000276341 001__ 276341 000276341 005__ 20250216000753.0 000276341 0247_ $$2doi$$a10.1016/j.exger.2025.112684 000276341 0247_ $$2pmid$$apmid:39824235 000276341 0247_ $$2ISSN$$a0531-5565 000276341 0247_ $$2ISSN$$a1873-6815 000276341 0247_ $$2altmetric$$aaltmetric:173429399 000276341 037__ $$aDZNE-2025-00289 000276341 041__ $$aEnglish 000276341 082__ $$a610 000276341 1001_ $$aLohner, Valerie$$b0 000276341 245__ $$aAssociations of blood-based biomarkers of neurodegenerative diseases with mortality, cardio- and cerebrovascular events in persons with chronic coronary syndrome. 000276341 260__ $$aAmsterdam [u.a.]$$bElsevier Science$$c2025 000276341 3367_ $$2DRIVER$$aarticle 000276341 3367_ $$2DataCite$$aOutput Types/Journal article 000276341 3367_ $$0PUB:(DE-HGF)16$$2PUB:(DE-HGF)$$aJournal Article$$bjournal$$mjournal$$s1739354471_25680 000276341 3367_ $$2BibTeX$$aARTICLE 000276341 3367_ $$2ORCID$$aJOURNAL_ARTICLE 000276341 3367_ $$00$$2EndNote$$aJournal Article 000276341 520__ $$aIn light of growing evidence highlighting interactions between cardiac and brain health, we investigated associations of biomarkers of neurodegenerative diseases with adverse outcomes (all-cause and cardiovascular mortality, major cardiovascular events, and stroke) in persons with chronic coronary syndrome (CCS).We used data from a cohort of persons with CCS for whom major adverse events were recorded over a follow-up of 20 years. We measured biomarkers of neurodegenerative diseases in baseline blood samples, using the Single-Molecule Array Technology on a HD-1 Analyzer. These include biomarkers of neuronal (neurofilament light chain (NfL) (n = 379)) and glial neurodegeneration (glial fibrillary acidic protein (GFAP) (n = 379)), and Alzheimer's disease pathology (phosphorylated tau181 (n = 379), total tau (n = 377), and amyloid β (Aβ40, Aβ42, Aβ42/Aβ40) (n = 377)). We applied Cox-proportional hazards models to evaluate associations of these biomarkers with adverse outcomes, adjusting for covariates and exploring interactions with apolipoprotein E (ApoE) ε4 genotype.Participants with higher NfL levels had increased rates of all-cause and cardiovascular mortality (Hazard ratio per increase by one standard deviation (95 % confidence interval): all-cause mortality: 1.36 (1.10-1.68); cardiovascular mortality: 1.42 (1.05-1.93)). The Aβ40/Aβ42-ratio was linked to incident stroke (0.72 (0.52-1.00)). Associations of GFAP with all-cause mortality and incident stroke were depending on ApoE ε4 genotype. The other biomarkers were not significantly associated with the studied outcomes.In persons with CSS, NfL and the Aβ40/Aβ42-ratio were related to mortality and incident stroke, respectively, whereas associations of GFAP with adverse outcomes varied by ApoE genotype. These biomarkers might play a role in linking aging, cardiovascular and neurodegenerative diseases. 000276341 536__ $$0G:(DE-HGF)POF4-353$$a353 - Clinical and Health Care Research (POF4-353)$$cPOF4-353$$fPOF IV$$x0 000276341 588__ $$aDataset connected to CrossRef, PubMed, , Journals: pub.dzne.de 000276341 650_7 $$2Other$$aBlood-based biomarkers of neurodegenerative diseases 000276341 650_7 $$2Other$$aCerebrovascular events 000276341 650_7 $$2Other$$aChronic coronary syndrome 000276341 650_7 $$2Other$$aCoronary heart disease 000276341 650_7 $$2Other$$aEpidemiology 000276341 650_7 $$2Other$$aMajor cardiovascular events 000276341 650_7 $$2Other$$aMortality 000276341 650_7 $$2NLM Chemicals$$aBiomarkers 