Cholesterol balance studies were carried out twice in a young male patient with homozygous familial hypercholesterolemia. At 13 mo, cholesterol balance in this patient averaged 31.3 mg/kg per d, and bile acid excretion was 12.0 mg/kg per d; at 3 yr, results were similar, 27.3 and 15.5 mg/kg per d for cholesterol balance and bile acids, respectively. A normal boy of 3 yr was also studied for comparison with the second study in our patient. Cholesterol balance and bile acid outputs in the normal child were 11.5 and 3.3 mg/kg per d, respectively. Thus, in comparison with the normal child, the patient with homozygous familial hypercholesterolemia had a marked increase in synthesis of cholesterol and bile acids. Although synthesis of bile acids was high in this patient, the fraction of newly synthesized cholesterol converted into bile acids (40-56%) was in the normal range; this suggests that the enhanced output of bile acids was secondary to an increased synthesis of cholesterol and not to malabsorption of bile acids, which likely would have produced a higher fractional conversion. Although our patient has been studied at a younger age than any reported in the literature, two similar children 5 and 6 yr of age were also observed to have elevated cholesterol synthesis. This finding contrasts with those in older children with the homozygous as well as heterozygous forms of this disease who appear to have normal synthesis of cholesterol and bile acids. Therefore, increased synthesis of cholesterol seems to be characteristic of early homozygous familial hypercholesterolemia, and may be a manifestation of a loss of feedback inhibition of cholesterol synthesis secondary to an absence of specific cell-surface receptors for low density lipoproteins. However, as children with this disease grow older, other mechanisms may come into play to restore cholesterol synthesis to normal levels.
Kathleen B. Schwarz, Joseph Witztum, Gustav Schonfeld, Scott M. Grundy, William E. Connor
Title and authors | Publication | Year |
---|---|---|
Determination of Fecal Sterols Following a Diet with and without Plant Sterols
M Cuevas-Tena, A Alegría, MJ Lagarda |
Lipids | 2017 |
Treatment of homozygous familial hypercholesterolemia
M France, J Schofield, S Kwok, H Soran |
Clinical Lipidology | 2014 |
Inhibition of cholesterol synthesis by atorvastatin in homozygous familial hypercholesterolaemia
FJ Raal, AS Pappu, DR Illingworth, GJ Pilcher, AD Marais, JC Firth, MJ Kotze, TM Heinonen, DM Black |
Atherosclerosis | 2000 |
Sterol balance in the Smith-Lemli-Opitz syndrome: reduction in whole body cholesterol synthesis and normal bile acid production
RD Steiner, LM Linck, DP Flavell, DS Lin, WE Connor |
Journal of lipid research | 2000 |
ApoB metabolism in familial hypercholesterolemia. Inconsistencies with the LDL receptor paradigm
WR Fisher, LA Zech, PW Stacpoole |
Arteriosclerosis Thrombosis and Vascular Biology | 1994 |
Influence of short term dietary cholesterol and fat on human plasma Lp[a] and LDL levels
SA Brown, J Morrisett, , R Reeves, AM Gotto, W Patsch |
Journal of lipid research | 1991 |
Three different schedules of low-density lipoprotein apheresis compared with plasmapheresis in patients with homozygous familial hypercholesterolemia
GM Berger, JC Firth, P Jacobs, L Wood, AD Marais, A Horak |
The American Journal of Medicine | 1990 |
Reduction in plasma low-density lipoprotein cholesterol and urinary mevalonic acid by lovastatin in patients with heterozygous familial hypercholesterolemia
AS Pappu, DR Illingworth, S Bacon |
Metabolism | 1989 |
The Bile Acids: Chemistry, Physiology, and Metabolism
KD Setchell, D Kritchevsky, PP Nair |
1988 | |
Diversity in expression of heterozygous familial hypercholesterolemia. Characterization of a unique kindred
RA Levy, RE Ostlund, CF Semenkovich, JL Witztum |
Journal of Clinical Investigation | 1986 |
Long-term changes in cholesterol biosynthesis and the effect of plasmapheresis therapy in a hypercholesterolemia homozygote
RA Levy, RE Ostlund, AC Goldberg, SM Grundy |
Metabolism | 1986 |
Liver, Nutrition, and Bile Acids
G Galli, E Bosisio |
1985 | |
Homozygous familial hypercholesterolemia occurring with apoprotein E3 deficiency. Report of two cases
PJ Nestel, MF Reardon, NH Fidge |
Arteriosclerosis (Dallas, Tex.) | 1984 |
Long term steroid metabolism balance studies in subjects on cholesterol-free and cholesterol-rich diets: comparison between normal and hypercholesterolemic individuals
RC Maranhão, EC Quintão |
Journal of lipid research | 1983 |
An improved gas-liquid chromatographic method for the determination of fecal neutral sterols
M Arca, A Montali, S Ciocca, F Angelico, A Cantafora |
Journal of lipid research | 1983 |
Familial hypercholesterolemia. Evidence for a newly recognized mutation determining increased fibroblast receptor affinity but decreased capacity for low density lipoprotein in two siblings
RE Ostlund, RA Levy, JL Witztum, G Schonfeld |
Journal of Clinical Investigation | 1982 |
Cholesterol reduction by a high-glucose diet in a patient with homozygous familial hypercholesterolemia
PW Stacpoole, LL Swift, HL Greene, AE Slonim, RK Younger, IM Burr |
The American Journal of Medicine | 1982 |
The LDL Receptor Defect in Familial Hypercholesterolemia: Implications for Pathogenesis and Therapy
JL Goldstein, MS Brown |
Medical Clinics of North America | 1982 |
Characterization of lipoprotein in a kindred with familial hypercholesterolemia
W Patsch, R Ostlund, I Kuisk, R Levy, G Schonfeld |
Journal of lipid research | 1982 |
Elevated cholesterol and bile acid synthesis in an adult patient with homozygous familial hypercholesterolemia. Reduction by a high glucose diet
PW Stacpoole, SM Grundy, LL Swift, HL Greene, AE Slonim, IM Burr |
Journal of Clinical Investigation | 1981 |
Analysis of lipids and endothelial and smooth muscle cells of umbilical cord in familial homozygous hypercholesterolemia
RE Ostlund, SV Hajek, RA Levy, JL Witztum |
Metabolism | 1981 |
Structure, Immunology, and Cell Reactivity of Low Density Lipoprotein from Umbilical Vein of a Newborn Type II Homozygote
W Patsch, JL Witztum, R Ostlund, G Schonfeld |
Journal of Clinical Investigation | 1980 |
Successful plasmapheresis in a 4-year-old child with homozygous familial hypercholesterolemia
JL Witztum, JC Williams, R Ostlund, L Sherman, G Siccard, G Schonfeld |
The Journal of Pediatrics | 1980 |
Advances in Lipid Research
AM Scanu |
Advances in Lipid Research | 1965 |