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100 1 _ |a Trares, Kira
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245 _ _ |a Association of the inflammation-related proteome with dementia development at older age: results from a large, prospective, population-based cohort study.
260 _ _ |a London
|c 2022
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520 _ _ |a Chronic inflammation is a central feature of several forms of dementia. However, few details on the associations of blood-based inflammation-related proteins with dementia incidence have been explored yet.The Olink Target 96 Inflammation panel was measured in baseline serum samples (collected 07/2000-06/2002) of 1782 older adults from a German, population-based cohort study in a case-cohort design. Logistic regression models were used to assess the associations of biomarkers with all-cause dementia, Alzheimer's disease, and vascular dementia incidence.During 17 years of follow-up, 504 participants were diagnosed with dementia, including 163 Alzheimer's disease and 195 vascular dementia cases. After correction for multiple testing, 58 out of 72 tested (80.6%) biomarkers were statistically significantly associated with all-cause dementia, 22 with Alzheimer's disease, and 33 with vascular dementia incidence. We identified four biomarker clusters, among which the strongest representatives, CX3CL1, EN-RAGE, LAP TGF-beta-1, and VEGF-A, were significantly associated with dementia endpoints independently from other inflammation-related proteins. CX3CL1 (odds ratio [95% confidence interval] per 1 standard deviation increase: 1.41 [1.24-1.60]) and EN-RAGE (1.41 [1.25-1.60]) were associated with all-cause dementia incidence, EN-RAGE (1.51 [1.25-1.83]) and LAP TGF-beta-1 (1.46 [1.21-1.76]) with Alzheimer's disease incidence, and VEGF-A (1.43 [1.20-1.70]) with vascular dementia incidence. All named associations were stronger among APOE ε4-negative subjects.With this large, population-based cohort study, we show for the first time that the majority of inflammation-related proteins measured in blood samples are associated with total dementia incidence. Future studies should concentrate not only on single biomarkers but also on the complex relationships in biomarker clusters.
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650 _ 7 |a Alzheimer’s disease
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650 _ 7 |a Biomarker
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650 _ 7 |a Cohort study
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650 _ 7 |a Dementia
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650 _ 7 |a Inflammation
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650 _ 7 |a Vascular dementia
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650 _ 7 |a Proteome
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650 _ 7 |a Transforming Growth Factor beta1
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650 _ 7 |a Vascular Endothelial Growth Factor A
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650 _ 2 |a Aged
|2 MeSH
650 _ 2 |a Alzheimer Disease: epidemiology
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650 _ 2 |a Cohort Studies
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650 _ 2 |a Dementia, Vascular: epidemiology
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650 _ 2 |a Humans
|2 MeSH
650 _ 2 |a Inflammation: epidemiology
|2 MeSH
650 _ 2 |a Prospective Studies
|2 MeSH
650 _ 2 |a Proteome
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650 _ 2 |a Transforming Growth Factor beta1
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650 _ 2 |a Vascular Endothelial Growth Factor A
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700 1 _ |a Bhardwaj, Megha
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700 1 _ |a Perna, Laura
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700 1 _ |a Stocker, Hannah
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700 1 _ |a Petrera, Agnese
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700 1 _ |a Hauck, Stefanie M
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700 1 _ |a Beyreuther, Konrad
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700 1 _ |a Brenner, Hermann
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700 1 _ |a Schöttker, Ben
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773 _ _ |a 10.1186/s13195-022-01063-y
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