A cohort study and meta-analysis of isolated diastolic hypertension: searching for a threshold to guide treatment

Author:

Jacobsen Alan P1,Al Rifai Mahmoud2,Arps Kelly3ORCID,Whelton Seamus P1ORCID,Budoff Matthew J4ORCID,Nasir Khurram5ORCID,Blaha Michael J1,Psaty Bruce M6,Blumenthal Roger S1ORCID,Post Wendy S1,McEvoy John W17ORCID

Affiliation:

1. Ciccarone Center for the Prevention of Cardiovascular Disease, Division of Cardiology, Department of Medicine, Johns Hopkins Medical Institutions, Baltimore, MD, USA

2. Department of Medicine, Section of Cardiology, Baylor College of Medicine, Houston, TX, USA

3. Department of Medicine, Duke University School of Medicine, Durham, NC, USA

4. Division of Cardiology, Harbor-UCLA Medical Center, Torrance, CA, USA

5. Division of Cardiovascular Prevention and Wellness, Department of Cardiology, Houston Methodist DeBakey Heart & Vascular Center, Houston, TX, USA

6. Cardiovascular Health Research Unit, Departments of Medicine, Epidemiology, and Health Services, University of Washington and Kaiser Permanente Health Research Institute, Seattle, WA, USA

7. National Institute for Prevention and Cardiovascular Health, National University of Ireland Galway School of Medicine, Moyola Lane, Newcastle, Galway, H91 FF68, Ireland

Abstract

Abstract Aims  Whether isolated diastolic hypertension (IDH), as defined by the 2017 American College of Cardiology (ACC)/American Heart Association (AHA) guideline, is associated with cardiovascular disease (CVD) has been disputed. We aimed to further study the associations of IDH with (i) subclinical CVD in the form of coronary artery calcium (CAC), (ii) incident systolic hypertension, and (iii) CVD events. Methods and results  We used multivariable-adjusted logistic and Cox regression to test whether IDH by 2017 ACC/AHA criteria (i.e. systolic blood pressure <130 mmHg and diastolic blood pressure ≥80 mmHg) was associated with the above outcomes in the Multi-Ethnic Study of Atherosclerosis (MESA). In a random-effects meta-analysis of the association between IDH and CVD events, we combined the MESA results with those from seven other previously published cohort studies. Among the 5104 MESA participants studied, 7.5% had IDH by the 2017 ACC/AHA criteria. There was no association between IDH and CAC [e.g. adjusted prevalence odds ratio for CAC >0 of 0.88 (95% CI 0.66, 1.17)]. Similarly, while IDH was associated with incident systolic hypertension, there was no statistically significant associations with incident CVD [hazard ratio 1.19 (95% CI 0.77, 1.84)] or death [hazard ratio 0.94 (95% CI 0.65, 1.36)] over 13 years in MESA. In a stratified meta-analysis of eight cohort studies (10 037 843 participants), the 2017 IDH definition was also not consistently associated with CVD and the relative magnitude of any potential association was noted to be numerically small [e.g. depending on inclusion criteria applied in the stratification, the adjusted hazard ratios ranged from 1.04 (95% CI 0.98, 1.10) to 1.09 (95% 1.03, 1.15)]. Conclusion  The lack of consistent excess in CAC or CVD suggests that emphasis on healthy lifestyle rather than drug therapy is sufficient among the millions of middle-aged or older adults who now meet the 2017 ACC/AHA criteria for IDH, though they require follow-up for incident systolic hypertension. These findings may not extrapolate to adults younger than 40 years, motivating further study in this age group.

Funder

National Heart, Lung, and Blood Institute

National Center for Advancing Translational Sciences

Publisher

Oxford University Press (OUP)

Subject

Cardiology and Cardiovascular Medicine

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