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DIABETES MELLITUS PATHOGENESIS, CLASSIFICATION, DIAGNOSIS
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DIABETES MELLITUS A group of metabolic diseases characterized by hyperglycemia and: abnormal carbohydrate metabolism due to absolute deficiency of insulin (type 1 DM) or a relative deficiency of insulin (type 2 DM)
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DIABETES MELLITUS INCIDENCE: 600 000 PER YEAR IN U.S. PREVALENCE: 8-10 MILLION IN U.S. TYPE 1 DM: 10% OF ALL DIABETICS TYPE 2 DM: 90% OF ALL DIABETICS
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DIABETES MELLITUS MORTALITY TYPE 1 DM: 11 TIMES GREATER TYPE 2 DM: 2-3 TIMES GREATER ECONOMIC IMPACT DIRECT HEALTH CARE: $7,9 BILLION DRUG TREATMENT: $380 MILLION
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DIABETES MELLITUS PATHOGENESIS OF TYPE 1 DM CELLULAR-MEDIATED AUTOIMMUNE DESTRUCTION OF -CELLS RESPONSIBLE FOR INSULIN PRODUCTION AND SECRETION
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DIABETES MELLITUS PATHOGENESIS OF TYPE 1 DM GENETIC SUSCEPTIBILITY ENVIROMENTAL FACTORS AUTOIMMUNITY LYMPHOCYTIC INFILTRATION PANCREATIC AUTOANTIBODIES
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HLA Region Chromosome 6 Class II Class III Class I DP DQ DR 21 C4 B C2 TNF B C A Ring 3 Ring 4 DPB2 DPA2 DPB1 DPA1 DNA DOB DQB2 DQA2 DQB1 DQA1 DRB1 DRB2 DRB3 DRB4 DRA1 Subregion DP Subregion DQ Subregion DR
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HLA-DR AND HLA-DQ: A RISK OF TYPE 1 DM Susceptibility Susceptibility DR3 DR4 DR (< DR3 or DR4) DQA1*0301 DQA1*0501 DQB1*0201 DQB1*0302 Resistance DR2 DR5 (<DR2) DQBI*0602 DQBI*0301
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TYPE 1 DM ENVIROMENTAL FACTORS Viruses Viruses Mumps, Coxackie B4, retroviruse, rubella, cytomegalovirus, Epstein-Barr virus Diet Diet Cow’s milk (BSA) Nitrosamines (smoked and cured meat) Coffee Gluten and other proteins (experimental data) Stress Stress
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PROPOSED PATHOGENESIS OF TYPE 1 DIABETES MELLITUS Normal islet ?Viral infection in pancreatic beta cells Secretion of interferon- by pancreatic -cells Hyperexpression of class I MHC antigen within islets Insulitis Selective destruction of -cells Insulin-deficient islet
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DIABETES MELLITUS PATHOGENESIS OF TYPE 1 DM Markers of the immune destruction of the -cell islet cell autoantibodies (icas) autoantibodies to insulin (iaas) autoantibodies to glutamic acid decarboxylase (GAD 65 ) autoantibodies to the tyrosine phosphatases One and usually more of these autoantibodies are present in 85–90% of individuals when fasting hyperglycemia is initially detected.
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DIABETES MELLITUS PHASES OF TYPE 1 DM DEVELOPMENT Geneticpredisposition ? Promoting factor factor OvertImmunologicalabnormalities Decrease in insulin secretion Symptomaticdiabetes Normal NormalglycemiaC-peptidepresentC-peptideabsent Age (years) Beta cells mass
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DIABETES MELLITUS PATHOGENESIS OF TYPE 2 DM HYPERGLYCEMIA DUE TO A RELATIVE DEFICIENCY OF INSULIN RELATED TO INSULIN RESISTANCE AND BETA CELL DYSFUNCTION
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DIABETES MELLITUS PATHOGENESIS OF TYPE 2 DM GENETIC PREDISPOSITION RELATIVE INSULIN DEFICIENCY LOSS OF FIRST PHASE SECRETION DECREASED GLUT-2
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Insulin resistance genes Insulin secretion genes -cells number genes Obesity genes ObesityDiet Physical activity Age Time Decreased insulin secretion Desensitisation of -cells for glucose Increased insulin secretion Increased insulin secretion Decreased insulin and glucose sensitivity Decreased insulin and glucose sensitivity Genetic factors Enviromental factors DMtype II II
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DIABETES MELLITUS MECHANISMS OF INSULIN RESISTANCE DECREASE IN INSULIN RECEPTORS DECREASE IN INSULIN BINDING POST-RECEPTOR DEFECTS DECREASE IN GLUT-4 INCREASED HEPATIC GLUCOSE PRODUCTION
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DIABETES MELLITUS Characteristics TYPE 1 DM TYPE 2 DM Duration of symptoms weeks months to years Complications at diagnosis No20% Age at onset < 40 yrs > 50 yrs AutoantibodiesYesNo Family History ---Strong ObesityRarelyOften History of DKA CommonRare
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DIABETES MELLITUS OTHER SPECIFIC TYPES OF DIABETES Genetic defects of the –cell Genetic defects in insulin action Diseases of the exocrine pancreas Endocrinopathies Drug- or chemical-induced diabetes Infections Uncommon forms of immune-mediated diabetes Other genetic syndromes sometimes associated with diabetes.
