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中华妇幼临床医学杂志(电子版) ›› 2018, Vol. 14 ›› Issue (02) : 213 -217. doi: 10.3877/cma.j.issn.1673-5250.2018.02.014

所属专题: 文献

论著

血浆催产素和精氨酸后叶加压素水平与儿童孤独症谱系障碍的相关性研究
郑萍1, 李尔珍1,(), 赵晓荣2, 刘翠英2, 赵秋芬3, 王珺1, 陈倩1, 关宏岩1   
  1. 1. 100020 北京,首都儿科研究所神经科
    2. 101314 北京首儿李桥儿童医院康复中心
    3. 101314 北京首儿李桥儿童医院检验科
  • 收稿日期:2017-11-18 修回日期:2018-03-01 出版日期:2018-04-01
  • 通信作者: 李尔珍

Correlation between levels of plasma oxytocin, arginine vasopressin and autism spectrum disorder in children

Ping Zheng1, Erzhen Li1,(), Xiaorong Zhao2, Cuiying Liu2, Qiufen Zhao3, Jun Wang1, Qian Chen1, Hongyan Guan1   

  1. 1. Department of Neurology, Capital Institute of Pediatrics, Beijing 100020, China
    2. Rehabilitation Center, Beijing Shou Er Li Qiao Children′s Hospital, Beijing 101314, China
    3. Department of Clinical Laboratory, Beijing Shou Er Li Qiao Children′s Hospital, Beijing 101314, China
  • Received:2017-11-18 Revised:2018-03-01 Published:2018-04-01
  • Corresponding author: Erzhen Li
  • About author:
    Corresponding author: Li Erzhen, Email:
引用本文:

郑萍, 李尔珍, 赵晓荣, 刘翠英, 赵秋芬, 王珺, 陈倩, 关宏岩. 血浆催产素和精氨酸后叶加压素水平与儿童孤独症谱系障碍的相关性研究[J/OL]. 中华妇幼临床医学杂志(电子版), 2018, 14(02): 213-217.

Ping Zheng, Erzhen Li, Xiaorong Zhao, Cuiying Liu, Qiufen Zhao, Jun Wang, Qian Chen, Hongyan Guan. Correlation between levels of plasma oxytocin, arginine vasopressin and autism spectrum disorder in children[J/OL]. Chinese Journal of Obstetrics & Gynecology and Pediatrics(Electronic Edition), 2018, 14(02): 213-217.

目的

探讨孤独症谱系障碍(ASD)患儿血浆催产素和精氨酸后叶加压素(AVP)水平与ASD发病的关系。

方法

选择2014年1月1日至2016年12月31日在首都儿科研究所就诊的40例ASD患儿为研究对象,年龄为2.0~12.0岁,并纳入ASD组。选择同期于同一医院进行体格检查的34例健康儿童纳入对照组,年龄为2.4~7.4岁。应用《儿童期孤独症评定量表》(CARS)和《精神疾病诊断与统计手册》第5版(DSM-5)对40例ASD患儿进行孤独症诊断及孤独症症状严重程度进行评定。采用酶联免疫吸附试验(ELISA)法定量检测2组受试儿血浆催产素和AVP水平。采用成组t检验,比较2组受试儿血浆催产素和AVP水平;采用直线相关性分析,对血浆催产素、血浆AVP水平与CARS评分的相关性进行分析。本研究遵循的程序符合首都儿科研究所人体试验委员会制定的伦理学标准,得到该委员会批准(审批号为[2012]-004),均与所有受试儿的法定监护人签署临床研究知情同意书。

结果

①2组受试儿的年龄、性别构成比比较,差异均无统计学意义(P>0.05)。② ASD组患儿血浆催产素水平为(359.2±103.3)pg/mL,显著低于对照组的(484.1±50.1)pg/mL,2组比较,差异有统计学意义(t=-6.43,P<0.001);ASD组患儿血浆AVP水平为(342.8±61.2)pg/mL,显著高于对照组的(312.2±39.2)pg/mL,2组比较,差异亦有统计学意义(t=2.51,P=0.014)。③相关性分析结果显示,ASD组患儿血浆催产素水平与CARS评分呈负相关关系(r=-0.155,P=0.032),血浆AVP水平与CARS评分无相关关系(r=0.032,P=0.841),血浆催产素水平与血浆AVP水平无相关关系(r=0.191,P=0.220)。对照组中,患儿血浆催产素水平与血浆AVP水平呈正相关关系(r=0.631,P<0.001)。

结论

ASD患儿血浆催产素水平降低,而血浆AVP水平升高,血浆催产素和AVP水平变化可能与ASD发病相关。

Objective

To investigate correlation between levels of plasma oxytocin, arginine vasopressin (AVP) and autism spectrum disorder (ASD) in children.

Methods

A total of 40 ASD children aged 2.0 to 12.0 years were admitted in the Capital Institute of Pediatrics from January 1, 2014 to December 31, 2016, and included in ASD group. Meanwhile, another 34 healthy children aged 2.4 to 7.4 years were selected as control group during the same period in the same hospital. Childhood Autism Rating Scale (CARS) and Diagnostic and Statistical Manual of Mental Disorders-fifth edition (DSM-5) were used to evaluate the severity of autistic symptoms. The levels of plasma oxytocin and AVP were detected by enzyme-linked immunosorbent assay (ELISA). The levels of plasma oxytocin and AVP between two groups were compared by independent-samples t test. And the correlation between levels of plasma oxytocin, AVP and CARS scores were analyzed by linear correlation analysis. The study protocol was approved by the Ethnical Review Board of Investigation in Human Beings of Capital Institute of Pediatrics (approval number: [2012]-004). Informed consent was obtained from each participant′s guardians.

