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Published on: February 14, 2021
Baroreflex sensitivity in asymptomatic coronary atherosclerosis
Sakari Simula1, Tomi Laitinen, Esko Vanninen
1Department of Neurology, Mikkeli Central Hospital, Mikkeli, Finland.
Insights
Reduced baroreflex sensitivity (BRS) is linked to early signs of coronary artery disease (CAD) in asymptomatic individuals. This finding suggests that impaired BRS may indicate underlying subclinical atherosclerosis in those at high risk for heart disease.
Area of Science:
- Cardiology
- Autonomic Nervous System Function
- Vascular Physiology
Background:
- Baroreflex sensitivity (BRS) is a key indicator of cardiac parasympathetic regulation.
- Impaired BRS is observed in established coronary artery disease (CAD) and post-myocardial infarction, with prognostic value.
- The presence of impaired BRS in asymptomatic individuals with subclinical coronary atherosclerosis remains unclear.
Purpose of the Study:
- To investigate the association between baroreflex sensitivity (BRS) and subclinical coronary atherosclerosis in asymptomatic individuals at high familial risk for CAD.
- To determine if impaired BRS is present in individuals with early, undetected coronary atherosclerosis.
Main Methods:
- Evaluated 31 asymptomatic subjects with high familial risk for CAD.
- Assessed BRS using the phenylephrine technique.
- Quantified coronary atherosclerosis severity using quantitative coronary angiography (QCA), calculating percentage of diameter stenosis (PDS).
- Ruled out myocardial perfusion defects using single photon emission tomography (SPECT).
Main Results:
- BRS showed an inverse correlation with the percentage of diameter stenosis (PDS) in proximal coronary artery segments (r = -0.315, P<0.05) and the most severe single coronary artery stenosis (r = -0.374, P<0.05).
- Subjects with severely blunted BRS (≤ 3 ms mmHg(-1)) exhibited significantly more severe PDS in proximal coronary segments (24 ± 7%) compared to those with higher BRS (> 3 ms mmHg(-1), 13 ± 11%, P<0.05).
Conclusions:
- Impaired baroreflex sensitivity (BRS) is associated with the severity of subclinical coronary atherosclerosis in asymptomatic individuals with familial risk for CAD.
- Severely blunted BRS in asymptomatic subjects may indicate the presence of advanced coronary atherosclerosis, suggesting BRS as a potential early marker.
Background:
Baroreflex sensitivity (BRS) reflects the effectiveness of cardiac parasympathetic regulation. BRS becomes impaired in stable coronary artery disease (CAD) and after myocardial infarction and carries prognostic information in these patients. Whether impaired BRS is found already in asymptomatic subjects, with subclinical coronary atherosclerosis, has remained elusive.
Methods:
The relationship between BRS and coronary atherosclerosis was evaluated in 31 subjects with high familial risk for CAD but without evidence of angina pectoris or myocardial ischaemia. Single photon emission tomography was performed with (99m) Tc-sestamibi to rule out myocardial perfusion defects at rest and during exercise. BRS was assessed by phenylephrine technique. Coronary atherosclerosis was analysed by quantitative coronary angiography (QCA). Percentage of diameter stenosis (PDS) was calculated separately for LAD, LCX, RCA coronary arteries as well as for proximal (PROX), middle (MID) and distal (DIST) coronary artery regions; and for all coronary artery regions (global PDS).
Results:
Baroreflex sensitivity averaged 7·8 ± 5·4 ms mmHg(-1) . BRS showed inverse correlation to PDS of the proximal coronary artery segments (r = -0·315; P<0·05) and with the most severe single coronary artery stenosis (r = -0·374; P<0·05). Five (16%) subjects had BRS ≤ 3 ms mmHg(-1) . They had more severe PDS of proximal coronary artery segment than subjects with BRS > 3 ms mmHg(-1) (24 ± 7% versus 13 ± 11%, P<0·05, respectively).
Conclusions:
Impairment of BRS was found to be associated with the severity of subclinical coronary atherosclerosis in healthy asymptomatic subjects with familial risk of CAD. Asymptomatic subjects with severely blunted BRS may have advanced coronary atherosclerosis.
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