Standing Blood Pressure and Risk of Falls, Syncope, Coronary Heart Disease, and Mortality

Jordan K Kondo1, William B Earle2, Ruth-Alma N Turkson-Ocran1,2

  • 1Harvard Medical School, Boston, Massachusetts, USA.

Insights

Low standing systolic blood pressure (SBP) is common and not linked to falls or syncope. However, it is associated with reduced risk of coronary heart disease (CHD) and mortality in adults.

Area of Science:

  • Cardiology
  • Gerontology
  • Public Health

Background:

  • Current ACC/AHA guidelines recommend caution with antihypertensive therapy for low standing systolic blood pressure (SBP) <110 mm Hg due to uncertain benefits.
  • Low SBP is a common finding in clinical practice, prompting investigation into its clinical significance.

Purpose of the Study:

  • To investigate the association between low standing SBP (<110 mm Hg) and the risk of adverse outcomes.
  • To evaluate the relationship between low standing SBP and falls, syncope, coronary heart disease (CHD), and mortality.

Main Methods:

  • Utilized data from the Atherosclerosis Risk in Communities (ARIC) Study, measuring SBP in adults aged 45-64 years (1987-1989).
  • Employed Cox regression to analyze associations between low standing SBP and outcomes, with follow-up through December 31, 2019.
  • Ascertained falls and syncope via claims data; adjudicated CHD events. Analyzed associations across various demographic and clinical strata.

Main Results:

  • Among 12,467 participants, 24% had standing SBP <110 mm Hg.
  • Low standing SBP was not significantly associated with increased risk of falls or syncope (HRs 1.02, 1.02).
  • Low standing SBP was associated with a significantly lower risk of CHD events (HR 0.88) and mortality (HR 0.91).

Conclusions:

  • Low standing SBP is prevalent in the community and not a significant risk factor for falls or syncope.
  • Low standing SBP is associated with reduced risk of coronary heart disease and mortality.
  • Findings do not support screening for low standing blood pressure as a predictor of adverse events.
Abstract

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