Abstract
Purpose
Insulin resistance (IR) and increased oxidative stress (OS) are the characteristics of polycystic ovary syndrome (PCOS). In this study, we aimed to evaluate the effects of oral glucose tolerance (OGTT) and mixed meal tests (MMT) on plasma total oxidant (TOS) and total antioxidant status (TAS) in patients with PCOS and the relationship between these parameters and IR, calculated via homeostasis of model assessment-IR (HOMA-IR) and Matsuda’s insulin sensitivity index (ISI) derived from OGTT and MMT.
Methods
Twenty-two patients with PCOS, and age- and body mass index (BMI)-matched 20 women as controls were enrolled into the study. Five-hour OGTT and MMT were performed on different days, and before and after these tests, plasma TOS and TAS levels were investigated. IR was calculated with HOMA-IR and Matsuda’s ISI.
Results
HOMA-IR levels were higher in patients with PCOS, compared to controls, while Matsuda’s ISI derived from OGTT and MMT was higher in controls. Plasma TOS levels before OGTT and MMT were higher in patients with PCOS than controls, while TAS levels were similar. After OGTT, plasma TOS levels became decreased at 5th hour, when compared to baseline values in PCOS group. Likewise, the same decrement was found in controls, but the decrement was not significant. After OGTT and MMT at 5th hour, no changes were observed in TAS levels, compared to baseline.
Conclusion
Matsuda’s ISIs derived from OGTT and MMT can be used instead of each other, and interestingly, we found a decrease in TOS levels after OGTT in patients with PCOS.
Similar content being viewed by others
References
Fauser BC, Tarlatzis BC, Rebar RW, Legro RS, Balen AH, Lobo R, Carmina E, Chang J, Yildiz BO, Laven JS, Boivin J, Petraglia F, Wijeyeratne CN, Norman RJ, Dunaif A, Franks S, Wild RA, Dumesic D, Barnhart K (2012) Consensus on women’s health aspects of polycystic ovary syndrome (PCOS): the Amsterdam ESHRE/ASRM-Sponsored 3rd PCOS Consensus Workshop Group. Fertil Steril 97(1):28–38. doi:10.1016/j.fertnstert.2011.09.024
Nandi A, Chen Z, Patel R, Poretsky L (2014) Polycystic ovary syndrome. Endocrinol Metab Clin North Am 43(1):123–147. doi:10.1016/j.ecl.2013.10.003
Chen L, Xu WM, Zhang D (2014) Association of abdominal obesity, insulin resistance, and oxidative stress in adipose tissue in women with polycystic ovary syndrome. Fertil. Steril 102(4):1167–1174. doi:10.1016/j.fertnstert.2014.06.027
Macut D, Antic IB, Bjekic-Macut J (2015) Cardiovascular risk factors and events in women with androgen excess. J Endocrinol Invest 38(3):295–301. doi:10.1007/s40618-014-0215-1
Cakiroglu Y, Vural F, Vural B (2016) The inflammatory markers in polycystic ovary syndrome: association with obesity and IVF outcomes. J Endocrinol Invest. doi:10.1007/s40618-016-0446-4
Ciampelli M, Leoni F, Cucinelli F, Mancuso S, Panunzi S, De Gaetano A, Lanzone A (2005) Assessment of insulin sensitivity from measurements in the fasting state and during an oral glucose tolerance test in polycystic ovary syndrome and menopausal patients. The J Clin Endocrinol Metab 90(3):1398–1406. doi:10.1210/jc.2004-0410
Ovalle F, Azziz R (2002) Insulin resistance, polycystic ovary syndrome, and type 2 diabetes mellitus. Fertil Steril 77(6):1095–1105
DeUgarte CM, Bartolucci AA, Azziz R (2005) Prevalence of insulin resistance in the polycystic ovary syndrome using the homeostasis model assessment. Fertil Steril 83(5):1454–1460. doi:10.1016/j.fertnstert.2004.11.070
Amato MC, Vesco R, Vigneri E, Ciresi A, Giordano C (2015) Hyperinsulinism and polycystic ovary syndrome (PCOS): role of insulin clearance. J Endocrinol Invest 38(12):1319–1326. doi:10.1007/s40618-015-0372-x
DeFronzo RA, Tobin JD, Andres R (1979) Glucose clamp technique: a method for quantifying insulin secretion and resistance. The Am J Physiol 237(3):E214–E223
Matthews DR, Hosker JP, Rudenski AS, Naylor BA, Treacher DF, Turner RC (1985) Homeostasis model assessment: insulin resistance and beta-cell function from fasting plasma glucose and insulin concentrations in man. Diabetologia 28(7):412–419
