A clinical and laboratory evaluation of methionine cycle-transsulfuration and androgen pathway markers in children with autistic disorders

被引:81
作者
Geier, David A.
Geier, Mark R.
机构
[1] Genet Ctr Amer, Silver Spring, MD 20905 USA
[2] MedCon Inc, Silver Spring, MD 20905 USA
关键词
precocious puberty; pervasive developmental delay; sex steroid hormones; sexual development;
D O I
10.1159/000094467
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background/Aims: The prevalence of autism spectrum disorders (ASDs) is 1 in 300 children in the US. ASDs are characterized by impairments in social relatedness and communication, repetitive behaviors, abnormal movement patterns, and sensory dysfunction. Pre-pubertal age children with ASDs were assessed for metabolites in the methionine cycle-transsulfuration and androgen pathways, and for present physical development/behaviors indicative of hyperandrogenicity. Methods: The Institutional Review Board of the Institute for Chronic Illnesses (Office for Human Research Protections, US Department of Health and Human Services IRB number: IRB00005375) approved the present study. Sixteen consecutive pre-pubertal age children (<= 11 years old; mean SD: 5.9 +/- 2.1 years old) with previously diagnosed ASDs that presented to the Genetic Centers of America for outpatient care were evaluated. Results: Significantly (p < 0.01) increased levels of serum/plasma dehydroepiandrosterone and serum total testosterone relative to the age- and sex-specific normal laboratory reference ranges were observed. Conversely, serum follicle-stimulating hormone levels were significantly (p < 0.01) decreased. Plasma-reduced glutathione (p < 0.01), plasma cysteine (p < 0.01), plasma methionine (p < 0.01), serum cystathionine (p < 0.05), and serum homocysteine (p < 0.01) were all significantly decreased. Conclusion: The results suggest a possible cyclical interaction between the methionine cycle-transsulfuration and androgen pathways in some children with ASDs. Copyright (c) 2006 S. Karger AG, Basel.
引用
收藏
页码:182 / 188
页数:7
相关论文
共 18 条
[1]   Sex differences in the brain: Implications for explaining autism [J].
Baron-Cohen, S ;
Knickmeyer, RC ;
Belmonte, MK .
SCIENCE, 2005, 310 (5749) :819-823
[2]   Prevalence of autism in a United States population: The Brick Township, New Jersey, investigation [J].
Bertrand, J ;
Mars, A ;
Boyle, C ;
Bove, F ;
Yeargin-Allsopp, M ;
Decoufle, P .
PEDIATRICS, 2001, 108 (05) :1155-1161
[3]   The relation between general cognitive level and adaptive behavior domains in individuals with autism with and without co-morbid mental retardation [J].
Bölte, S ;
Poustka, F .
CHILD PSYCHIATRY & HUMAN DEVELOPMENT, 2002, 33 (02) :165-172
[4]  
Boris M., 2004, J Am Phys Surg, V9, P106
[5]   A systems neuroscience approach to autism: Biological, cognitive, and clinical perspectives [J].
Eigsti, IM ;
Shapiro, T .
MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS, 2003, 9 (03) :205-215
[6]   The potential importance of steroids in the treatment of autistic spectrum disorders and other disorders involving mercury toxicity [J].
Geier, MR ;
Geier, DA .
MEDICAL HYPOTHESES, 2005, 64 (05) :946-954
[7]   Oral and transdermal estrogens both lower plasma total homocysteine in male-to-female transsexuals [J].
Giltay, EJ ;
Verhoef, P ;
Gooren, LJG ;
Geleijnse, JM ;
Schouten, EG ;
Stehouwer, CDA .
ATHEROSCLEROSIS, 2003, 168 (01) :139-146
[8]   Effects of sex steroids on plasma total homocysteine levels: A study in transsexual males and females [J].
Giltay, EJ ;
Hoogeveen, EK ;
Elbers, JMH ;
Gooren, LJG ;
Asscheman, H ;
Stehouwer, CDA .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1998, 83 (02) :550-553
[9]   Metabolic biomarkers of increased oxidative stress and impaired methylation capacity in children with autism [J].
James, SJ ;
Cutler, P ;
Melnyk, S ;
Jernigan, S ;
Janak, L ;
Gaylor, DW ;
Neubrander, JA .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 2004, 80 (06) :1611-1617
[10]   High levels of homocysteine and low serum paraoxonase 1 arylesterase activity in children with autism [J].
Pasca, SP ;
Nemes, B ;
Vlase, L ;
Gagyi, CE ;
Dronca, E ;
Miu, AC ;
Dronca, M .
LIFE SCIENCES, 2006, 78 (19) :2244-2248