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血浆胰岛素样生长因子-1与老年人新发谵妄

Plasma insulin growth factor-1 and incident delirium in older people.

作者信息

Wilson K, Broadhurst C, Diver M, Jackson M, Mottram P

机构信息

Elderly Mental Health Academic Unit, University of Liverpool, Liverpool, UK.

出版信息

Int J Geriatr Psychiatry. 2005 Feb;20(2):154-9. doi: 10.1002/gps.1265.

DOI:10.1002/gps.1265
PMID:15660412
Abstract

BACKGROUND

A variety of demographic and clinical variables are acknowledged as risk factors for delirium; a syndrome thought to be mediated by abnormalities in a wide range of neurotransmitters. However, little research has been conducted in this field and the role of neuro-immunological factors as a mechanism of medication has received very little attention.

AIMS

To determine if low base line (on admission) IGF-1 levels (a protective cytokine released by brain cells in response to insult) is a risk factor for incident delirium in patients aged 75 and over admitted to an acute medical ward.

METHOD

Base line demographic and clinical variables and serum IGF-1 levels were measured in a consecutive series of 100 non-delirious subjects on inpatient admission. Subjects were assessed daily regarding the development of delirium during the inpatient episode.

RESULTS

Twelve patients developed incident delirium. IGF-1 (OR: 0.822, CI: 0.69, 0.97, p = 0.027), pre-admission cognitive deterioration (assessed by IQCODE) (OR; 3.26, CI: 1.18, 9.04, p = 0.023) and depression (GDS four item: cut-off score > or = 3) (OR; 8.99, CI 1.59,50.76, p = 0.013) were identified as risk factors for developing subsequent delirium.

CONCLUSIONS

Despite the small size of this study our findings suggest that low, pre-morbid IGF-1 is a risk factor for subsequent delirium in this population, emphasizing the potential protective role of this anabolic cytokine and the need for replication of these findings.

摘要

背景

多种人口统计学和临床变量被认为是谵妄的危险因素;谵妄是一种被认为由多种神经递质异常介导的综合征。然而,该领域的研究很少,神经免疫因素作为谵妄发病机制的作用很少受到关注。

目的

确定低基线(入院时)胰岛素样生长因子-1(IGF-1)水平(一种脑细胞在受到损伤时释放的保护性细胞因子)是否是入住急性内科病房的75岁及以上患者发生谵妄的危险因素。

方法

对连续入院的100名无谵妄的受试者测量基线人口统计学和临床变量以及血清IGF-1水平。在住院期间每天评估受试者是否发生谵妄。

结果

12名患者发生了谵妄。IGF-1(比值比:0.822,可信区间:0.69,0.97,p = 0.027)、入院前认知功能恶化(通过IQCODE评估)(比值比:3.26,可信区间:1.18,9.04,p = 0.023)和抑郁(老年抑郁量表四项:临界值≥3)(比值比:8.99,可信区间1.59,50.76,p = 0.013)被确定为发生后续谵妄的危险因素。

结论

尽管本研究规模较小,但我们的研究结果表明,病前低IGF-1水平是该人群发生后续谵妄的危险因素,强调了这种合成代谢细胞因子的潜在保护作用以及重复这些研究结果的必要性。

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