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重性抑郁障碍易感基因EHD3与疾病认知功能相关 被引量:3

Association between EHD3 Gene and the Cognitive Function of Patients with Major Depressive Disorder
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摘要 目的探讨EHD3基因与重性抑郁障碍(MDD)患者认知功能的相关性。方法以47例MDD患者与40例正常对照者为研究对象,分析其认知功能的差异,然后将MDD患者的各项量表得分作为数量性状,采用UNPHASED软件的数量性状模块,分析认知功能与EHD3基因多态性的相关性。结果 MDD组WAIS-RC和WMS-R量表的各项评分均显著低于正常对照组(P均<0.05)。EHD3基因的rs3769621等位基因及基因型分别与WAIS-RC图形拼凑原始分(χ2=10.561,P=0.001;χ2=7.922,P=0.019)和图形拼凑量表分(χ2=12.627,P=0.00038;χ2=11.775,P=0.0027),以及WMS-R心智(1-100)原始分(χ2=8.762,P=0.003;χ2=17.399,P=0.00016)和心智(1-100)量表分(χ2=10.356,P=0.001;χ2=14.958,P=0.00056)显著相关;经过Bonferroni法校正后,上述结果差异仍显著。结论在中国北方汉族人群中,EHD3基因可能与MDD认知功能内表型相关。 Objective To analyze the potential association between the EHD3 gene and the cognitive function of patients with major depressive disorder (MDD).Methods A total of 47 MDD patients and 40 healthy controls were enrolled in this study.After their cognitive functions were analyzed,the scores of the MDD patients were used as the quantitative traits; by using the quantitative trait module in the UNPHASED soft ware,we analyzed the potential association of the cognitive traits with the EHD3 gene.Results The cognitive scores (WAIS-RC and WMS-R) of MDD patients were significantly lower than those of controls (P < 0.05).The rs3769621 allele and genotype of EHD3 gene were significantly associated with the raw score and scaled score ofWAIS-RC (x2=10.561,P=0.001; x2=7.922,P=0.019; x2=12.627,P=0.00038; x2 =11.775,P=0.0027) andWMS-R (x2=8.762,P=0.003; x2=17.399,P=0.00016; x2=10.356,P =0.001 ; x2 =14.958,P =0.00056).Such associations remained statistically significant after Bonferroni correction.Conclusion The EHD3 gene may be associated with the endophenotype of cognitive function in MDD patients.
出处 《中国医学科学院学报》 CAS CSCD 北大核心 2014年第3期227-233,共7页 Acta Academiae Medicinae Sinicae
基金 国家自然科学基金(31222031) 中央高校基本科研业务费专项资金(2012S05) 协和青年科研基金(2012J09) "新世纪优秀人才支持计划"(NCET-12-0071)~~
关键词 重性抑郁障碍 认知功能 EHD3基因 major depressive disorder cognitive function EHD3 gene
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  • 1Robbins TW,Cognition:the uhimate brain function[J].Neumpsychopharmacology,2011,36 (1):1-2.
  • 2Papakostas GI,Petersen T,Mahal Y,et al.Quality of life assessments in major depressive disorder:a review of the literature[J].Gen Hosp Psychiatry,2004,26(1):13-17.
  • 3Almasy L,Blangem J.Endophenotypes as quantitative risk factors for psychiatric disease:rationale and study design[J].AmJMedGenet,2001,105(1):42-44.
  • 4Gould TD,Gottesman II.Psychiatric endophenotypes and the development of valid animal models[J].Genes Brain Behav,2006,5(2):113-119.
  • 5Gottesman II,Gould TD.The endophenotype concept in psychiatry:etymology and strategic intentions[J].Am J Psychiatry,2003,160(4):636-645.
  • 6Blume JJ,Halbach A,Behrendt D,et al.EHD proteins are associated with tubular and vesicular compartments and interact with specific phospholipids[J].Exp Cell Res,2007,313(2):219-231.
  • 7Naslavsky N,Rahajeng J,Sharma M,et al.Interactions between EHD proteins and Rab11-FIP2:a role for EHD3 in early endosomal transpo[J].Mol Biol Cell,2006,17(1):163-177.
  • 8Muglia P,Tozzi F,Galwey NW,et al.Genome-wide association study of recurrent major depressive disorder in two European case-control cohorts[J].Mol Psychiatry,2010,15(6):589-601.
  • 9Shi C,Zhang K,Wang K,et al.A study of the combined effects of the EHD3 and FREM3 genes in patients with major depressive disorder[J].Am J Med Genet B Neuropsychiatr Genet,2012,159B(3):336-342.
  • 10龚耀先.修订韦氏成人智力量表手册[M].长沙:湖南地图出版社,1992:1-188.

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  • 1Lee RS, Hermens DF, Porter MA, et al. A meta-analysis of cognitive deficits in first-episode Major Depressive Disorder [J]. J Affect Disord, 2012,140(2) : 113- 124.
  • 2Wagner S, Muller C, Helmreich I, et al. A meta-analysis of cognitive functions in children and adolescents with major depressive disorder[J]. Eur Child Adolesc Psychiatry, 2015,24 (1):5-19.
  • 3Yeh YC, Tsang HY, Lin PY, et al. Subtypes of mind cogni tive impairment among the elderly with major depressive disor der in remission [J]. Am J Geriatr Psychiatry, 2011,19 (11) 923-931.
  • 4Van den Berg MD, Oldehinkel AJ, Bouhuys AL. Depression in later life: three etiologically different subgroups [J]. J Affect Disord,2001,65(1) : 19-26.
  • 5Wang X, Hou Z, Yuan Y, et al. Association study between plasma GDNF and cognitive function in late-onset depression [J]. J Affect Disord,2011,132(3) :418-421.
  • 6Talarowska M, Zajaezkowska M, Galeeki P. Cognitive functions in first-episode depression and recurrent depressive disorder. Psyehiatr Danub[J],2015,27(1):38-43.
  • 7Wang X, Wang Z, Wu Y, et al. Association analysis of the catechol- O- methyltransferase/methyle- netetrahydrofolate reductase genes and cognition in late- onset depression[J]. Psychiatry Clin Neurosci, 2014,68 (5) : 344- 352.
  • 8Wang X, Wang Z, Wu Y, et al. Tryptophan hydroxylase 2 gene is associated with cognition in late-onset depression in a Chinese Han population[J]. Neurosci Lett, 2015, 600: 98- 103.
  • 9Rajan KB, Wilson RS, Skarupski KA, et al. Gene-behavior interaction of depressive symptoms and the apolipoprotein E ( varepsilon) 4 allele on cognitive decline[J]. Psychosom Med, 2014,76(2) :101-108.
  • 10Guo J, Liu Z, Dai H, et al. Preliminary investigation of the influence of CREB1 gene polymorphisms on cognitive dysfunction in Chinese patients with major depression[J]. Int J Neurosci,2014,124(1) :22-29.

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