精神分裂症神经变性的生物标志物:系统回顾和荟萃分析。

0 PSYCHIATRY
Jack Christopher Wilson, Kathy Y Liu, Katherine Jones, Jansher Mahmood, Utkarsh Arya, Rob Howard
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引用次数: 0

摘要

问题神经退行性疾病是否是导致老年精神分裂症患者痴呆症发病率增加的原因?多项研究报告显示,与普通人群相比,精神分裂症患者中痴呆症的发病率更高。这可能反映出精神分裂症患者罹患血管性痴呆或阿尔茨海默病(AD)等神经退行性疾病的风险较高。或者,这也可能反映了认知储备较低的人群非病理性、与年龄相关的认知能力下降:我们查阅了将有认知障碍证据的精神分裂症患者(年龄≥45岁)与对照组的尸检结果、海马磁共振成像体积或脑脊液(CSF)中的AD标记物进行比较的论文。随后,我们对死后研究进行了荟萃分析,这些研究比较了认知功能受损的精神分裂症患者与正常对照组或AD组的淀粉样β斑块(APs)或神经纤维缠结(NFTs):与对照组相比,没有研究发现认知功能受损的精神分裂症患者的AP或NFT明显增加。所有将精神分裂症患者的AP或NFT与AD组患者的AP或NFT进行比较的尸检研究均发现,AD组患者的AP或NFT明显增多。没有任何研究发现精神分裂症患者与对照组患者的脑脊液总tau或磷酸化tau存在明显差异。有两项研究比较了精神分裂症患者和对照组的脑脊液Aβ42,发现精神分裂症患者的脑脊液Aβ42明显低于对照组。海马体积的研究结果不一:结论:研究并未发现认知功能受损的精神分裂症患者与对照组相比,AD 相关病变的发生率更高。人群研究中发现的痴呆症发病率较高,这可能反映出用于诊断痴呆症的临床诊断工具缺乏特异性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Biomarkers of neurodegeneration in schizophrenia: systematic review and meta-analysis.

Question: Does neurodegenerative disease underlie the increased rate of dementia observed in older people with schizophrenia? Several studies have reported a higher prevalence of dementia in people with schizophrenia compared with the general population. This may reflect a higher risk of developing neurodegenerative diseases such as vascular dementia or Alzheimer's disease (AD). Alternatively, this may reflect non-pathological, age-related cognitive decline in a population with low cognitive reserve.

Study selection and analysis: We reviewed papers that compared postmortem findings, hippocampal MRI volume or cerebrospinal fluid (CSF) markers of AD, between patients with schizophrenia with evidence of cognitive impairment (age ≥45 years) with controls. We subsequently performed a meta-analysis of postmortem studies that compared amyloid-β plaques (APs) or neurofibrillary tangles (NFTs) in cognitively impaired patients with schizophrenia to normal controls or an AD group.

Findings: No studies found a significant increase of APs or NFTs in cognitively impaired patients with schizophrenia compared with controls. All postmortem studies that compared APs or NFTs in patients with schizophrenia to an AD group found significantly more APs or NFTs in AD. No studies found a significant differences in CSF total tau or phosphorylated tau between patients with schizophrenia and controls. The two studies which compared CSF Aβ42 between patients with schizophrenia and controls found significantly decreased CSF Aβ42 in schizophrenia compared with controls. Hippocampal volume findings were mixed.

Conclusions: Studies have not found higher rates of AD-related pathology in cognitively impaired individuals with schizophrenia compared with controls. Higher rates of dementia identified in population studies may reflect a lack of specificity in clinical diagnostic tools used to diagnose dementia.

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