Home LiteratureArticle Details
PMID: 172531 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Reduction in cholesterol and low density lipoprotein synthesis after portacaval shunt surgery in a patient with homozygous familial hypercholesterolemia.

The Journal of clinical investigation ·Vol. 56 ·No. 6 ·1975-12-00 ·Pages 1420-30

Bilheimer DW, Goldstein JL, Grundy SM, Brown MS

Abstract

The turnover of 125I-labeled low density lipoprotein (LDL) and the total body balance of cholestrol were studied in a 6-yr-old girl with the homozygous form of familial hypercholesterolemia (FH) before and after the surgical creation of an end-to-side portacaval shunt. The results were compared with those of similar studies simultaneously performed in untreated patients with the heterozygous form of FH and with the results of earlier studies performed on normolipidemic subjects. Before shunt surgery, the rate of synthesis of LDL in the FH homozygote (mg/kg per day) was fourfold higher than in normolipidemic subjects and twofold higher than in her heterozygous mother. The fractional catabolic rate for LDL in the homozygote was decreased to 33% of normal control values. The rate of cholesterol synthesis, estimated by chemical sterol balance, was higher in the FH homozygote than in two FH heterozygotes of similar age studied simultaneously. When considered in relation to the markedly elevated level of plasma cholesterol, the observed rate of cholesterol synthesis in the FH homozygote was inappropriately elevated. Bile acid production was normal in all three children. 5 mo after shunt surgery, the rate of LDL synthesis in the homozygote had declined by 48% as compared with the preoperative value, and this caused a 39% drop in the plasma LDL cholesterol level despite a 17% reduction in the fractional catabolic rate of the lipoprotein. The rate of cholesterol synthesis fell by 62% as compared with the preoperative value. The findings of an inappropriately elevated rate of production of both cholesterol and LDL as well as a reduced fractional catabolic rate for the lipoprotein in the untreated FH homozygote are consistent with results of studies in cultured fibroblasts indicating that the primary genetic defect in FH involves a deficiency in a cell-surface receptor for LDL that regulates both cholesterol synthesis and LDL degradation. Although the mechanism for the decline in production of cholesterol and LDL after portacaval shunt surgery is unknown, it was observed that these changes were associated with marked increases in the plasma concentrations of bile acids and glucagon.

