Effects of Dietary Cholesterol and Simvastatin on Cholesterol Synthesis in Smith-Lemli-Opitz Syndrome

被引:37
作者
Chan, Yen-Ming [1 ]
Merkens, Louise S. [2 ]
Connor, William E. [3 ]
Roullet, Jean-Baptiste [2 ]
Penfield, Jennifer A. [2 ]
Jordan, Julia M. [4 ]
Steiner, Robert D. [2 ,4 ,5 ]
Jones, Peter J. H. [1 ]
机构
[1] Univ Manitoba, Richardson Ctr Funct Foods & Nutraceut, Winnipeg, MB R3T 6C5, Canada
[2] Oregon Hlth & Sci Univ, Dept Pediat, Portland, OR 97239 USA
[3] Oregon Hlth & Sci Univ, Dept Med, Portland, OR 97239 USA
[4] Oregon Hlth & Sci Univ, Oregon Clin & Translat Res Inst, Portland, OR 97239 USA
[5] Oregon Hlth & Sci Univ, Dept Mol & Med Genet, Portland, OR 97239 USA
基金
美国国家卫生研究院;
关键词
FAMILIAL HYPERCHOLESTEROLEMIA; CONTROLLED-TRIAL; STATIN THERAPY; SYNDROME SLOS; CHILDREN; SUPPLEMENTATION; EFFICACY; MULTICENTER; ADOLESCENTS; POPULATION;
D O I
10.1203/PDR.0b013e31819ea4eb
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Deficient cholesterol and/or excessive 7-dehydrocholesterol (7-DHC) may be responsible for the pathology of Smith-Lemli-Opitz syndrome (SLOS). Both high-cholesterol diets given to ameliorate cholesterol deficiency while decreasing 7-DHC and cholesterol-enriched diets plus simvastatin to further decrease sterol synthesis have been used as potential therapies. However, the effect of dietary cholesterol and simvastatin on cholesterol synthesis in SLOS has not been reported. Twelve subjects with SLOS enrolled in the Study: Nine had received a high cholesterol diet (HI) for 3 y and three were studied after 4 wk on a low cholesterol diet (LO). Cholesterol fractional synthesis rate (FSR) was measured after oral administration of deuterium oxide, using gas chromatography isotope ratio mass spectrometry. FSR was lower in HI compared with LO (HI: 1.46 +/- 0.62%/d; LO: 4.77 +/- 0.95%/d; p < 0.001). Three HI subjects were retested after 0.8 y taking simvastatin (HI + ST). Simvastatin tended to reduce FSR and significantly decreased) < 0.01) plasma 7-DHC compared with cholesterol supplementation alone. The study demonstrates the utility of the deuterium incorporation method to understand the effect of therapeutic interventions in SLOS. The data suggest that dietary cholesterol supplementation reduces cholesterol synthesis in SLOS and further support the rationale for the combined treatment of SLOS with a cholesterol-enriched diet and simvastatin. (Pediatr Res 65: 681-685, 2009)
引用
收藏
页码:681 / 685
页数:5
相关论文
共 39 条
[1]  
BATTA AK, 1995, J LIPID RES, V36, P705
[2]   Smith-Lemli-Opitz syndrome: The first malformation syndrome associated with defective cholesterol synthesis [J].
Battaile, KP ;
Steiner, RD .
MOLECULAR GENETICS AND METABOLISM, 2000, 71 (1-2) :154-162
[3]   FEMALE EXTERNAL GENITALIA AND MULLERIAN DUCT DERIVATIVES IN A 46,XY INFANT WITH THE SMITH-LEMLI-OPITZ SYNDROME [J].
BIALER, MG ;
PENCHASZADEH, VB ;
KAHN, E ;
LIBES, R ;
KRIGSMAN, G ;
LESSER, ML .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1987, 28 (03) :723-731
[4]   Development and characterization of a hypomorphic Smith-Lemli-Opitz syndrome mouse model and efficacy of simvastatin therapy [J].
Correa-Cerro, LS ;
Wassif, CA ;
Kratz, L ;
Miller, GF ;
Munasinghe, JP ;
Grinberg, A ;
Fliesler, SJ ;
Porter, FD .
HUMAN MOLECULAR GENETICS, 2006, 15 (06) :839-851
[5]  
Cunniff C, 1997, AM J MED GENET, V68, P263, DOI 10.1002/(SICI)1096-8628(19970131)68:3<263::AID-AJMG4>3.3.CO
[6]  
2-5
[7]  
Daniels SR, 2008, PEDIATRICS, V122, P198, DOI 10.1542/peds.2008-1349
[8]   Early statin therapy restores endothelial function in children with familial hypercholesterolemia [J].
de Jongh, S ;
Lilien, MR ;
Roodt, JO ;
Stroes, ESG ;
Bakker, HD ;
Kastelein, JJP .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2002, 40 (12) :2117-2121
[9]   SIMVASTATIN USE IN CHILDREN [J].
DUCOBU, J ;
BRASSEUR, D ;
CHAUDRON, JM ;
DESLYPERE, JP ;
HARVENGT, C ;
MULS, E ;
THOMSON, M .
LANCET, 1992, 339 (8807) :1488-1488
[10]  
Elias ER, 1997, AM J MED GENET, V68, P305, DOI 10.1002/(SICI)1096-8628(19970131)68:3<305::AID-AJMG11>3.0.CO