Causal effect of systolic blood pressure on myocardial injury and mortality: insights from Mendelian randomization and a prospective group study
- PMID: 40833557
- DOI: 10.1007/s11010-025-05373-1
Causal effect of systolic blood pressure on myocardial injury and mortality: insights from Mendelian randomization and a prospective group study
Abstract
This study aimed to examine the causal relationship between systolic blood pressure (SBP) and myocardial injury (MI), and to evaluate its prognostic implications for all-cause and cardiovascular mortality. A two-stage analytical approach was used. First, Mendelian randomization (MR) was conducted to assess the independent causal effects of SBP on six MI-related phenotypes, with adjustment for potential confounders, including lipid profiles, glycemic indices, and anthropometric traits. Second, data from 4459 participants in the National Health and Nutrition Examination Survey, with a follow-up period of up to 15 years, were analyzed. The dose-response relationship between SBP and MI was assessed using restricted cubic spline analysis. Thresholds based on sex-, age-, and comorbidities were identified using the Johnson-Neyman interaction model. MR analysis demonstrated a causal association between elevated SBP and increased risks of acute heart failure (odds ratio [OR] = 1.523), MI (OR = 1.014), and ischemic stroke (OR = 33.339). In the prospective group analysis, SBP ≥ 180 mmHg was associated with a 213.4% increased risk of MI (OR = 3.134, p = 0.003), and a graded increase in mortality was observed (hazard ratio [HR] = 2.783 for all-cause death; HR = 1.888 for cardiovascular death). Sex-stratified analysis demonstrated that the lowest MI risk occurred at SBP levels of 120-150 mmHg in men and extended to 162 mmHg in women. Among individuals aged ≥ 43 years, the risk of all-cause mortality significantly increased when SBP exceeded 135 mmHg (p < 0.001). A U-shaped relationship between SBP and mortality was observed in individuals aged ≥ 58 years with MI, with the lowest risk at 113 mmHg. Genetic and observational evidence support a causal role of elevated SBP in the development of MI. The findings demonstrate sex- and age-specific thresholds, along with a U-shaped mortality curve, providing a nuanced framework for individualized blood pressure management strategies.
Keywords: Mendelian randomization analysis (MR); Mortality; Myocardial injury (MI); NHANES cohort analysis; Systolic blood pressure (SBP).
© 2025. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.
Conflict of interest statement
Declarations. Ethics approval and consent to participate: Not applicable. Consent for publication: Not applicable. Competing interests: The authors declare no competing interests.
Similar articles
-
Effects of a gluten-reduced or gluten-free diet for the primary prevention of cardiovascular disease.Cochrane Database Syst Rev. 2022 Feb 24;2(2):CD013556. doi: 10.1002/14651858.CD013556.pub2. Cochrane Database Syst Rev. 2022. PMID: 35199850 Free PMC article.
-
Prescription of Controlled Substances: Benefits and Risks.2025 Jul 6. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan–. 2025 Jul 6. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan–. PMID: 30726003 Free Books & Documents.
-
Reassessing the association between age at menarche and cardiovascular disease: observational and Mendelian randomization analyses.Eur J Prev Cardiol. 2025 Mar 18:zwaf051. doi: 10.1093/eurjpc/zwaf051. Online ahead of print. Eur J Prev Cardiol. 2025. PMID: 40099743 Free PMC article.
-
Quality improvement strategies for diabetes care: Effects on outcomes for adults living with diabetes.Cochrane Database Syst Rev. 2023 May 31;5(5):CD014513. doi: 10.1002/14651858.CD014513. Cochrane Database Syst Rev. 2023. PMID: 37254718 Free PMC article.
-
Altered albumin/neutrophil to lymphocyte ratio are associated with all-cause and cardiovascular mortality for advanced cardiovascular-kidney-metabolic syndrome.Front Nutr. 2025 Jul 16;12:1595119. doi: 10.3389/fnut.2025.1595119. eCollection 2025. Front Nutr. 2025. PMID: 40740647 Free PMC article.
References
-
- Sun J, Qiao Y, Zhao M et al (2023) Global, regional, and national burden of cardiovascular diseases in youths and young adults aged 15–39 years in 204 countries/territories, 1990–2019: a systematic analysis of global burden of disease study 2019. BMC Med 21(1):222. https://doi.org/10.1186/s12916-023-02925-4 - DOI - PubMed - PMC
-
- Tran J, Norton R, Canoy D et al (2021) Multi-morbidity and blood pressure trajectories in hypertensive patients: a multiple landmark cohort study. PLoS Med 18(6):e1003674. https://doi.org/10.1371/journal.pmed.1003674 - DOI - PubMed - PMC
-
- Blood Pressure Lowering Treatment Trialists’ Collaboration (2021) Age-stratified and blood-pressure-stratified effects of blood-pressure-lowering pharmacotherapy for the prevention of cardiovascular disease and death: an individual participant-level data meta-analysis. Lancet 398(10305):1053–1064. https://doi.org/10.1016/S0140-6736(21)01921-8 - DOI
-
- Zhang W, Zhang S, Deng Y et al (2021) Trial of intensive blood-pressure control in older patients with hypertension. N Engl J Med 385(14):1268–1279. https://doi.org/10.1056/NEJMoa2111437 - DOI - PubMed
-
- Puelacher C, Gualandro DM, Glarner N et al (2023) Long-term outcomes of perioperative myocardial infarction/injury after non-cardiac surgery. Eur Heart J 44(19):1690–1701. https://doi.org/10.1093/eurheartj/ehac798 - DOI - PubMed - PMC
Grants and funding
LinkOut - more resources
Full Text Sources