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一种用于早期检测阿尔茨海默病的新型血液检测方法。

A novel blood test for the early detection of Alzheimer's disease.

机构信息

DiaGenic ASA, Oslo, Norway.

出版信息

J Alzheimers Dis. 2011;23(1):121-9. doi: 10.3233/JAD-2010-101521.

Abstract

Despite a variety of testing approaches, it is often difficult to make an accurate diagnosis of Alzheimer's disease (AD), especially at an early stage of the disease. Diagnosis is based on clinical criteria as well as exclusion of other causes of dementia but a definitive diagnosis can only be made at autopsy. We have investigated the diagnostic value of a 96-gene expression array for detection of early AD. Gene expression analysis was performed on blood RNA from a cohort of 203 probable AD and 209 cognitively healthy age matched controls. A disease classification algorithm was developed on samples from 208 individuals (AD = 103; controls = 105) and was validated in two steps using an independent initial test set (n = 74; AD = 32; controls = 42) and another second test set (n = 130; AD = 68; controls = 62). In the initial analysis, diagnostic accuracy was 71.6 ± 10.3%, with sensitivity 71.9 ± 15.6% and specificity 71.4 ± 13.7%. Essentially the same level of agreement was achieved in the two independent test sets. High agreement (24/30; 80%) between algorithm prediction and subjects with available cerebrospinal fluid biomarker was found. Assuming a clinical accuracy of 80%, calculations indicate that the agreement with underlying true pathology is in the range 85%-90%. These findings suggest that the gene expression blood test can aid in the diagnosis of mild to moderate AD, but further studies are needed to confirm these findings.

摘要

尽管有多种测试方法,但要准确诊断阿尔茨海默病(AD),尤其是在疾病的早期阶段,通常非常困难。诊断基于临床标准以及排除其他痴呆原因,但只有在尸检时才能做出明确诊断。我们研究了 96 个基因表达阵列检测早期 AD 的诊断价值。对来自 203 例可能 AD 和 209 例认知健康年龄匹配对照者的血液 RNA 进行了基因表达分析。在来自 208 名个体的样本上(AD=103;对照=105)开发了疾病分类算法,并通过两个独立的初始测试集(n=74;AD=32;对照=42)和另一个第二测试集(n=130;AD=68;对照=62)进行了两步验证。在初步分析中,诊断准确率为 71.6±10.3%,灵敏度为 71.9±15.6%,特异性为 71.4±13.7%。在两个独立的测试集中,基本达到了相同的一致性水平。在具有可用脑脊液生物标志物的受试者中,算法预测与实际情况之间的一致性非常高(24/30;80%)。假设临床准确率为 80%,计算表明与潜在真实病理的一致性在 85%-90%之间。这些发现表明,基因表达血液测试可以帮助诊断轻度至中度 AD,但需要进一步研究来证实这些发现。

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