Share:
Share this content in WeChat
X
Original Article
Study on diffusion kurtosis imaging of the caput nuclei caudate in children with autism spectrum disorder
SUN Yongbing  ZHAO Xin  LU Lin  XING Qingna  HE Xiongpeng  ZHANG Xiaoan 

Cite this article as: Sun YB, Zhao X, Lu L, et al. Study on diffusion kurtosis imaging of the caput nuclei caudate in children with autism spectrum disorder[J]. Chin J Magn Reson Imaging, 2022, 13(4): 69-74. DOI:10.12015/issn.1674-8034.2022.04.012.


[Abstract] Objective To investigate the clinical value of diffusional kurtosis imaging (DKI) in evaluating caput nuclei caudate changes in children with autism spectrum disorder (ASD) accompanied by language impairment.Materials and Methods A total of 34 children with ASD were collected as a case group and 30 healthy children in the same period as a control group. The independent sample t-test was used to analyze the differences in brain volume between the two groups. The DKI parameters of bilateral and right/left (R0) caudate nuclei in the two groups showed anisotropy fraction, mean diffusivity coefficient, axial diffusivity (Da), radial diffusivity (Dr), mean kurtosis (Mk), axial kurtosis, radial kurtosis (Kr) was used to analyze the relationship between DKI parameters of caudate nucleus and communication, language comprehension, and language expression scores by using Spearman correlation analysis.Results Compared with the control group, an increase in white matter volume and gray matter volume of the ASD group (P<0.05), decreased in the scores of communication, language comprehension, and language expression (P<0.05). The R0-Da value (P=0.049), the Kr value of the left caput nuclei caudat, and the Mk value of the left caput nuclei caudate in the ASD group were greater than those in the control group, and the R0-Mk value less than the control group (P all<0.05); In the control group, the left caput nuclei caudate Kr was negatively correlated with language comprehension scores (r=-0.514, P=0.004), and the left caput nuclei caudate Mk values were negatively correlated with language comprehension and language expression scores (r=-0.701, P<0.001), (r=-0.614, P<0.001), the R0-Mk values are positively correlated with language comprehension and language expression scores (r=0.481, P=0.007), (r=0.410, P=0.025 ), there was no correlation between the bilateral caput nuclei caudate and R0-DKI characteristic values and language scores of children in the ASD group (P>0.05).Conclusions DKI can be used to evaluate caudate head abnormalities in children with ASD, whose lateralization affects normal language expression.
[Keywords] autism spectrum disorder;diffusion kurtosis imaging;caput nuclei caudate;language lateralization;Psychoeducational Profile (Third Edition)

SUN Yongbing1, 2   ZHAO Xin1, 2   LU Lin1, 2   XING Qingna1, 2   HE Xiongpeng1, 2   ZHANG Xiaoan1, 2*  

1 Department of Radiology, the Third Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, China

2 Institute of Neuroscience, Zhengzhou University, Zhengzhou 450052, China

Zhang XA, E-mail: zxa@zzu.edu.cn

Conflicts of interest   None.

ACKNOWLEDGMENTS National Natural Science Foundation of China (No. 81870983).
Received  2021-12-25
Accepted  2022-03-25
DOI: 10.12015/issn.1674-8034.2022.04.012
Cite this article as: Sun YB, Zhao X, Lu L, et al. Study on diffusion kurtosis imaging of the caput nuclei caudate in children with autism spectrum disorder[J]. Chin J Magn Reson Imaging, 2022, 13(4): 69-74. DOI:10.12015/issn.1674-8034.2022.04.012.

