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Diastolic Blood Pressure, Subclinical Myocardial Damage, and Cardiac Events: Implications for Blood Pressure Control
John W McEvoy1, Yuan Chen2, Andreea Rawlings2
1Department of Epidemiology and the Welch Center for Prevention, Epidemiology and Clinical Research, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland; Ciccarone Center for the Prevention of Heart Disease, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Insights
Low diastolic blood pressure (DBP) is linked to myocardial damage and coronary heart disease (CHD) events, especially in those with high systolic blood pressure (SBP). Maintaining DBP above 60-70 mm Hg is advised during SBP treatment.
Area of Science:
- Cardiology
- Hypertension Research
- Clinical Trials
Background:
- The optimal systolic blood pressure (SBP) treatment target remains debated, with some trials suggesting a goal of 120 mm Hg.
- Achieving very low SBP may inadvertently lower diastolic blood pressure (DBP) to levels potentially compromising heart muscle blood supply.
Purpose of the Study:
- To investigate the independent association between DBP and myocardial damage, measured by high-sensitivity cardiac troponin-T (hs-cTnT).
- To examine the relationship between DBP and the risk of coronary heart disease (CHD), stroke, and all-cause mortality over a 21-year period.
Main Methods:
- Analysis of data from 11,565 adults in the Atherosclerosis Risk In Communities (ARIC) cohort.
- Assessment of associations between baseline DBP and hs-cTnT levels, and the change in hs-cTnT over time.
- Prospective evaluation of DBP's association with incident CHD, stroke, and mortality.
Main Results:
- Lower baseline DBP (<60 mm Hg and 60-69 mm Hg) was independently associated with higher odds of prevalent myocardial damage (hs-cTnT ≥14 ng/l).
- Low DBP was linked to progressive myocardial damage and increased risk of incident CHD and mortality, but not stroke.
- These associations were most pronounced in individuals with baseline SBP ≥120 mm Hg, indicating elevated pulse pressure.
Conclusions:
- Low DBP is associated with subclinical myocardial damage and CHD events, particularly in adults with SBP ≥120 mm Hg.
- When treating to lower SBP, clinicians should monitor DBP, aiming to keep it above 70 mm Hg, and especially above 60 mm Hg, to avoid potential harm.
Background:
The optimal systolic blood pressure (SBP) treatment goal is in question, with SPRINT (Systolic Blood Pressure Intervention Trial) suggesting benefit for 120 mm Hg. However, achieving an SBP this low may reduce diastolic blood pressure (DBP) to levels that could compromise myocardial perfusion.
Objectives:
This study sought to examine the independent association of DBP with myocardial damage (using high-sensitivity cardiac troponin-T [hs-cTnT]) and with coronary heart disease (CHD), stroke, or death over 21 years.
Methods:
The authors studied 11,565 adults from the ARIC (Atherosclerosis Risk In Communities) cohort, analyzing DBP and hs-cTnT associations as well as prospective associations between DBP and events.
Results:
Mean baseline age was 57 years, 57% of patients were female, and 25% were black. Compared with persons who had DBP between 80 to 89 mm Hg at baseline (ARIC visit 2), the adjusted odds ratio of having hs-cTnT ≥14 ng/l at that visit was 2.2 and 1.5 in those with DBP <60 mm Hg and 60 to 69 mm Hg, respectively. Low DBP at baseline was also independently associated with progressive myocardial damage on the basis of estimated annual change in hs-cTnT over the 6 years between ARIC visits 2 and 4. In addition, compared with a DBP of 80 to 89 mm Hg, a DBP <60 mm Hg was associated with incident CHD and mortality, but not with stroke. The DBP and incident CHD association was strongest with baseline hs-cTnT ≥14 ng/l (p value for interaction <0.001). Associations of low DBP with prevalent hs-cTnT and incident CHD were most pronounced among patients with baseline SBP ≥120 mm Hg.
Conclusions:
Particularly among adults with an SBP ≥120 mm Hg, and thus elevated pulse pressure, low DBP was associated with subclinical myocardial damage and CHD events. When titrating treatment to SBP <140 mm Hg, it may be prudent to ensure that DBP levels do not fall below 70 mm Hg, and particularly not below 60 mm Hg.
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