Key result
Novel Bayesian risk model predicts incident cardiometabolic multimorbidity with an AUC of ~0.89.
Why the study?
Current risk prediction models usually focus on single diseases and rarely incorporate social determinants, despite cardiometabolic diseases frequently clustering as multimorbidity.
Cohort (n=11,964)
Yes
A Bayesian risk prediction model incorporating social and cardiometabolic risk factors demonstrated good discrimination for predicting cardiometabolic multimorbidity in middle-aged Swedish adults.
May improve multimorbidity risk stratification incorporating social factors; leaves open external validation and clinical utility.
Cardiometabolic diseases often cluster as multimorbidity, yet current risk prediction models typically focus on a single disease and rarely incorporate social determinants. This study aims to develop a Bayesian risk prediction model for cardiometabolic multimorbidity in middle-aged Swedish adults. This prospective cohort included 11,964 adults without prior cardiometabolic disease from the Swedish CArdioPulmonary bioImage Study (SCAPIS; enrolment 2013–2016). Cardiometabolic disease was defined as incident type 2 diabetes (T2D), ischaemic heart disease/heart failure, or stroke. Regularised Bayesian logistic regression models were developed to predict any cardiometabolic disease (≥ 1 condition) and cardiometabolic multimorbidity (≥ 2 conditions) within 2–5 years. Twenty-two social and cardiometabolic risk predictors were considered. During follow-up, 6.0% of participants developed cardiometabolic disease(s) (5.7% with a single cardiometabolic disease and 0.3% with multimorbidity). The prediction model showed fair discrimination for any cardiometabolic disease (AUC 0.76, 95% CI 0.74–0.78) and good discrimination for multimorbidity (AUC 0.89, 95% CI 0.86–0.93). The highest predicted risks were observed among older foreign-born males with hypertension, low HDL-C, high waist circumference, and current/ex-smoker, with predicted risks of 34.7% (95% CrI 30.3%–39.5%) for any cardiometabolic disease and 4.4% (95% CrI 2.0%–7.9%) for multimorbidity. These findings suggest that social determinants and uncertainty estimates may provide useful information for cardiometabolic disease prediction, though further validation is needed before use in clinical practice.
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Anindya et al. (2026) conducted a cohort in Cardiometabolic multimorbidity (n=11,964). Social and cardiometabolic risk factors was evaluated on Discrimination for cardiometabolic multimorbidity (≥ 2 conditions) (AUC 0.89, 95% CI 0.86-0.93). A regularised Bayesian risk prediction model incorporating social and cardiometabolic risk factors demonstrated good discrimination for predicting cardiometabolic multimorbidity (AUC 0.89).
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