Results

① There were no significant differences between two groups in age and constituent ratio of gender (P>0.05). ② The level of plasma oxytocin was (359.2±103.3) pg/mL in ASD group, which was significant lower than (484.1±50.1) pg/mL in control group, and the difference between two groups was statistically significant (t=-6.43, P<0.001). Besides, the level of plasma AVP was (342.8±61.2) pg/mL in ASD group, which was significant higher than (312.2±39.2) pg/mL in control group, and the difference between two groups was statistically significant (t=2.51, P=0.014). ③ In ASD group, there was a negative correlation between plasma oxytocin level and CARS score in children with ASD (r=-0.155, P=0.032), and plasma AVP level was not correlated with CARS score (r=0.032, P=0.841), plasma oxytocin level also was not associated with plasma AVP level (r=0.191, P=0.220). In control group, plasma oxytocin level was positively correlated with plasma AVP level (r=0.631, P<0.001).

Conclusions

Plasma oxytocin level decreases and plasma AVP level increases in children with ASD. The changes of plasma oxytocin and AVP may be involved in the pathogenesis of ASD.

表1 2组受试儿的一般临床资料比较
表2 2组受试儿血浆催产素与AVP水平比较(pg/mL,±s)
[1]
Bonnet-BrilhaultF. Autism: an early neurodevelopmental disorder [J]. Arch Pediatr, 2017, 24(4): 384-390.
[2]
BairdG,SimonoffE,PicklesA, et al. Prevalence of disorders of the autism spectrum in a population cohort of children in South Thames: the Special Needs and Autism Project (SNAP) [J]. Lancet, 2006, 368(9531): 210-215.
[3]
HollanderE,BartzJ,ChaplinW, et al. Oxytocin increases retention of social cognition in autism [J]. Biol Psychiatry, 2007, 61(4): 498-503.
[4]
GreenL,FeinD,ModahlC, et al. Oxytocin and autistic disorder: alterations in peptide forms [J]. Biol Psychiatry, 2001, 50(8): 609-613.
[5]
ZhangR,ZhangHF,HanJS, et al. Genes related to oxytocin and arginine-vasopressin pathways: associations with autism spectrum disorders [J]. Neurosci Bull, 2017, 33(2): 238-246.
[6]
TomovaA,HusarovaV,LakatosovaS, et al. Gastrointestinal microbiota in children with autism in Slovakia [J]. Physiol Behav, 2015, 138: 179-187.
[7]
MillerM,BalesKL,TaylorSL, et al. Oxytocin and vasopressin in children and adolescents with autism spectrum disorders: sex differences and associations with symptoms [J]. Autism Res, 2013, 6(2): 91-102.
[8]
BosoM,EmanueleE,PolitiP, et al. Reduced plasma apelin levels in patients with autistic spectrum disorder [J]. Arch Med Res, 2007, 38(1): 70-74.
[9]
American Psychological Association.Diagnostic and statistical manual of mental disorders (DSM)[M].5th ed. Washington DC: American Psychological Association, 2013: 15-18.
[10]
中华人民共和国卫生部. 儿童孤独症诊疗康复指南 [EB/OL]. (2010-07-23)[2017-11-08].

URL    
[11]
OoiYP,WengSJ,KossowskyJ, et al. Oxytocin and autism spectrum disorders: a systematic review and Meta-analysis of randomized controlled trials [J]. Pharmacopsychiatry, 2017, 50(1): 5-13.
[12]
LeeSY,LeeAR,HwangboR, et al. Is oxytocin application for autism spectrum disorder evidence-based? [J]. Exp Neurobiol, 2015, 24(4): 312-324.
[13]
GordonI,JackA,PretzschCM, et al. Intranasal oxytocin enhances connectivity in the neural circuitry supporting social motivation and social perception in children with autism [J]. Sci Rep, 2016, 6: 35054.
[14]
ModahlC,FeinD,WaterhouseL, et al. Does oxytocin deficiency mediate social deficits in autism? [J]. J Autism Dev Disord, 1992, 22(3): 449-451.
[15]
MunesueT,YokoyamaS,NakamuraK, et al. Two genetic variants of CD38 in subjects with autism spectrum disorder and controls [J]. Neurosci Res, 2010, 67(2): 181-191.
[16]
AlvaresGA,QuintanaDS,WhitehouseAJ. Beyond the hype and hope: critical considerations for intranasal oxytocin research in autism spectrum disorder [J]. Autism Res, 2017, 10(1): 25-41.
[17]
WalumH,LichtensteinP,NeiderhiserJM, et al. Variation in the oxytocin receptor gene is associated with pair-bonding and social behavior [J]. Biol Psychiatry, 2012, 71(5): 419-426.
[18]
FeldmanR,Zagoory-SharonO,WeismanO, et al. Sensitive parenting is associated with plasma oxytocin and polymorphisms in the OXTR and CD38 genes [J]. Biol Psychiatry, 2012, 72(3): 175-181.
[19]
LabuschagneI,PhanKL,WoodA, et al. Oxytocin attenuates amygdala reactivity to fear in generalized social anxiety disorder [J]. Neuropsychopharmacology, 2010, 35(12): 2403-2413.
[20]
ZhangHF,DaiYC,WuJ, et al. Plasma oxytocin and arginine-vasopressin levels in children with autism spectrum disorder in china: associations with symptoms [J]. Neurosci Bull, 2016, 32(5): 423-432.
[21]
Al-AyadhiLY. Altered oxytocin and vasopressin levels in autistic children in Central Saudi Arabia [J]. Neurosciences (Riyadh), 2005, 10(1): 47-50.
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