Prevalence of Latent Autoimmune Diabetes in Adult (LADA) Among Clinically Diagnosed Type 2 Diabetic Patients

Authors

  • Meroj A. Jasem Department of Biology, College of Science, AL-Mustansyria University, Iraq
  • Alia A. Al-Ubaidi Department of Biology, College of Science, AL-Mustansyria University, Iraq
  • Anni Admon Immunology Department, Central Public Health Laboratories, Baghdad, Iraq
  • Khadeja N. Zwaer Biochemistry Department, Al-Kindy Endocrinology and Diabetic Center, Baghdad, Iraq

Keywords:

LADA, GADA, Type2 diabetic patients, Pancreatic islet cells autoantibodies

Abstract

Background and Objectives: Identification of LADA represents a major interest for many diabetologists, because its prevalence is relatively high and seems to be underestimated. Also, correct diagnosis of LADA patients allows an early and accurate therapeutic intervention.
Aim of the Study: The purpose of this study was the evaluation of the prevalence of latent autoimmune diabetes in adults (LADA) among group of clinically diagnosed type2 diabetic patients.

Methods: Seventy four type 2 diabetic patients were tested for the presence of autoantibodies ICA, GAD, IA-2. All patients were also characterized according to clinical symptoms preceeding the onset of the disease, age, BMI. ICA was measured by indirect immunofluorescence on cryostat sections of human pancreas of blood group O. GADab and IA-2ab were measured by ELISA assay.

Results: The presence of at least one autoantibody was revealed in 14/74 patients. That allowed us to recognize LADA in these cases. The coexistence of two antibodies was   observed in 3/14 patients. None of the patients had three examined autoantibodies. GADab were detected more frequently (12/14) than GADab and IA-2ab, which were found with the same frequency (2/14) (P < 0.004).

Conclusions: Among patients with diagnosed type2 diabetes there is a group with autoimmune diabetes, called LADA. Phenotype similarity between diabetes type 2 and LADA makes the proper diagnosis impossible without more specific tests. The diagnosis of LADA is based on the presence of autoantibodies.

Metrics

Metrics Loading ...

References

WHO/ADA. Report for the expert commetii on the diagnosis and classification of diabetes militus. Diabetes Care 1997; 20:1183-1197.

Alberti KG and Zimmet PZ. Definition, diagnosis and classification of diabetes mellitus and its complications. Part 1: diagnosis and classification of diabetes mellitus provisional report of a WHO consultation. Diabet Med 1998; 15: 539–553.

Stenström G, Gottsäter A, Bakhtadze E, Berger B, Sundkvist G. Diabetes. Latent autoimmune diabetes in adults: definition, prevalence, beta-cell function, and treatment. 2005;54 Suppl 2:S68-72

Borg H; Gottsater A; Landin-Olsson M; Fernlund P; Sundkvist G .High levels of antigen-specific islet antibodies predict future beta-cell failure in patients with onset of diabetes in adult age. J Clin Endocrinol Metab 2001; 86(7):3032-3038.

Fourlanos S; Perry C; Stein MS; Stankovich J; Harrison LC; Colman PG. A clinical screening tool identifies autoimmune diabetes in adults. Diabetes Care. 2006; 29(5):970-5.

Van Deutekom AW, Heine RJ, Simsek S. The islet autoantibody titres: their clinical relevance in latent autoimmune diabetes in adults (LADA) and the classification of diabetes mellitus. Diabet Med. 2008;25(2):117-25.

Schiel R, Müller UA.GAD autoantibodies in a selection-free population of insulin-treated diabetic patients: indicator of a high prevalence of LADA? Diabetes Res Clin Pract. 2000,49:33-40.

Pietropaolo M, Barinas-Mitchell E, Pietropaolo SL, Kuller LH, Trucco M. Evidence of islet cell autoimmunity in elderly patients with Type 2 diabetes. Diabetes 2000; 49: 32–38.

Lohmann T, Keller K, Verlohren HJ, Krug J, Steindorf J, Scherbaum W.A, Sessielr J. Titre and combination of ICA and autoantibodies to glutamic acid decarboxylase disrimate two clinically distinct types of latent autoimmune diabetes in adults (LADA). Diabetologia 2001; 44:1005-1010.

Turner, R., Stratton, I., Horton, V., Manley, S., Zimmet, P., Mackay, I. R., Shattock, M., Bottazzo, G. F., for UK Prospective Diabetes Study (UKPDS) Group. UKPDS 25: Autoantibodies to islet-cell cytoplasm and glutamic acid decarboxylase for prediction of insulin requirement in type 2 diabetes. Lancet. 1997; 350: 1288– 1293.

