Serum Levels of Anti Glutamic Acid Decarboxylase and Insulin Auto Antibodies in First Degree Relatives of Patients with Diabetes Mellitus

Main Article Content

U Ali
IY Mohammed
https://orcid.org/0000-0002-4856-218X
IA Yahaya

Abstract

Antibodies to Glutamic Acid Decarboxylase (anti-GAD) and Insulin Auto Antibodies (IAA) mediate the autoimmune destruction of pancreatic islet cells and have been used to predict the risk of future development of Diabetes Mellitus (DM). These circulating antibodies are usually detected in body fluids and tissues several years before the onset of hyperglycemia. This helps in identifying individuals at risk of future development of DM thereby providing a good lead time for secondary preventive measures such as Therapeutic Lifestyle Changes to be introduced. This study determined the prevalence of Anti-GAD and IAA as a major risk factor for developing DM among First Degree Relatives (FDR) of DM patients in Kano, Northwestern Nigeria. This was a cross-sectional descriptive study carried out on 100 randomly selected FDR of individuals with DM in the diabetic clinic of Aminu Kano Teaching Hospital (AKTH). Control group recruited were 100 apparently healthy subjects with no family history of DM. Anti-GAD and IAA were measured using Enzyme Linked Immunosorbent Assay (ELISA) based technique. GAD Ab levels >32 ng/mL and IAA levels >39 ng/ml were considered positive for Antibodies. Data obtained was analyzed using statistical package for social sciences (SPSS) version 20.0. Anti-GAD and IAA were present in 81% (O.R= 1.9, 95% CI= 1.0-3.7, p= 0.050) and 66% (O.R= 1.9, 95% CI= 1.7-5.6), p <0.001) of FDR of DM patients compared to controls 69% and 34%. The mean level of Anti-GAD was also higher among the FDR of diabetics compared to controls (68.4±31.9 vs 45.3±22.4, p <0.001). The mean IAA level was also higher among the FDR of diabetics compared to controls (61.0±20.7 vs 51.8±11.7, p <0.001). This study demonstrated a high Anti-GAD and IAA positivity among first degree relatives of diabetics compared to controls underscoring the importance of screening for risk factors. Preventive measures like lifestyle changes can be appropriately applied among to slow the progression to diabetes mellitus.

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1.
Ali U, Mohammed I, Yahaya I. Serum Levels of Anti Glutamic Acid Decarboxylase and Insulin Auto Antibodies in First Degree Relatives of Patients with Diabetes Mellitus. Wes J Med Biomed Sci [Internet]. 2021 Apr. 30 [cited 2024 May 21];2(1):51-6. Available from: https://www.wjmbs.com.ng/index.php/wjmbs/article/view/37
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References

