fkg sept 2012 lecture

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    DIABETES MELLITUS

    NINA TRISTINA

    DEPARTEMEN PATOLOGI KLINIK

    FKUP/RSHS BANDUNG

    2012

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    CARBOHYDRATE METABOLISM

    CARBOHYDRATE

    BLOOD

    GLUCOSE

    GLYCOGEN FFA TRIGLYCERIDE

    AMINO ACID

    PYRUVATE - LACTATE

    ENERGY ATP + H2O + CO2

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    NORMAL BLOOD SUGAR CONTROLE

    BY HORMONAL REGULATION

    BLOOD SUGAR (CONC.)

    1. INSULIN

    2. GLUCAGON

    3. THYROXINE

    4. GROWTH HORMONE

    5. A.C.T.H

    6. CORTICOSTEROID

    7. EPINEPHRINE

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    NORMAL BLOOD SUGAR CONTROL BY INTER-

    MEDIARY REGULATION:

    1. GLYCOGENESIS

    2. GLYCOGENOLYSIS3. GLUCONEOGENESIS

    4. GLUCOLYSIS

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    BLOOD GLUCOSE CONCENTRATION

    NORMAL DM

    1. FASTING 70-100mg/dl 126 mg/dl

    2. POST PRAN

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    DIABETES MELLITUS

    : IS CHARACTERIZED BY CHANGES IN THE

    METABOLISM OF EACH OF THE MAJOR BODY

    FUELS (CARBOHYDRATE - FAT AND PROTEIN)

    AND IS ASSOCIATED BY DISTURBANCES OF A

    VARIETY OF HORMONES.

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    1. URINE GLUCOSE2. BLOOD GLUCOSE (diagnostic)

    3. ORAL GLUCOSE TOLERANCE TEST (confirmatory test)

    4. IV- GLUCOSE TOLERANCE TEST (confirmatory test)

    5. HbA1C TEST (follow-up)

    6. FRUCTOSAMIN TEST (follow-up)

    7. C-PEPTIDE CONC (confirmatory test)

    8. URINARY KETON (complication)9. BLOOD KETON (complication)

    10. MICROALBUMIN IN URINE (complication)

    LABORATORY EXAMINATIONS

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    *Fasting plasma glucose(FPG)

    ADA- the screening test of choice

    *Random plasma glucose(RPG)

    (measuring plasma glucose without regard to the last food intake).

    RPG (8.9 mmol/L) or above to be abnormal

    *Oral glucose tolerance test(OGTT)(2 hours after ingestion of a glucose load of 75 g a plasma glucose value of 11.1

    mmol/L) or more is abnormal

    *Glycosylated hemoglobin(HbA1c)

    6,5%

    Urinalysis and fingerstick glucose not to be used in screening!!!

    SCREENING FOR TYPE II DIABETES

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    ORAL GLUCOSE TOLERANCE TEST

    (OGTT)

    100

    200

    300

    100

    200

    300

    1 2 30 1 2 30Hours Hours

    BG mg/dlNORMAL DM

    SEVERE

    MILD

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    PRE-ANALYTIC STEPS(contd.)

    Specimens handling :

    Glycolysis 7 mg/dl/h in WB w/o inhibitors

    At 4C 2 mg/dl/h will lost Bacterial contamination will decrease glucose

    level

    Delay time in serum containing blood clot :< 90 minutes

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    BLOOD GLUCOSE

    PRE-ANALYTIC STEPS (contd.)

    OGTT

    Diet : must consists of > 150g of carbohy-

    drate/day, over a period of 3 days

    Discontinue any drugs that can affect glucose

    plasma level 3 days before the test

    Fasting : 12 hours

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    BLOOD GLUCOSE

    PRE-ANALYTIC STEPS (contd.)OGTT A parallel urine sample must be taken for

    fasting glucose and ketone. A positive test strip

    results is a contraindication for OGTT

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    POST-ANALYTICAL STEPS

    INTERPRETATION :

    Normoglycemia

    Hyperglycemia

    Hypoglycemia

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    INTERFERING FACTORS :

    Falsely high : dextrose iv-infusion, steroids,

    stress, infection, caffeine, nicotine, -blockers,

    adrenal gland infection, total parenteralnutrition (TPN), diuretics, estrogen, phenytoin

    Falsely low : insulin, alcohol, anabolic steroids,OAD

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    Glycohemoglobin =Glycated Hemoglobin

    = Hb A1C = A1c

    - Not recomended for D/ of DM

    - 2011: ADA, D/ if 6.5%

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    RESULTS: HbA1c

    GOOD 2,5-6,0%

    FAIR 6,1-8,0%POOR > 8%

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    Criteria for testing for diabetes in asymptomatic

    adult individuals

    1. Testing should be considered in all adults

    who are overweight (BMI 25 kg/m2*)

    and have additional risk factors:

    physical inactivity

    first-degree relative with diabetes

    high-risk race/ethnicity (e.g., African American,Latino, Native American, Asian American, Pacific

    Islander)

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    A1C 5.7%, IGT, or IFG on previous testing

    other clinical conditions associated with insulin

    resistance (e.g., severe obesity, acanthosis

    nigricans)

    history of CVD

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    2. In the absence of the above criteria, testingfor diabetes should begin at age 45years.

    3. If results are normal, testing should be repeatedat least at 3-year intervals, with consideration of

    more frequent testing depending on initial results

    and risk status.