Volume 13 Supplement 1

Abstracts of the 2011 SCMR/Euro CMR Joint Scientific Sessions

Open Access

Measurement of myocardial blood flow response to the cold pressor test with myocardial perfusion CMR

  • Timothy A Fairbairn1,
  • Adam Mather1,
  • Adbul Larghat1,
  • John Greenwood1 and
  • Sven Plein1
Journal of Cardiovascular Magnetic Resonance201113(Suppl 1):P312

DOI: 10.1186/1532-429X-13-S1-P312

Published: 2 February 2011

Objective

To measure Cold Pressor Test (CPT)-induced changes in MBF and compare them to adenosine induced (endothelial-independent) changes in MBF.

Background

The CPT induces endothelial-dependent vasodilation with increased myocardial blood flow (MBF) in normal coronary arteries. It has been used to demonstrate abnormal coronary vasomotion by invasive (angiography) and non-invasive techniques (SPECT and PET). Cardiovascular Magnetic Resonance (CMR) allows the assessment of MBF in separate myocardial layers due to its high spatial resolution, but has not previously been used to measure physiological responses to CPT.

Methods

Eleven healthy volunteers (age 23±5.4, 64% male) attended for a CMR perfusion scan (Phillips Intera 1.5T, 0.05mmol/kg Gd-DTPA, spatial resolution 2.3 x 2.3mm), performed at rest, during CPT (120s of foot immersion in 0-4°C water) and adenosine hyperaemia (140mcg/kg/min for 4 minutes). Each perfusion scan was separated by 15 minutes. Heart rate (HR) and blood pressure (BP) were simultaneously recorded .This information was then used to calculate mean arterial pressure (MAP= 2*Diastolic BP (DBP)+ Systolic BP (SBP)/3), rate-pressure product (RPP= HR x SBP) and coronary vascular resistance (CVR= MAP/ MBF). MBF (ml/g/min) was estimated for a mid-ventricular slice by Fermi-constrained deconvolution.

Results

MBF increased significantly from rest to CPT (1.5±0.5 to 2.3±0.6 ml/g/min, p=0.004) and from CPT to stress (4.4±0.8, p<0.001) (Table 1). Endocardial MBF was significantly higher than epicardial MBF at rest (p<0.001) and during CPT (p=0.008), however during adenosine hyperaemia epicardial MBF was higher (p=0.043). Regression analysis of haemodynamic factors identified Coronary Vascular Resistance (CVR) as the only independent predictor of MBF during rest, CPT and adenosine, (Figure 1).
Table 1

Haemodynamic parameters and Myocardial Blood Flow (ml/g/min), measured at rest, peak cold pressor test (CPT) and adenosine stress

 

REST

P value

CPT

P value

ADENOSINE

Heart Rate (bpm)

70 ±9

0.001

84 ±12

0.02

97 ±12

Systolic Blood Pressure (mmHg)

120 ±10

0.025

132 ±16

0.002

114 ±14

Diastolic Blood Pressure (mmHg)

66 ±7

0.001

78 ±9

<0.001

60 ±9

Mean Arterial Pressure (mmHg)

84 ±6

0.022

94 ±15

<0.001

78 ±10

Rate Pressure Product (mmHg/min)

8441 ±1198

<0.001

11157 ±2018

0.972

11184 ±2031

Coronary Vascular Resistance (mmHg/ml min g)

60.5 ±14.8

0.01

43.9 ±15.4

<0.001

18.5 ±4.2

Myocardial Blood Flow (ml/g/min)

1.48 ±0.15

0.004

2.31 ±0.18

<0.001

4.36 ±0.25

Endocardial Blood Flow (ml/g/min)

1.7 ±0.6

NA

2.38 ±0.5

NA

4.09 ±0.7

Epicardial Blood Flow (ml/g/min)

1.38 ±0.5

NA

2.09 ±0.7

NA

4.53 ±1.1

Figure 1

A scatter plot demonstrating the negative relationship between Coronary Vascular Resistance (CVR) and Myocardial Blood Flow (MBF, ml/g/min) for each perfusion examination.

Discussion

Perfusion-CMR permits assessment of endothelial-dependent (CPT) and endothelial-independent (adenosine) MBF in a single examination. Furthermore, CMR demonstrates differences in the physiological response to CPT and maximal hyperaemia between the endocardium and epicardium. Future studies should establish the role of this new method in at risk groups such as those with diabetes or smokers.

Authors’ Affiliations

(1)
University of Leeds

Copyright

© Fairbairn et al; licensee BioMed Central Ltd. 2011

This article is published under license to BioMed Central Ltd. This is an open access article distributed under the terms of the Creative Commons Attribution License (<url>http://creativecommons.org/licenses/by/2.0</url>), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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