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Karen Leffondre

Publications and source records attributed to Karen Leffondre.

2 recordsLinked to original sources

Efficient Bayesian inference for non-linear association structures in joint models: A hierarchical approach via INLA

Joint models for longitudinal and time-to-event data are increasingly used in health research to characterize the association between biomarker trajectories and the risk of clinical events. However, these models usually assume a linear relationship between the longitudinal marker and the log-hazard of the event. This assumption is rarely verified and often fails to capture complex biological mechanisms, such as U-shaped risk profiles or plateau effects. In this paper, we propose a fast and stable hierarchical framework for non-linear association structures in joint models using Integrated Nested Laplace Approximations (INLA), implemented in the INLAjoint R package. Our approach builds upon a unified framework where the scaling effect of the marker is decomposed into a parametric baseline (constant and linear components) and a data-driven smooth deviation modeled via an orthogonal basis derived from a second-order random walk. This natural hierarchy allows researchers to adapt model flexibility directly and verify the linearity assumption using standard information criteria. Through simulation studies, we demonstrate that the proposed method accurately recovers complex non-linear trajectories. We illustrate the practical utility of our framework by analyzing the joint association of the current value and current slope of body mass index (BMI) with all-cause mortality in the Health and Retirement Study. This analysis reveals a U-shaped mortality risk for the BMI value, and a non-linear effect for the rate of weight change, where a declining weight trajectory is associated with higher mortality risk.

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Time-varying exposure history and subsequent health outcomes: a two-stage approach to identify critical windows

Long-term behavioral and health risk factors constitute a primary focus of research on the etiology of chronic diseases. Yet, identifying critical time-windows during which risk factors have the strongest impact on disease risk is challenging. To assess the trajectory of association of an exposure history with an outcome, the weighted cumulative exposure index (WCIE) has been proposed, with weights reflecting the relative importance of exposures at different times. However, WCIE is restricted to a complete observed error-free exposure whereas exposures are often measured with intermittent missingness and error. Moreover, it rarely explores exposure history that is very distant from the outcome as usually sought in life-course epidemiology. We extend the WCIE methodology to (i) exposures that are intermittently measured with error, and (ii) contexts where the exposure time-window precedes the outcome time-window using a landmark approach. First, the individual exposure history up to the landmark time is estimated using a mixed model that handles missing data and error in exposure measurement, and the predicted complete error-free exposure history is derived. Then the WCIE methodology is applied to assess the trajectory of association between the predicted exposure history and the health outcome collected after the landmark time. In our context, the health outcome is a longitudinal marker analyzed using a mixed model. A simulation study first demonstrates the correct inference obtained with this approach. Then, applied to the Nurses' Health Study (19,415 women) to investigate the association between BMI history (collected from midlife) and subsequent cognitive decline after age 70. In conclusion, this approach, easy to implement, provides a flexible tool for studying complex dynamic relationships and identifying critical time windows while accounting for exposure measurement errors.

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