A 4-year trial of simvastatin in the treatment of patients with heterozygous familial hypercholesterolemia

被引:0
|
作者
Kitatani, M
Koizumi, J
Inazu, A
Kajinami, K
Mabuchi, H
机构
关键词
D O I
暂无
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
A study was conducted to determine the clinical efficacy and tolerability of simvastatin, an inhibitor of 3-hydroxy-3-methylglutaryl coenzyme A reductase in seven patients with heterozygous familial hypercholesterolemia (FH) (defined as primary hypercholesterolemia with tendon xanthoma or primary hypercholesterolemia without tendon xanthomas and at least one first-degree relative with familial hypercholesterolemia), These patients were administrated 10 mg/d of simvastatin for up to 4 years, Simvastatin significantly reduced levels of both total cholesterol and low-density lipoprotein cholesterol during treatment; respective reduction rates were 28% and 34% after 1 month and 32% and 40% after 4 years, Serum high-density lipoprotein cholesterol levels slightly and insignificantly increased, Serum triglyseride levels fell significantly by 24% at month 6, After this study, all xanthomas had reduced in size, No adverse events related to simvastatin were observed. We conclude that long-term simvastatin therapy is clinically useful and well tolerated in patients with FH.
引用
收藏
页码:62 / 71
页数:10
相关论文
共 50 条
  • [21] Similar response to simvastatin in patients heterozygous for familial hypercholesterolemia with mRNA negative and mRNA positive mutations
    Sijbrands, EJG
    Lombardi, MP
    Westendorp, RGJ
    Leuven, JAG
    Meinders, AE
    Van der Laarse, A
    Frants, RR
    Havekes, LM
    Smelt, AHM
    ATHEROSCLEROSIS, 1998, 136 (02) : 247 - 254
  • [22] The effects of lovastatin and simvastatin on the diurnal periodicity of plasma mevalonate concentrations in patients with heterozygous familial hypercholesterolemia
    Pappu, AS
    Illingworth, DR
    ATHEROSCLEROSIS, 2002, 165 (01) : 137 - 144
  • [23] Disparities in Diagnosis and Treatment of Heterozygous Familial Hypercholesterolemia
    Shustak, Rachel
    Perlstein, Abigail
    Artis, Amanda
    Zavez, Alexis
    Tam, Vicky
    Martino, Giordana
    Brothers, Julie
    CIRCULATION, 2024, 150
  • [24] A case of sitosterolemia misdiagnosed as familial hypercholesterolemia: A 4-year follow-up
    Wang, Wei
    Jiang, Long
    Chen, Pan-Pan
    Wu, Yue
    Su, Peng-Yu
    Wang, Lu-Ya
    JOURNAL OF CLINICAL LIPIDOLOGY, 2018, 12 (01) : 236 - 239
  • [25] Influence of simvastatin on LDL-subtypes in patients with heterozygous familial hypercholesterolemia and in patients with diabetes mellitus and mixed hyperlipoproteinemia
    Geiss, HC
    Schwandt, P
    Parhofer, KG
    EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES, 2002, 110 (04) : 182 - 187
  • [26] Alirocumab in Pediatric Patients With Heterozygous Familial Hypercholesterolemia
    Santos, Raul D.
    Wiegman, Albert
    Caprio, Sonia
    Cariou, Bertrand
    Averna, Maurizio
    Poulouin, Yann
    Scemama, Michel
    Manvelian, Garen
    Garon, Genevieve
    Daniels, Stephen
    JAMA PEDIATRICS, 2024, 178 (03) : 283 - 293
  • [27] Lipoprotein(a) metabolism in patients with heterozygous familial hypercholesterolemia
    Parhofer, KG
    Ritter, MM
    Geiss, C
    Schwandt, P
    ATHEROSCLEROSIS, 1997, 134 (1-2) : 146 - 146
  • [28] Colesevelam: In pediatric patients with heterozygous familial hypercholesterolemia
    Perry C.M.
    Pediatric Drugs, 2010, 12 (2) : 133 - 140
  • [29] Sitostanol ester margarine without and with simvastatin in dietary treatment or families heterozygous of familial hypercholesterolemia North Karelia deletion
    Vuorio, AF
    Gylling, H
    Turtola, H
    Kontula, K
    Miettinen, TA
    CIRCULATION, 1998, 98 (17) : 533 - 534
  • [30] COMBINATION TREATMENT WITH CHOLESTYRAMINE AND BEZAFIBRATE FOR HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA
    CURTIS, LD
    DICKSON, AC
    LING, KLE
    BETTERIDGE, J
    BRITISH MEDICAL JOURNAL, 1988, 297 (6642): : 173 - 175