Correlation of Interleukin-10, Superoxide Dismutase (SOD), and Malondialdehyde (MDA) Levels with HbA1c in Pediatric Type 1 Diabetes Mellitus
DOI:
https://doi.org/10.11594/jtls.07.03.15Keywords:
Type 1 diabetes mellitus, superoxide dismutase, malondialdehyde, interleukin 10, HbA1c.Abstract
Type 1 diabetes mellitus (T1DM) is an autoimmune disease characterized by pancreatic β-cell destruction and considered to be correlated with oxidative stress. This study aimed to investigate the association of oxidative stress [superoxide dismutase (SOD) and malondialdehyde (MDA) levels], inflammation [interleukin 10 (IL-10)], and glycemic control (HbA1c) in pediatric T1DM patients. This study included 25 T1DM subjects and 25 healthy control subjects and was designed as a cross- sectional study. SOD, MDA, and IL-10 levels were measured by ELISA. We obtained that that IL-10 and SOD levels were significantly decreased in the T1DM group, but MDA and HbA1c levels were significantly elevated in the T1DM group. IL-10 levels were positively correlated with SOD levels and negatively correlated with MDA and HbA1c. SOD levels were negatively correlated with HbA1c levels. MDA was positively correlated with HbA1c levels. IL-10 and SOD levels were significantly decreased, but MDA and HbA1c levels were significantly elevated in the T1DM group.References
Zóka A, Műzes G, Somogyi A et al. (2013) Altered im-mune regulation in type 1 diabetes. Clinical and Develop-mental Immunology 10 (7): 1-17. doi: 10.1155/2013/254874.
Craig ME, Hattersley A, Donaghue K (2009) Definition, epidemiology and classification of diabetes in children and adolescents. Pediatric Diabetes 7 (10): 3 – 12. doi: 10.1111/j.1399-5448.2009.00568.x.
Pulungan AB, Mansyoer R, Batubara JRL, Tridjaja B, (2012) Gambaran diabetes melitus tipe 1. Sari Pediatri 15 (6): 57 – 62.
Cahyono HA, Wulandari D, Ratnasari V (2013) Short term complication of type 1 diabetes melitus. Pediatrica Indonesiana 53 (5): 92.
Rabinovitch A (2004) Roles of cell-mediated immunity and cytokines in the pathogenesis of type 1 diabetes mellitus. diabetes mellitus: A fundamental and clinical text 3rd edition. Philadelphia, Lippincott Williams and Wilkins.
Maritim AC, Sanders RA, Watkins JB (2003) Diabetes, oxidative stress, and antioxidants: a review. Journal of Biochemical and Molecular Toxicology 17 (2): 24 – 38. doi: 10.1002/jbt.10058.
Bouillon R, Geert C, Lieve V et al. (2008) Vitamin D and human health: Lessons from vitamin D receptor null mice. Endocrine Reviews 29 (6): 726 – 776. doi: 10.1210/er.2008-0004.
Costacou T, Zgibor JC, Evans RW et al. (2006) Antioxidants and coronary artery disease among individuals with type 1 diabetes: Findings from the Pittsburgh Epidemiology of Diabetes Complications Study. Journal of Diabetes and its Complications 20 (1): 387 – 394. doi: 10.1016/j.jdiacomp.2005.10.007.
Derr R, Gareet E, Stacy AG (2003) Is HbA1c affected by glycemic instability?. Diabetes Care 26 (10) : 2728 – 2732. doi: 10.2337/diacare.26.10.2728.
R and D (2011) Human IL-10 Immunoassay. USA and Canada. R and D Systems, Inc. http://www.rndsystems.com/
pdf/ D1000B.pdf. Accessed: February 2014
Sacks BD, Arnold M, Bakris GL et al. (2002) Guidelines and recommendations for laboratory analysis in the diagnosis and management of diabetes mellitus. Diabetes Care 34 (6): e61 – e99. doi: 10.2337/dc11-9998.
Asadullah K, Sterry W, Volk HD (2003) Interleukin-10 therapy – Review of a new approach. Pharmacological Reviews 55 (5): 241 – 269. doi: 10.1124/pr.55.2.4.
