Key result
High systolic blood pressure converged across all evidence streams as the leading metabolic stroke risk factor, accounting for 53-71% of attributable DALYs and a cohort SHR of 1.37 (95% CI 1.26-1.48).
Why the study?
In regional blocs spanning multiple GBD super-regions and genetic ancestry groups, population, individual, and genetic evidence for stroke-prevention priorities face different transportability limits, and earlier combined studies did not prespecify what counts as disagreement.
How do five metabolic risk factors (systolic blood pressure, LDL cholesterol, body-mass index, fasting glucose, and kidney dysfunction) rank and converge across population attributable burden, individual cohort incidence, and genetic Mendelian randomisation evidence for stroke prevention priority setting in the Shanghai Cooperation Organisation?
Observational (n=7,896)
Yes
How do five metabolic risk factors (systolic blood pressure, LDL cholesterol, body-mass index, fasting glucose, and kidney dysfunction) rank and converge across population attributable burden, individual cohort incidence, and genetic Mendelian randomisation evidence for stroke prevention priority setting in the Shanghai Cooperation Organisation?
Across the structurally and genetically heterogeneous Shanghai Cooperation Organisation, systolic blood pressure is the only metabolic risk factor for stroke with robust, convergent support across population, individual cohort, and genetic evidence streams, whereas LDL cholesterol, BMI, fasting glucose, and kidney dysfunction exhibit structural discordance or unexplained divergence.
Supports systolic blood pressure as top metabolic stroke priority; confirms convergence across DALY, cohort, and genetic streams but leaves practice change open.
BACKGROUND Regional stroke-prevention priorities usually rest on what a bloc’s members share. Where members span multiple Global Burden of Disease (GBD) super-regions and genetic ancestry groups, population, individual, and genetic evidence face different transportability limits, and earlier combined studies did not prespecify what counts as disagreement. METHODS We studied the Shanghai Cooperation Organisation, which spans four super-regions and five ancestry groups and is land-contiguous. For five metabolic risk factors we triangulated GBD 2023 attributable fractions of stroke DALYs in ten states, incident stroke among 7896 adults in the China Health and Retirement Longitudinal Study (2011–18; SHRs per 1 SD), and subtype-specific Mendelian randomisation in three ancestries. An explicit rule set, with one pre-submission amendment, classified convergence and divergence by whether a listed mechanism accounted for it. FINDINGS High systolic blood pressure converged: 53–71% of attributable DALYs, the strongest cohort exposure (SHR 1·37, 95% CI 1·26–1·48), and genetically supported in both ancestries. LDL cholesterol (GBD attribution restricted to ischaemic stroke; European genetic evidence for that subtype; no cohort association) and body-mass index (last in attribution but second in the cohort, with a 1·80-fold [1·48–2·18] gradient inside the 20–25 kg/m² minimum-risk window) showed structural discordance. The cohort lacked subtype data to establish LDL dilution. Fasting glucose and kidney dysfunction diverged without such a mechanism. INTERPRETATION Systolic blood pressure had the strongest cross-stream support. LDL cholesterol and body-mass index require qualified interpretation; fasting glucose and kidney dysfunction could not be ranked reliably. The framework identifies where priorities require scrutiny.
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Wang et al. (2026) conducted an observational in Stroke (n=7,896). High systolic blood pressure (among 5 metabolic risk factors: SBP, BMI, LDL cholesterol, fasting glucose, kidney dysfunction) vs. Per 1-SD lower exposure / theoretical minimum-risk exposure level was evaluated on Incident stroke (CHARLS cohort) and stroke DALYs / subtype-specific stroke (GBD and Mendelian randomization) (SHR 1.37, 95% CI 1.26-1.48). High systolic blood pressure converged across all evidence streams as the leading metabolic stroke risk factor, accounting for 53-71% of attributable DALYs and a cohort SHR of 1.37 (95% CI 1.26-1.48).
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