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Telomere length among Chinese oldest old

Yeung, S. S. Y.; Wang, X.; Ma, S. L.; Chen, Y.; Kwok, S. W. T.; Leung, N. S. T.; Woo, J.

2022-07-29 geriatric medicine
10.1101/2022.07.26.22278044 medRxiv
Show abstract

IntroductionTelomere length (TL) is generally regarded as a biomarker of aging. TL, which is influenced by sociodemographic factors, has been shown to be inversely associated with morbidity. However, most studies were examined in the youngest old and whether the findings can be extended to the oldest old is less clear. This study examined TL and its associated factors in Chinese oldest old in Hong Kong. MethodsFollow-up data collected after 14 years from the baseline of the Mr. and Ms. Osteoporosis cohort were analyzed. A structured interview on sociodemographic factors and physical measurement was conducted. Frailty and sarcopenia status were respectively determined by Frieds criteria and Asian Working Group for Sarcopenia definition. TL was measured by a molecular inversion probe - quantitative PCR (MIP-qPCR) assay and expressed as telomere / a single copy reference gene (T/S) ratio. Adjusted binary logistic regressions were used to examine the associations between TL and the presence of multimorbidity, age-related diseases, frailty and sarcopenia. ResultsAmong 555 participants (mean age 83.6{+/-}3.8 years, 41.3% women), the mean T/S ratio was 1.01{+/-}0.20. Males had lower T/S ratio (0.97{+/-}0.20) compared with females (1.07{+/-}0.18) (p<0.001). A lower education level was related to a longer TL (p=0.016). Being a current smoker was related to a shorter TL (p=0.007). TL was not significantly different across categories of age, subjective socioeconomic status, drinking status, physical activity level and body mass index (p>0.05). There were no associations between TL and the presence of multimorbidity, diabetes, stroke, cardiovascular diseases, cognitive impairment, frailty and sarcopenia. ConclusionAmong Chinese oldest old, males had shorter TL compared with females. TL was not associated with age-related diseases, frailty and sarcopenia in this age group. TL may not be a biological marker of aging among the oldest old.

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