparoscopic gastric banding failure? Surg Obes Relat Dis 2011 (Epub ahead of print).         [ Links ]

37. Buchwald H, Avidor Y, Braunwald E, Jensen MD, Pories W, Fahrbach K, Schoelles K. Bariatric surgery: a systematic review and meta-analysis. JAMA2004; 292: 1724-1737.         [ Links ]

38. Pontiroli AE, Laneri M, Veronelli A, Frigè F, Micheletto G, Folli F, Adami G, Scopinaro N. Biliary pancreatic diversion and laparoscopic adjustable gastric banding in morbid obesity: their long-term effects on metabolic syndrome and on cardiovascular parameters. Cardiovasc Diabetol 2009; 20 (8): 37.         [ Links ]

39. Repa JJ, Mangelsdorf DJ. Nuclear receptor regulation of cholesterol and bile acid metabolism. Curr Opin Biotechnol 1999; 10: 557-563.         [ Links ]

40. Bays HA: Current and investigational antiobesity agents and obesity therapeutic treatment targets. Obes Res 2004; 12: 1197-1211.         [ Links ]

41. Prachand VN, Alverdy JC. The role of malabsorption in bariatric surgery. World J Surg 2009; 33: 1989-1994.         [ Links ]

42. Zhang H, DiBaise JK, Zuccolo A, Kudrna D, Braidotti M, Yu Y, Parameswaran P, Crowell MD, Wing R, Rittmann BE, Krajmalnik-Brown R. Human gut microbiota in obesity and after gastric bypass. Proc Natl Acad Sci USA 2009; 106:2365-2370.         [ Links ]

43. Folini L, Merlotti C, Benetti A, Veronelli A, Frigè F, Miele L, Micheletto G, Masci E, Rovati M, Pontiroli AE. Cholesterol levels are reduced after malabsorptive surgey, not after restrictive surgery or diet. Submitted.         [ Links ]

44. Benetti A, Del Puppo M, Crosignani A, Veronelli A, Masci E, Micheletto G, Pontiroli AE. Glucose and cholesterol metabolism after bariatric surgery in grade-3-obesity; differences between malabsorptive and restrictive surgery. Submitted.         [ Links ]

45. Buchwald H, Estok R, Fahrbach K, Banel D, Jensen MD, Pories WJ, Bantle JP, Sledge I. Weight and type 2 diabetes after bariatric surgery: systematic review and meta-analysis. Am J Med 2009; 122: 248-256.         [ Links ]

46. Pontiroli AE, Morabito A. Long-term prevention of mortality in morbid obesity through bariatric surgery. a systematic review and meta-analysis of trials performed with gastric banding and gastric bypass. Ann Surg 2011; 253: 484-487.         [ Links ]

 

 

Correspondence:
A. E. Pontiroli
Dipartamento di Medicina, Chirurgia e Odonoiatria
Universitá degli Studi di Milano
AEP, Medicina 2, Ospedale San Palo, Via A di Rudini 8
20142 Milano, Italy
E-mail: antonio.pontiroli@unimi.it

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