Zeyda M, Stulnig TM (2009) Obesity, inflammation, and insulin resistance – A mini-review. Gerontology 55 (4): 379 –386. doi: 10.1159/000212758.
Atkinson MA, Leiter EH (1999) The NOD mouse model of type 1 diabetes: As good as it gets? Nature Medicine 5: 601 – 604. doi: 10.1038/9442.
Pennline, KJ, Roque-Gaffney E, Monahan M (1994) Recombinant human IL-10 prevents the onset of diabetes in the nonobese diabetic mouse. Clinical Immunology and Immunopathology 71 (2): 169 – 175. doi: 10.1006/clin.1994.1068.
Goodarzi MT, Varmaziar L, Navidi AA, Parivar K (2008) Study of oxidative stress in type 2 diabetic patients and its relationship with glycated hemoglobin. Saudi Medical Journal 29 (4): 503 – 506.
Hsu WT, Tsai LY, Lin SK et al. (2006) Effects of diabetes duration and glycemic control on free radicals in children with type 1 diabetes mellitus. Annals of Clinical and Laboratory Science 36 (2): 174 – 178.
Abou-Seif MA, Youssef AA (2004) Evaluation of some biochemical changes in diabetic patients. Clinica Chimica Acta. 346: 161 – 170. 10.1016/j.cccn.2004.03.030.
Suys B, de Beeck LO, Rooman R et al. (2007) Impact of oxidative stress on the endothelial dysfunction of children and adolescents with type 1 diabetes mellitus: Protection by superoxide dismutase?. Pediatric Research 62: 456 – 461. doi: 10.1203/PDR.0b013e318142581a.
Dominguez C, Ruiz E, Gussinye M, Carascosa A (1998) Oxidative stress at onset and in early stages of type 1 diabetes in children and adolescent. Diabetes Care 21 (10): 1736 – 1742. doi: 10.2337/diacare.21.10.1736.
Hogg N, Kalyanaraman B (1998) The use of NO gas in biological systems. In: Titheradge MA (eds) Nitric Oxide Protocols. New York, Humana Press. pp 231 – 236. doi: 10.1385/1-59259-749-1:231
Nishikawa T, Edelstein D, Du X et al. (2007) Normalizing mitochondrial superoxide production blocks three pathways of hyperglycemic damage. Nature 404: 787 – 790. doi:10.1038/35008121.
Brownlee M (2001) Biochemistry and molecular cell biology of diabetic complications. Nature 414: 813 – 820. doi: 10.1038/414813a.
Firoozrai M, Nourbakhsh M, Razzaghy-Azar M (2007) Erythrocyte susceptibility to oxidative stress and antioxidant status in patients with type 1 diabetes. Diabetes Research and Clinical Practice 77 (3): 427 – 432. doi: 10.1016/j.diabres.2007.02.001.
Siu AW, To CH (2002) Nitric oxide and hydroxyl radical-induced retinal lipid peroxidation in vitro. Clinical and Experimental Optometry 85 (6): 378 – 382. doi: 10.1111/j.1444-0938.2002.tb02389.x.
Ferretti G, Bacchetti T, Busni D et al. (2004) Protective effect of paraoxonase activity in high-density lipoproteins against erythrocyte membranes peroxidation: A comparison between healthy subjects and type 1 diabetic patients. The Journal of Clinical Endocrinology and Metabolism 89 (6): 2957 – 2962. doi: 10.1210/jc.2003-031897.
Acworth IN, McCabe DR, Maher TJ (1997) The analysis of free radicals, their reaction products, and antioxidants. In: Baskin SI, Salem H (Eds.) Oxidants, Antioxidants and Free Radicals. Washington D.C., Taylor and Francis.
Gugliucci A (2000) Glycation as the glucose link to diabetic complications. The Journal of the American Osteopathic Association 100 (10): 621 – 634.
Cohen RM, Holmes YR, Chenier TC, Joiner CH (2002) Discordance between HbA1c and fructosamine: Evidence for a glycosylation gap and its relation to diabetic nephropathy. Diabetes Care 26 (1): 163 – 167. doi: 10.2337/diacare.26.1.163.