1. Atkinson MA, Eisenbarth GS. Type 1 diabetes: new perspectives on disease pathogenesis and treatment. Lancet 2001; 358(9277): 221-229.
2. Sacks DB, Bruns DE, Goldstein DE, Maclaren NK, McDonald JM, Parrott M. Guidelines and recommendations for laboratory analysis in the diagnosis and management of diabetes mellitus. Clin Chem 2002;48(3):436–472.
3. Carl A Buntis, Edward R. Ashwood and David E.Bruns. TIETZ Fundamentals of clinical chemistry 380 - 381p.
4. Al Alwan I, Bin Dajim N, Jawdat D, Tamimi W, Al Ahmdi R, Albuhairan F. Prevalence of autoantibodies in children newly diagnosed with type 1 diabetes mellitus. Br J Biomed Sci 2012; 69(1):31–33.
5. Bruining GJ, Molenaar JL, Grobbee DE, Hofman A, Scheffer GJ, Bruining H A, et al. Ten-year follow-up study of islet-cell antibodies and childhood diabetes mellitus. Lancet 1989;1:1100–1103.
6. Aanstoot HJ, Sigurdsson E, Jaffe M, Shi Y, Christgau S, Grobbee D, et al. Value of antibodies to GAD65 combined with islet cell cytoplasmic antibodies for predicting IDDM in a childhood population. Diabetologia 1994;37(9):917–924.
7. Krischer JP, Schatz D, Riley WJ, Spillar RP, Silverstein JH, Schwartz S, et al. Insulin and islet cell autoantibodies as time-dependent covariates in the development of insulin-dependent diabetes: a prospective study in relatives. J Clin Endocrinol Metab 1993;77(3):743–749.
8. Karjalainen J, Váhślo P, Knip M, Tuomilehto-wolf E, Virtala E, Åkerblom HK. Islet cell autoimmunity and progression to insulin-dependent diabetes mellitus in genetically high- and low-risk siblings of diabetic children. Eur J Clin Invest 1996;26(8):640–649.
9. Rheeder P, Stolk RP, Grobbee DE. Ethnic differences in C-peptide levels and anti-GAD antibodies in South African patients with diabetic ketoacidosis. QJM. 2001;94(1):39–43.
10. Lutale J, Thordarson H, Holm P, Eide G, Vetvik K. Islet cell autoantibodies in African patients with Type 1 and Type 2 diabetes in Dar es Salaam Tanzania: a cross sectional study. J Autoimmune Dis 2007;4:4.
11. Singha P. Determination of adequate sample size. In: Biostatistics. 1st ed. Dabco Ltd 2000. p. 204–205.
12. Eagle bio-science-anti-GAD ELISA kit. Enzyme immunoassay for the determination of autoantibodies to Glutamic acid decarboxylase (GAD65 Abs) in human serum. p. 1–10.
13. Eagle bio-science. Enzyme immunoassay for the determination of autoantibodies to insulin in human (IAA), IAA ELISA kit. p. 1–7.
14. GI Ahaneku, CU Osuji, BC Anisiuba, VO Ikeh, OC Oguejiofor, JE Ahaneku. Evaluation of blood pressure and indices of obesity in a typical rural community in eastern Nigeria. Annals of African Medicine. Vol 10, No 2: 120 (2011)
15. Theodore A. Kotchen; Obesity-Related Hypertension: Epidemiology, Pathophysiology, and Clinical Management. Am J Hypertens 2010; 23 (11): 1170-1178. doi: 10.1038/ajh.2010.172
16. Lundgren VM, Isomaa B, Lyssenko V, Laurila E, Korhonen P, Groop LC, Tuomi T, Botnia Study Group. GAD antibody positivity predicts type 2 diabetes in an adult population. Diabetes. 2010 Feb 1;59(2):416-422.
17. Siewko K, Popławska-Kita A, Telejko B, Maciulewski R, Zielińska A, Nikołajuk A, Górska M, Szelachowska M. Prognostic markers for the development of type 1 diabetes in first-degree relatives of diabetic patients. Endokrynologia Polska. 2014;65(3):176-180.
18. Al-Abady HL, Mahdi NK, Al-Naama LM, Mahdi JK. The prevalence of autoantibodies among relatives for type 1 and 2 diabetic patients. JPMA. The Journal of the Pakistan Medical Association. 2016 Sep;66(9):1064-1067.
19. Notkins, A. L., & Lernmark, Åke. (2001). Autoimmune type 1 diabetes: resolved and unresolved issues. Journal of Clinical Investigation, 108(9), 1247–1252.
20. Lyssenko V, Almgren P, Anevski D, Perfekt R, Lahti K, Nisse´n M, Isomaa B, Forsen B, Homstro¨m N, Saloranta C, Taskinen MR, Groop L, Tuomi T, Botnia Study Group. Botnia study group: predictors of and longitudinal changes in insulin sensitivity and secretion preceding onset of type 2 diabetes. Diabetes 2005;54:166–174
21. Lutale, J., Thordarson, H., Holm, P., Eide, G., & Vetvik, K. (2007). Islet cell autoantibodies in African patients with Type 1 and Type 2 diabetes in Dar es Salaam Tanzania: a cross sectional study. Journal of Autoimmune Diseases, 4, 4. http://doi.org/10.1186/1740-2557-4-4
22. Pugliese A, Bugawan T, Moromisato R, Awdeh ZL, Alper CA, Jackson RA, Erlich HA, Eisenbarth GS. Two subsets of HLA-DQA1 alleles mark phenotypic variation in levels of insulin autoantibodies in first degree relatives at risk for insulin-dependent diabetes. Journal of Clinical Investigation. 1994 Jun;93(6):2447.
23. Siewko K, Popławska-Kita A, Telejko B, Abdelrazek SS, Górska M, Szelachowska M. Organ-specific antibodies in first-degree relatives of patients with type 1 diabetes. Polskie Archiwum Medycyny Wewnetrznej. 2015 Jan 1;125(1-2):95-97.
24. Ebtissam M. Salah, Hesham El-Hafnawy, Mona Anwar M. , Samar M.E. Salem , Mai M. Youssef , Atef Bassyoni and Marry Aziz. Prevalence of Diabetes-associated Antibodies and Impaired Insulin Response to Glucose in First Degree Relatives of Diabetic Patients. Journal of Medical Sciences. 2006, 6: 139-148.