期刊文献+

5-羟色胺转运体基因长度多态性与孤独症谱系障碍易感性关系的Meta分析 被引量:3

An Integrated Meta-analysis of the Association between 5-HTTLPR and Autism Spectrum Disorder
暂未订购
导出
摘要 目的采用Meta分析的方法综合评价5-羟色胺转运体基因长度多态性(5-hydroxytryptamine transporterlength polymorphism,5-HTTLPR)与孤独症谱系障碍(autism spectrum disorder,ASD)易感性之间的关系。方法在多个数据库中全面检索相关文献,收集2012年10月前有关5-HTTLPR与ASD易感性关系的病例对照研究及以家系为基础的传递/不平衡检验(TDT)的数据,采用R软件的Catmap软件包进行Meta分析。结果该研究共纳入25篇文献。Meta分析结果显示合并后OR值为1.10(95%CI=0.95~1.26,Pheterogeneity=0.000)。敏感性分析进一步表明该结果具有良好的稳定性。分层分析显示,病例对照研究和TDT研究的合并OR值分别为1.19(95%CI=0.83~1.72)和1.07(95%CI=0.92~1.25);样本量大于150和小于等于150的研究的合并OR值分别为1.14(95%CI=0.98~1.34)和1.09(95%CI=0.92~1.29);美洲人群、欧洲人群和亚洲人群的合并OR值分别为1.25(95%CI=1.12~1.40)、1.03(95%CI=0.84~1.28)和0.81(95%CI=0.66~0.99)。结论 5-HTTLPR与ASD易感性之间不存在明显关联,但这种关系在不同地域人群中可能存在较大差异。 Objective To clarify the relationship between fi-hydroxytryptamine transporter length polymorphism(5-HTTL- PR) and autism spectrum disorder(ASD) by using a meta-analysis. Methods Multiple electronic databases were searched to re- trieve the literatures about the association between 5-HTTLPR and ASD susceptibility. These literatures were published before October 2012. Data of case-control studies and transmission/disequilibrium test(TDT) studies were collected and analyzed using the Catmap package in R software. Results Twenty-five studies were included in this recta-analysis. The combined result showed the lack of association between 5-HTTLPR and ASD(OR= 1.10,95 %CI= 0. 95-1.26, Phet*mgendty = 0. 000) in the ran- dom-effects model and the sensitivity analysis further indicated the stability of this result. By stratified analysis, no evidence of significant association between this polymorphism and ASD was found either in the case-control studies(OR = 1.19,95 % CI= 0.83-1.72,) or in the TDT studies(OR= 1.07,95%CI= 0. 92-1. 25). The pooled OR for studies of sample size 〉150 and sample size≤150 was 1.14(95%CI=0.98-1.34) and 1.09(95%CI=0. 92-1.29) ,respectively. However,the stratified anal- ysis by population source demonstrated that the significant association was present in American(OR = 1.25,95 % CI= 1.12- 1.40) and Asian(OR = 0. 81,95% CI= 0. 66 - 0. 99) populations, but for the European population, no positive result was ob- tained(OR=1 03,95%CI=0.84--1.28). Conclusion 5-HTTLPR may not contribute to the risk of ASD. This association be- tween 5-HTTLPR and ASD susceptibility may vary across different populations.
出处 《华中科技大学学报(医学版)》 CAS CSCD 北大核心 2013年第2期181-186,共6页 Acta Medicinae Universitatis Scientiae et Technologiae Huazhong
基金 国家自然科学基金资助项目(No.81273092)
关键词 孤独症谱系障碍 5-羟色胺转运体基因长度多态性 META分析 autism spectrum disorder b-hydroxytryptamine transporter length polymorphisml meta-analysls
  • 相关文献

参考文献40

  • 1Elsabbagh M, Divan G, Koh Y J, et al. Global prevalence of autism and other pervasive developmental disorders[J]. Au- tism Res,2012,5(3) : 160-179.
  • 2王佳,于聪,孙彩虹,夏薇,梁爽,武丽杰.孤独症患儿236名家庭疾病负担状况调查[J].中国学校卫生,2010,31(2):138-140. 被引量:28
  • 3Freitag C M. The genetics of autistic disorders and its clinicalrelevancet a review of the literature [J]. Mol Psychiatry, 2006,12(1) z2-22.
  • 4Bailey A, Le Couteur A, Gottesman I, et al. Autism as a strongly genetic disorder: evidence from a British twin study [J]. Psyehol Med,1995,25(1) :63-77.
  • 5Muhle R, Trentacoste S V, Rapin I. The genetics of autism [J]. Pediatrics,2004,113(5):e472-e486.
  • 6Murphy D L, Lerner A,Rudnick G, et al. Serotonin transport- er:gene,genetic disorders,and pharmacogenetics[J]. Mol In- terv,2004,4(2) : 109-123.
  • 7Abramson R K, Wright H H, Carpenter R, et al. Elevated blood serotonin in autistic probands and their first-degree rel- atives[J]. J Autism Dev Disord, 1989,19(3) :397-407.
  • 8Piven J,Tsai G, Nehme E, et al. Platelet serotonin, a possible marker for familial autism[J]. J Autism Dev Disord, 1991,21 (1) :51-59.
  • 9Anderson G M, Freedman D X,Cohen D J, et al. Whole blood serotonin in autistic and normal subjects[J]. J Child Psychol Psyc,1987,28(6) :885-900.
  • 10McDougle C J,Naylor S T,Cohen D J,et al. A double-blind, placebo-controlled study of fluvoxamine in adults with autis- tic disorder[J]. Arch Gen Psychiat, 1996,63(11) : 1001-1008.

