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100 | 1 | _ | |a Trares, Kira |0 P:(DE-He78)b09508a4c4afe85c57dd131eefa689ea |b 0 |e First author |u dkfz |
245 | _ | _ | |a Addition of inflammation-related biomarkers to the CAIDE model for risk prediction of all-cause dementia, Alzheimer's disease and vascular dementia in a prospective study. |
260 | _ | _ | |a London |c 2024 |b BioMed Central |
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520 | _ | _ | |a It is of interest whether inflammatory biomarkers can improve dementia prediction models, such as the widely used Cardiovascular Risk Factors, Aging and Dementia (CAIDE) model.The Olink Target 96 Inflammation panel was assessed in a nested case-cohort design within a large, population-based German cohort study (n = 9940; age-range: 50-75 years). All study participants who developed dementia over 20 years of follow-up and had complete CAIDE variable data (n = 562, including 173 Alzheimer's disease (AD) and 199 vascular dementia (VD) cases) as well as n = 1,356 controls were selected for measurements. 69 inflammation-related biomarkers were eligible for use. LASSO logistic regression and bootstrapping were utilized to select relevant biomarkers and determine areas under the curve (AUCs).The CAIDE model 2 (including Apolipoprotein E (APOE) ε4 carrier status) predicted all-cause dementia, AD, and VD better than CAIDE model 1 (without APOE ε4) with AUCs of 0.725, 0.752 and 0.707, respectively. Although 20, 7, and 4 inflammation-related biomarkers were selected by LASSO regression to improve CAIDE model 2, the AUCs did not increase markedly. CAIDE models 1 and 2 generally performed better in mid-life (50-64 years) than in late-life (65-75 years) sub-samples of our cohort, but again, inflammation-related biomarkers did not improve their predictive abilities.Despite a lack of improvement in dementia risk prediction, the selected inflammation-related biomarkers were significantly associated with dementia outcomes and may serve as a starting point to further elucidate the pathogenesis of dementia. |
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650 | _ | 7 | |a Alzheimer’s disease |2 Other |
650 | _ | 7 | |a Cohort study |2 Other |
650 | _ | 7 | |a Dementia |2 Other |
650 | _ | 7 | |a Inflammation |2 Other |
650 | _ | 7 | |a Risk prediction |2 Other |
650 | _ | 7 | |a Vascular dementia |2 Other |
700 | 1 | _ | |a Wiesenfarth, Manuel |0 P:(DE-He78)1042737c83ba70ec508bdd99f0096864 |b 1 |u dkfz |
700 | 1 | _ | |a Stocker, Hannah |0 P:(DE-He78)104fae0755c89365b7ae32238b3f1f52 |b 2 |u dkfz |
700 | 1 | _ | |a Perna, Laura |b 3 |
700 | 1 | _ | |a Petrera, Agnese |b 4 |
700 | 1 | _ | |a Hauck, Stefanie M |b 5 |
700 | 1 | _ | |a Beyreuther, Konrad |b 6 |
700 | 1 | _ | |a Brenner, Hermann |0 P:(DE-He78)90d5535ff896e70eed81f4a4f6f22ae2 |b 7 |u dkfz |
700 | 1 | _ | |a Schöttker, Ben |0 P:(DE-He78)c67a12496b8aac150c0eef888d808d46 |b 8 |e Last author |u dkfz |
773 | _ | _ | |a 10.1186/s12979-024-00427-2 |g Vol. 21, no. 1, p. 23 |0 PERI:(DE-600)2168941-6 |n 1 |p 23 |t Immunity & ageing |v 21 |y 2024 |x 1742-4933 |
856 | 4 | _ | |u https://inrepo02.dkfz.de/record/289223/files/s12979-024-00427-2.pdf |
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