Skip to main content

Advertisement

Log in

Roux-en-Y Bypass Gastroplasty: Markers of Oxidative Stress 6 Months After Surgery

  • Clinical Research
  • Published:
Obesity Surgery Aims and scope Submit manuscript

Abstract

Background

This study examined the effect of weight loss on energy intake, vitamin C, E, β-carotene (diet/blood), reduced glutathione (GSH), C-reactive protein (CRP), thiobarbituric acid reactive substances (TBARS), catalase, and myeloperoxidase, in patients with Roux-en-Y bypass gastroplasty.

Methods

Prospective clinical study with control (C) and bariatric (B) groups (n = 20 each). Age was 38.8 ± 11.1 (C) and 37.8 ± 11.2 years (B), and body mass indices (BMI) were 22.4 ± 2.4 and 48.1 ± 8.7 kg/m2, respectively. Group C was assessed on a single occasion and B at three time points (basal period and 3 and 6 months after gastroplasty).

Results

BMI was decreased at three (38.3 ± 1.7, P = 0.018) and 6 months after surgery (34.9 ± 1.7, P < 0.001). Mean weight loss was 20.53 ± 1.1 after three and 27.96 ± 1.3 kg after 6 months. Serum vitamin C and β-carotene (P < 0.01 and P < 0.001, respectively) were increased at 6 months compared to basal. Basal serum vitamin C (P = 0.001) and β-carotene (P < 0.001) were lower compared to controls. Serum vitamin E corrected for cholesterol and triglycerides was higher in group B at three (P = 0.01) and 6 months (P = 0.001) and lower at basal (P < 0.001) compared to controls. GSH was higher in controls (P < 0.001) compared to basal. Catalase (P = 0.01) and TBARS (P < 0.001) were higher in group B at 6 months. TBARS were higher (P < 0.001) at basal compared to controls. Myeloperoxidase and CRP decreased in group B after three (P = 0.028, P = 0.010) and 6 months (P < 0.001, P = 0.001), respectively.

Conclusions

Roux-en-Y bypass gastroplasty led to decreased proinflammatory parameters together with increased nutritional antioxidants, catalase, and TBARS, and decreased GSH 6 months after surgery.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. World Health Organization (WHO). Obesity: preventing and managing the global epidemic. Report of a WHO consultation on obesity. Geneva: WHO/NUT/NCD/981, 1998.

  2. Higdon JV, Frei B. Obesity and oxidative stress: a direct link to CVD? Arterioscler Thromb Vasc Biol. 2003;23:365–7.

    Article  CAS  PubMed  Google Scholar 

  3. Uzun H, Zengin K, Taskin M, et al. Changes in leptin, plasminogen activator factor and oxidative stress in morbidly obese patients following open and laparoscopic Swedish adjustable gastric banding. Obes Surg. 2004;14:659–65.

    Article  PubMed  Google Scholar 

  4. Halliwell B, Gutteridge JMC. Oxygen is a toxic gas – an introduction to oxygen toxicity and reactive oxygen species. In: Free Radicals in Biology and Medicine. Oxford: Clarendon Press 1999:1-35.

  5. Fang YZ, Yang S, Wu G. Free radicals, antioxidants and nutrition. Nutrition. 2002;18:872–9.

    Article  CAS  PubMed  Google Scholar 

  6. Kelling PL, Smith LL. Relevance of NADPH depletion and mixed disulphide formation in rat lung to the mechanism of cell damage following paraquat administration. Biochem Pharmacol. 1982;31:3243–9.

    Article  Google Scholar 

  7. Mohn A, Catino M, Capanna R, et al. Increased oxidative stress in prepubertal severely obese children: effect of a dietary restriction-weight loss program. J Clin Endocrinol Metab. 2005;90:2653–8.

    Article  CAS  PubMed  Google Scholar 

  8. Arnhold J. Properties, functions, and secretion of human myeloperoxidase. Biochemistry. 2004;69:8–15.

    Google Scholar 

  9. Galan P, Viteri FE, Bertrais S, et al. Serum concentrations of β-carotene, vitamins C and E, zinc and selenium are influenced by sex, age, diet, smoking status, alcohol consumption and corpulence in a general French adult population. Eur J Clin Nutr. 2005;59:1181–90.

    Article  CAS  PubMed  Google Scholar 

  10. Strauss RS. Comparison of serum concentrations of alpha-tocopherol and beta-carotene in a cross-sectional sample of obese and non-obese children (NHANES III). J Pediatr. 1999;134:160–5.

    Article  CAS  PubMed  Google Scholar 

  11. Sies H, Stahl W. Vitamins E and C, β-carotene and other carotenoids as antioxidants. Am J Clin Nutr. 1995;62:15S–21S. Suppl 13.

    Google Scholar 

  12. Jung R. Obesity as a disease. Br Med Bull. 1997;53:307–21.

    CAS  PubMed  Google Scholar 

  13. Deitel M, Shahi B, Deitel FH. Effect of weight loss in the morbidly obese patient with severe disability. Obes Surg. 1991;1:419–21.

