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[饮食失调中的遗传标记与人格特质——初步结果]

[Genetic markers and personality traits in eating disorders--preliminary results].

作者信息

Abrahám Ildikó, Bokor Szilvia, Fenyvesi Ilona, Molnár Dénes, Vörös Viktor, Osváth Péter, Gáti Agnes

机构信息

PTE Pszichiátriai Klinika, Pécs.

出版信息

Neuropsychopharmacol Hung. 2007 Dec;9(4):175-81.

Abstract

INTRODUCTION

The multidimensional approach of the ethiopathogenesis of eating disorders include the genetic, biologic, psychosocial effects, and premorbid personality markers.

AIM/METHOD: To determine the potential relation between genetic and personality trate and state factors, and also to investigate the connection of clinical symptoms and diagnostic subgroups. The serotonin transporter gene (VNTR) polymorphism was investigated by polymerase chain reaction (PCR) technology, the personality factors were determined by the Temperament and Character Inventory (TCI) inventory.

RESULTS

Among patients with bulimia nervosa (BN) the short allele of serotonin transporter gene was more frequent than in anorexia nervosa (78% vs. 67%), and in both groups it was more common than in the general population (43%). Patients with anorexia nervosa (AN) have higher scores in the scale of harm avoidance (61,2 vs. 51.4), but in bulimia nervosa the novelty seeking (54.5 vs. 44.2) and the reward dependence factors (53.2 vs. 46.5) were more significant. In the self-directedness (BN: 42.7; AN: 44.3) and the cooperativeness scales (BN: 51.2; AN: 44.6) both groups show lower scores, which could implicate personality disorder in the background of the eating disorders. Anorexic patients with the 10 allele show similar personality factors like patients with bulimia nervosa, while with the 12 allele (homozygotes), their factors were more likely the factors of patients with classic anorexic symptoms.

CONCLUSION

Our data strength the role of specific personality factors in the background of the symptoms of eating disorders. Among patients with bulimia nervosa the 10 allele were more frequent, which could indicate the role of the serotonin system in developing eating disorders. Two subgroups were differentiated among patients with anorexia nervosa in relation with personality factors; the factors of patients with the 12 allele homozygotes were similar to the classical factors of anorexia nervosa, while patients with the 10 allele were like bulimic patients. Our results could improve our knowledge with newer aspects concerning the etiology of eating disorders, that might be used in broadening our preventive and therapeutic facilities in the future.

摘要

引言

饮食失调的病因发病机制的多维方法包括遗传、生物学、心理社会影响以及病前人格特征。

目的/方法:确定遗传与人格特质及状态因素之间的潜在关系,并研究临床症状与诊断亚组之间的联系。通过聚合酶链反应(PCR)技术研究血清素转运体基因(VNTR)多态性,通过气质与性格量表(TCI)确定人格因素。

结果

在神经性贪食症(BN)患者中,血清素转运体基因的短等位基因比神经性厌食症患者更常见(78%对67%),且在两组中都比一般人群更常见(43%)。神经性厌食症(AN)患者在回避伤害量表上得分更高(61.2对51.4),但在神经性贪食症中,寻求新奇(54.5对44.2)和奖励依赖因素(53.2对46.5)更显著。在自我导向(BN:42.7;AN:44.3)和合作性量表(BN:51.2;AN:44.6)上,两组得分均较低,这可能意味着饮食失调背后存在人格障碍。携带10等位基因的厌食症患者表现出与神经性贪食症患者相似的人格因素,而携带12等位基因(纯合子)的患者,其因素更可能是具有典型厌食症状患者的因素。

结论

我们的数据强化了特定人格因素在饮食失调症状背景中的作用。在神经性贪食症患者中,10等位基因更常见,这可能表明血清素系统在饮食失调发展中的作用。在神经性厌食症患者中,根据人格因素区分出两个亚组;携带12等位基因纯合子的患者因素与神经性厌食症的经典因素相似,而携带10等位基因的患者则类似贪食症患者。我们的结果可以从饮食失调病因的新方面增进我们的知识,这可能用于未来扩大我们的预防和治疗手段。

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