Relationship Between Ascending Thoracic Aortic Diameter and Blood Pressure: A Mendelian Randomization Study

Author:

DePaolo John1ORCID,Levin Michael G.2ORCID,Tcheandjieu Catherine34ORCID,Priest James R.5ORCID,Gill Dipender67ORCID,Burgess Stephen89ORCID,Damrauer Scott M.11011ORCID,Chirinos Julio A.2ORCID

Affiliation:

1. Department of Surgery (J.D., S.M.D.), Perelman School of Medicine, University of Pennsylvania, Philadelphia.

2. Division of Cardiovascular Medicine, Department of Medicine (M.G.L., J.A.C.), Perelman School of Medicine, University of Pennsylvania, Philadelphia.

3. Gladstone Institute of Data Science and Biotechnology, Gladstone Institutes, San Francisco, CA (C.T.).

4. Department of Epidemiology and Biostatistics, University of California San Francisco (C.T.).

5. Division of Pediatric Cardiology, Department of Pediatrics, Stanford University School of Medicine, CA (J.R.P.).

6. Chief Scientific Advisor Office, Research and Early Development, Novo Nordisk, Copenhagen, Denmark (D.G.).

7. Department of Epidemiology and Biostatistics, School of Public Health, Imperial College London, United Kingdom (D.G.).

8. MRC Integrative Epidemiology Unit, University of Bristol, United Kingdom (S.B.).

9. Department of Public Health and Primary Care, University of Cambridge, United Kingdom (S.B.).

10. Department of Genetics (S.M.D.), Perelman School of Medicine, University of Pennsylvania, Philadelphia.

11. Corporal Michael Crescenz VA Medical Center, Philadelphia, PA (S.M.D.).

Abstract

Background: Observational studies identified elevated blood pressure (BP) as a strong risk factor for thoracic aortic dilation, and BP reduction is the primary medical intervention recommended to prevent progression of aortic aneurysms. However, although BP may impact aortic dilation, aortic size may also impact BP. The causal relationship between BP and thoracic aortic size has not been reliably established. Methods: Genome-wide association studies summary statistics were obtained for BP and ascending thoracic aortic diameter (AscAoD). Causal effects of BP on AscAoD were estimated using 2-sample Mendelian randomization using a range of pleiotropy-robust methods. Results: Genetically predicted increased systolic BP, diastolic BP, and mean arterial pressure all significantly associate with higher AscAoD (systolic BP: β estimate, 0.0041 mm/mm Hg [95% CI, 0.0008–0.0074]; P =0.02, diastolic BP: β estimate, 0.0272 mm/mm Hg [95% CI, 0.0224–0.0320]; P <0.001, and mean arterial pressure: β estimate, 0.0168 mm/mm Hg [95% CI, 0.0130–0.0206]; P <0.001). Genetically predicted pulse pressure, meanwhile, had an inverse association with AscAoD (β estimate, −0.0155 mm/mm Hg [95% CI, −0.0213 to −0.0096]; P <0.001). Multivariable Mendelian randomization analyses showed that genetically predicted increased mean arterial pressure and reduced pulse pressure were independently associated with AscAoD. Bidirectional Mendelian randomization demonstrated that genetically predicted AscAoD was inversely associated with pulse pressure (β estimate, −2.0721 mm Hg/mm [95% CI, −3.1137 to −1.0306]; P <0.001) and systolic BP (β estimate, −1.2878 mm Hg/mm [95% CI, −2.3533 to −0.2224]; P =0.02), while directly associated with diastolic BP (0.8203 mm Hg/mm [95% CI, 0.2735–1.3672]; P =0.004). Conclusions: BP likely contributes causally to ascending thoracic aortic dilation. Increased AscAoD likely contributes to lower systolic BP and pulse pressure, but not diastolic BP, consistent with the hemodynamic consequences of a reduced aortic diameter.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

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