    Article  PubMed  Google Scholar 

  14. Mango VL, Frishman WH. Physiologic, psychologic, and metabolic consequences of bariatric surgery. Cardiol Rev. 2006;14:232–7.

    Article  PubMed  Google Scholar 

  15. Buchwald H. The future of bariatric surgery. Obes Surg. 2005;15:598–605.

    Article  PubMed  Google Scholar 

  16. van Stijn MFM, Boelens PG, Richir MC, et al. Antioxidant-enriched enteral nutrition and immuno-inflammatory response after major gastrointestinal tract surgery. Br J Nutr. 2010;103:314–8.

    Article  PubMed  Google Scholar 

  17. Xu J, Yunshi Z, Li R. Immunonutrition in surgical patients. Curr Drug Targets. 2009;10:771–7.

    Article  CAS  PubMed  Google Scholar 

  18. Kücükakin B, Gögenur I, Reiter RJ, et al. Oxidative stress in relation to surgery: is there a role for the antioxidant melatonin? J Surg Res. 2009;152:338–47.

    Article  PubMed  Google Scholar 

  19. Malinowski SS. Nutritional and metabolic complications of bariatric surgery. Am J Med Sci. 2006;331:219–25.

    Article  PubMed  Google Scholar 

  20. Alvarez-Leite J. Nutrient deficiencies secondary to bariatric surgery. Curr Opin Clin Nutr Metab Care. 2004;7:569–75.

    Article  PubMed  Google Scholar 

  21. Melissas J, Malliaraki N, Papadakis JA, et al. Plasma antioxidant capacity in morbidly obese patients before and after weight loss. Obes Surg. 2006;16:314–20.

    Article  PubMed  Google Scholar 

  22. World Medical Association (WMA). Declaration of Helsinki. Edinburgh, Scotland: 52nd General Assembly-WMA. 2000. [cited 2006 Feb 25]; Available from: URL: http://www.wma.net

  23. World Health Organization (WHO). Physical Status: the use and interpretation of anthropometry. WHO technical report series 854. Geneva: WHO, 1995. 453p.

  24. Sichieri R, Everhart JE. Validity of a Brazilian frequency questionnaire against dietary recalls and estimated energy intake. Nutr Res. 1998;18:1649–59.

    Article  CAS  Google Scholar 

  25. Willet W, Stampfer MJ. Total energy intake: implications for epidemiologic analyses. Am J Epidemiol. 1986;124:17–27.

    Google Scholar 

  26. United States Department of Agriculture (USDA). Available at: http://www.nal.usda.gov/fnic/foodcomp/search/. Accessed on: 6 May 2007.

  27. Bessey OA. Ascorbic acid microchemical methods. In: Gyorgy P, editor. Vitamin methods. New York: Academic Press; 1960. p. 303.

    Google Scholar 

  28. Arnauld J, Fortis I, Blachier S, et al. Simultaneous determination of retinol, alpha-tocopherol and beta-carotene in serum by isocratic high-performance liquid chromatography. J Chromatogr. 1991;572:103–16.

    Article  Google Scholar 

  29. Nagaya T, Nakaya K, Yoshida I, et al. Comparison of indices for serum vitamin E status in healthy subjects. Clin Chim Acta. 1998;276:103–8.

    Article  CAS  PubMed  Google Scholar 

  30. Beutler E, Duron O, Kelly BM. Improved method for the determination of blood glutathione. J Lab Clin Med. 1963;61:882–90.

    CAS  PubMed  Google Scholar 

  31. Aebi H. Catalase in vitro. Methods Enzymol. 1984;105:121–6.

    Article  CAS  PubMed  Google Scholar 

  32. Rao TS, Curie JL, Shaffer AF, et al. Comparative evaluation of arachidonic acid (AA) and tetradecanoylphorbol acetate (TPA)-induced dermal inflammation. Inflamm. 1993;17:723–41.

    Article  CAS  Google Scholar 

  33. Whicher JT, Ritchie RF, Johnson AM, et al. New international reference preparation for proteins in human serum (RRPHS). Clin Chem. 1994;40:934–8.

    CAS  PubMed  Google Scholar 

  34. Baudner S, Bienvenu J, Blirup-Jensen S et al. The certification of a matrix reference material for immunochemical measurement of 14 human serum proteins. CRM 470. Brussels: community bureau of reference, commission of the European communities, 1993:1-172.

  35. Ohkawa H, Oshishi N, Yagi K. Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Anal Biochem. 1979;95:351–8.

    Article  CAS  PubMed  Google Scholar 

  36. Bird RP, Draper AH. Comparative studies on different methods of malondyaldehyde determination. Meth Enzymol. 1984;105:295–305.

    Google Scholar 

  37. Kisakol G, Guney E, Bayraktar F, et al. Effect of surgical weight loss on free radical and antioxidant balance: a preliminary report. Obes Surg. 2002;12:795–800.

    Article  PubMed  Google Scholar 

  38. Dias MCG, Ribeiro AG, Scabim VM, et al. Dietary intake of female bariatric patients after anti-obesity gastroplasty. Clinics. 2006;61:93–8.