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DIABETES MELLITUS GESTATIONAL DIABETES any degree of glucose intolerance with onset or first recognition during pregnancy. 3% of pregnancies onset: 24-28 th week of gestation risk factors previous gestational dm obesity previous macrosomia
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DIABETES MELLITUS GESTATIONAL DIABETES CONSEQUENCES: increased perinatal mortality macrosomia neonatal hyperbilirubinaemia hypocalcemiahypoglycemia obesity in children
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DIABETES MELLITUS GLUCOSE INTOLERANCE IMPAIRED GLUCOSE TOLERANCE IMPAIRED FASTING GLUCOSE
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DIABETES MELLITUS CLINICAL MANIFESTATIONS HYPERGLYCEMIA Normal Fasting Glucose: 70-110 mg/dL Absolute/relative deficiency of insulin Impaired glucose uptake Increased production
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DIABETES MELLITUS CLINICAL MANIFESTATIONS HYPERGLYCEMIA Assessment of severity Mild: 126-200 mg/dL Moderate: 200-300 mg/dL Severe: 300-500 mg/dL Very severe: > 500 mg/dL Also evaluate symptoms
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DIABETES MELLITUS CLINICAL MANIFESTATIONS GLUCOSURIA When ability of kidney to reabsorb glucose is exceeded POLYURIA Due to osmotic diuresis from glucose not reabsorbed POLYDIPSIA Response to increase fluid loss
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DIABETES MELLITUS CLINICAL MANIFESTATIONS POLYPHAGIA Due to proteolysis/gluconeogenesis WEIGHT LOSS Excretion of ingested calories Metabolism of fat/proteins Fluid loss WEAKNESS, FATIGUE Decreased ATP production
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DIABETES MELLITUS CLINICAL MANIFESTATIONS OTHER SYMPTOMS acetone breath nausea, vomiting abdominal pain Kussmaul respirations
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DIABETES MELLITUS DIAGNOSIS 3 CRITERIA BY WHICH DIAGNOSIS IS MADE: casual PG > 200 mg/dL + symptoms FPG 126 mg/dL 2-Hr PG 200 mg/dL during OGTT confirm on a subsequent day confirm on a subsequent day
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DIABETES MELLITUS DIAGNOSIS ORAL GLUCOSE TOLERANCE TEST (OGTT) SHOULD BE PERFORMED IN A MORNING USE A GLUCOSE LOAD CONTAINING THE EQUIVALENT OF 75 G ANHYDROUS GLUCOSE DISSOLVED IN 250-300 ML OF WATER.
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DIABETES MELLITUS DIAGNOSIS IMPAIRED GLUCOSE TOLERANCE 2-hr PG: 140-200 mg/dL 2-hr PG: 140-200 mg/dL IMPAIRED FASTING GLUCOSE FPG = 110 –125 mg/dL FPG = 110 –125 mg/dL
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DIABETES MELLITUS DIAGNOSIS GESTATIONAL DIABETES Screening test during 24-28 th week of pregnancy
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DIABETES MELLITUS 56 year-old male in office feeling tired, less energy x 6 months UA: 2+ glucose FPG = 140 mg/dL Fulfill the criteria for diabetes? Why or Why not? Type of diabetes
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