Matsuda M, DeFronzo RA (1999) Insulin sensitivity indices obtained from oral glucose tolerance testing: comparison with the euglycemic insulin clamp. Diabetes Care 22(9):1462–1470
Halliwell B (1994) Free radicals, antioxidants, and human disease: curiosity, cause, or consequence? Lancet 344(8924):721–724
Baynes JW (1991) Role of oxidative stress in development of complications in diabetes. Diabetes 40(4):405–412
Matthews AT, Ross MK (2015) Oxyradical stress, endocannabinoids, and atherosclerosis. Toxics 3(4):481–498. doi:10.3390/toxics3040481
Moti M, Amini L, Mirhoseini Ardakani SS, Kamalzadeh S, Masoomikarimi M, Jafarisani M (2015) Oxidative stress and anti-oxidant defense system in Iranian women with polycystic ovary syndrome. Iranian J Reprod Med 13(6):373–378
Das P, Biswas S, Mukherjee S, Bandyopadhyay SK (2016) Association of Oxidative Stress and Obesity with Insulin Resistance in Type 2 Diabetes Mellitus. Mymensingh Med J: MMJ 25(1):148–152
Meigs JB, Larson MG, Fox CS, Keaney JF Jr, Vasan RS, Benjamin EJ (2007) Association of oxidative stress, insulin resistance, and diabetes risk phenotypes: the Framingham offspring study. Diabetes Care 30(10):2529–2535. doi:10.2337/dc07-0817
Riemersma RA, Wood DA, Macintyre CC, Elton RA, Gey KF, Oliver MF (1991) Risk of angina pectoris and plasma concentrations of vitamins A, C, and E and carotene. Lancet 337(8732):1–5
Sies H (2015) Oxidative stress: a concept in redox biology and medicine. Redox Biol 4:180–183. doi:10.1016/j.redox.2015.01.002
Fisher-Wellman KH, Bloomer RJ (2010) Exacerbated postprandial oxidative stress induced by the acute intake of a lipid meal compared to isoenergetically administered carbohydrate, protein, and mixed meals in young, healthy men. J Am Coll Nutr 29(4):373–381
Fisher-Wellman KH, Bloomer RJ (2010) Lack of effect of a high-calorie dextrose or maltodextrin meal on postprandial oxidative stress in healthy young men. Int J Sport Nutr Exerc Metab 20(5):393–400
von Bibra H, St John Sutton M, Schuster T, Ceriello A, Siegmund T, Schumm-Draeger PM (2013) Oxidative stress after a carbohydrate meal contributes to the deterioration of diastolic cardiac function in nonhypertensive insulin-treated patients with moderately well controlled type 2 diabetes. Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme 45(6):449–455. doi:10.1055/s-0033-1333752
Serin O, Konukoglu D, Firtina S, Mavis O (2007) Serum oxidized low density lipoprotein, paraoxonase 1 and lipid peroxidation levels during oral glucose tolerance test. Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme 39(3):207–211. doi:10.1055/s-2007-970419
Savic-Radojevic A, Bozic Antic I, Coric V, Bjekic-Macut J, Radic T, Zarkovic M, Djukic T, Pljesa-Ercegovac M, Panidis D, Katsikis I, Simic T, Macut D (2015) Effect of hyperglycemia and hyperinsulinemia on glutathione peroxidase activity in non-obese women with polycystic ovary syndrome. Hormones 14(1):101–108. doi:10.14310/horm.2002.1525
Mohanty P, Hamouda W, Garg R, Aljada A, Ghanim H, Dandona P (2000) Glucose challenge stimulates reactive oxygen species (ROS) generation by leucocytes. The J Clin Endocrinol Metab 85(8):2970–2973. doi:10.1210/jcem.85.8.6854
Erel O (2005) A new automated colorimetric method for measuring total oxidant status. Clin Biochem 38(12):1103–1111. doi:10.1016/j.clinbiochem.2005.08.008
Erel O (2004) A novel automated direct measurement method for total antioxidant capacity using a new generation, more stable ABTS radical cation. Clin Biochem 37(4):277–285. doi:10.1016/j.clinbiochem.2003.11.015
Campbell PJ, Mandarino LJ, Gerich JE (1988) Quantification of the relative impairment in actions of insulin on hepatic glucose production and peripheral glucose uptake in non-insulin-dependent diabetes mellitus. Metab: Clin Exp 37(1):15–21
de Paula Martins W, Santana LF, Nastri CO, Ferriani FA, de Sa MF, Dos Reis RM (2007) Agreement among insulin sensitivity indexes on the diagnosis of insulin resistance in polycystic ovary syndrome and ovulatory women. Eur J Obstet Gynecol Reprod Biol 133(2):203–207. doi:10.1016/j.ejogrb.2006.10.038
