USE OF 3-HYDROXY-3-METHYLGLUTARYL COENZYME A REDUCTASE INHIBITORS IN VARIOUS FORMS OF DYSLIPIDEMIA

被引:7
作者
GRUNDY, SM
VEGA, GL
GARG, A
机构
[1] UNIV TEXAS,SW MED CTR,CTR HUMAN NUTR,DEPT BIOCHEM,DALLAS,TX 75235
[2] UNIV TEXAS,SW MED CTR,CTR HUMAN NUTR,DEPT CLIN NUTR,DALLAS,TX 75235
关键词
D O I
10.1016/0002-9149(90)90438-7
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The inhibitors of 3-hydroxy-3-methylglutaryl coenzyme A (HMG CoA) reductase are highly effective in treating severe elevations of serum cholesterol, and are being widely used for this purpose. In our laboratory, these drugs have been used for the treatment of other forms of dyslipidemia including primary moderate hypercholesterolemia, primary mixed hyperlipidemia, diabetic dyslipidemia, hyperlipidemia of the nephrotic syndrome, and primary hypoalphalipoproteinemia. In these conditions, the HMG CoA reductase inhibitors proved effective in substantially decreasing levels of both low-density lipoproteins and very low density lipoproteins, as well as apolipoprotein B. In some patients, they may even increase levels of high-density lipoproteins. The primary mode of action of HMG CoA reductase inhibitors appears to be to increase the synthesis of hepatic receptors for lipoproteins containing apolipoprotein B, although a reduction in synthesis of these lipoproteins has not been ruled out with certainty. Regardless of mechanisms, drugs of this type appear to have the potential for effective therapy of various forms of dyslipidemia beyond primary severe hypercholesterolemia. © 1990.
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收藏
页码:B31 / B38
页数:8
相关论文
共 41 条
[1]   MEVINOLIN AND COLESTIPOL STIMULATE RECEPTOR-MEDIATED CLEARANCE OF LOW-DENSITY LIPOPROTEIN FROM PLASMA IN FAMILIAL HYPERCHOLESTEROLEMIA HETEROZYGOTES [J].
BILHEIMER, DW ;
GRUNDY, SM ;
BROWN, MS ;
GOLDSTEIN, JL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1983, 80 (13) :4124-4128
[2]   A RECEPTOR-MEDIATED PATHWAY FOR CHOLESTEROL HOMEOSTASIS [J].
BROWN, MS ;
GOLDSTEIN, JL .
SCIENCE, 1986, 232 (4746) :34-47
[3]   COMBINATION-DRUG THERAPY FOR FAMILIAL COMBINED HYPERLIPIDEMIA [J].
EAST, C ;
BILHEIMER, DW ;
GRUNDY, SM .
ANNALS OF INTERNAL MEDICINE, 1988, 109 (01) :25-32
[4]   HELSINKI HEART-STUDY - PRIMARY-PREVENTION TRIAL WITH GEMFIBROZIL IN MIDDLE-AGED MEN WITH DYSLIPIDEMIA - SAFETY OF TREATMENT, CHANGES IN RISK-FACTORS, AND INCIDENCE OF CORONARY HEART-DISEASE [J].
FRICK, MH ;
ELO, O ;
HAAPA, K ;
HEINONEN, OP ;
HEINSALMI, P ;
HELO, P ;
HUTTUNEN, JK ;
KAITANIEMI, P ;
KOSKINEN, P ;
MANNINEN, V ;
MAENPAA, H ;
MALKONEN, M ;
MANTTARI, M ;
NOROLA, S ;
PASTERNACK, A ;
PIKKARAINEN, J ;
ROMO, M ;
SJOBLOM, T ;
NIKKILA, EA .
NEW ENGLAND JOURNAL OF MEDICINE, 1987, 317 (20) :1237-1245
[5]   MANAGEMENT OF DYSLIPIDEMIA IN NIDDM [J].
GARG, A ;
GRUNDY, SM .
DIABETES CARE, 1990, 13 (02) :153-169
[6]   LOVASTATIN FOR LOWERING CHOLESTEROL LEVELS IN NON-INSULIN-DEPENDENT DIABETES-MELLITUS [J].
GARG, A ;
GRUNDY, SM .
NEW ENGLAND JOURNAL OF MEDICINE, 1988, 318 (02) :81-86
[7]   GEMFIBROZIL ALONE AND IN COMBINATION WITH LOVASTATIN FOR TREATMENT OF HYPERTRIGLYCERIDEMIA IN NIDDM [J].
GARG, A ;
GRUNDY, SM .
DIABETES, 1989, 38 (03) :364-372
[8]   HYPERLIPIDEMIA IN CORONARY HEART-DISEASE .2. GENETIC ANALYSIS OF LIPID-LEVELS IN 176 FAMILIES AND DELINEATION OF A NEW INHERITED DISORDER, COMBINED HYPERLIPIDEMIA [J].
GOLDSTEIN, JL ;
SCHROTT, HG ;
HAZZARD, WR ;
BIRMAN, EL ;
MOTULSKY, AG .
JOURNAL OF CLINICAL INVESTIGATION, 1973, 52 (07) :1544-1568
[9]  
GOLDSTEIN JL, 1983, METABOLIC BASIS INHE, P672
[10]   LOVASTATIN IN THE TREATMENT OF MULTIFACTORIAL HYPERLIPIDEMIA ASSOCIATED WITH PROTEINURIA [J].
GOLPER, TA ;
ILLINGWORTH, DR ;
MORRIS, CD ;
BENNETT, WM .
AMERICAN JOURNAL OF KIDNEY DISEASES, 1989, 13 (04) :312-320