Sawah SIA (2011) A cross-sectional study of vitamin D, glycemic control, and inflammatory cytokines in children and adolescents with type 1 diabetes mellitus. Doctoral Thesis. University of Pennsylvania.
Rubio-Cabezas O, Hattersley AT, Njølstad PR et al. (2011) The Diagnosis and Management of Monogenic diabetes. In: Sperling MA (Eds) Diabetes in Childhood and adoles-cence. ISPAD Clinical Practice Consensus Guidelines 2014. pp 47 – 64. http://www.ispad.org/?page=ISPADClinicalPract. Ac-cessed: February 2014.
Gunnett CA, Donald D, Heistad, Faraci FM (2002) Interleukin-10 protects nitric oxide-dependent relaxation during diabetes role of superoxide. Diabetes 51 (8): 1931 – 1937. doi: 10.2337/diabetes.51.6.1931.
Mayhan WG (1997) Superoxide dismutase partially restores impaired dilatation of the basilar artery during diabetes mellitus. Brain Research 760 (1 – 2): 204 – 209.
Moore KW, O’Garra A, de Waal Malefyt R et al. (1993) Interleukin-10. Annual Review of Immunology 11 (1): 165 –190. doi: 10.1146/annurev.iy.11.040193.001121.
Kuga S, Otsuka T, Niiro H et al. (1996) Suppression of superoxide anion production by interleukin-10 is accompanied by a downregulation of the genes for subunit proteins of NADPH oxidase. Experimental Hematology 24 (2): 151 – 157.
Guizhen Z, Meihua L, Yang S et al. (2007) Effects of micronutrients on oxidative stress and islet function in type 1 diabetes mellitus rats: Relationships to Th2 type cytokines, interleukin-4, and interleukin-10. Chemical Research in Chinese Universities 23 (6): 701 – 704.
Foss-Freitas MC, Foss NT, Donadi EA, Foss MC (2007) Effect of metabolic control on interferon-γ and interleukin-10 production by peripheral blood mononuclear cells from type 1 and type 2 diabetic patients. Brazilian Journal of Medical and Biological Research 40 (5): 671 – 677. doi: 10.1590/S0100-879X2006005000107.
Reznick AZ, Shehadeh N, Shafir Y, Nagler RM (2006) Free radicals related effects and antioxidants in saliva and serum of adolescents with type 1 diabetes mellitus. Archives of Oral Biology 51 (8): 640 – 648. doi: 10.1016/j.archoralbio.2006.02.004.
Rahbani-Nobar ME, Rahimi-Pour, Rahbani-Nobar M et al. (2013) Total antioxidant capacity, superoxide dismutase and glutathione peroxidase in diabetic patients. Medical Journal of Islamic Academy of Sciences 12 (4): 109 – 114.
Belce A, Uslu E, Kucur M et al. (2000) Evaluation of salivary sialic acid level and Cu-Zn superoxide dismutase activity in type 1 diabetes mellitus. The Tohoku Journal of Experimental Medicine 192 (3): 219 – 225. doi: 10.1620/tjem.192.219.
Erciyas F, Taneli F, Arslan B, Uslu Y (2004) Glycemic control, oxidative stress, and lipid profile in children with type 1 diabetes mellitus. Archives of Medical Research 35: 134 – 140. doi: 10.1016/j.arcmed.2003.10.002.
Indran M, Rokiah, Chan SP, Kuppusamy UR (2004) Alteration of lipid peroxidation and antioxidant enzymes in young Malaysian IDDM patients. The Medical Journal of Malaysia 59 (2): 166 – 170.
Vessby J, Basu S, Mohsen R et al. (2002) Oxidative stress and antioxidant status in type 1 diabetes mellitus. Journal of Internal Medicine 251 (1): 69 – 76.
Celec P, Cervenka T, Hodosy J et al. (2004) Salivary thiobarbituric acid reacting substances and their relation to the gingival inflammation. Timisoara Medical Journal 54 (1): 81 – 85.
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