Goji Aya, Ito Hiromichi, Mori Kenji, Harada Masafumi, Hisaoka Sonoka, Toda Yoshihiro, Mori Tatsuo, Abe Yoko, Miyazaki Masahito, Kagami Shoji
Department of Pediatrics, Institute of Biomedical Sciences, Tokushima University Graduate School, Tokushima, Japan.
Department of Child Health & Nursing, Institute of Biomedical Sciences, Tokushima University Graduate School, Tokushima, Japan.
PLoS One. 2017 Jan 6;12(1):e0169288. doi: 10.1371/journal.pone.0169288. eCollection 2017.
Proton magnetic resonance spectroscopy (1H MRS) is a noninvasive neuroimaging method to quantify biochemical metabolites in vivo and it can serve as a powerful tool to monitor neurobiochemical profiles in the brain. Asperger's syndrome (AS) is a type of autism spectrum disorder, which is characterized by impaired social skills and restrictive, repetitive patterns of interest and activities, while intellectual levels and language skills are relatively preserved. Despite clinical aspects have been well-characterized, neurometabolic profiling in the brain of AS remains to be clear. The present study used proton magnetic resonance spectroscopy (1H MRS) to investigate whether pediatric AS is associated with measurable neurometabolic abnormalities that can contribute new information on the neurobiological underpinnings of the disorder.
Study participants consisted of 34 children with AS (2-12 years old; mean age 5.2 (±2.0); 28 boys) and 19 typically developed children (2-11 years old; mean age 5.6 (±2.6); 12 boys) who served as the normal control group. The 1H MRS data were obtained from two regions of interest: the anterior cingulate cortex (ACC) and left cerebellum.
In the ACC, levels of N-acetylaspartate (NAA), total creatine (tCr), total choline-containing compounds (tCho) and myo-Inositol (mI) were significantly decreased in children with AS compared to controls. On the other hand, no significant group differences in any of the metabolites were found in the left cerebellum. Neither age nor sex accounted for the metabolic findings in the regions.
The finding of decreased levels of NAA, tCr, tCho, and mI in the ACC but not in left cerebellar voxels in the AS, suggests a lower ACC neuronal density in the present AS cohort compared to controls.
质子磁共振波谱(1H MRS)是一种用于在体内定量生化代谢物的非侵入性神经成像方法,它可作为监测大脑神经生化特征的有力工具。阿斯伯格综合征(AS)是自闭症谱系障碍的一种类型,其特征是社交技能受损以及兴趣和活动模式受限、重复,而智力水平和语言技能相对保留。尽管临床特征已得到充分描述,但AS患者大脑中的神经代谢特征仍不清楚。本研究使用质子磁共振波谱(1H MRS)来调查儿童AS是否与可测量的神经代谢异常相关,这些异常可为该疾病的神经生物学基础提供新信息。
研究参与者包括34名AS儿童(2至12岁;平均年龄5.2(±2.0)岁;28名男孩)和19名发育正常的儿童(2至11岁;平均年龄5.6(±2.6)岁;12名男孩),后者作为正常对照组。1H MRS数据从两个感兴趣区域获取:前扣带回皮质(ACC)和左侧小脑。
在ACC中,与对照组相比,AS儿童的N-乙酰天门冬氨酸(NAA)、总肌酸(tCr)、总含胆碱化合物(tCho)和肌醇(mI)水平显著降低。另一方面,在左侧小脑中未发现任何代谢物存在显著的组间差异。年龄和性别均不能解释这些区域的代谢结果。
AS患者ACC中NAA、tCr、tCho和mI水平降低,而左侧小脑体素中未降低,这一发现表明与对照组相比,本AS队列中的ACC神经元密度较低。