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Citations to this article

Elevated Cholesterol and Bile Acid Synthesis in a Young Patient with Homozygous Familial Hypercholesterolemia
Kathleen B. Schwarz, … , Scott M. Grundy, William E. Connor
Kathleen B. Schwarz, … , Scott M. Grundy, William E. Connor
Published September 1, 1979
Citation Information: J Clin Invest. 1979;64(3):756-760. https://doi.org/10.1172/JCI109520.
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Research Article

Elevated Cholesterol and Bile Acid Synthesis in a Young Patient with Homozygous Familial Hypercholesterolemia

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Abstract

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.

Authors

Kathleen B. Schwarz, Joseph Witztum, Gustav Schonfeld, Scott M. Grundy, William E. Connor

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Total citations by year

Year: 2017 2014 2000 1994 1991 1990 1989 1988 1986 1985 1984 1983 1982 1981 1980 1965 Total
Citations: 1 1 2 1 1 1 1 1 2 1 1 2 4 2 2 1 24
Citation information
This citation data is accumulated from CrossRef, which receives citation information from participating publishers, including this journal. Not all publishers participate in CrossRef, so this information is not comprehensive. Additionally, data may not reflect the most current citations to this article, and the data may differ from citation information available from other sources (for example, Google Scholar, Web of Science, and Scopus).

Citations to this article (24)

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

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