[1]
Anandhi B, Jerritta S, Anusuya IG, et al. Time domain analysis of heart rate variability signals in valence recognition for children with autism spectrum disorder (ASD)[J]. IRBM, 2021 DOI: 10.1016/j.irbm.2021.06.002.
[2]
Zhou H, Xu X, Yan WL, et al. Prevalence of autism spectrum disorder in China: a nationwide multi-center population-based study among children aged 6 to 12 years[J]. Neurosci Bull, 2020, 36(9): 961-971. DOI: 10.1007/s12264-020-00530-6.
[3]
Developmental Behavior Group of Pediatrics Branch of Chinese Medical Association, Child Health Care Professional Committee of Pediatrics Branch of Chinese Medical Doctor Association, an expert group of children autism diagnosis and prevention technology and standard research project. Early identification, screening, and early intervention of children with autism spectrum disorder[J]. Chin J Pediatr, 2017, 55(12): 890-897. DOI: 10.3760/cma.j.issn.0578-1310.2017.12.004.
[4]
Naigles LR. Input and language development in children with autism[J]. Semin Speech Lang, 2013, 34(4): 237-248. DOI: 10.1055/s-0033-1353446.
[5]
D'Mello AM, Moore DM, Crocetti D, et al. Cerebellar gray matter differentiates children with early language delay in autism[J]. Autism Res, 2016, 9(11): 1191-1204. DOI: 10.1002/aur.1622.
[6]
Dominey PF, Inui T, Hoen M. Neural network processing of natural language: Ⅱ. Towards a unified model of corticostriatal function in learning sentence comprehension and non-linguistic sequencing[J]. Brain Lang, 2009, 109(2/3): 80-92. DOI: 10.1016/j.bandl.2008.08.002.
[7]
Branzi FM, Della Rosa PA, Canini M, et al. Language control in bilinguals: monitoring and response selection[J]. Cereb Cortex, 2016, 26(6): 2367-2380. DOI: 10.1093/cercor/bhv052.
[8]
Li L, Abutalebi J, Zou LJ, et al. Bilingualism alters brain functional connectivity between "control" regions and "language" regions: evidence from bimodal bilinguals[J]. Neuropsychologia, 2015, 71: 236-247. DOI: 10.1016/j.neuropsychologia.2015.04.007.
[9]
Umesh Rudrapatna S, Wieloch T, Beirup K, et al. Can diffusion kurtosis imaging improve the sensitivity and specificity of detecting microstructural alterations in brain tissue chronically after experimental stroke? Comparisons with diffusion tensor imaging and histology[J]. Neuroimage, 2014, 97: 363-373. DOI: 10.1016/j.neuroimage.2014.04.013.
[10]
Zou XB, Deng HZ. Expounding on the diagnosis criteria of autistic spectrum disorders of diagnostic and statistical manual of mental disorders-fifth edition, DSM-V[J]. Chin J Pract Pediatr, 2013, 28(8): 561-563.
[11]
Zhang Y, Huang XH. The value of the third edition of pep-3 autism assessment scale in early screening and efficacy evaluation of children with ASD[J]. Sichuan Med J, 2021, 42(2): 149-152. DOI: 10.16252/j.cnki.issn1004-0501-2021.02.010.
[12]
Yankowitz LD, Herrington JD, Yerys BE, et al. Evidence against the "normalization" prediction of the early brain overgrowth hypothesis of autism[J]. Mol Autism, 2020, 11(1): 51. DOI: 10.1186/s13229-020-00353-2.
[13]
Sokol DK, Maloney B, Westmark CJ, et al. Novel contribution of secreted amyloid-β precursor protein to white matter brain enlargement in autism spectrum disorder[J]. Front Psychiatry, 2019, 10: 165. DOI: 10.3389/fpsyt.2019.00165.
[14]
Bonilha L, Cendes F, Rorden C, et al. Gray and white matter imbalance: typical structural abnormality underlying classic autism?[J]. Brain Dev, 2008, 30(6): 396-401. DOI: 10.1016/j.braindev.2007.11.006.
[15]
