Article Text
Abstract
Objective To examine the association between low-intensity smoking (10 or less cigarettes per day) and all-cause and cause-specific mortality risk among women who smoke and by age at cessation among women who previously smoked.
Methods In this study, 104 717 female participants of the Mexican Teachers’ Cohort Study were categorised according to self-reported smoking status at baseline (2006/2008) and were followed for mortality through 2019. We estimated HRs and 95% CIs for all-cause and cause-specific mortality using multivariable Cox proportional hazards regression models with age as the underlying time metric.
Results Smoking as few as one to two cigarettes per day was associated with higher mortality risk for all causes (HR: 1.36; 95% CI 1.10 to 1.67) and all cancers (HR: 1.46; 95% CI 1.05 to 2.02), compared with never smoking. Similarly, slightly higher HRs were observed among participants smoking ≥3 cigarettes per day (all causes HR: 1.43; 95% CI 1.19 to 1.70; all cancers HR: 1.48; 95% CI 1.10 to 1.97; cardiovascular disease HR: 1.58; 95% CI 1.09 to 2.28).
Conclusions In this large study of Mexican women, low-intensity smoking was associated with higher mortality risk for all causes and all cancers. Interventions are needed to promote cessation among women who smoke at low-intensity in Mexico, regardless of how few cigarettes they smoke per day.
- Low/Middle income country
- Smoking Caused Disease
- Prevention
- Priority/special populations
Data availability statement
Data are available on reasonable request. The data that support the findings of this study are available from the corresponding author, ML, on reasonable request. We have adopted a data enclave approach and guidelines are available on our website https://esmaestras.org/available-mtc-data/.
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Data availability statement
Data are available on reasonable request. The data that support the findings of this study are available from the corresponding author, ML, on reasonable request. We have adopted a data enclave approach and guidelines are available on our website https://esmaestras.org/available-mtc-data/.
Footnotes
Contributors Guarantor: ML. Conceptualisation: DSG-T, ML and NDF. Data curation: DS and AC-V. Methodology: TB-G, DSG-T, MI-C and NDF. Formal analysis and writing – original draft: DSG-T. Investigation: JEH-A, EM-C, MB and ML. Funding acquisition and supervision: NDF. Writing – review and editing: all authors.
Funding This study was supported by National Cancer Institute, Division of Cancer Epidemiology and Genetics, Intramural Research Program.
Disclaimer The comments and opinions expressed in this paper are those of the authors and does not reflect the official policy of the Department of Health and Human Service, National Institutes of Health and National Cancer Institute.
Competing interests None declared.
Provenance and peer review Not commissioned; externally peer reviewed.
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