Effect of optimal dietary therapy upon visual function in children with long-chain 3-hydroxyacyl CoA dehydrogenase and trifunctional protein deficiency

被引:51
作者
Gillingham, MB [1 ]
Weleber, RG
Neuringer, M
Connor, WE
Mills, M
van Calcar, S
ver Hoeve, J
Wolff, J
Harding, CO
机构
[1] Oregon Hlth Sci Univ, Dept Pediat, Portland, OR 97239 USA
[2] Oregon Hlth Sci Univ, Dept Mol & Med Genet, Portland, OR 97239 USA
[3] Oregon Hlth Sci Univ, Dept Ophthalmol, Portland, OR 97239 USA
[4] Oregon Hlth Sci Univ, Dept Med, Portland, OR 97239 USA
[5] Oregon Hlth Sci Univ, Casey Eye Inst, Portland, OR 97239 USA
[6] Oregon Hlth Sci Univ, Oregon Natl Primate Res Ctr, Portland, OR 97239 USA
[7] Univ Wisconsin, Sch Med, Dept Ophthalmol, Madison, WI 53705 USA
[8] Univ Wisconsin, Sch Med, Dept Visual Sci, Madison, WI 53705 USA
[9] Univ Wisconsin, Sch Med, Waisman Ctr, Madison, WI 53705 USA
[10] Univ Wisconsin, Sch Med, Dept Pediat, Madison, WI 53705 USA
关键词
long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency; trifunctional protein deficiency; hydroxyacylcarnitines; docosahexaenoic acid; chorioretinopathy;
D O I
10.1016/j.ymgme.2005.06.001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The objective of this prospective cohort study was to determine if dietary therapy including docosahexacnoic acid (DHA; C22:6 omega-3) supplementation prevents the progression of the severe chorioretinopathy that develops in children with long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) or trifunctional protein (TFP) deficiency. Physical, biochemical, and ophthalmological evaluations, including electroretinogram (ERG) and visual acuity by evoked potential (VEP), were performed at baseline and annually following the initiation of 65-130mg/day DHA supplementation and continued treatment with a low-fat diet. Fourteen children with LCHAD or TFP deficiency, 1-12 years of age at enrollment, were followed for 2-5 years. Three subjects with TFP beta-subunit mutations had normal appearance of the posterior pole of the ocular fundi at enrollment and no changes over the course of the study. Eleven subjects who were homozygote and heterozygote for the common mutation, c.1528G > C, had no change to severe progression of atrophy of the choroid and retina with time. Of these, four subjects had marked to severe chorioretinopathy associated with high levels of plasma hydroxyacylcarnitines and decreased color, night and/or central vision during the study. The plasma level of long-chain 3-hydroxyacylcarnitines, metabolites that accumulate as a result of LCHAD and TFP deficiency, was found to be negatively correlated with maximum ERG amplitude (R-max) (p = 0.0038, R-2 = 0.62). In addition, subjects with sustained low plasma long-chain 3-hydroxyacylcarnitines maintained higher ERG amplitudes with time compared to subjects with chronically high 3-hydroxyacylcarnitines. Visual acuity, as determined with the VEP, appeared to increase with time on DHA supplementation (p = 0.051) and there was a trend for a positive correlation with plasma DHA concentrations (p = 0.075, R-2 = 0.31). Thus, optimal dietary therapy as indicated by low plasma 3-hydroxyacylearnitine and high plasma DHA concentrations was associated with retention of retinal function and visual acuity in children with LCHAD or TFP deficiency. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:124 / 133
页数:10
相关论文
共 41 条
[1]  
ANDREASSON S, 1993, ACTA OPHTHALMOL, V71, P491
[2]  
BIRCH EE, 1992, INVEST OPHTH VIS SCI, V33, P3242
[3]  
Birch Eileen E., 1997, P183
[4]   Clinical aspects of essential fatty acid metabolism: Jonathan Rhoads lecture [J].
Bistrian, BR .
JOURNAL OF PARENTERAL AND ENTERAL NUTRITION, 2003, 27 (03) :168-175
[5]  
Costa CG, 1998, CLIN CHEM, V44, P463
[6]   Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: Clinical presentation and follow-up of 50 patients [J].
den Boer, MEJ ;
Wanders, RJA ;
Morris, AAM ;
Ijlst, L ;
Heymans, HSA ;
Wijburg, FA .
PEDIATRICS, 2002, 109 (01) :99-104
[7]  
FLIESLER SJ, 1983, PROG LIPID RES, V22, P79
[8]   Dietary management of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency (LCHADD). A case report and survey [J].
Gillingham, M ;
Van Calcar, S ;
Ney, D ;
Wolff, J ;
Harding, C .
JOURNAL OF INHERITED METABOLIC DISEASE, 1999, 22 (02) :123-131
[9]   Optimal dietary therapy of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency [J].
Gillingham, MB ;
Connor, WE ;
Matern, D ;
Rinaldo, P ;
Burlingame, T ;
Meeuws, K ;
Harding, CO .
MOLECULAR GENETICS AND METABOLISM, 2003, 79 (02) :114-123
[10]   THE DEVELOPMENT OF MONOCULAR AND BINOCULAR VEP ACUITY [J].
HAMER, RD ;
NORCIA, AM ;
TYLER, CW ;
HSUWINGES, C .
VISION RESEARCH, 1989, 29 (04) :397-408