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Updated: Jul 12, 2025

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Telomere Length and Telomerase Activity; A Yin and Yang of Cell Senescence
Published on: May 22, 2013
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Telomere Length among Chinese Aged 75+ Years.
Suey S Y Yeung1, Suk Ling Ma2, Xingyan Wang3,4,5,6
1Department of Medicine and Therapeutics, Faculty of Medicine, The Chinese University of Hong Kong, Hong Kong, Hong Kong, China.
Gerontology
|October 19, 2023
Summary
Telomere length (TL) in Chinese adults aged 75+ was shorter in males than females. Unlike previous findings, TL was not associated with age-related diseases, frailty, or sarcopenia in this older population.
Area of Science:
- Gerontology
- Molecular Biology
- Public Health
Background:
- Telomere length (TL) is a recognized biomarker of aging, often inversely associated with morbidity.
- Previous research primarily focused on younger populations, leaving the association in older adults less clear.
- Limited studies have investigated TL and its determinants in Chinese older adults.
Purpose of the Study:
- To examine telomere length (TL) in Chinese individuals aged 75 years and older.
- To identify factors associated with TL in this demographic.
- To determine the relationship between TL and multimorbidity, age-related diseases, frailty, and sarcopenia.
Main Methods:
- Cross-sectional study of 555 Chinese participants (mean age 83.6 years) from the Mr. and Ms. Osteoporosis cohort.
- TL measured using a molecular inversion probe-quantitative PCR assay (T/S ratio).
- Associations examined using adjusted binary logistic regressions.
Main Results:
- Males exhibited shorter TL (mean T/S ratio 0.97) compared to females (1.07) (p < 0.001).
- Lower education level correlated with longer TL (p = 0.016), while current smoking was linked to shorter TL (p = 0.007).
- No significant associations were found between TL and multimorbidity, specific age-related diseases, frailty, or sarcopenia.
Conclusions:
- In Chinese adults aged 75+, males have shorter telomere length (TL) than females.
- TL was not significantly associated with age-related diseases, frailty, or sarcopenia in this cohort.
- These findings suggest TL may not serve as a reliable biological marker of aging in older individuals.
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