Elevated blood pressure and risk of aortic valve disease: a cohort analysis of 5.4 million UK adults. (12th September 2018)

• Record Type: Journal Article
• Authors: Rahimi, Kazem; Mohseni, Hamid; Kiran, Amit; Tran, Jenny; Nazarzadeh, Milad; Rahimian, Fatemeh; Woodward, Mark; Dwyer, Terence; MacMahon, Stephen; Otto, Catherine M
• Is Part Of: European heart journal. Volume 39:Number 39(2018)
• Page Start: 3596
• Page End: 3603
• Publication Date: 2018-09-12
• Subjects: Blood pressure -- Aortic valve disease -- Cohort study -- Aortic stenosis -- Aortic regurgitation; Cardiology -- Periodicals; Heart -- Diseases -- Periodicals; 616.12005
• DOI: 10.1093/eurheartj/ehy486
• Languages: English
• ISSNs: 0195-668X

Abstract

Abstract: Aims: To test two related hypotheses that elevated blood pressure (BP) is a risk factor for aortic valve stenosis (AS) or regurgitation (AR). Methods and results: In this cohort study of 5.4 million UK patients with no known cardiovascular disease or aortic valve disease at baseline, we investigated the relationship between BP and risk of incident AS and AR using multivariable-adjusted Cox regression models. Over a median follow-up of 9.2 years, 20 680 patients (0.38%) were diagnosed with AS and 6440 (0.12%) patients with AR. Systolic BP (SBP) was continuously related to the risk of AS and AR with no evidence of a nadir down to 115 mmHg. Each 20 mmHg increment in SBP was associated with a 41% higher risk of AS (hazard ratio 1.41, 95% confidence interval 1.38–1.45) and a 38% higher risk of AR (1.38, 1.31–1.45). Associations were stronger in younger patients but with no strong evidence for interaction by gender or body mass index. Each 10 mmHg increment in diastolic BP was associated with a 24% higher risk of AS (1.24, 1.19–1.29) but not AR (1.04, 0.97–1.11). Each 15 mmHg increment in pulse pressure was associated with a 46% greater risk of AS (1.46, 1.42–1.50) and a 53% higher risk of AR (1.53, 1.45–1.62). Conclusion: Long-term exposure to elevated BP across its whole spectrum was associated with increased risk of AS and AR. The possible causal nature of the observed associations warrants further investigation.