Predicted lean body mass trajectories, and cancer risk and cancer‐specific and all‐cause mortality: A prospective cohort study

Abstract

BackgroundAlthough many studies have investigated the association between body composition, cancer risk and mortality, predicting these risks through a single body composition measurement undoubtedly increases the limitations of the study. Few studies have explored the association between the trajectory of changes in body composition and the risk of cancer and death. We aimed to explore the association of predicted lean mass trajectories with cancer risk, cancer‐specific mortality and all‐cause mortality.MethodsThe participants in this study were all from the Kailuan cohort, a prospective, periodic, resurvey cohort study initiated in 2006. Latent mixture modelling was used to identify predicted lean mass trajectories for 2006–2010. The hazard ratios (HRs) and 95% confidence intervals (95% CIs) of the Cox proportional hazard models were used to describe the association between predicted lean mass trajectories and cancer risk and cancer‐specific and all‐cause mortality during follow‐up (2010–2021).ResultsA total of 44 374 participants (average age, 53.01 ± 11.41 years, 78.99% men and 21.01% women) were enrolled in this study. Five distinct trajectories were identified: low‐stable (n = 12 060), low‐increasing (n = 8027), moderately stable‐decreasing (n = 4725), moderately stable‐increasing (n = 8053) and high‐stable (n = 11 509). During the 11‐year follow‐up period, 2183 cancer events were recorded. After adjusting for age, predicted fat mass in 2010, sex, BMI, sedentary, physical activity, smoke, alcohol use, salt consumption, high‐fat diet, high‐sensitivity C‐reactive protein, serum creatinine, family history of tumour, hypertension, diabetes mellitus, compared with the low‐stable group, participants in the low‐increasing group (HR = 0.851, 95% CI, 0.748–0.969), moderately stable‐increasing group (HR = 0.803, 95% CI, 0.697–0.925) and high‐stable group (HR = 0.770, 95% CI, 0.659–0.901) had a lower cancer risk, but not in the moderately stable‐decreasing group (HR = 0.864, 95% CI, 0.735–1.015). Compared with the low‐stable group, the risk of cancer‐specific mortality was reduced by 25.4% (8.8–38.9%), 36.5% (20.3–49.4%) and 35.4% (17.9–49.2%), and the risk of all‐cause mortality was reduced by 24.2% (16.9–30.8%), 37.0% (30.0–43.2%) and 47.4% (41.0–53.1%) in the low‐increasing, moderately stable‐increasing group and high‐stable groups, respectively.ConclusionsPredicted lean mass trajectories may be closely associated with cancer risk and cancer‐specific and all‐cause mortality. Regular monitoring of body composition is necessary.

The association of metabolic syndrome score trajectory patterns with risk of all cancer types

“…This involved using the significance levels of the cubic, quadratic, and linear terms to determine the most appropriate functional form for each trajectory pattern. 10,13,14 Inflammation and MetS may interact in a synergistic manner to increase the risk of cancer. 15 To further investigate this association, we conducted a subgroup analysis by categorizing participants based on their CRP levels.…”