Sensory cognitive abnormalities of pain in autism spectrum disorder: a case-control study

被引:52
|
作者
Yasuda, Yuka [1 ]
Hashimoto, Ryota [1 ,2 ]
Nakae, Aya [3 ,4 ]
Kang, Hongling [3 ]
Ohi, Kazutaka [1 ]
Yamamori, Hidenaga [1 ]
Fujimoto, Michiko [1 ]
Hagihira, Satoshi [3 ]
Takeda, Masatoshi [1 ]
机构
[1] Osaka Univ, Grad Sch Med, Dept Psychiat, D3,2-2 Yamadaoka, Suita, Osaka 5650871, Japan
[2] Osaka Univ, United Grad Sch Child Dev, Mol Res Ctr Childrens Mental Dev, D3,2-2 Yamadaoka, Suita, Osaka 5650871, Japan
[3] Dept Anesthesiol & Intens Care Med, 2-2 Yamadaoka, Suita, Osaka 5650871, Japan
[4] Osaka Univ, Immunol Frontier Res Ctr, BioSyst Bldg,1-3 Yamadaoka, Osaka, Osaka 5650871, Japan
来源
关键词
Autism spectrum disorder (ASD); Sensory abnormality; Pain processing; Quality of pain; Visual Analog Scale (VAS); Short-form McGill Pain Questionnaire (SF-MPQ); BETA-ENDORPHIN; CHILDREN; INDIVIDUALS; PERCEPTION; QUESTIONNAIRE; ADOLESCENTS; EXPRESSION; INTENSITY; SYMPTOMS; VERSION;
D O I
10.1186/s12991-016-0095-1
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Background: The Diagnostic and Statistical Manual of Mental Disorders, 5th Edition (DSM-5) recently included sensory processing abnormalities in the diagnostic criteria for individuals with autism spectrum disorder (ASD). However, there is no standard method for evaluating sensory abnormalities in individuals with ASD. Methods: Fifteen individuals with ASD and 15 age-and sex-matched controls were enrolled in this study. We compared objective pain sensitivity by measuring the pain detection threshold and pain tolerance to three different stimuli (electricity, heat, and cold). Then, we compared both subjective pain sensitivity, assessed by the visual analog scale (VAS), and quality of pain, assessed by the short-form McGill Pain Questionnaire (SF-MPQ), to determine the maximum tolerable pain intensities of each stimulation. Results: The pain detection threshold and pain tolerance of individuals with ASD were not impaired, indicating that there were no differences in the somatic perception of pain between groups. However, individuals with ASD were hyposensitive to subjective pain intensity compared to controls (VAS; electrical: p = 0.044, cold: p = 0.011, heat: p = 0.042) and hyposensitive to affective aspects of pain sensitivity (SF-MPQ; electrical: p = 0.0071, cold: p = 0.042). Conclusions: Our results suggest that the cognitive pathways for pain processing are impaired in ASD and, furthermore, that our methodology can be used to assess pain sensitivity in individuals with ASD. Further investigations into sensory abnormalities in individuals with ASD are needed to clarify the pathophysiologic processes that may alter sensory processing in this disorder.
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页数:8
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