Herbert MR, Ziegler DA, Makris N, et al. Localization of white matter volume increase in autism and developmental language disorder[J]. Ann Neurol, 2004, 55(4): 530-540. DOI: 10.1002/ana.20032.
[16]
Khanbabaei M, Hughes E, Ellegood J, et al. Precocious myelination in a mouse model of autism[J]. Transl Psychiatry, 2019, 9(1): 251. DOI: 10.1038/s41398-019-0590-7.
[17]
Lo YC, Chen YJ, Hsu YC, et al. Reduced tract integrity of the model for social communication is a neural substrate of social communication deficits in autism spectrum disorder[J]. J Child Psychol Psychiatry, 2017, 58(5): 576-585. DOI: 10.1111/jcpp.12641.
[18]
Hu S, Li H, Zhang YQ, et al. Advances in neuroimaging studies of childhood autism[J]. Chin J Magn Reson Imaging, 2021, 12(11): 105-108. DOI: 10.12015/issn.1674-8034.2021.11.026.
[19]
Wegiel J, Flory M, Kuchna I, et al. Stereological study of the neuronal number and volume of 38 brain subdivisions of subjects diagnosed with autism reveals significant alterations restricted to the striatum, amygdala and cerebellum[J]. Acta Neuropathol Commun, 2014, 2: 141. DOI: 10.1186/s40478-014-0141-7.
[20]
Zhang L, Zhao LP, Liu SR, et al. Analysis of microstructure and blood perfusion in thalamus and basal Ganglia in patients with untreated depressive disorder[J]. Chin J Med Imaging Technol, 2018, 34(2): 176-180. DOI: 10.13929/j.1003-3289.201709068.
[21]
Steven AJ, Zhuo JC, Melhem ER. Diffusion kurtosis imaging: an emerging technique for evaluating the microstructural environment of the brain[J]. AJR Am J Roentgenol, 2014, 202(1): W26-W33. DOI: 10.2214/AJR.13.11365.
[22]
Irie R, Kamagata K, Kerever A, et al. The relationship between neurite density measured with confocal microscopy in a cleared mouse brain and metrics obtained from diffusion tensor and diffusion kurtosis imaging[J]. Magn Reson Med Sci, 2018, 17(2): 138-144. DOI: 10.2463/mrms.mp.2017-0031.
[23]
Levitt JG, O'Neill J, Blanton RE, et al. Proton magnetic resonance spectroscopic imaging of the brain in childhood autism[J]. Biol Psychiatry, 2003, 54(12): 1355-1366. DOI: 10.1016/s0006-3223(03)00688-7.
[24]
Friederici AD. Towards a neural basis of auditory sentence processing[J]. Trends Cogn Sci, 2002, 6(2): 78-84. DOI: 10.1016/s1364-6613(00)01839-8.
[25]
Tan AP, Ngoh ZM, Yeo SSP, et al. Left lateralization of neonatal caudate microstructure affects emerging language development at 24 months[J]. Eur J Neurosci, 2021, 54(2): 4621-4637. DOI: 10.1111/ejn.15347.
[26]
Sui YV, Donaldson J, Miles L, et al. Diffusional kurtosis imaging of the corpus callosum in autism[J]. Mol Autism, 2018, 9: 62. DOI: 10.1186/s13229-018-0245-1.
[27]
Hattori A, Kamagata K, Kirino E, et al. White matter alterations in adult with autism spectrum disorder evaluated using diffusion kurtosis imaging[J]. Neuroradiology, 2019, 61(12): 1343-1353. DOI: 10.1007/s00234-019-02238-5.
[28]
McKenna F, Miles L, Donaldson J, et al. Diffusion kurtosis imaging of gray matter in young adults with autism spectrum disorder[J]. Sci Rep, 2020, 10(1): 21465. DOI: 10.1038/s41598-020-78486-w.

PREV Alterations in amplitude of low frequency fluctuation and regional homogeneity in patients with neuromyelitis optica spectrum disorder and cognitive impairment: A resting-state functional magnetic resonance imaging study
NEXT Functional connectivity and regional homogeneity of resting state functional magnetic resonance imaging in patients with Ménière Disease
  



Tel & Fax: +8610-67113815    E-mail: editor@cjmri.cn