Madeline Schwid1, Hannah Recht1, Kai Lin1, Jeremy Collins1, Michael Markl1, Dan Lee1, and James Carr1
1Northwestern University, Chicago, IL, United States
Synopsis
This study evaluated semiquantitative measures of ischemia
using noninvasive stress perfusion CMR for the detection and quantification of
CAV using invasive coronary angiography as the standard reference on a cohort
of chronic heart transplant patients. Based on angiogram results, patients were
divided into groups by disease severity. The upslope and myocardial perfusion
reserve was measured per segment for each patient based on the AHA 16 segment
model. These values were then correlated to the angiogram results and averaged
by segment to create bullseye plots for each group. As disease severity
increases, both myocardial perfusion reserve and stress upslope decrease. Background
Chronic allograft vasculopathy (CAV) is a
progressive disease of the small vessels that affects heart transplant patients
and is a significant cause of morbidity and mortality. Traditional methods for diagnosing CAV rely on catheter
based angiography and intravascular ultrasound (IVUS), which are both invasive
and associated with potential adverse events. Stress perfusion cardiac MRI
(CMR) is frequently used to noninvasively diagnose ischemic heart disease and
has also been used to assess CAV in heart transplant patients. However, since
CAV is primarily a disease of the microvasculature, sparing the larger more
proximal epicardial coronary arteries, quantitative measures of myocardial
perfusion may be more valuable than relying on subjective assessment alone.
Purpose
The purpose of this study was to evaluate semiquantitative measures of ischemia using noninvasive stress
perfusion CMR in the detection of CAV using invasive coronary angiography as
the standard reference.
Methods
A
cohort of 41 chronic heart transplant patients was studied using both stress
CMR and coronary angiography. Stress CMR was performed in the standard manner
using an IV injection of regadenoson and 0.2 mM/kg of an extracellular
gadolinium based contrast agent. Based on the distribution of disease on the coronary
angiogram, the patients were sub-divided into groups of no disease (group 1),
mild chronic allograft vasculopathy (CAV) (group 2), and moderate to severe CAV
(group 3), based on the International Heart Lung Transplantation (IHLT)
guidelines for diagnosis of CAV. The time between the angiogram and perfusion
results varied from less than 6 months to just over 2 years, with an average of
about 1 year between studies. The rest and stress perfusion images were
analyzed by segment based on the AHA 16 segment model of the heart using
dedicated myocardial perfusion software (Argus, Siemens Healthcare). The
upslope was measured for each segment on both stress and rest images. The
myocardial perfusion reserve was calculated by dividing the upslope values of
rest and stress images. The semiquantitative results of the perfusion studies,
both stress perfusion upslope values and myocardial perfusion reserve, were
then correlated to the angiogram results. Bullseye plots based on the 16
segment model were created and compared for each of the CAV groups.
Results
There
were 18 patients with no evidence of CAV on angiography (group 1), 18 patients
with mild CAV (group 2), and 5 patients with moderate to severe CAV (group 3). Both
stress perfusion upslope and myocardial perfusion reserve tended to decrease with
increasing disease severity (fig 1). This is exhibited in the bullseye plots (fig
2) by the decreasing average value as well as overall lower values for both
stress upslope and myocardial perfusion reserve, demonstrated by an increase in
dark red colored segments.
Conclusions
Semiquantitative
parameters of upslope and myocardial perfusion reserve as measured from stress
perfusion CMR can detect both mild and moderate to severe CAV in heart transplant
patients. Stress perfusion CMR is a promising noninvasive tool for detecting
CAV potentially obviating the need for regular invasive coronary angiography.
Acknowledgements
No acknowledgement found.References
No reference found.