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多巴胺D4受体(DRD4)基因在依恋紊乱中作用的进一步证据:外显子III 48碱基对重复序列与-521 C/T启动子多态性的相互作用

Further evidence for the role of the dopamine D4 receptor (DRD4) gene in attachment disorganization: interaction of the exon III 48-bp repeat and the -521 C/T promoter polymorphisms.

作者信息

Lakatos K, Nemoda Z, Toth I, Ronai Z, Ney K, Sasvari- Szekely M, Gervai J

机构信息

Social Development Group, Institute of Psychology, Hungarian Academy of Sciences, Budapest, POB 398, Hungary-1394.

出版信息

Mol Psychiatry. 2002;7(1):27-31. doi: 10.1038/sj.mp.4000986.

Abstract

In non-clinical low-risk populations 15% of infants show disorganized attachment behavior(1,2) with their caregivers in the Strange Situation,(3) a mildly stressful laboratory procedure testing infants' ability to cope with separation anxiety. Disorganization of early attachment has been primarily ascribed to inadequate parenting,(2,4,5) and has been associated with childhood behavior problems(6,7)and adolescent psychopathological tendencies.(5) We have recently reported an association between the DRD4 exon III 48 basepair repeat polymorphism and disorganization of infants' attachment behavior towards their mother in a low-social-risk group of 1-year-old infants:(8) the risk for disorganized attachment among infants carrying the 7-repeat allele was fourfold. Here we report further evidence for the involvement of the dopamine D4 receptor gene in attachment disorganization. The same group of infants was genotyped for the functional -521 C/T single nucleotide polymorphism (SNP) in the upstream regulatory region of the DRD4 gene(9) in order to test the association with attachment disorganization both alone and in interaction with the DRD4 exon III 7-repeat allele. While the -521 C/T genotype itself had no effect on attachment status (chi(2) = 0.41, df = 2, P = 0.82), there was an interaction between the structural 48-bp repeat polymorphism and the -521 C/T promoter polymorphism: the association between disorganized attachment and the 7-repeat allele was enhanced in the presence of the -521 T allele (chi(2) = 6.61 and 6.67, df = 1, P < 0.025 for CT and TT genotypes, respectively). In the presence of both risk alleles the odds ratio for disorganized attachment increased tenfold. This result supports our previous postulation that the DRD4 gene plays a role in the development of attachment behavior in low-risk, non-clinical populations.

摘要

在非临床低风险人群中,15%的婴儿在陌生情境中与其照料者表现出紊乱型依恋行为(1,2),陌生情境是一种轻度应激的实验室程序,用于测试婴儿应对分离焦虑的能力(3)。早期依恋的紊乱主要归因于养育方式不当(2,4,5),并与儿童期行为问题(6,7)以及青少年心理病理倾向(5)相关。我们最近报告了在一组低社会风险的1岁婴儿中,多巴胺D4受体基因(DRD4)外显子III 48碱基对重复多态性与婴儿对母亲的依恋行为紊乱之间的关联:携带7重复等位基因的婴儿出现紊乱型依恋的风险是四倍。在此,我们报告了多巴胺D4受体基因参与依恋紊乱的进一步证据。对同一组婴儿进行了DRD4基因上游调控区功能性-521 C/T单核苷酸多态性(SNP)的基因分型(9),以测试其与依恋紊乱的单独关联以及与DRD4外显子III 7重复等位基因的相互作用。虽然-521 C/T基因型本身对依恋状态没有影响(χ² = 0.41,自由度 = 2,P = 0.82),但结构48碱基对重复多态性与-521 C/T启动子多态性之间存在相互作用:在存在-521 T等位基因的情况下,紊乱型依恋与7重复等位基因之间的关联增强(对于CT和TT基因型,χ²分别为6.61和6.67,自由度 = 1,P < 0.025)。在同时存在两种风险等位基因的情况下,紊乱型依恋的优势比增加了十倍。这一结果支持了我们之前的假设,即DRD4基因在低风险、非临床人群依恋行为的发展中起作用。

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