Show simple item record

dc.contributor.authorStaerk, Laila
dc.contributor.authorWang, Biqi
dc.contributor.authorLunetta, Kathryn L.
dc.contributor.authorHelm, Robert H.
dc.contributor.authorKo, Darae
dc.contributor.authorSherer, Jason A.
dc.contributor.authorEllinor, Patrick T.
dc.contributor.authorLubitz, Steven A.
dc.contributor.authorMcManus, David D.
dc.contributor.authorVasan, Ramachandran S.
dc.contributor.authorBenjamin, Emelia J.
dc.contributor.authorTrinquart, Ludovic
dc.date2022-08-11T08:09:49.000
dc.date.accessioned2022-08-23T16:44:29Z
dc.date.available2022-08-23T16:44:29Z
dc.date.issued2017-11-14
dc.date.submitted2018-03-22
dc.identifier.citation<p>J Am Heart Assoc. 2017 Nov 14;6(11). pii: e006541. doi: 10.1161/JAHA.117.006541. <a href="https://doi.org/10.1161/JAHA.117.006541">Link to article on publisher's site</a></p>
dc.identifier.issn2047-9980 (Linking)
dc.identifier.doi10.1161/JAHA.117.006541
dc.identifier.pmid29138179
dc.identifier.urihttp://hdl.handle.net/20.500.14038/40508
dc.description.abstractBACKGROUND: Advancing age is a prominent risk factor for atrial fibrillation (AF). Shorter telomere length is a biomarker of biological aging, but the link between shorter telomere length and increased risk of AF remains unclear. We examined the association between shorter leukocyte telomere length (LTL) and incident AF. METHODS AND RESULTS: We included AF-free participants from the observational Framingham Heart Study Offspring cohort from 1995 to 1998, who had LTL measurements. We examined the association between baseline LTL and incident AF with multivariable Cox models adjusted for age, sex, current smoking, height, weight, systolic and diastolic blood pressure, use of antihypertensive medication, diabetes mellitus, history of myocardial infarction, and history of heart failure. The study sample comprised 1143 AF-free participants (52.8% women), with mean age of 60+/-8 years. The mean LTL at baseline was 6.95+/-0.57 kb. During 15.1+/-4.2 years mean follow-up, 184 participants (64 women) developed AF. Chronological age was associated with increased risk of AF (hazard ratio per 10-year increase, 2.16; 95% confidence interval, 1.71-2.72). There was no significant association between LTL and incident AF (hazard ratio per 1 SD decrease LTL, 1.01; 95% confidence interval, 0.86-1.19). Our study was observational in nature; hence, we could not exclude residual confounding and we were unable to establish causal pathways. CONCLUSIONS: In our moderate-sized community-based cohort, we did not find evidence for a significant association between LTL and risk of incident AF.
dc.language.isoen_US
dc.relation<p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=29138179&dopt=Abstract">Link to Article in PubMed</a></p>
dc.rightsCopyright 2017: The Authors. Published on behalf of the American Heart Association, Inc., by Wiley. This is an open access article under the terms of the Creative Commons Attribution-NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/
dc.subjectaging
dc.subjectatrial fibrillation
dc.subjectbiomarker
dc.subjectepidemiology
dc.subjecttelomere genetics
dc.subjectCardiology
dc.subjectCardiovascular Diseases
dc.subjectEpidemiology
dc.subjectGenetics
dc.subjectPhysiological Processes
dc.titleAssociation Between Leukocyte Telomere Length and the Risk of Incident Atrial Fibrillation: The Framingham Heart Study
dc.typeJournal Article
dc.source.journaltitleJournal of the American Heart Association
dc.source.volume6
dc.source.issue11
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=4322&amp;context=oapubs&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/oapubs/3311
dc.identifier.contextkey11825456
refterms.dateFOA2022-08-23T16:44:29Z
html.description.abstract<p>BACKGROUND: Advancing age is a prominent risk factor for atrial fibrillation (AF). Shorter telomere length is a biomarker of biological aging, but the link between shorter telomere length and increased risk of AF remains unclear. We examined the association between shorter leukocyte telomere length (LTL) and incident AF.</p> <p>METHODS AND RESULTS: We included AF-free participants from the observational Framingham Heart Study Offspring cohort from 1995 to 1998, who had LTL measurements. We examined the association between baseline LTL and incident AF with multivariable Cox models adjusted for age, sex, current smoking, height, weight, systolic and diastolic blood pressure, use of antihypertensive medication, diabetes mellitus, history of myocardial infarction, and history of heart failure. The study sample comprised 1143 AF-free participants (52.8% women), with mean age of 60+/-8 years. The mean LTL at baseline was 6.95+/-0.57 kb. During 15.1+/-4.2 years mean follow-up, 184 participants (64 women) developed AF. Chronological age was associated with increased risk of AF (hazard ratio per 10-year increase, 2.16; 95% confidence interval, 1.71-2.72). There was no significant association between LTL and incident AF (hazard ratio per 1 SD decrease LTL, 1.01; 95% confidence interval, 0.86-1.19). Our study was observational in nature; hence, we could not exclude residual confounding and we were unable to establish causal pathways.</p> <p>CONCLUSIONS: In our moderate-sized community-based cohort, we did not find evidence for a significant association between LTL and risk of incident AF.</p>
dc.identifier.submissionpathoapubs/3311
dc.contributor.departmentDivision of Cardiovascular Medicine, Department of Medicine


Files in this item

Thumbnail
Name:
e006541.full.pdf
Size:
1.344Mb
Format:
PDF

This item appears in the following Collection(s)

Show simple item record

Copyright 2017: The Authors. Published on behalf of the American Heart Association, Inc., by Wiley. This is an open access article under the terms of the Creative Commons Attribution-NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
Except where otherwise noted, this item's license is described as Copyright 2017: The Authors. Published on behalf of the American Heart Association, Inc., by Wiley. This is an open access article under the terms of the Creative Commons Attribution-NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.