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1-30 Lipids

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Questions in this quiz (30)

  1. 16.1. Select the regulatory effects of cholesterol delivered to cells via LDL receptors:
    1. Aa) inhibits the enzyme hydroxymethylglutaryl-CoA reductase (HMG)
    2. Bb) inhibits the enzyme acylcholesterol acyl transferase (ACAT)
    3. Cc) inhibits the synthesis of LDL-receptors
    4. Dd) activates the enzyme lecithincholesterol acyl transferase (LCAT)
    5. Ee) activates cholesterol ester transfer protein (CETP)
  2. 26.2. Select the correct statements regarding lipoprotein(a):
    1. Aa) represents a lipoprotein with an antiatherogenic role
    2. Bb) possesses structural analogy with HDL
    3. Cc) contains a lot of cholesterol
    4. Dd) contains apo B-100 and apo(a)
    5. Ee) is catabolized by means of LDL-receptors
  3. 36.3. Select the most common causes of familial hyperchylomicronemia (HLP type I):
    1. Aa) lecithincholesterol acyl transferase (LCAT) enzyme deficiency
    2. Bb) lipoprotein lipase (LPL) deficiency
    3. Cc) apolipoprotein C-II deficiency
    4. Dd) LDL-receptor mutations
    5. Ee) apolipoprotein E polymorphism
  4. 46.4. Select lipid profile changes characteristic of familial hyperchylomicronemia
    (HLP type I):
    1. Aa) increase in plasma values of apoA
    2. Bb) severe hypertriglyceridemia
    3. Cc) increase in HDL-cholesterol concentration
    4. Dd) the presence of chylomicronsto fastin blood
    5. Ee) lack of VLDL and LDL
  5. 56.5. Select the hereditary defects associated with familial hypercholesterolemia:
    1. Aa) ABCA1 membrane transporter defect
    2. Bb) apolipoprotein A-II deficiency
    3. Cc) apolipoprotein B-100 deficiency
    4. Dd) LDL-receptor mutations
    5. Ee) mutations with "loss of function" of PCSK9 (proprotein convertase subtilisin/kexin type
  6. 66.6. Select lipid profile changes characteristic of familial hypercholesterolemia:
    1. Aa) high level of HDL-cholesterol
    2. Bb) increased values of LDL-cholesterol
    3. Cc) low concentration of apoB-100
    4. Dd) high concentrations of total cholesterol
    5. Ee) lack of chylomicrons and VLDL
  7. 76.7. Select the correct statements regarding sitosterolemia:
    1. Aa) is caused by high expression of ABCA-1
    2. Bb) is determined by ABCG-5 and ABCG-8 deficiency
    3. Cc) is associated with a high cardiovascular risk
    4. Dd) is characterized by an increase in the plasma concentration of plant sterols and cholesterol
    5. Ee) a distinctive clinical sign of the disease is moderate hemolysis
  8. 86.8. Regarding LCAT (lecithincholesterolacyl transferase) enzyme deficiency, the statements are
    correct:
    1. Aa) is characterized by the excessive accumulation of triglycerides in the tissues
    2. Bb) is characterized by the excessive accumulation of cholesterol esters in HDL
    3. Cc) leads to early atherosclerosis
    4. Dd) is accompanied by a decrease in the concentration of HDL in the blood
    5. Ee) is clinically manifested by acute pancreatitis attacks
  9. 96.9. Select the correct answers regarding familial a-beta-lipoproteinemia:
    1. Aa) is caused by defective synthesis of apoproteins B
    2. Bb) is determined by the high expression of LDL-receptors
    3. Cc) is characterized by hypertriglyceridemia
    4. Dd) is characterized by malabsorption of lipids and fat-soluble vitamins
    5. Ee) leads to early atherosclerosis
  10. 106.10. Select the correct answers regarding familial an-alpha-lipoproteinemia (Tangier disease):
    1. Aa) is determined by the hereditary defect of the ABCA-1 transporter
    2. Bb) can be caused by mutations of ABCG-5 and ABCG-8 transporters
    3. Cc) causes the accumulation of cholesterol esters in the tissues
    4. Dd) is characterized by low plasma values of LDL-cholesterol
    5. Ee) presents antiatherogenic protection

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Quiz on 1-30 Lipids, created by ppppp oooo on 08/05/2026.
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