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024 | 7 | _ | |a 10.1016/j.exger.2025.112684 |2 doi |
024 | 7 | _ | |a 10.1016/j.exger.2025.112684 |2 doi |
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041 | _ | _ | |a English |
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100 | 1 | _ | |a Lohner, Valerie |b 0 |
245 | _ | _ | |a Associations of blood-based biomarkers of neurodegenerative diseases with mortality, cardio- and cerebrovascular events in persons with chronic coronary syndrome. |
260 | _ | _ | |a Amsterdam [u.a.] |c 2025 |b Elsevier Science |
336 | 7 | _ | |a article |2 DRIVER |
336 | 7 | _ | |a Output Types/Journal article |2 DataCite |
336 | 7 | _ | |a Journal Article |b journal |m journal |0 PUB:(DE-HGF)16 |s 1738587517_22142 |2 PUB:(DE-HGF) |
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336 | 7 | _ | |a Journal Article |0 0 |2 EndNote |
500 | _ | _ | |a #LA:C120# / Volume 200, February 2025, 112684 |
520 | _ | _ | |a In light of growing evidence highlighting interactions between cardiac and brain health, we investigated associations of biomarkers of neurodegenerative diseases with adverse outcomes (all-cause and cardiovascular mortality, major cardiovascular events, and stroke) in persons with chronic coronary syndrome (CCS).We used data from a cohort of persons with CCS for whom major adverse events were recorded over a follow-up of 20 years. We measured biomarkers of neurodegenerative diseases in baseline blood samples, using the Single-Molecule Array Technology on a HD-1 Analyzer. These include biomarkers of neuronal (neurofilament light chain (NfL) (n = 379)) and glial neurodegeneration (glial fibrillary acidic protein (GFAP) (n = 379)), and Alzheimer's disease pathology (phosphorylated tau181 (n = 379), total tau (n = 377), and amyloid β (Aβ40, Aβ42, Aβ42/Aβ40) (n = 377)). We applied Cox-proportional hazards models to evaluate associations of these biomarkers with adverse outcomes, adjusting for covariates and exploring interactions with apolipoprotein E (ApoE) ε4 genotype.Participants with higher NfL levels had increased rates of all-cause and cardiovascular mortality (Hazard ratio per increase by one standard deviation (95 % confidence interval): all-cause mortality: 1.36 (1.10-1.68); cardiovascular mortality: 1.42 (1.05-1.93)). The Aβ40/Aβ42-ratio was linked to incident stroke (0.72 (0.52-1.00)). Associations of GFAP with all-cause mortality and incident stroke were depending on ApoE ε4 genotype. The other biomarkers were not significantly associated with the studied outcomes.In persons with CSS, NfL and the Aβ40/Aβ42-ratio were related to mortality and incident stroke, respectively, whereas associations of GFAP with adverse outcomes varied by ApoE genotype. These biomarkers might play a role in linking aging, cardiovascular and neurodegenerative diseases. |
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650 | _ | 7 | |a Blood-based biomarkers of neurodegenerative diseases |2 Other |
650 | _ | 7 | |a Cerebrovascular events |2 Other |
650 | _ | 7 | |a Chronic coronary syndrome |2 Other |
650 | _ | 7 | |a Coronary heart disease |2 Other |
650 | _ | 7 | |a Epidemiology |2 Other |
650 | _ | 7 | |a Major cardiovascular events |2 Other |
650 | _ | 7 | |a Mortality |2 Other |
700 | 1 | _ | |a Perna, Laura |b 1 |
700 | 1 | _ | |a Schöttker, Ben |0 P:(DE-He78)c67a12496b8aac150c0eef888d808d46 |b 2 |u dkfz |
700 | 1 | _ | |a Perneczky, Robert |b 3 |
700 | 1 | _ | |a Brenner, Hermann |0 P:(DE-He78)90d5535ff896e70eed81f4a4f6f22ae2 |b 4 |u dkfz |
700 | 1 | _ | |a Mons, Ute |0 P:(DE-He78)1b59582b6c05ac4e57aa8b90dd9667f9 |b 5 |e Last author |u dkfz |
773 | _ | _ | |a 10.1016/j.exger.2025.112684 |0 PERI:(DE-600)2005397-6 |p 112684 |t Experimental gerontology |v 200 |y 2025 |x 0531-5565 |
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