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Background: Researchers have suggested that longitudinal trajectories of mammographic breast density (MD) can be used to understand changes in breast cancer (BC) risk over a woman's lifetime. Some have suggested, based on biological arguments, that the cumulative trajectory of MD encapsulates the risk of BC across time. Others have tried to connect changes in MD to the risk of BC. Methods: To summarize the MD–BC association, we jointly model longitudinal trajectories of MD and time to diagnosis using data from a large ( N = 40 , 087 ) mammography cohort of Swedish women aged 40–80 years. Five hundred eighteen women were diagnosed with BC during follow-up. We fitted three joint models (JMs) with different association structures; Cumulative, current value and slope, and current value association structures. Results: All models showed evidence of an association between MD trajectory and BC risk ( P < 0.001 for current value of MD, P < 0.001 and P = 0.005 for current value and slope of MD respectively, and P < 0.001 for cumulative value of MD). Models with cumulative association structure and with current value and slope association structure had better goodness of fit than a model based only on current value. The JM with current value and slope structure suggested that a decrease in MD may be associated with an increased (instantaneous) BC risk. It is possible that this is because of increased screening sensitivity rather than being related to biology. Conclusion: We argue that a JM with a cumulative association structure may be the most appropriate/biologically relevant model in this context. [ABSTRACT FROM AUTHOR]

Conflicting results have appeared in the literature on whether the amount of non-dense, adipose tissue in the breast is a risk factor or a protective factor for breast cancer, and biological hypotheses supporting both have been proposed. We suggest here that limitations in study design and statistical methodology could potentially explain the inconsistent results. Specifically, we exploit recent advances in methodology and software developed for the joint analysis of multiple longitudinal outcomes and time-to-event data to jointly analyze dense and non-dense tissue trajectories and the risk of breast cancer in a large, Swedish, screening cohort. We also perform extensive sensitivity analyses by mimicking analyses/designs of previously published studies, e.g. ignoring available longitudinal data. Overall, we did not find strong evidence supporting an association between non-dense tissue and the risk of incident breast cancer. We hypothesize that (1) previous studies have not been able to isolate the effect of non-dense tissue from dense tissue or adipose tissue elsewhere in the body, that (2) estimates of the effect of non-dense tissue on risk are strongly sensitive to modeling assumptions, or that (3) the effect size of non-dense tissue on breast cancer risk is likely to be small/not clinically relevant., (© The Author(s) 2024. Published by Oxford University Press on behalf of the Johns Hopkins Bloomberg School of Public Health.)