Fig. 6From: Multi-platform proteomic analysis of Alzheimer’s disease cerebrospinal fluid and plasma reveals network biomarkers associated with proteostasis and the matrisomeBrain M42 matrisome coverage and SMOC1 levels in CSF and plasma. A–G Coverage of the M42 matrisome module by proteomic platform in CSF and plasma (A). B Differences in SMOC1 relative abundance as measured by Olink between control and AD cases in CSF (left) and plasma (right). C Differences in SMOC1 relative abundance as measured by Olink between control and PD cases in CSF (left) and plasma (right) in the Accelerating Medicines Partnership – Parkinson’s Disease (AMP-PD) cohort. D Differences in SMOC1 relative abundance as measured by TMT-MS among control (n=18), AD (n=17), amyotrophic lateral sclerosis (ALS, n=19), PD (n=13), and frontotemporal dementia (FTD, n=11) subjects, a cohort previously described in Higginbotham et al. [7]. E Correlation of relative SMOC1 levels between CSF and plasma. F Correlation of SMOC1 relative abundance with CSF Aβ/T-Tau ratio in CSF (left) and plasma (right). G Correlation of SMOC1 relative abundance with age in CSF (left) and plasma (right) in the AMP-PD cohort. Differences between groups were assessed by t test or one-way ANOVA with Tukey test. Correlations were performed using Pearson correlation. Aβ, amyloid-β; TMT-MS, tandem mass tag mass spectrometry; SMOC1, SPARC-related modular calcium-binding protein 1; T-Tau, total tau. *<0.05, **<0.01, ***<0.001Back to article page