
Hyperlipoproteinemia
DISORDERS OF PLASMA LIPOPROTEINS (DYSLIPOPROTEINEMIA)
HYPERLIPOPROTEINEMIA
- There is an elevation of circulating lipoproteins.
- Fredrickson’s Classification of hyperlipoproteinemia are of 5 types-
I. Type I (familial lipoprotein lipase deficiency)
- Deficiency of lipoprotein lipase or apo C-II.
- Elevated levels of chylomicrons
- Triglyceride level is increased.
Clinical features-
- Acute pancreatitis
- Eruptive xanthoma
- Hepatosplenomegaly
Treatment-
- Gene therapy.
II. Type II- 2 types
-
Type IIa ( familial hypercholesterolemia)
- Due to deficiency of functional LDL receptors.
- LDL cholesterol is raised.
- Four classes of mutation have been defined for LDL receptors-
- Class I (most common)- loss of receptor synthesis
- Class II- receptors are synthesized but not translocated to cell membrane
- Class III- Receptor binds poorly to apo B-100
- Class IV- receptor binds to apo B-100 but no interilization.
2. Type IIb ( familial combined hyperlipedimia)
- LDL and VLDL are increased
III. Type III (familial dysbetalipoproteinemia)- Broad β- disease
- Due to abnormalities in apo- E
- Chylomicron remnants and VLDL remnants(IDL) are increased.
- Triglyceride and cholesterol increased.
IV. Type IV (familial hypertriglyceridemia)
- Deficiency of apo-A- V.
- Increased VLDL level
V. Type V (Endogenous hypertriglyceridemia)
- Increased VLDL and chylomicrons.
Exam Question
- Fredrickson’s Classification of hyperlipoproteinemia are of 5 types
- Type I (familial lipoprotein lipase deficiency)- Deficiency of lipoprotein lipase or apo C-II.
– Elevated levels of chylomicrons
- Type IIa ( familial hypercholesterolemia)- Due to deficiency of functional LDL receptors.
- Four classes of mutation have been defined for LDL receptors- Class I (most common)- loss of receptor synthesis
- Type IIb ( familial combined hyperlipedimia)- LDL and VLDL are increased
- Type III (familial dysbetalipoproteinemia)- Broad β- disease- Due to abnormalities in apo- E and Chylomicron remnants and VLDL remnants(IDL) are increased.
- Type IV (familial hypertriglyceridemia)- Deficiency of apo-A- V.
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