    Article  PubMed  Google Scholar 

  39. Bernet CP, Ciangura C, Coupaye M, et al. Nutritional deficiency after gastric bypass: diagnosis, prevention and treatment. Diabete Metab. 2007;33:13–24.

    Article  Google Scholar 

  40. Khan NI, Naz L, Yasmeen G. Obesity: an independent risk factor for systemic oxidative stress. Pak J Pharm Sci. 2006;19:62–5.

    CAS  PubMed  Google Scholar 

  41. Moor de Burgos A, Wartanowicz M, Ziemlanski S. Blood vitamin and lipid levels in overweight and obese women. Eur J Clin Nutr. 1992;46:803–8.

    CAS  PubMed  Google Scholar 

  42. Faber P, Johnstone AM, Gibney ER, et al. The effect of rate of weight loss on erythrocyte glutathione concentration and synthesis in healthy obese men. Clin Sci. 2002;102:569–77.

    Article  CAS  PubMed  Google Scholar 

  43. Uzun H, Konukoglu D, Gelisgen R, et al. Plasma protein carbonyl and thiol stress before and after laparoscopic gastric banding in morbidly obese patients. Obes Surg. 2007;17:1367–73.

    Article  PubMed  Google Scholar 

  44. Furukawa S, Fujita T, Shimabukuro M, et al. Increased oxidative stress in obesity and its impact on metabolic syndrome. J Clin Invest. 2004;114:1752–61.

    CAS  PubMed  Google Scholar 

  45. Dandona P, Mohanty P, Ghanim H, et al. The suppressive effect of dietary restriction and weight loss in the obese on the generation of reactive oxygen species by leukocytes, lipid peroxidation, and protein carbonylation. J Clin Endocrinol Metab. 2001;86:355–62.

    Article  CAS  PubMed  Google Scholar 

  46. Kirkman HN, Gaetani GF. Mammalian catalase: a venerable enzyme with new mysteries. Trends Biochem Sci. 2007;32:44–50.

    Article  CAS  PubMed  Google Scholar 

  47. Zhang R, Brennan ML, Zhongzhou S, et al. Myeloperoxidase functions as a major enzymatic catalyst for initiation of lipid peroxidation at sites of inflammation. J Biol Chem. 2002;277:46116–22.

    Article  CAS  PubMed  Google Scholar 

  48. Cabrera EJ, Valezi AC, Delfino VDA, et al. Reduction in plasma levels of inflammatory and oxidative stress indicators after Roux-en-Y Gastric Bypass. Obes Surg. 2010;20:42–9.

    Article  Google Scholar 

  49. van Dielen FMH, Buurman WA, Hadfoune M, et al. Macrophage inhibitory factor, plasminogen activator inhibitor-1, other acute phase proteins, and inflammatory mediators normalize as a result of weight loss in morbidly obese subjects treated with gastric restrictive surgery. J Clin Endocrinol Metab. 2004;89:4062–8.

    Article  PubMed  Google Scholar 

  50. Barbosa E, Faintuch J, Moreira EAM, et al. Supplementation of vitamin E, C and zinc attenuates oxidative stress in burned children: a randomized, double-blind, placebo-controlled pilot study. J Burn Care Res. 2009;30:859–66.

    Article  PubMed  Google Scholar 

Download references

Acknowledgments

The authors are grateful to the following for financial support: Fundação de Apoio à Pesquisa Científica e Tecnológica do Estado de Santa Catarina (FAPESC): Grant no. CON 14191/2007-7; Conselho Nacional de Desenvolvimento Científico e Tecnológico - CNPq, Programa Institucional de Bolsa de Iniciação Científica - Conselho Nacional de Desenvolvimento Científico e Tecnológico, and Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - CAPES. Statement of authorships: Moreira, Fröde, Wilhelm Filho had full access to all of the data in the study and take responsibility for the integrity of the data and the accuracy of the data analysis. Study concept and design: Moreira, Fröde, Wilhelm Filho. Acquisition of data: Boesing. Analysis and interpretation of data: Vigil, Parizotto, Inácio, Portinari, Trindade, Jordão Júnior. Drafting of the manuscript: Moreira, Fröde, Wilhelm Filho. Critical revision of the manuscript for important intellectual content: Moreira, Fröde, Wilhelm Filho. Statistical analysis: Boesing, Moreira. Final approval of the version to be submitted: Moreira, Fröde, Wilhelm Filho. Obtained funding: Moreira, Trindade.

Conflict of Interest Statement

No conflict of interest needs to be reported; the funding agency had no role in the analysis or interpretation of the data or in the decision to submit the report for publication.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Emilia Addison Machado Moreira.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Boesing, F., Moreira, E.A.M., Wilhelm-Filho, D. et al. Roux-en-Y Bypass Gastroplasty: Markers of Oxidative Stress 6 Months After Surgery. OBES SURG 20, 1236–1244 (2010). https://doi.org/10.1007/s11695-010-0196-x

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11695-010-0196-x

Keywords

Navigation