THE EFFECT OF CHOLESTEROL-LOWERING AGENTS ON HEPATIC AND PLASMA-CHOLESTEROL IN NIEMANN-PICK DISEASE TYPE-C

被引:84
作者
PATTERSON, MC
DIBISCEGLIE, AM
HIGGINS, JJ
ABEL, RB
SCHIFFMANN, R
PARKER, CC
ARGOFF, CE
GREWAL, RP
YU, K
PENTCHEV, PG
BRADY, RO
BARTON, NW
机构
[1] NINCDS, DEV & METAB NEUROL BRANCH, BLDG 10, ROOM 3D03, BETHESDA, MD 20892 USA
[2] NINCDS, BIOMETRY & FIELD STUDIES BRANCH, BETHESDA, MD 20892 USA
[3] NATL INST DIABET & DIGEST & KIDNEY DIS, LIVER DIS SECT, BETHESDA, MD USA
[4] NATL INST DIABET & DIGEST & KIDNEY DIS, DIGEST DIS BRANCH, BETHESDA, MD USA
关键词
D O I
10.1212/WNL.43.1_Part_1.61
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Niemann-Pick disease type C (NP-C) is a neurovisceral lipidosis characterized by defective intracellular trafficking of cholesterol and lysosomal accumulation of unesterified cholesterol, believed to be an offending metabolite. We studied the effect of cholesterol-lowering agents on hepatic and plasma cholesterol levels in NP-C by randomly assigning 25 patients with NP-C to one of five treatment regimens containing different combinations of cholestyramine, lovastatin, nicotinic acid, or dimethyl sulfoxide (DMSO). Unesterified cholesterol content was measured in liver biopsies before and after 4 months' treatment. All drug regimens except DMSO alone reduced hepatic and plasma cholesterol levels. Toxicity was limited and did not prevent any patient from completing the study. The combination of cholestyramine, lovastatin, and nicotinic acid lowered cholesterol levels in liver and blood with minimal side effects. A controlled clinical study will be necessary to determine if this regimen influences the rate of neurologic progression.
引用
收藏
页码:61 / 64
页数:4
相关论文
共 16 条
[1]  
BAROWN MS, 1990, GOODMAN GILMANS PHAR, P874
[2]   TYPE-C NIEMANN-PICK DISEASE - LOW-DENSITY LIPOPROTEIN UPTAKE IS ASSOCIATED WITH PREMATURE CHOLESTEROL ACCUMULATION IN THE GOLGI-COMPLEX AND EXCESSIVE CHOLESTEROL STORAGE IN LYSOSOMES [J].
BLANCHETTEMACKIE, EJ ;
DWYER, NK ;
AMENDE, LM ;
KRUTH, HS ;
BUTLER, JD ;
SOKOL, J ;
COMLY, ME ;
VANIER, MT ;
AUGUST, JT ;
BRADY, RO ;
PENTCHEV, PG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (21) :8022-8026
[3]   CLINICAL SPECTRUM OF NIEMANN-PICK DISEASE TYPE-C [J].
FINK, JK ;
FILLINGKATZ, MR ;
SOKOL, J ;
COGAN, DG ;
PIKUS, A ;
SONIES, B ;
SOONG, B ;
PENTCHEV, PG ;
COMLY, ME ;
BRADY, RO ;
BARTON, NW .
NEUROLOGY, 1989, 39 (08) :1040-1049
[4]   IMPORTANCE OF BETA, TYPE-II ERROR AND SAMPLE-SIZE IN DESIGN AND INTERPRETATION OF RANDOMIZED CONTROL TRIAL - SURVEY OF 71 NEGATIVE TRIALS [J].
FREIMAN, JA ;
CHALMERS, TC ;
SMITH, H ;
KUEBLER, RR .
NEW ENGLAND JOURNAL OF MEDICINE, 1978, 299 (13) :690-694
[5]  
LOWRY OH, 1951, J BIOL CHEM, V193, P265
[6]   TYPE-C NIEMANN-PICK DISEASE - DIMETHYL-SULFOXIDE MODERATES ABNORMAL LDL-CHOLESTEROL PROCESSING IN MUTANT FIBROBLASTS [J].
MACKIE, EJB ;
DWYER, NK ;
VANIER, MT ;
SOKOL, J ;
MERRICK, HF ;
COMLY, ME ;
ARGOFF, CE ;
PENTCHEV, PG .
BIOCHIMICA ET BIOPHYSICA ACTA, 1989, 1006 (02) :219-226
[7]   COMPLEMENTARITY OF COLESTIPOL, NIACIN, AND LOVASTATIN IN TREATMENT OF SEVERE FAMILIAL HYPERCHOLESTEROLEMIA [J].
MALLOY, MJ ;
KANE, JP ;
KUNITAKE, ST ;
TUN, P .
ANNALS OF INTERNAL MEDICINE, 1987, 107 (05) :616-623
[8]  
MONTGOMERY DC, 1984, DESIGN ANAL EXPT, P59
[9]   REDUCTION OF SERUM CHOLESTEROL LEVELS AND BETA-LIPOPROTEIN CHOLESTEROL LEVELS BY NICOTINIC ACID [J].
PARSONS, WB ;
FLINN, JH .
ARCHIVES OF INTERNAL MEDICINE, 1959, 103 (05) :783-790
[10]  
PENTCHEV PG, 1986, J BIOL CHEM, V261, P2772