Pathophysiology of Type 1 Diabetes 1. Type 1 Diabetes Mellitus Characterized by absolute insulin deficiency Pathophysiology and etiology –Result of pancreatic.

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Presentation transcript:

Pathophysiology of Type 1 Diabetes 1

Type 1 Diabetes Mellitus Characterized by absolute insulin deficiency Pathophysiology and etiology –Result of pancreatic beta cell destruction Prone to ketosis –Total deficit of circulating insulin –Autoimmune –Idiopathic 2

Type of Diabetes in Youth by Race/Ethnicity and Etiology 3 AA, African American; AI, American Indian; API, Asian/Pacific Islander; IR, insulin resistant; IS, insulin sensitive; NHW, non-Hispanic white. Dabelea D, et al. Diabetes Care. 2011;34: SEARCH for Diabetes in Youth Study (N=2291) Distribution of etiologic categories by race/ethnicity

Type 1 Diabetes Pathophysiology 4 Inflammation T cell TNF-  IFN-  FasL Autoimmune Reaction Macrophage  -cell CD8 + T cell TNF-  IL-1 NO Class I MHC Dendritic cell  -cell Destruction Class II MHC CD8, cluster of differentiation 8; FasL, Fas ligand; IFN- , interferon  ; IL-1, interleukin 1; MHC, major histocompatibility complex; NO, nitric oxide; TNF- , tumor necrosis factor . Maahs DM, et al. Endocrinol Metab Clin North Am. 2010;39:  -cell destruction –Usually leading to absolute insulin deficiency Immune mediated Idiopathic

Pathophysiologic Features of Type 1 Diabetes Chronic autoimmune disorder –Occurs in genetically susceptible individuals –May be precipitated by environmental factors Autoimmune response against –Altered pancreatic  -cell antigens –Molecules in  -cells that resemble a viral protein Antibodies –Approximately 85% of patients: circulating islet cell antibodies –Majority: detectable anti-insulin antibodies –Most islet cell antibodies directed against GAD within pancreatic  -cells 5 GAD, glutamic acid decarboxylase. Maahs DM, et al. Endocrinol Metab Clin North Am. 2010;39:

Trends in T1D Immunophenotype at Diagnosis Prevalence of IA-2A and ZnT8A has increased significantly, mirrored by raised levels of IA-2A, ZnT8A, and IA-2β autoantibodies (IA-2βA) IAA and GADA prevalence and levels have not changed Increases in IA-2A, ZnT8A, and IA-2βA at diagnosis during a period of rising incidence suggest that the process leading to type 1 diabetes is now characterized by a more intense humoral autoimmune response 6 Autoantibodies to insulin, IAA; GAD, GADA; islet antigen-2, IA-2A; T1D, type 1 diabetes; zinc transporter 8, ZnT8A. Long AE, et al. Diabetes. 2012;61:

Autoimmune Basis for Type 1 Diabetes Atkinson MA. Diabetes. 2005;54: GADA, ICA512A, ICA Environmental triggers and regulators Time  -Cell mass Interactions between genes imparting susceptibility and resistance Variable insulinitis  -cell sensitivity to injury Prediabetes Overt T1D Immune dysregulation IAA C-peptide undetec- table Loss of first-phase insulin response (IVGTT) Glucose intolerance 7

Models for Pathogenesis of T1D 8 van Belle TL, et al. Physiol Rev. 2011;91:

Models for Pathogenesis of T1D 9 van Belle TL, et al. Physiol Rev. 2011;91:

Models for Pathogenesis of T1D: Fertile Field Hypothesis 10 van Belle TL, et al. Physiol Rev. 2011;91:

How Type 1 Diabetes Might Arise 11 van Belle TL, et al. Physiol Rev. 2011;91:

Insulin and Glucose Metabolism 12 Stimulates glucose uptake into muscle and adipose cells Inhibits hepatic glucose production Major Metabolic Effects of Insulin Hyperglycemia  osmotic diuresis and dehydration Consequences of Insulin Deficiency

Major Metabolic Effects of Insulin and Consequences of Insulin Deficiency Insulin effects: inhibits breakdown of triglycerides (lipolysis) in adipose tissue Consequences of insulin deficiency: elevated FFA levels Insulin effects: inhibits ketogenesis Consequences of insulin deficiency: ketoacidosis, production of ketone bodies Insulin effects in muscle: stimulates amino acid uptake and protein synthesis, inhibits protein degradation, regulates gene transcription Consequences of insulin deficiency: muscle wasting 13