Differentiating slowly developing type 1 from true type 2? www.medscape.com, Experts And Viewpoint, Medscape Diabetes & Endocrinology, August 2000

Schranz DB, Bekris L, Landin-Olsson M. Newly diagnosed latent autoimmune diabetes in adults (LADA) is associated with low level glutamat decarboxylase (GAD65) and IA-2 antibodies. Diabetes Incidence Study in Sweden (DISS). Horm Metab Res 2000; 32:133-138.

Borg H, Gottsäter A, Fernlund P, Sundkvist G . 12-Year Prospective Study of the Relationship Between Islet Antibodies and ß-Cell Function at and After the Diagnosis in Patients With Adult-Onset Diabetes. Diabetes. 2002;51(6): 1754-1762

David D, Leslie G, Williams R, Pozzilli P.: Type 1 Diabetes and Latent Autoimmune Diabetes in Adults: One End of the Rainbow The Journal of Clinical Endocrinology & Metabolism 2006; 91(5):1654–1659

Fourlanos S, Dotta F, Greenbaum CJ, Palmer JP, Rolandsson O, Colman PG, Harrison LC . Latent autoimmune diabetes in adults (LADA) should be less latent. Diabetologia 2005;48:2206–2212

Juneja R, Hirsch IB, Naik RG, Brooks-Worrell BM, Greenbaum CJ, Palmer JP Islet cell antibodies and glutamic acid decarboxylase antibodies, but not the clinical phenotype, help to identify type 1(1/2) diabetes in patients presenting with type 2 diabetes. Metabolism 2001;50:1008–1013.

Torn C, Landin-Olsson M, Ostman J. Glutamic acid decarboxylase antibodies (GADA) is the most important factor for prediction of insulin therapy within 3 years in young adult diabetic patients not classified as Type 1 diabetes on clinical grounds. Diabetes Metab Res Rev 2000; 16:442–447.

Humphrey ARG, McCarty DJ, Mackay IR, Rowley MJ, Dwyer T, Zimmet PZ: Autoantibodies to glutamic acid decarboxylase and phenotypic features associated with early insulin treatment in individuals with adult-onset diabetes mellitus. Diabet Med 1998; 15:113–119.

Takeda H, Kawasaki E, Shimizu I, Konoue E, Fujiyama M, Murao S, Tanaka K, Mori K, Tarumi Y, Seto I, Fujii Y, Kato K, Kondo S, Takada Y, Kitsuki N, Kaino Y, Kida K, Hashimoto N, Yamane Y, Yamawaki T, Onuma H, Nishimiya T, Osawa H, Saito Y, Makino H . Clinical, autoimmune, and genetic characteristics of adult-onset diabetic patients with GAD autoantibodies in Japan (Ehime Study). Diabetes Care2002;25:995–1001

Lutale JJK, Thordarson H, Holm PI, Eide GE , 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; 4:4-8

Park Y, Lee HK, Koh CS, Min H, Rowley M, Mackay IR. The low prevalence of immunogenetic markers in Korean adult-onset IDDM patients. Diabetes Care 1996; 19: 241–245.

Thai AC, Ng WY, Loke KY, Lee WRW, Lui KE & Cheah JS. Anti- GAD antibodies in Chinese patients with youth and adult-onset IDDM and NIDDM. Diabetologia 1997, 40 :1425–1430.

Maioli M, Alejandro E, Tonolo G, Gilliam LK, Bekris L, Hampe CS,. Obinu D, Manconi A, Puddu L, Lynch C Lernmark A. Epitope-Restricted 65-Kilodalton Glutamic Acid Decarboxylase Autoantibodies among New-Onset Sardinian Type 2 Diabetes Patients Define Phenotypes of Autoimmune Diabetes The Journal of Clinical Endocrinology & Metabolism2004; 89, (11) :5675-5682.

Gale EA. Latent autoimmune diabetes in adults: a guide for the perplexed. Diabetologia 2005; 48: 2195–2199.

. Yang L, Zhou Z.G., Tan S.Z., Huang G., Jin P., Yan X, Li X., Peng H., Hagopianb W. Carboxypeptidase-H Autoantibodies Differentiate a More Latent Subset of Autoimmune Diabetes from Phenotypic Type 2 Diabetes among Chinese Adults Immunology of Diabetes V: Ann. N.Y. Acad. Sci.;2008.1150: 263–266

Downloads

Published

2018-11-06

How to Cite

Jasem, M. A., Al-Ubaidi, A. A., Admon, A., & Zwaer, K. N. (2018). Prevalence of Latent Autoimmune Diabetes in Adult (LADA) Among Clinically Diagnosed Type 2 Diabetic Patients. Zanco Journal of Medical Sciences (Zanco J Med Sci), 14(1 Special), 181–187. Retrieved from https://zjms.hmu.edu.krd/index.php/zjms/article/view/572

Issue

Section

Original Articles