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. 2021 Jul 2;144(11):3505–3516. doi: 10.1093/brain/awab223

Table 2.

Diagnostic accuracy of plasma and CSF biomarkers to detect amyloid-β positivity on PET or CSF amyloid-β42/40

AUC Accuracy Sensitivity Specificity
Whole sample
Plasma GFAP 0.761 70.6% 71.3% 70.4%
CSF GFAP** 0.694 60.1% 81.2% 51.8%
CSF sTREM2*** 0.643 61.5% 68.6% 58.6%
CSF YKL-40 0.706 59.5% 83.5% 50.0%
All cognitively unimpaired individuals
Plasma GFAP 0.754 70.8% 73.1% 70.3%
CSF GFAP* 0.675 66.0% 67.3% 65.7%
CSF sTREM2 0.699 61.8% 78.9% 58.1%
CSF YKL-40 0.735 57.5% 88.5% 50.6%
All cognitively impaired individuals
Plasma GFAP 0.779 70.9% 71.4% 70.4%
CSF GFAP* 0.679 65.3% 87.1% 43.7%
CSF sTREM2** 0.601 61.4% 73.9% 49.3%
CSF YKL-40** 0.639 62.9% 81.2% 45.1%
Non-Alzheimer’s disease patients
Plasma GFAP 0.755 70.0% 83.3% 62.8%
CSF GFAP 0.624 73.3% 29.2% 94.1%
CSF sTREM2 0.526 60.0% 58.3% 60.8%
CSF YKL-40* 0.585 58.1% 66.7% 54.0%

The analyses conducted in the whole sample, cognitively unimpaired and cognitively impaired individuals were performed using amyloid-β-PET, whereas the analyses conducted in a separate non-Alzheimer’s disease group were performed using CSF amyloid-β42/40.

*

P < 0.05 versus plasma GFAP.

**

P < 0.01 versus plasma GFAP.

***

P < 0.001 versus plasma GFAP.