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在巴尔的摩纵向衰老研究参与者中,寻求新奇行为与多巴胺D4受体(D4DR)外显子III七重复等位基因之间无关联。

No association between novelty seeking and dopamine D4 receptor (D4DR) exon III seven repeat alleles in Baltimore Longitudinal Study of Aging participants.

作者信息

Vandenbergh D J, Zonderman A B, Wang J, Uhl G R, Costa P T

机构信息

Molecular Neurobiology Branch, Intramular Research, NIDA, NIH, USA.

出版信息

Mol Psychiatry. 1997 Sep;2(5):417-9. doi: 10.1038/sj.mp.4000309.

Abstract

Recent studies by Ebstein et al and Benjamin et al found associations between long repeat polymorphisms in the D4 dopamine receptor gene (D4DR) and individual variation in a human personality trait, identified as 'Novelty Seeking' (NS). Ebstein et al used the Tridimensional Personality Questionnaire (TPQ) to measure NS scores; Benjamin et al used the Revised NEO Personality Inventory (NEO-PI-R) to estimate NS scores. However, Malhotra et al failed to replicate the association between the direct measure of NS using the TPQ and the long alleles of the D4DR genotypes in two Finnish samples. In an attempt to confirm the association found by Benjamin et al using NEO-PI-R estimated NS, the present study used an alternative design extreme groups strategy to select high and low novelty seeking research volunteers from the Baltimore Longitudinal Study of Aging (BLSA). There were no significant associations between long alleles (7-repeat allele) and high novelty seeking groups. The findings of Ebstein and colleagues and those of Benjamin and colleagues do not generalize to this American middle-aged, mixed-gender sample, a conclusion also consistent with the findings of a recent Swedish study. Demographic factors such as the age and gender composition of the samples are important sources of variation in allelic association studies and future research must carefully address whether the D4DR genetic polymorphisms vary substantially across demographic groups.

摘要

埃布斯坦等人以及本杰明等人最近的研究发现,D4多巴胺受体基因(D4DR)中的长重复多态性与一种被确定为“新奇寻求”(NS)的人格特质的个体差异之间存在关联。埃布斯坦等人使用三维人格问卷(TPQ)来测量新奇寻求得分;本杰明等人使用修订的大五人格量表(NEO-PI-R)来估计新奇寻求得分。然而,马尔霍特拉等人未能在两个芬兰样本中重现使用TPQ直接测量新奇寻求与D4DR基因型的长等位基因之间的关联。为了证实本杰明等人使用NEO-PI-R估计的新奇寻求所发现的关联,本研究采用了一种替代设计的极端组策略,从巴尔的摩纵向衰老研究(BLSA)中挑选高新奇寻求和低新奇寻求的研究志愿者。长等位基因(7重复等位基因)与高新奇寻求组之间没有显著关联。埃布斯坦及其同事以及本杰明及其同事的研究结果并不适用于这个美国中年、混合性别的样本,这一结论也与最近一项瑞典研究的结果一致。样本的年龄和性别构成等人口统计学因素是等位基因关联研究中变异的重要来源,未来的研究必须仔细探讨D4DR基因多态性在不同人口群体中是否存在显著差异。

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