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Lethal atherosclerosis associated with abnormal plasma and tissue sterol composition in sitosterolemia with
Insights
Sitosterolemia with xanthomatosis leads to premature deposition of plant sterols and saturated stanols in tissues, accelerating atherosclerosis. This study compared sterol deposition in a sitosterolemic subject versus a control.
Area of Science:
- Biochemistry
- Cardiovascular Medicine
- Genetics
Background:
- Sitosterolemia is a rare genetic disorder characterized by impaired transport of plant sterols from tissues back into the plasma.
- Elevated plant sterol levels in plasma and tissues are associated with increased risk of cardiovascular disease.
Abstract:
Tissue sterol composition was determined in an 18-year-old male with sitosterolemia with xanthomatosis who died suddenly and whose coronary and aortic vessels showed extensive atherosclerosis and, for comparison, in an 18-year-old male with minimal atherosclerosis who died accidently. Sterols in the control tissues (plasma, erythrocytes, cardiac muscle, lung, liver, aorta, and brain) contained cholesterol with only trace amounts of cholestanol. In contrast, sterols in corresponding tissues of the sitosterolemic subject (except brain) were composed of cholesterol, increased amounts of plant sterols, campesterol and sitosterol, and 5 alpha-saturated stanols, cholestanol, 5 alpha-campestanol, and 5 alpha-sitostanol, that were deposited in approximately the same ratio as present in plasma. However, sitosterolemic brain sterol composition resembled that of the control brain with cholesterol and only trace amounts (less than 1%) of cholestanol and phytosterols. The sitosterolemic aorta was extensively atherosclerotic and contained more than twice the quantity of sterols as the control aorta (5.6 mg/g versus 2.6 mg/g) with increased amounts of cholesterol, plant sterols, and 5 alpha-saturated stanols. These results indicate that cholesterol, plant sterols, and 5 alpha-stanols are deposited prematurely and are associated with accelerated atherosclerosis in subjects with sitosterolemia with xanthomatosis.