Rodriguez-Moran M, Guerrero-Romero F (2003) Insulin resistance is independently related to age in Mexican women. J Endocrinol Invest 26(1):42–48. doi:10.1007/BF03345121
Haffner SM, D’Agostino R, Saad MF, Rewers M, Mykkanen L, Selby J, Howard G, Savage PJ, Hamman RF, Wagenknecht LE et al (1996) Increased insulin resistance and insulin secretion in nondiabetic African-Americans and Hispanics compared with non-Hispanic whites. The insulin resistance atherosclerosis study. Diabetes 45(6):742–748
Karter AJ, Mayer-Davis EJ, Selby JV, D’Agostino RB Jr, Haffner SM, Sholinsky P, Bergman R, Saad MF, Hamman RF (1996) Insulin sensitivity and abdominal obesity in African-American, Hispanic, and non-Hispanic white men and women. The insulin resistance and atherosclerosis study. Diabetes 45(11):1547–1555
Creutzfeldt W, Nauck M (1992) Gut hormones and diabetes mellitus. Diabetes Metab Rev 8(2):149–177
Rodriguez-Diaz R, Caicedo A (2014) Neural control of the endocrine pancreas. Best practice & research. Clin Endocrinol Metab 28(5):745–756. doi:10.1016/j.beem.2014.05.002
Newsholme P, Cruzat V, Arfuso F, Keane K (2014) Nutrient regulation of insulin secretion and action. The J Endocrinol 221(3):R105–R120. doi:10.1530/JOE-13-0616
Berthiaume N, Zinker BA (2002) Metabolic responses in a model of insulin resistance: comparison between oral glucose and meal tolerance tests. Metab, Clin Exp 51(5):595–598
Selimoglu H, Duran C, Kiyici S, Guclu M, Ersoy C, Ozkaya G, Erturk E, Tuncel E, Imamoglu S (2009) Comparison of composite whole body insulin sensitivity index derived from mixed meal test and oral glucose tolerance test in insulin resistant obese subjects. Endocrine 36(2):299–304. doi:10.1007/s12020-009-9213-z
Lee HC, Wei YH (2007) Oxidative stress, mitochondrial DNA mutation, and apoptosis in aging. Exp Biol Med 232(5):592–606
Ceriello A, Bortolotti N, Crescentini A, Motz E, Lizzio S, Russo A, Ezsol Z, Tonutti L, Taboga C (1998) Antioxidant defences are reduced during the oral glucose tolerance test in normal and non-insulin-dependent diabetic subjects. Eur J Clin Invest 28(4):329–333
Ceriello A, Bortolotti N, Motz E, Crescentini A, Lizzio S, Russo A, Tonutti L, Taboga C (1998) Meal-generated oxidative stress in type 2 diabetic patients. Diabetes Care 21(9):1529–1533
Malin SK, Kirwan JP, Sia CL, Gonzalez F (2014) Glucose-stimulated oxidative stress in mononuclear cells is related to pancreatic beta-cell dysfunction in polycystic ovary syndrome. The J Clin Endocrinol Metab 99(1):322–329. doi:10.1210/jc.2013-3177
Cavalot F, Petrelli A, Traversa M, Bonomo K, Fiora E, Conti M, Anfossi G, Costa G, Trovati M (2006) Postprandial blood glucose is a stronger predictor of cardiovascular events than fasting blood glucose in type 2 diabetes mellitus, particularly in women: lessons from the San Luigi Gonzaga Diabetes Study. The J Clin Endocrinol Metab 91(3):813–819. doi:10.1210/jc.2005-1005
Monnier L, Mas E, Ginet C, Michel F, Villon L, Cristol JP, Colette C (2006) Activation of oxidative stress by acute glucose fluctuations compared with sustained chronic hyperglycemia in patients with type 2 diabetes. JAMA 295(14):1681–1687. doi:10.1001/jama.295.14.1681
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
This study was supported by Konya Training and Research Hospital’s Research Fund.
Conflicts of interest
Authors declare that they have no conflict of interest.
Ethical approval
All procedures in the study involving human participants were performed in accordance with the ethical standards of the institutional research committee and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards.
Informed consent
Informed consent was obtained from all individual participants included in the study.
Rights and permissions
About this article
Cite this article
Kucukaydın, Z., Duran, C., Basaran, M. et al. Plasma total oxidant and antioxidant status after oral glucose tolerance and mixed meal tests in patients with polycystic ovary syndrome. J Endocrinol Invest 39, 1139–1148 (2016). https://doi.org/10.1007/s40618-016-0498-5
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s40618-016-0498-5