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SOAT-1基因多态性在心脏搭桥手术后认知功能下降和谵妄中的作用。

The role of SOAT-1 polymorphisms in cognitive decline and delirium after bypass heart surgery.

作者信息

Tagarakis G I, Tsolaki-Tagaraki F, Tsolaki M, Diegeler A, Kazis D, Rouska E, Papassotiropoulos A

机构信息

Anaximandrou 24, 3rd Department of Neurology, Papanikolaou Hospital, Thessaloniki, Greece.

出版信息

Clin Res Cardiol. 2007 Sep;96(9):600-3. doi: 10.1007/s00392-007-0539-3. Epub 2007 Jun 27.

Abstract

BACKGROUND

Cognitive decline (CD) and delirium (PD) are commonly observed complications after bypass heart surgery. In this study we aimed to investigate whether certain genetic factors (alleles of the SOAT-1 gene) play a role in their appearance.

PATIENTS AND METHODS

We examined 137 patients receiving coronary bypass surgery with a neuropsychiatric test battery consisting of the Mini Mental State Examination (MMSE), the Brief Psychiatric Rating Scale (BPRS), the Wechsler's Memory Scale-Revised (WMS-R) on admission and one month after surgery, and the Delirium Rating Scale postoperatively, when indicated, and genotyped them in relation to the SOAT-1 genotypes (AA positive group with augmented protection of the nerve cells against stress and the AA negative group--AC and CC subgroups--with diminished protection against stress).

RESULTS

We noted a significant decline in test results postoperatively and a high frequency of delirium (29.92% of the patients). None of these complications could be associated to the SOAT-1 genotypes.

CONCLUSIONS

Our study confirmed the expected cognitive decline and highly frequent delirium after bypass heart surgery and excluded the possible role of SOAT-1 genotype polymorphisms in their genesis.

摘要

背景

认知功能减退(CD)和谵妄(PD)是心脏搭桥手术后常见的并发症。在本研究中,我们旨在调查某些遗传因素(SOAT-1基因的等位基因)在其发生过程中是否起作用。

患者与方法

我们对137例行冠状动脉搭桥手术的患者进行了神经精神测试,包括入院时和术后1个月的简易精神状态检查表(MMSE)、简明精神病评定量表(BPRS)、韦氏记忆量表修订版(WMS-R),以及术后必要时的谵妄评定量表,并对他们进行了与SOAT-1基因分型相关的基因分型(AA阳性组神经细胞对应激的保护增强,AA阴性组——AC和CC亚组——对应激的保护减弱)。

结果

我们注意到术后测试结果显著下降,且谵妄发生率很高(占患者的29.92%)。这些并发症均与SOAT-1基因分型无关。

结论

我们的研究证实了心脏搭桥手术后预期的认知功能减退和高发性谵妄,并排除了SOAT-1基因多态性在其发生过程中的可能作用。

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