MeSH Terms
Adult Arginine Bile Acids and Salts/blood Child Cholesterol/biosynthesis Female Glucagon/blood Homozygote Humans Hypercholesterolemia/blood,genetics,surgery Lipoproteins, LDL/biosynthesis,blood Lipoproteins, VLDL/blood Male Portacaval Shunt, Surgical Triglycerides/blood
Chemicals
Bile Acids and Salts Lipoproteins, LDL Lipoproteins, VLDL Triglycerides Glucagon Arginine Cholesterol
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Bilheimer D W
Goldstein J L
Grundy S M
Brown M S
References (35)
35 references, click to expand
  1. Cholesterol synthesis by cultured fibroblasts: decreased feedback inhibition in familial hypercholesterolemia.
    J Lab Clin Med. 1974 Jan;83(1):7-15 PMID: 4855550
  2. The regulation of cholesterol metabolism as related to familial hypercholesterolaemia.
    Sci Basis Med Annu Rev. 1970;:230-59 PMID: 4920181
  3. Studies of pancreatic alpha cell function in normal and diabetic subjects.
    J Clin Invest. 1970 Apr;49(4):837-48 PMID: 4986215
  4. An evaluation of four methods for measuring cholesterol absorption by the intestine in man.
    J Lipid Res. 1971 Mar;12(2):221-32 PMID: 5108132
  5. Cholesterol metabolism in patients with coronary heart disease.
    Ann Clin Res. 1971 Dec;3(6):313-22 PMID: 5156891
  6. The metabolism of cholesterol in two hypercholesterolaemic patients treated with cholestyramine.
    Clin Sci. 1969 Oct;37(2):443-54 PMID: 5359001
  7. Interruption of the enterohepatic circulation of bile acids in man: comparative effects of cholestyramine and ileal exclusion on cholesterol metabolism.
    J Lab Clin Med. 1971 Jul;78(1):94-121 PMID: 5569253
  8. Studies in the metabolism of cholesterol in subjects with normal plasma cholesterol levels and in patients with essential hypercholesterolaemia.
    Clin Sci. 1967 Apr;32(2):201-13 PMID: 6022815
  9. Cholesterol ester formation in cultured human fibroblasts. Stimulation by oxygenated sterols.
    J Biol Chem. 1975 May 25;250(10):4025-7 PMID: 1126942
  10. The distribution and chemical composition of ultracentrifugally separated lipoproteins in human serum.
    J Clin Invest. 1955 Sep;34(9):1345-53 PMID: 13252080
  11. Simple rapid microtechnic for serum total cholesterol.
    Am J Clin Pathol. 1957 May;27(5):583-8 PMID: 13435243
  12. The theory of tracer experiments with 131I-labelled plasma proteins.
    Phys Med Biol. 1957 Jul;2(1):36-53 PMID: 13484460
  13. Distribution and degradation of human serum albumin labeled with I 131 by different techniques.
    Ann N Y Acad Sci. 1957 Aug 30;70(1):109-21 PMID: 13488259
  14. Studies on the synthesis and secretion of serum lipoproteins by rat liver slices.
    J Clin Invest. 1960 Oct;39:1560-9 PMID: 13738935
  15. Estimation of cholesterol in serum by means of improved technics.
    Tech Bull Regist Med Technol. 1963 Feb;33:19-23 PMID: 13929259
  16. Protein measurement with the Folin phenol reagent.
    J Biol Chem. 1951 Nov;193(1):265-75 PMID: 14907713
  17. Familial hypercholesterolemia. A genetic regulatory defect in cholesterol metabolism.
    Am J Med. 1975 Feb;58(2):147-50 PMID: 163579
  18. Role of the low density lipoprotein receptor in regulating the content of free and esterified cholesterol in human fibroblasts.
    J Clin Invest. 1975 Apr;55(4):783-93 PMID: 164482
  19. The metabolism of the apoprotein of plasma low density lipoprotein in familial hyperbetalipoproteinaemia in the homozygous form.
    Atherosclerosis. 1975 Mar-Apr;21(2):283-98 PMID: 165827
  20. Effects of polyunsaturated fats on lipid metabolism in patients with hypertriglyceridemia.
    J Clin Invest. 1975 Feb;55(2):269-82 PMID: 233943
  21. Genetic heterogeneity in familial hypercholesterolemia: evidence for two different mutations affecting functions of low-density lipoprotein receptor.
    Proc Natl Acad Sci U S A. 1975 Mar;72(3):1092-6 PMID: 236556
  22. Receptor-dependent hydrolysis of cholesteryl esters contained in plasma low density lipoprotein.
    Proc Natl Acad Sci U S A. 1975 Aug;72(8):2925-9 PMID: 241998
  23. Portacaval shunt in hyperlipoproteinaemia.
    Lancet. 1973 Oct 27;2(7835):940-4 PMID: 4126562
  24. Electrophoretic separation of plasma lipoproteins in agarose gel.
    J Lipid Res. 1968 Nov;9(6):693-700 PMID: 4176473
  25. Practical methods for plasma lipoprotein analysis.
    Adv Lipid Res. 1968;6:1-68 PMID: 4179999
  26. The metabolism of very low density lipoprotein proteins. I. Preliminary in vitro and in vivo observations.
    Biochim Biophys Acta. 1972 Feb 21;260(2):212-21 PMID: 4335139
  27. The metabolism of low density lipoprotein in familial type II hyperlipoproteinemia.
    J Clin Invest. 1972 Jun;51(6):1528-36 PMID: 4336943
  28. Familial hypercholesterolemia: identification of a defect in the regulation of 3-hydroxy-3-methylglutaryl coenzyme A reductase activity associated with overproduction of cholesterol.
    Proc Natl Acad Sci U S A. 1973 Oct;70(10):2804-8 PMID: 4355366
  29. Regulation of 3-hydroxy-3-methylglutaryl coenzyme A reductase activity in cultured human fibroblasts. Comparison of cells from a normal subject and from a patient with homozygous familial hypercholesterolemia.
    J Biol Chem. 1974 Feb 10;249(3):789-96 PMID: 4359767
  30. Familial hypercholesterolemia: defective binding of lipoproteins to cultured fibroblasts associated with impaired regulation of 3-hydroxy-3-methylglutaryl coenzyme A reductase activity.
    Proc Natl Acad Sci U S A. 1974 Mar;71(3):788-92 PMID: 4362634
  31. Expression of the familial hypercholesterolemia gene in heterozygotes: mechanism for a dominant disorder in man.
    Science. 1974 Jul 5;185(4145):61-3 PMID: 4366052
  32. Binding and degradation of low density lipoproteins by cultured human fibroblasts. Comparison of cells from a normal subject and from a patient with homozygous familial hypercholesterolemia.
    J Biol Chem. 1974 Aug 25;249(16):5153-62 PMID: 4368448
  33. The metabolism of low-density lipoprotein in a patient with familial hyperbetalipoproteinaemia.
    Clin Sci Mol Med. 1974 Dec;47(6):635-8 PMID: 4375014
  34. Expression of the familial hypercholesterolemia gene in heterozygotes: model for a dominant disorder in man.
    Trans Assoc Am Physicians. 1974;87:120-31 PMID: 4376290
  35. Postprandial serum bile acid for the detection of hepatobiliary disease.
    JAMA. 1973 Jul 16;225(3):292-3 PMID: 4740377
Article Info
Journal
The Journal of clinical investigation
Abbr.
J Clin Invest
ISSN
0021-9738
Published
1975-12-00
Pages
1420-30
Language
English
Region
United States
NLM ID
7802877
PMCID
PMC333120
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]