Leukocyte telomere length is associated with disability in older u.s. Population.
Journal Article (Journal Article)
Objectives
To determine whether mean leukocyte telomere length (LTL) serves as a biomarker of disability assessed according to activities of daily living (ADLs) and what factors may modify this relationship.Design
Retrospective cross-sectional study.Setting
A subset of the National Long Term Care Survey (NTLCS), a Medicare-based U.S. population longitudinal study focused on trends of overall health and functional status in older adults.Participants
Six hundred and twenty-four individuals from the 1999 wave of the NTLCS cohort.Measurements
Relative LTL determined according to quantitative polymerase chain reaction. LTL has previously been shown to correlate with common age-related disorders and mortality, as well as with socioeconomic status.Results
A sex difference in LTL was observed but not age-dependent shortening or association with socioeconomic status. LTL was associated with disability and functional status assessed according to ADLs. The association between ADLs and LTL was stronger in subjects without diabetes mellitus, whereas associations were not seen when only subjects with diabetes mellitus were analyzed. Associations between LTL and cardiovascular disease (CVD) and cancer were also present in the group without diabetes mellitus but not in the group with diabetes mellitus.Conclusion
These findings support the concept that LTL is a biomarker of overall well-being that is predictive of disability of older individuals in the U.S. population. Diabetes mellitus plays an important role as a modifier of the association between LTL and disability, CVD, and cancer. These associations have clinical implications because of the potential predictive value of LTL and deserve further investigation.Full Text
Duke Authors
Cited Authors
- Risques, RA; Arbeev, KG; Yashin, AI; Ukraintseva, SV; Martin, GM; Rabinovitch, PS; Oshima, J
Published Date
- July 2010
Published In
Volume / Issue
- 58 / 7
Start / End Page
- 1289 - 1298
PubMed ID
- 20579170
Pubmed Central ID
- PMC2918372
Electronic International Standard Serial Number (EISSN)
- 1532-5415
International Standard Serial Number (ISSN)
- 0002-8614
Digital Object Identifier (DOI)
- 10.1111/j.1532-5415.2010.02948.x
Language
- eng