|
Journal of Lipid Research, Vol. 41, 1339-1346, August 2000
Copyright © 2000 by Lipid Research, Inc.
Simvastatin: a new therapeutic approach for Smith-Lemli-Opitz syndrome
Petr E. Jiraa,
Ron A. Weversb,
Jan de Jongb,
Estela Rubio-Gozalboa,
Fokje S. M. Janssen-Zijlstrab,
Arno F. J. van Heystc,
Rob C. A. Sengersa, and
Jan A. M. Smeitinka
a Department of Metabolic Diseases, University Hospital Nijmegen, 6500 HB Nijmegen, The Netherlands
b Institute of Pediatrics, Laboratory of Pediatrics and Neurology, University Hospital Nijmegen, 6500 HB Nijmegen, The Netherlands
c Department of Neonatology, University Hospital Nijmegen, 6500 HB Nijmegen, The Netherlands
Correspondence to:
Jan A. M. Smeitink
The Smith-Lemli-Opitz syndrome (SLOS) is caused by deficient 7-dehydrocholesterol reductase, which catalyzes the final step of the cholesterol biosynthetic pathway, resulting in low cholesterol and high concentrations of its direct precursors 7-dehydrocholesterol (7DHC) and 8DHC. We hypothesized that i) 7DHC and 8DHC accumulation contributes to the poor outcome of SLOS patients and ii) blood exchange transfusions with hydroxymethylglutaryl (HMG)-CoA reductase inhibition would improve the precursor-to-cholesterol ratio and may improve the clinical outcome of SLO patients. First, an in vitro study was performed to study sterol exchange between plasma and erythrocyte membranes. Second, several exchange transfusions were carried out in vivo in two SLOS patients. Third, simvastatin was given for 23 and 14 months to two patients. The in vitro results illustrated rapid sterol exchange between plasma and erythrocyte membranes. The effect of exchange transfusion was impressive and prompt but the effect on plasma sterol levels lasted only for 3 days. In contrast, simvastatin treatment for several months demonstrated a lasting improvement of the precursor-to-cholesterol ratio in plasma, erythrocyte membranes, and cerebrospinal fluid (CSF). Plasma precursor concentrations decreased to 28 and 33% of the initial level, respectively, whereas the cholesterol concentration normalized by a more than twofold increase. During the follow-up period all morphometric parameters improved. The therapy was well tolerated and no unwanted clinical side effects occurred.
This is the first study in which the blood cholesterol level in SLOS patients is normalized with a simultaneous significant decrease in precursor levels. There was a lasting biochemical improvement with encouraging clinical improvement. Statin therapy is a promising novel approach in SLOS that deserves further studies in larger series of patients.Jira, P. E., R. A. Wevers, J. de Jong, E. Rubio-Gozalbo, F. S. M. Janssen-Zijlstra, A. F. J. van Heyst, R. C. A. Sengers, and J. A. M. Smeitink. Simvastatin: a new therapeutic approach for Smith-Lemli-Opitz syndrome. J. Lipid Res. 2000. 41: 1339;1346.
Supplementary key words:
cholesterol biosynthesis, Smith-Lemli-Opitz syndrome, simvastatin, exchange transfusion

CiteULike Complore Connotea Del.icio.us Digg Reddit Technorati What's this?
This article has been cited by other articles:

|
 |

|
 |
 
B. Manzi, A. L. Loizzo, G. Giana, and P. Curatolo
Autism and Metabolic Diseases
J Child Neurol,
March 1, 2008;
23(3):
307 - 314.
[Abstract]
[PDF]
|
 |
|

|
 |

|
 |
 
L. S. Correa-Cerro, C. A. Wassif, L. Kratz, G. F. Miller, J. P. Munasinghe, A. Grinberg, S. J. Fliesler, and F. D. Porter
Development and characterization of a hypomorphic Smith-Lemli-Opitz syndrome mouse model and efficacy of simvastatin therapy
Hum. Mol. Genet.,
March 15, 2006;
15(6):
839 - 851.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
G. E. Herman
Disorders of cholesterol biosynthesis: prototypic metabolic malformation syndromes
Hum. Mol. Genet.,
April 2, 2003;
12(90001):
R75 - 88.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
A. S. Pappu, R. D. Steiner, S. L. Connor, D. P. Flavell, D. S. Lin, L. Hatcher, D. R. Illingworth, and W. E. Connor
Feedback inhibition of the cholesterol biosynthetic pathway in patients with Smith-Lemli-Opitz syndrome as demonstrated by urinary mevalonate excretion
J. Lipid Res.,
October 1, 2002;
43(10):
1661 - 1669.
[Abstract]
[Full Text]
[PDF]
|
 |
|
Copyright © 2000 by the American Society for Biochemistry and Molecular Biology.
|
Advertisement
Advertisement
|