二级参考文献38

  • 1Matthew WS, Paul JL, David LP, et al. The genetics of childhood psychiatric disorders: a decade of progress, J Am Acad Child Adolesc Psychiatry, 2000, 39(8):946.
  • 2Kim S-J, Cox N, Courchesne R, et al. Transmission disequilbrium mapping at the serotonin transporter gene (SLC6A4) region in autistic disorder. Molecular Psychiatry, 2002, 7 (3): 278.
  • 3Veenstra-Vander Weele J, Anderson GM, Cook EH. Pharmacogenetics and the serotonin system: initial studies and future directions. Eur J Pharmacol, 2000, 410(2 - 3): 165.
  • 4Cook EH, Crotts M, Leventhal BL. Autistic disorder and other pervasive developmental disorders. In: Klykylo WM, Kay J, Rube Deds. Clinical Child Psychiatry. 1st ed. Philadelphia: Saunders, 1998. 337-355.
  • 5Lesch KP, Bengel D, Heil A, et al. Association of anxiety-related traits with a polymorphism in the serotonin transporter gene regulatory region.Science, 1996, 274(5292): 1527.
  • 6Tordjman S, Gutknecht L, Carlier M, et al. Role of the serotoniin transporter gene in the behavioral expression of autism. Mol Psychiatry, 2001,6(4) :434.
  • 7Maestrini E, Lai C, Marlow A, et al. Serotonin transporter (5-HTT) and gamma-aminobutyric acid receptor subunit beta3 (GABRB3) gene polymorphisms are not associated with autism in the IMGSA families. Am J Med Genet, 1999, 88(5) :492.
  • 8Persico AM, Militerni R, Bravaccio C, et al. Lack of association between serotonin transporter gene promoter variants and autistic disorder in two ethnically distinct samples. Am J Med Genet, 2000, 96(1):123.
  • 9Zhong N, Ye L, Ju W, et al. 5-HTTLPR variants not associated with autistic spectrum disorders. Neurogenetics, 1999, 2(2): 129.
  • 10Cook EH Jr, Courchesne R, Lord C, et al. Evidence of linkage between the serotonin transporter and autistic disorder. Mol Psychiatry, 1997, 2(3): 247.

共引文献35

同被引文献59

  • 1Taqhizadeh N, Davidson A,Williams K,et al. Autism spectrum disorder ( ASD ) and its perioperative management [J]. Paediatr Anaesth, 2015, 25 ( 11 ) : 1076 - 1084.
  • 2Tzagkaraki E, Sofocleous C, Fryssira-Kanioura H, et al. Screening of UBE3A gene in patients referred for Angelman Syndrome [J]. Eur J Paediatr Neurol, 2013, 17 (4) : 366 - 373.
  • 3Liu X, Takumi T. Genomic and genetic aspects of autism spectrum disorder [ J ]. Biochem Biophys Res Commun, 2014, 452 (2) : 244 -253.
  • 4Szatmari P, Paterson AD, Zwaigenbaum L, et al. Mapping autism risk loci using genetic linkage and chromosomal rearrangements [ J ]. Nat Genet, 2007, 39 (3) : 319 - 328.
  • 5Cai G, Edelmann L, Goldsmith JE, et al. Multiplex ligation- dependent probe amplification for genetic screening in autism spectrum disorders : efficient identification of known microduplications and identification of a novel microduplication in ASMT [J]. BMC Med Genomics, 2008, 16(1): 50.
  • 6Lintas C, Persico AM. Autistic phenotypes and genetic testing: state-of-the-art for the clinical geneticist [J]. J Med Genet, 2009, 46 (1): 1-8.
  • 7Takumi T. A humanoid mouse model of autism [ J]. Brain Dev, 2010, 32 (9) : 753 -758.
  • 8Yoo HK, Chung S, Hong JP, et al. Microsatellite marker in gamma-aminobutyric acid-a receptor beta 3 subunit gene and autism spectrum disorders in Korean trios [ J ]. Yonsei Med J, 2009, 50 (2) : 304 -306.
  • 9Gadow KD, DeVincent CJ, Siegal VI, et al. Allele-specific associations of 5-HTTLPR/rs25531 with ADHD and autism spectrum disorder [ J ]. Prog Neuropsychopharmacol Biol Psychiatry, 2013, 10(40) : 292 - 297.
  • 10Meguid NA, Gebril OH, Khalil RO. A study of blood serotonin and serotonin transporter promoter variant (5- HTTLPR) polymorphism in Egyptian autistic children [ J]. Adv Biomed Res, 2015, (4) :94.

引证文献3

二级引证文献16

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部