International Meeting for Autism Research: Dyslipidemia in Male Patients with High-Functioning Autism

Dyslipidemia in Male Patients with High-Functioning Autism

Thursday, May 20, 2010
Franklin Hall B Level 4 (Philadelphia Marriott Downtown)
1:00 PM
H. Matsuzaki , Molecular Reserach Center for Child Mental Development, Osaka University School of Medicine, Suita, Japan
K. Iwata , Research Center for Child Mental Development, Hamamatsu University School of Medicine, Hamamatsu, Japan
S. Suda , Research Center for Child Mental Development, Hamamatsu University School of Medicine, Hamamatsu, Japan
K. J. Tsuchiya , Research Center for Child Mental Development, Hamamatsu University School of Medicine, Hamamatsu, Japan
K. Suzuki , Research Center for Child Mental Development, Hamamatsu University School of Medicine, Hamamatsu, Japan
K. Nakamura , Psychiatry and Neurology, Hamamatsu University School of Medicine, Hamamatsu, Japan
M. Tsujii , Faculty of Sociology, Chukyo University, Nagoya, Japan
N. Takei , Research Center for Child Mental Development, Hamamatsu University School of Medicine, Hamamatsu, Japan
N. Mori , Psychiatry and Neurology, Hamamatsu University School of Medicine, Hamamatsu, Japan
Background: The neurobiological basis for autism remains poorly understood, but evidence is mounting in support of lipid metabolism playing a role in autism. In order to clarify the role of lipids in autism, we examined whether serum lipid profiles are altered in high-functioning autism patients (male: 6-31y.o.) enrolled in Asperger Society Japan.

Objectives: In this study, we measured serum levels of cholesterol and triacylglycerol in the 112 male subjects with high-functioning autism and 106 age-matched healthy male subjects.

Methods: The size distribution of serum lipoprotein particles was evaluated by high sensitivity lipoprotein profiling system with high-performance liquid chromatography (Skylight Biotech, Inc., Akita, Japan). Samples were diluted 20 times and analyzed at a flow rate of 350 ml/min by monitoring the concentrations of total cholesterol and triacylglycerol.

Results: The serum levels of total cholesterol and triacylglycerol in the infant subjects with high-functioning autism were significantly lower (Mann-Whitney U test: p < 0.001) than those of normal control subjects. In each fraction, there were significant differences in the serum levels of very-low density lipoprotein (VLDL) and high density lipoprotein (HDL) fraction. In particular, it’s remarkable in VLDL fraction of triacylglycerol (p< 0.00003). However, there were no differences between the patients with autism and healthy subjects in serum chylomicron and low density lipoprotein (LDL)levels.

Conclusions: The association between autism and abnormal serum lipid profile suggests that individuals with high-functioning autism may be at increased risk for VLDL hypolipidemia in infancy and which might be implicated in the pathophysiology of autism.

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