Key result
Genetic liability to high blood pressure linked to ~35% higher odds of ischemic heart disease.
Why the study?
Ischemic heart disease and ischemic stroke are major contributors to health loss in Europe with regional heterogeneity, yet comparisons of disease burden, attributable risks, and genetic evidence remain limited.
How have the regional burdens and attributable risk profiles of ischemic heart disease and ischemic stroke evolved across Europe from 1990 to 2023, and what is the complementary genetic evidence linking cardiometabolic traits to these outcomes?
Observational
Yes
How have the regional burdens and attributable risk profiles of ischemic heart disease and ischemic stroke evolved across Europe from 1990 to 2023, and what is the complementary genetic evidence linking cardiometabolic traits to these outcomes?
Despite widespread declines in age-standardized ischemic heart disease and ischemic stroke rates across Europe from 1990 to 2023, Eastern Europe retains a disproportionately high burden, and convergent epidemiological and genetic evidence underscores the primacy of blood pressure and LDL-C control alongside regional environmental risks like lead exposure.
Answers are grounded in this paper and cite their sources.
Genetic liability to high BP was associated with IHD and stroke; leaves open targeted prevention integrating MR with regional GBD trends.
Background Ischemic heart disease (IHD) and ischemic stroke (IS) remain major contributors to health loss in Europe, with regional heterogeneity. Comparisons of burden, attributable risks, and genetic evidence remain limited. Methods Global Burden of Disease (GBD) 2023 estimates for Central, Eastern, and Western Europe from 1990 to 2023 were analyzed. Age‐standardized prevalence, incidence, mortality, and disability‐adjusted life‐year rates were summarized; temporal trends were assessed by Joinpoint regression and 2023 cross‐country concordance by Spearman correlation. GBD risk profiles were compared between 1990 and 2023. Complementary Mendelian randomization (MR) evaluated high blood pressure, fasting glucose, and low‐density lipoprotein cholesterol (LDL‐C). Results Eastern Europe had the highest 2023 burden. IHD and IS rates were positively concordant across countries (Spearman ρ = 0.681–0.820; all p < 0.001), and regional 1990–2023 average annual percent changes were negative. High systolic blood pressure and high LDL‐C remained leading GBD‐attributable risks. In MR, genetic liability to high blood pressure was associated with IHD (odds ratio [OR] = 1.354, 95% confidence interval [CI] 1.281–1.433) and IS (OR = 1.351, 95% CI 1.295–1.409), and LDL‐C with IHD (OR = 1.610, 95% CI 1.508–1.719); these met the Bonferroni threshold. Fasting glucose showed nominal evidence for IHD, whereas fasting glucose and LDL‐C showed no statistically significant associations with overall IS. Conclusions IHD and IS burdens declined across Europe, but regional inequalities persisted. GBD attribution and MR provide complementary evidence; cardiometabolic risks remain central, while genetic associations differ between IHD and overall IS.
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Hu et al. (2026) conducted an observational in Ischemic heart disease (IHD) and ischemic stroke (IS). Genetic liability to high blood pressure, LDL-C, and fasting glucose (MR) / GBD modifiable risk factors was evaluated on Ischemic heart disease (IHD) odds in inverse-variance weighted Mendelian randomization for genetic liability to high blood pressure (OR 1.354, 95% CI 1.281-1.433, p=<0.001). Genetic liability to high blood pressure increased odds of ischemic heart disease (OR 1.354) and ischemic stroke (OR 1.351), while European disease burdens declined from 1990 to 2023.
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