Lack of Effect of Cholesterol Esterase Inhibitor CVT-1 on Cholesterol Absorption and LDL cholesterol in Humans

被引:0
|
作者
Matthew S. Bosner
Andrew A. Wolff
Richard E. Ostlund
机构
[1] Washington University School of Medicine,Divisions of Cardiology, Department of Medicine
[2] Washington University School of Medicine,Divisions of Endocrinology, Diabetes and Metabolism, Department of Medicine
[3] CV Therapeutics,undefined
[4] Inc.,undefined
[5] Washington University School of Medicine,undefined
来源
Cardiovascular Drugs and Therapy | 1999年 / 13卷
关键词
cholesterol; cholesterol absorption; cholesterol esterase; clinical trial; mass spectrometry;
D O I
暂无
中图分类号
学科分类号
摘要
Two clinical trials were performed to test the hypothesis that CVT-1, a potent inhibitor of pancreatic cholesterol esterase, reduces percent cholesterol absorption and LDL cholesterol in humans. Measurements of cholesterol absorption were made with deuterated cholesterol tracers given orally and intravenously and detected in plasma by a new technique using negative ion mass spectrometry. Study 1 was a randomized, double-blind parallel study of CVT-1 treatment of doses of 0, 300, 1500, and 3000 mg/day in 19 subjects. Percent cholesterol absorption measured at baseline and again after 2 and 6 weeks showed no treatment effect and LDL cholesterol was unchanged. Study II was a randomized open-label crossover comparison between CVT-1 given as 1000 mg three times daily for 2 weeks and 187.5 mg hourly 16 hours/day for 2 weeks. Percent cholesterol absorption and plasma LDL cholesterol were not different between periods. We conclude that cholesterol esterase is not required for unesterified cholesterol absorption in human subjects.
引用
收藏
页码:449 / 454
页数:5
相关论文
共 50 条
  • [41] Degree of serum LDL cholesterol reduction by simvastatin and ezetimibe is dependent on baseline LDL cholesterol concentration but not on baseline values and changes of cholesterol synthesis and absorption parameters
    Luetjohann, Dieter
    Stellaard, Frans
    INTERNATIONAL JOURNAL OF CLINICAL PHARMACOLOGY AND THERAPEUTICS, 2024, 62 (07) : 295 - 306
  • [42] EFFECT OF LOVASTATIN ON CHOLESTEROL ABSORPTION IN CHOLESTEROL-FED RABBITS
    NIELSEN, LB
    STENDER, S
    KJELDSEN, K
    PHARMACOLOGY & TOXICOLOGY, 1993, 72 (03): : 148 - 151
  • [43] EFFECT OF MONOGLYCERIDES ON ABSORPTION OF CHOLESTEROL AND TURNOVER RATE OF CHOLESTEROL ESTERS
    PINTER, KG
    MILLER, ON
    HAMILTON, JG
    FEDERATION PROCEEDINGS, 1963, 22 (02) : 376 - &
  • [44] The effect of adjusting LDL-cholesterol for Lipoprotein(a)-cholesterol on the diagnosis of Familial Hypercholesterolaemia
    Thayabaran, D.
    Tsui, A. P. T.
    Ebmeier, S. J.
    Cegla, J.
    David, A.
    Jones, B.
    ATHEROSCLEROSIS PLUS, 2022, 49 : S3 - S3
  • [45] The effect of adjusting LDL-cholesterol for Lp(a)-cholesterol on the diagnosis of familial hypercholesterolaemia
    Thayabaran, Darmiga
    Tsui, Anson P. T.
    Ebmeier, Stefan
    Cegla, Jaimini
    David, Alessia
    Jones, Ben
    JOURNAL OF CLINICAL LIPIDOLOGY, 2023, 17 (02) : 244 - 254
  • [46] THE EFFECT OF UGTIA1 POLYMORPHISM ON ATORVASTAIN PHARMACOKINECTICS AND RESPONSE OF TOTAL CHOLESTEROL AND LDL CHOLESTEROL.
    Cho, S.
    Park, K.
    Chung, J.
    CLINICAL PHARMACOLOGY & THERAPEUTICS, 2012, 91 : S106 - S107
  • [47] Effect of absolute reduction in LDL cholesterol on cardiovascular events: Does final LDL cholesterol acheived matter?
    Rahilly, C. R.
    Gaziano, J.
    Scranton, R.
    VALUE IN HEALTH, 2006, 9 (06) : A340 - A341
  • [48] RICE BRAN OIL DECREASES PLASMA LDL CHOLESTEROL BY INHIBITING DIETARY-CHOLESTEROL ABSORPTION
    RONG, N
    AUSMAN, L
    NICOLOSI, R
    FASEB JOURNAL, 1994, 8 (04): : A162 - A162
  • [49] GENETIC-FACTORS REGULATE SERUM LDL CHOLESTEROL LEVEL AND CHOLESTEROL ABSORPTION IN FAMILIAL HYPERCHOLESTEROLEMIA
    GYLLING, H
    AALTOSETALA, K
    KONTULA, K
    MIETTINEN, TA
    ARTERIOSCLEROSIS, 1990, 10 (05): : A843 - A843
  • [50] Inhibition of cholesterol absorption with CP-148,623 lowers serum cholesterol in humans
    Harris, WS
    Windsor, SL
    Newton, FA
    Gelfand, RA
    CLINICAL PHARMACOLOGY & THERAPEUTICS, 1997, 61 (03) : 385 - 389