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Questions and Answers

What is the target level for Serum Cystatin-C?

  • 0.50-0.60 mg/L
  • 0.78-0.86 mg/L (correct)
  • 0.90-1.00 mg/L
  • 1.10-1.20 mg/L
  • What is the most common cause of liver enzyme elevation in diabetic patients?

  • Autoimmune hepatitis
  • Non-alcoholic liver disease (NAFLD) (correct)
  • Alcoholic liver disease
  • Hemochromatosis
  • How often should patients with Type 1 Diabetes Mellitus (T1DM) have their Serum Cystatin-C measured?

  • Once every six months
  • Twice a year
  • Once a year after 5 years (correct)
  • Only when symptoms arise
  • What fasting target level is recommended for LDL cholesterol?

    <p>&lt; 2.60 mmol/L</p> Signup and view all the answers

    What is the role of HbA1c in diabetic patients?

    <p>To evaluate risk of chronic complications</p> Signup and view all the answers

    Why is routine monitoring of liver enzymes necessary in diabetes management?

    <p>To screen for treatable causes of chronic liver disease</p> Signup and view all the answers

    What is dyslipidemia a strong predisposition for in diabetic patients?

    <p>Cardiovascular complications</p> Signup and view all the answers

    When should the screening for liver enzymes begin in diabetes management?

    <p>With the start of drug therapy</p> Signup and view all the answers

    Which of the following statements is true regarding hsCRP?

    <p>It evaluates inflammation and cardiovascular disease risk</p> Signup and view all the answers

    What is a significant flaw in microalbuminuria detection in patients taking ACE inhibitors?

    <p>It becomes unreliable</p> Signup and view all the answers

    Study Notes

    Limitations of 1,5-AG

    • Low levels of 1,5-AG indicate hyperglycemia in the preceding 24 hours.
    • It is not reliable in patients with renal disease and gestational diabetes mellitus (GDM).

    Monitoring of Glycemic Control

    • Long-term monitoring methods include:
      • HbA1c
      • Glycated Albumin
      • Fructosamine
      • Advanced Glycation End-products (AGE)
      • C-peptide
      • Insulin

    Glycated Haemoglobin (HbA1c)

    • Non-enzymatic glucose attachment to hemoglobin signifies average glycemic control over 90-120 days.
    • Gold standard for monitoring diabetes mellitus (DM), sensitive to changes in the last month.
    • No fasting required for testing.
    • Decreasing HbA1c levels correlates with reduced risk for microvascular disease (37%), myocardial infarction (14%), and death (21%).
    • Should be measured 2-4 times per year in DM patients.

    Limitations of HbA1c

    • Results may be skewed by erythrocyte turnover, hemoglobinopathies, chronic kidney disease (CKD), or alcoholism.
    • It does not measure glycemic variability or hypoglycemia.
    • Levels increase with age, and there are racial disparities in results.
    • Less reliable in rapidly evolving Type 1 diabetes mellitus (T1DM).

    HbA1c and Plasma Glucose Relationship

    • Strong relationship exists between HbA1c and plasma glucose:
      • Average Plasma Glucose (mg/dL) = (HbA1c x 35.6) - 77.3
      • Average Plasma Glucose (mmol/L) = (HbA1c x 1.98) - 4.29

    Glycated Albumin and Fructosamine

    • Glycated Albumin and fructosamine measure glycemic state over 2-3 weeks, useful when HbA1c is unreliable.
    • Fructosamine indicates recent glycemic control changes.
    • Glycated albumin is advantageous for DM patients with CKD.

    Clinical Utility and Limitations of Glycated Albumin and Fructosamine

    • Useful in monitoring poorly controlled DM and predicting complications.
    • Limitations include underestimation in obesity and effects of systemic illness on serum proteins.

    C-peptide

    • C-peptide indicates insulin production, reflecting residual beta-cell function.
    • Helps assess insulin replacement adequacy and dosage adjustments.
    • Higher C-peptide levels correlate with lower complication rates in T1DM and better control in T2DM.
    • Distinguishes DM types: low in T1DM, high or normal in early T2DM.

    Detection and Management of Diabetic Complications

    • Acute Complications:
      • Diabetic Ketoacidosis (DKA)
      • Hyperglycemic Hyperosmolar State (HHS)
      • Hypoglycemia
      • Lactic acidosis
    • Chronic Complications:
      • Microvascular: nephropathy, neuropathy, retinopathy
      • Macrovascular: coronary heart disease, peripheral vascular disease, cerebrovascular disease

    Monitoring Acute Complications

    • Key tests for diagnosis include glucose, lactate, creatine kinase, electrolytes, and ketone levels.
    • Blood urea nitrogen (BUN) and creatinine levels monitor risk for acute kidney injury during DKA and HHS.
    • Liver enzymes (AST, ALT) track potential liver dysfunction associated with DKA and HHS.

    Monitoring Chronic Complications

    • Urine Albumin and ACR should target <30 mg/g for early nephropathy detection.
    • Serum creatinine and estimated glomerular filtration rate (eGFR) help assess kidney function.
    • Serum cystatin-C is more sensitive for renal impairment assessment in diabetics.
    • Monitor lipid profiles annually due to cardiovascular risk association.
    • Regular HbA1c testing helps identify risk for chronic complications related to DM.

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