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RESEARCH PAPER / 2024-11-13

Telomere length and chronotype among women in the California Teachers Study (CTS).

Mia Blanchard, Jue Lin, Susan Hurley, Debbie Goldberg, Julie Von Behren, Sophia S Wang, Peggy Reynolds, Jessica Clague DeHart

School of Community and Global Health, Claremont Graduate University, Claremont, California, USA.School of Community and Global Health, Claremont Graduate University, Claremont, California, USA. · pubmed

Abstract

While links between certain chronotypes and poorer health outcomes have been well established in previous studies, few studies have examined the relationship between chronotype and cellular aging. Using data from the California Teachers Study (CTS), the present study evaluates the relationship between cellular aging and chronobiology through an analysis of leukocyte telomere length (LTL) and chronotype among 817 predominantly postmenopausal women with no history of cancer and occupations not associated with night-shift work. Unconditional logistic regression models were run to estimate odds ratios (ORs) for each chronotype category, adjusted for age, ethnicity, and smoking status. Analyses were then stratified by potential modifiers to assess whether results varied among specific subgroups within the sample. Women who reported being current evening types and evening types from teen years to now were significantly less likely to have short LTL compared to women who reported being current morning types or morning types from teen years to now (OR = 0.72; 95% CI = 0.53-0.98; OR = 0.57; 95% CI = 0.39-0.84). Our results suggest that women with no history of cancer who identify as evening chronotypes may undergo decreased cellular aging compared to women in the same population who identify as morning types. Further studies on populations of postmenopausal women are warranted.

The following analysis is generated by AI and may contain errors. It is separate from the authors’ abstract and is not peer review.

Research summary

The paper explores the relationship between chronotype and leukocyte telomere length, which is a biomarker of cellular aging. While it provides insights into how chronotype may influence cellular aging in a specific population of postmenopausal women, the findings are relatively narrow in scope and do not address broader mechanisms of aging or longevity. The study contributes to the understanding of lifestyle factors affecting aging but does not present groundbreaking findings that would significantly advance the field of longevity research.

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