Volume 15 Supplement 1
Cardiac magnetic resonance imaging for myocardial perfusion and diastolic function - reference control values for women
© Mehta et al; licensee BioMed Central Ltd. 2013
Published: 30 January 2013
Diastolic dysfunction and angina in the absence of obstructive coronary artery disease are more common in women. Microvascular coronary dysfunction (MCD) and are associated with an adverse cardiovascular prognosis. Cardiac Magnetic resonance imaging (CMRI) is established for assessment of left ventricular (LV) systolic function however but has not been wildly used to assess diastolic function is unknown. Stress CMRI may be used for measurement of myocardial perfusion reserve index (MPRI) and LV diastolic function using routine imaging techniques, which may be particularly relevant for detection of MCD in women. Normal reference values for MPRI and LV diastolic function in asymptomatic middle-aged, overweight women have not previously been established.
Cardiac Magnetic Resonance Imaging
(n=21) (mean ± SD)
MPRI (Myocardial Perfusion Reserve Index)
2.19 + 0.38
Peak filling rate
366.5 ± 75.2 ml/s
Peak filling rate (adjusted for end diastolic volume)
2.9 ± 0.4 ml/s
Peak filling rate (adjusted for stroke volume)
4.2 ± 0.6 ml/s
Time to peak filling rate
200.0 ± 19.7 ms
End diastolic volume/ end diastolic volume index
128.6 ± 27.7/ 73.0 ± 14.5 ml
End systolic volume/ end systolic volume index
36.8 ± 7.9/ 20.9 ± 4.0 ml
Left ventricular ejection fraction
70.4 ± 3.9%
Mean age was 51.1 ± 8.3 yrs and mean BMI was 25.1 ± 3.8 kg/m2. Reference control values for MPRI and LV diastolic filling are shown in the table.
Automated CMRI segmentation can provide quantitative perfusion and LV diastolic function profiles that may offer insight into MCD. We report normal values for MPRI, and LV diastolic filling by CMRI in a reference group of asymptomatic, overweight middle-aged women. These data can be used in comparisons to suspected and known MCD and diastolic dysfunction populations.
This work was supported by contracts from the National Heart, Lung and Blood Institutes, nos. N01-HV-68161, N01-HV-68162, N01-HV-68163, N01-HV-68164, a GCRC grant MO1-RR00425 from the National Center for Research Resources, and grants from the Gustavus and Louis Pfeiffer Research Foundation, Denville, New Jersey, the Women's Guild of Cedars-Sinai Medical Center, Los Angeles, California, the Edythe L. Broad Women's Heart Research Fellowship, Cedars-Sinai Medical Center, Los Angeles, California, and the Barbra Streisand Women's Cardiovascular Research and Education Program, Cedars-Sinai Medical Center, Los Angeles.
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 (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.