Application of a ketogenic diet in children with autistic behavior: Pilot study

被引:176
作者
Evangeliou, A
Vlachonikolis, I
Mihailidou, H
Spilioti, M
Skarpalezou, A
Makaronas, N
Prokopiou, A
Christodoulou, P
Liapi-Adamidou, G
Helidonis, E
Sbyrakis, S
Smeitink, J
机构
[1] Univ Crete, Sch Med, Dept Paediat, Iraklion, Greece
[2] Univ Crete, Sch Med, Dept Neurol, Iraklion, Greece
[3] Univ Crete, Biostat Lab, Iraklion, Crete, Greece
[4] Childrens Hosp Agia Sofia, Inst Child Hlth, Athens, Greece
[5] Ctr Mental Hlth, Iraklion, Crete, Greece
[6] Ctr Mental Hlth, Khania, Crete, Greece
[7] Univ Crete, Sch Med, Dept Ear Nose & Throat, Iraklion, Greece
[8] Univ Athens, Dept Pediat 2, Athens, Greece
[9] Univ Nijmegen Hosp, Dept Pediat, NL-6500 HB Nijmegen, Netherlands
关键词
D O I
10.1177/08830738030180020501
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
A pilot prospective follow-up study of the role of the ketogenic diet was carried out on 30 children, aged between 4 and 10 years, with autistic behavior. The diet was applied for 6 months, with continuous administration for 4 weeks, interrupted by 2-week diet-free intervals. Seven patients could not tolerate the diet, whereas five other patients adhered to the diet for I to 2 months and then discontinued it. Of the remaining group who adhered to the diet, 18 of 30 children (60%), improvement was recorded in several parameters and in accordance with the Childhood Autism Rating Scale. Significant improvement (> 12 units of the Childhood Autism Rating Scale) was recorded in two patients (pre-Scale: 35.00 +/- 1.41 [mean +/- SD]), average improvement (> 8-12 units) in eight patients (pre-Scale: 41.88 +/- 3.14[mean SD]), and minor improvement (2-8 units) in eight patients (pre-Scale: 45.25 +/- 2.76 [mean +/- SD]). Although these data are very preliminary, there is some evidence that the ketogenic diet may be used in autistic behavior as an additional or alternative therapy.
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页码:113 / 118
页数:6
相关论文
共 32 条
[1]  
Armitage P., 2001, STAT METHODS MED RES, V4th
[2]   AUTISM AS A STRONGLY GENETIC DISORDER - EVIDENCE FROM A BRITISH TWIN STUDY [J].
BAILEY, A ;
LECOUTEUR, A ;
GOTTESMAN, I ;
BOLTON, P ;
SIMONOFF, E ;
YUZDA, E ;
RUTTER, M .
PSYCHOLOGICAL MEDICINE, 1995, 25 (01) :63-77
[3]  
Bujas-Petkovic Z, 1989, Lijec Vjesn, V111, P458
[4]   Ketone bodies and brain glutamate and GABA metabolism [J].
Daikhin, Y ;
Yudkoff, M .
DEVELOPMENTAL NEUROSCIENCE, 1998, 20 (4-5) :358-364
[5]  
EATON I, 1988, MANUAL DIETETIC PRAC, P489
[6]  
EATON J, 1994, CLIN DIETETICS, P168
[7]  
Erecinska M, 1996, J NEUROCHEM, V67, P2325
[8]   Selective screening for inborn errors of metabolism: the primary care-based model in rural Crete [J].
Evangeliou, A ;
Lionis, C ;
Michailidou, H ;
Spilioti, M ;
Kanitsakis, A ;
Nikitakis, P ;
Drakonakis, N ;
Giannakopoulou, C ;
Sbyrakis, S ;
Sewell, AC ;
Boehles, HJ ;
Smeitink, J ;
Wevers, RA .
JOURNAL OF INHERITED METABOLIC DISEASE, 2001, 24 (08) :877-880
[9]   High-dose pyridoxine and magnesium administration in children with autistic disorder: An absence of salutary effects in a double-blind, placebo-controlled study [J].
Findling, RL ;
Maxwell, K ;
ScoteseWojtila, L ;
Huang, J ;
Yamashita, T ;
Wiznitzer, M .
JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS, 1997, 27 (04) :467-478
[10]  
HAAS RH, 1986, AM J MED GENET, V24, P225