Key result
A per unit increase in square root serum digoxin concentration is associated with a 1.77 times higher hazard of all-cause mortality in patients with heart failure.
Why the study?
As the use of joint modelling increases, it is important to understand how and why it is being applied to heart failure research.
How is joint modelling applied in heart failure research, and what is the relationship between repeat measurements of serum digoxin and all-cause mortality?
Systematic Review (n=2,012)
How is joint modelling applied in heart failure research, and what is the relationship between repeat measurements of serum digoxin and all-cause mortality?
Joint modelling is increasingly used in heart failure research and can effectively link longitudinal biomarker measurements, such as serum digoxin, with time-to-event outcomes like mortality.
Joint modelling may refine dynamic biomarker-outcome links in HF cohorts; leaves open clinical adoption pending prospective validation.
BACKGROUND: Joint modelling combines two or more statistical models to reduce bias and increase efficiency. As the use of joint modelling increases it is important to understand how and why it is being applied to heart failure research. METHODS: A systematic review of major medical databases of studies which used joint modelling within heart failure alongside an exemplar; joint modelling repeat measurements of serum digoxin with all-cause mortality using data from the Effect of Digoxin on Mortality and Morbidity in Patients with Heart Failure (DIG) trial. RESULTS: Overall, 28 studies were included that used joint models, 25 (89%) used data from cohort studies, the remaining 3 (11%) using data from clinical trials. 21 (75%) of the studies used biomarkers and the remaining studies used imaging parameters and functional parameters. The exemplar findings show that a per unit increase of square root serum digoxin is associated with the hazard of all-cause mortality increasing by 1.77 (1.34-2.33) times when adjusting for clinically relevant covariates. CONCLUSION: Recently, there has been a rise in publications of joint modelling being applied to heart failure. Where appropriate, joint models should be preferred over traditional models allowing for the inclusion of repeated measures while accounting for the biological nature of biomarkers and measurement error.
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Field et al. (2023) conducted a systematic review in Heart failure (n=2,012). Serum digoxin concentration (square root transformed) vs. Lower serum digoxin concentration was evaluated on All-cause mortality (HR 1.77, 95% CI 1.34-2.33, p=<0.001). A per unit increase in square root serum digoxin concentration is associated with a 1.77 times higher hazard of all-cause mortality in patients with heart failure.
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