dc.contributor.author
Rennenberg, Regina von
dc.contributor.author
Liman, Thomas
dc.contributor.author
Nolte, Christian H.
dc.contributor.author
Nave, Alexander H.
dc.contributor.author
Scheitz, Jan F.
dc.contributor.author
Düzel, Sandra
dc.contributor.author
Regitz-Zagrosek, Vera
dc.contributor.author
Gerstorf, Denis
dc.contributor.author
Steinhagen-Thiessen, Elisabeth
dc.contributor.author
Demuth, Ilja
dc.contributor.author
Endres, Matthias
dc.date.accessioned
2024-09-23T13:14:44Z
dc.date.available
2024-09-23T13:14:44Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/44997
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-44708
dc.description.abstract
Introduction: There is evidence of an association between markers of cardiac injury and cognition in patients with cardiovascular disease. We hypothesized that levels of high-sensitivity cardiac troponin T (hs-cTnT) are associated with cognitive performance and cognitive decline in a population of predominantly healthy older adults. Methods: We included 1,226 predominantly healthy adults >= 60 years from the Berlin Aging Study II. Participants were recruited from the general population of the Berlin metropolitan area from 2009 to 2014. At baseline, participants underwent measurement of hs-cTnT and cognitive testing using the extended Consortium to Establish a Registry for Alzheimer's Disease (CERAD-Plus) battery. In addition, the Digit Symbol Substitution Test (DSST) was performed at baseline and at follow-up (7.3 +/- 1.4 years after the baseline visit). The CERAD test results were summarized into four cognitive domains (processing speed, executive function, visuo-construction, and memory). After summing-up the respective raw scores, we calculated standardized z scores. We performed unadjusted and adjusted linear regression models to assess links between hs-cTnT and cognitive domains. We used linear mixed models to analyze associations between hs-cTnT and cognitive decline according to changes in DSST scores over time. Results: The mean age of study participants at baseline was 68.5 (+/- 3.6) years, 49% were female, and median hs-cTnT levels were 6 ng/L (IQR 4-8 ng/L). We detected no significant association between hs-cTnT and different cognitive domains at baseline after adjustment for age, sex, education, and cardiovascular risk factors. Hs-cTnT was associated with cognitive decline, which remained statistically significant after full adjustment (adjusted beta-coefficient -0.82 (-1.28 to -0.36), p = 0.001). After stratification for sex, the association with hs-cTnT remained statistically significant in men but not in women. Conclusion: Higher hs-cTnT levels in older men are associated with cognitive decline measured with the DSST.
en
dc.subject
Cardiac troponin
en
dc.subject
Cognitive decline
en
dc.subject
Heart-brain axis
en
dc.subject.ddc
600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit::610 Medizin und Gesundheit
dc.title
High-Sensitivity Cardiac Troponin T and Cognitive Decline in Older Adults: Results of the Berlin Aging Study II
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.doi
10.1159/000523845
dcterms.bibliographicCitation.journaltitle
Gerontology
dcterms.bibliographicCitation.number
2
dcterms.bibliographicCitation.originalpublishername
Karger
dcterms.bibliographicCitation.pagestart
140
dcterms.bibliographicCitation.pageend
148
dcterms.bibliographicCitation.volume
69
dcterms.rightsHolder.note
Copyright applies in this work.
dcterms.rightsHolder.url
http://rightsstatements.org/vocab/InC/1.0/
refubium.affiliation
Charité - Universitätsmedizin Berlin
refubium.note.author
Dieser Beitrag ist mit Zustimmung des Rechteinhabers aufgrund einer (DFG geförderten) Allianz- bzw. Nationallizenz frei zugänglich.
de
refubium.note.author
This publication is shared with permission of the rights owner and made freely accessible through a DFG (German Research Foundation) funded license at either an alliance or national level.
en
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.bibliographicCitation.pmid
35512662
dcterms.isPartOf.issn
0304-324X
dcterms.isPartOf.eissn
1423-0003