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通过 p300 对同卵双胞胎中一致和不一致的精神分裂症遗传易感性进行测量。

Genetic liability to schizophrenia measured by p300 in concordant and discordant monozygotic twins.

机构信息

Department of General Psychiatry, Centre for Psychosocial Medicine, University of Heidelberg, Germany. Anuradha.Sharma @ med.uni-heidelberg.de

出版信息

Psychopathology. 2011;44(6):398-406. doi: 10.1159/000325883. Epub 2011 Sep 29.

Abstract

BACKGROUND

Differential effects of genes and environment can contribute to etiological heterogeneity in schizophrenia. Twins concordant and discordant for schizophrenia may differ in genetic predisposition to schizophrenia with concordant twins having a higher genetic liability and discordant twins having a lower genetic liability to schizophrenia. We aimed to investigate whether P300 amplitude (which has been postulated as a genetic marker for schizophrenia) reflected this heterogeneity.

SAMPLING AND METHODS

We compared P300 amplitudes across 36 monozygotic twin pairs (6 concordant for schizophrenia/schizoaffective disorder, 11 discordant and 19 healthy control pairs) performing an auditory oddball task, using multiple regression (age, gender, birth order, premorbid IQ as covariates). We further looked at the correlation between the Brief Psychiatric Rating Scale (BPRS) and P300 amplitude in affected twins, and compared concordant and discordant affected twins on the Global Assessment Scale (GAS).

RESULTS

Multiple regression yielded a highly significant model (p = 0.004) though the explained variance was limited (21%). The main effect of the group on P300 amplitude was significant (p = 0.0001): affected concordant twins showed a significantly lower P300 amplitude as compared to affected discordant (p = 0.005, Cohen's d = 1.08) and control twins (p = 0.000, d = 1.16). Discordant affected and unaffected twins did not differ significantly from each other or from control twins. P300 did not correlate significantly with the BPRS and the affected groups did not differ across the GAS.

CONCLUSIONS

Our results provide evidence for etiological heterogeneity within schizophrenia pointing to different pathophysiological mechanisms that may underlie more and less genetically determined forms of schizophrenia. They also indicate that P300 correlates with a differing degree of genetic liability to schizophrenia independently of the psychopathological status and even in the presence of similar functional profiles.

摘要

背景

基因和环境的差异效应可能导致精神分裂症的病因异质性。精神分裂症同卵双胞胎的一致性和不一致性可能在精神分裂症的遗传易感性上有所不同,一致性双胞胎的遗传易感性更高,而不一致性双胞胎的遗传易感性更低。我们旨在研究 P300 振幅(被推测为精神分裂症的遗传标志物)是否反映了这种异质性。

方法

我们比较了 36 对同卵双胞胎(6 对精神分裂症/分裂情感障碍一致,11 对不一致,19 对健康对照)在执行听觉Oddball 任务时的 P300 振幅,使用多元回归(年龄、性别、出生顺序、学前智商作为协变量)。我们进一步研究了受影响的双胞胎中 BPRS 和 P300 振幅之间的相关性,并比较了一致和不一致的受影响双胞胎的 GAS 评分。

结果

多元回归产生了一个高度显著的模型(p = 0.004),尽管解释的方差有限(21%)。组间对 P300 振幅的主要影响显著(p = 0.0001):与不一致的受影响的双胞胎相比,受影响的一致双胞胎的 P300 振幅明显较低(p = 0.005,Cohen's d = 1.08)和对照组双胞胎(p = 0.000,d = 1.16)。不一致的受影响和未受影响的双胞胎彼此之间以及与对照组双胞胎之间没有显著差异。P300 与 BPRS 无显著相关性,受影响的组在 GAS 上也没有差异。

结论

我们的研究结果为精神分裂症中的病因异质性提供了证据,表明不同的病理生理机制可能是导致遗传程度较高和较低的精神分裂症的原因。它们还表明,P300 与精神分裂症的遗传易感性程度相关,与精神病理学状态无关,甚至在存在相似的功能谱的情况下也是如此。

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