000276341 650_7 $$2NLM Chemicals$$aAmyloid beta-Peptides 000276341 650_7 $$2NLM Chemicals$$atau Proteins 000276341 650_7 $$2NLM Chemicals$$aGlial Fibrillary Acidic Protein 000276341 650_7 $$2NLM Chemicals$$aneurofilament protein L 000276341 650_7 $$2NLM Chemicals$$aGFAP protein, human 000276341 650_7 $$2NLM Chemicals$$aApolipoprotein E4 000276341 650_7 $$2NLM Chemicals$$aNeurofilament Proteins 000276341 650_2 $$2MeSH$$aHumans 000276341 650_2 $$2MeSH$$aBiomarkers: blood 000276341 650_2 $$2MeSH$$aFemale 000276341 650_2 $$2MeSH$$aMale 000276341 650_2 $$2MeSH$$aAged 000276341 650_2 $$2MeSH$$aMiddle Aged 000276341 650_2 $$2MeSH$$aAmyloid beta-Peptides: blood 000276341 650_2 $$2MeSH$$aNeurodegenerative Diseases: blood 000276341 650_2 $$2MeSH$$aNeurodegenerative Diseases: mortality 000276341 650_2 $$2MeSH$$atau Proteins: blood 000276341 650_2 $$2MeSH$$aGlial Fibrillary Acidic Protein: blood 000276341 650_2 $$2MeSH$$aStroke: blood 000276341 650_2 $$2MeSH$$aStroke: mortality 000276341 650_2 $$2MeSH$$aCardiovascular Diseases: mortality 000276341 650_2 $$2MeSH$$aCardiovascular Diseases: blood 000276341 650_2 $$2MeSH$$aProportional Hazards Models 000276341 650_2 $$2MeSH$$aApolipoprotein E4: genetics 000276341 650_2 $$2MeSH$$aNeurofilament Proteins 000276341 7001_ $$aPerna, Laura$$b1 000276341 7001_ $$aSchöttker, Ben$$b2 000276341 7001_ $$0P:(DE-2719)2812234$$aPerneczky, Robert$$b3$$udzne 000276341 7001_ $$aBrenner, Hermann$$b4 000276341 7001_ $$aMons, Ute$$b5 000276341 773__ $$0PERI:(DE-600)2005397-6$$a10.1016/j.exger.2025.112684$$gVol. 200, p. 112684 -$$p112684$$tExperimental gerontology$$v200$$x0531-5565$$y2025 000276341 8564_ $$uhttps://pub.dzne.de/record/276341/files/DZNE-2025-00289%20SUP.pdf 000276341 8564_ $$uhttps://pub.dzne.de/record/276341/files/DZNE-2025-00289.pdf$$yOpenAccess 000276341 8564_ $$uhttps://pub.dzne.de/record/276341/files/DZNE-2025-00289%20SUP.pdf?subformat=pdfa$$xpdfa 000276341 8564_ $$uhttps://pub.dzne.de/record/276341/files/DZNE-2025-00289.pdf?subformat=pdfa$$xpdfa$$yOpenAccess 000276341 909CO $$ooai:pub.dzne.de:276341$$pdnbdelivery$$pdriver$$pVDB$$popen_access$$popenaire 000276341 9101_ $$0I:(DE-588)1065079516$$6P:(DE-2719)2812234$$aDeutsches Zentrum für Neurodegenerative Erkrankungen$$b3$$kDZNE 000276341 9131_ $$0G:(DE-HGF)POF4-353$$1G:(DE-HGF)POF4-350$$2G:(DE-HGF)POF4-300$$3G:(DE-HGF)POF4$$4G:(DE-HGF)POF$$aDE-HGF$$bGesundheit$$lNeurodegenerative Diseases$$vClinical and Health Care Research$$x0 000276341 9141_ $$y2025 000276341 915__ $$0StatID:(DE-HGF)0200$$2StatID$$aDBCoverage$$bSCOPUS$$d2025-01-02 000276341 915__ $$0StatID:(DE-HGF)0160$$2StatID$$aDBCoverage$$bEssential Science Indicators$$d2025-01-02 000276341 915__ $$0StatID:(DE-HGF)1050$$2StatID$$aDBCoverage$$bBIOSIS Previews$$d2025-01-02 000276341 915__ $$0StatID:(DE-HGF)1190$$2StatID$$aDBCoverage$$bBiological Abstracts$$d2025-01-02 000276341 915__ $$0StatID:(DE-HGF)0600$$2StatID$$aDBCoverage$$bEbsco Academic Search$$d2025-01-02 000276341 915__ $$0StatID:(DE-HGF)0113$$2StatID$$aWoS$$bScience Citation Index Expanded$$d2025-01-02 000276341 915__ $$0LIC:(DE-HGF)CCBYNC4$$2HGFVOC$$aCreative Commons Attribution-NonCommercial CC BY-NC 4.0 000276341 915__ $$0StatID:(DE-HGF)0501$$2StatID$$aDBCoverage$$bDOAJ Seal$$d2023-06-13T12:49:31Z 000276341 915__ $$0StatID:(DE-HGF)0500$$2StatID$$aDBCoverage$$bDOAJ$$d2023-06-13T12:49:31Z 000276341 915__ $$0StatID:(DE-HGF)1030$$2StatID$$aDBCoverage$$bCurrent Contents - 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