Laura Saunders1, Andy Swift1, and Jim Wild1
1University of Sheffield, Sheffield, United Kingdom
Synopsis
This work explores lung T1
mapping as a contrast-free, radiation-free method of differentiating subgroups
in pulmonary hypertension, measured during both free breathing and inspiration
breath hold acquisitions. Inspiration lung T1 mapping is
significantly different between patients with pulmonary arterial hypertension
(PAH) and chronic thromboembolic
PH
(CTEPH), as well as between patients with idiopathic PAH and PAH due to
connective tissue disease (CTD) and congenital heart disease (CHD). Free
breathing lung T1 mapping was also significantly different between
patients with IPAH and PAH CTD and CHD and may be useful in patients who
struggle to maintain breath hold due to dyspnoea.
Background
Lung T1 mapping has been shown
to be sensitive to pulmonary perfusion and lung T1 reflects a
combination of tissue composition and density, blood volume and blood
oxygenation [1]. Pulmonary hypertension is a heterogeneous condition defined by
increased blood pressure in the pulmonary artery, which may have a variety of
causes including stiffening or thickening of the small pulmonary artery
branches (pulmonary arterial hypertension, PAH) or blood clots in the lungs
(chronic thromboembolic
pulmonary hypertension,
CTEPH). Patient treatment and outcome depends upon the cause (and therefore
subgroup) of pulmonary hypertension and therefore differentiating patients is
key to patient management and treatment. Lung T1 mapping may be a
contrast-free, radiation-free method of differentiating subgroups in pulmonary
hypertension however patients may struggle with a breath hold due to dyspnoea.Purpose
To explore lung T1 mapping as a contrast-free,
radiation-free method of differentiating subgroups in pulmonary hypertension,
measuring during both free breathing and inspiration breath hold acquisitions.Methods
65 patients with suspected pulmonary
hypertension and 9 healthy volunteers underwent lung T1 mapping on a
1.5T GE scanner using a Look-Locker inversion recovery sequence. T1 mapping
images were acquired during inspiration breath hold and also during an
identical acquisition during free breathing with post-processing image registration
for motion correction. The Look-Locker sequence comprises a global 180 degree
inversion pulse followed by 16 gradient echo readout images [2].
Imaging parameters were as follows: inversion time (TI): 229ms; TR=3.2ms; flip
angle: 7; phase x frequency: 128x128; slice thickness: 15mm; pixel bandwidth:
244.14; normal field of view 400-440mm. Breathing instructions for the free
breathing acquisition were to breathe normally.
For analysis, patients were grouped into
the 5 subcategories of pulmonary hypertension (PAH: n=29; pulmonary
hypertension with left heart disease (PH LHD): n=9; pulmonary hypertension due
to lung disease (PH-lung): n=7; CTEPH: n=8; other pulmonary hypertension
(MISC): n=3) and patients without pulmonary hypertension (no-PH: n=9). Of the
patients with PAH, 8 had a diagnosis of idiopathic PAH (IPAH), 10 had a
diagnosis of PAH due to connective tissue disease (PAH-CTD) and 8 had a
diagnosis of PAH due to congenital heart disease (PAH-CHD), 1 had PAH due to
drugs and 1 had PAH associated with portal hypertension.
For free breathing acquisitions,
post-processing image registration was used to spatially align acquired images
based creating spatially aligned synthetic images. Automatically selected ROIs
from the acquired images are input into a combined respiratory and inversion
recovery model to determine images which are in the similar respiratory states.
Spatially aligned images are then input into a simplified inversion recovery
model to create synthetic images. Acquired images are then co-registered to
synthetic images, see Figure 1. Image alignment before and after image
registration was evaluated using Dice Similarity Coefficient (DSC).
Results
Lung image alignment was significantly
improved after image registration for free breathing images (DSC before
registration: 0.93±0.02; DSC after registration: 0.95±0.02; p<0.001) and
post registration DSC was not significantly different from breath hold DSC
(p=0.651).
T1 maps were created for all
patients, see Figure 2. Mean lung T1 during inspiration was
significantly lower in CTEPH (T1=0.97±0.2s) than both healthy volunteers (T1=1.10±0.12s,
p=0.038) and PAH (T1=1.14±0.11, p=0.016), see Figure 3. Mean free
breathing T1 was significantly lower in patients with PH-Lung (T1=0.93±0.33s)
when compared to healthy volunteers (T1=1.22±0.3s, p=0.049). Within the
group of patients with PAH, during inspiration and free breathing acquisition,
mean lung T1 was significantly lower in patients with IPAH than
patients (T1=1.03±0.09s) with PAH-CTD (T1=1.22±0.06s, inspiration:
p<0.001; free breathing: p=0.019) or PAH-CHD (T1=1.16±0.07s, inspiration:
p=0.005; free breathing: p=0.004), see Figure 4. There was no significant
difference in mean lung T1 between patients with PAH-CHD and
PAH-CTD.
T1 values from inspiration and
breath hold significantly correlated with one another (r=0.534, p<0.001) and
did not differ from one another significantly in this patient cohort (p=0.461).Discussion and conclusion
Inspiration lung T1 mapping is
significantly different between patients with PAH and CTEPH, as well as between
patients with IPAH and PAH due to CTD and CHD. Free breathing lung T1
mapping was significantly lower in patients with PH-Lung when compared to
healthy volunteers, as well as being significantly different between patients
with IPAH and PAH due to CTD and CHD. Free breathing T1 mapping
acquisition may be particularly useful in patients who struggle to maintain
breath hold due to dyspnoea.Acknowledgements
No acknowledgement found.References
[1] Jobst et a., (2015). Functional Lung
MRI in Chronic Obstructive Pulmonary Disease: Comparison of T1
Mapping, Oxygen-enhanced T1 Mapping and Dynamic Contrast Enhanced
Perfusion.