Jessica Elizabeth Caterini1,2, Laura Banks3,4, Greg D Wells1,5, Brian McCrindle4,6, and Mike Seed4,6
1Physiology and Experimental Medicine, Hospital for Sick Children, Toronto, ON, Canada, 2Department of Exercise Sciences, University of Toronto, Toronto, ON, Canada, 3Faculty of Kinesiology and Physical Education, University of Toronto, ON, Canada, 4Labatt Family Heart Centre, Hospital for Sick Children, Toronto, ON, Canada, 5Faculty of Kinesiology and Physical Education, University of Toronto, Toronto, ON, Canada, 6Department of Pediatrics, Faculty of Medicine, University of Toronto, Toronto, ON, Canada
Synopsis
This
study provides a comparison of four commonly-used estimates of PWV to evaluate
aortic stiffness, and compares these estimates of PWV with factors indicating
cardiometabolic risk in obese youth. Hemodynamic parameters and phase-contrast
CMR of the aortic arch at 3.0T were measured in 19 participants (12 obese, 7
normal-weight). Four methods of estimating PWV were used (cross-correlation,
foot-to-foot, half-peak, area under the curve). There was an association
between increasing measures of inflammation (C-reactive protein) and BMI,
indicating that aortic PWV may be associated with changes in arterial stiffness in
adolescents with subclinical biomarkers of cardiovascular disease. Careful
consideration should be given to the method of PWV estimation due to
measurement bias.
Purpose
Phase
contrast magnetic resonance imaging can be used to estimate pulse wave velocity
as a non-invasive marker to detect early changes in vascular structure and
function[1]. While aortic PWV (aPWV) measured by velocity-encoded CMR may
uncover early vascular abnormalities in obese youth at risk for cardiovascular
disease, numerous techniques can be used to measure the time-shift (Δt) between
two points in the pulse wave, which results in measurement error. This study assessed
inter-method agreement in aortic PWV (aPWV) using two standard algorithms
(cross-correlation (CC), time-to-foot (TTF)) and two methods interpolating time
points on the flow curve (half-peak (HP), integral (INT))[2]. We also investigated
the relationship between aPWV and markers of cardiometabolic risk in a cohort
of overweight/obese (Ow/Ob) adolescentsMethods
Nineteen
(n=12 Ow/Ob, Table 1) adolescents had cardiac imaging performed on a 3T MRI
system (Siemens Magnetom TrioTim, Germany). Flow waves were obtained using
phase-contrast images perpendicular to the ascending and descending aorta at
the level of the right pulmonary artery. PC images were acquired with a non-breath-hold single-slice ECG-gated
sequence. Imaging parameters were: TE/TR = 2.72/19.16ms, flip angle = 25°,
in-plane resolution = 1.6mm x1.6 mm, slice thickness = 4mm, venc=150cm/s,
NSA=2, iPAT= GRAPPA, acceleration factor 2. This resulted in an effective
temporal resolution for flow-velocity calculation of 10-14ms depending
on the heart rate. Aortic arch length
measurements were obtained with a turbo spin echo breath-hold sequence oriented
along the long axis of the aortic arch. Flow waves were analyzed with
commercially-available software Qflow (Medis, Netherlands), and aortic arch
distance measured between the ascending and descending aorta using Qmass
(Medis, Netherlands). aPWV was obtained for all four methods (CC, TTF, HP, INT)
using custom programs in MATLAB, and a mean aPWV was computed from the average
of the four methods. Bland-Altman analysis assessed inter-method agreement, and
regression analyses were used to compare aPWV with measures of cardiometabolic
risk. Results
Inter-method
results showed no significant bias across the CC and INT methods (mean
difference ± SD= 0.91±0.56 m/s), CC and HP (mean difference ± SD= 1.23±0.29 m/s),
or HP and INT (mean difference ± SD = 0.32±0.29 m/s). FTF had significant bias
against CC, HP, and INT methods. aPWV was significantly higher in Ow/Ob participants
versus healthy normal weight controls when corrected for age and sex (Ow/Ob=
3.8±0.49 m/s; control= 3.07±0.52 m/s, p=0.014). BMI z-score (β=0.51, r2=0.61,
p=0.017) and C-reactive protein significantly predicted increasing aPWV
(β=0.61, r2=0.61, p=0.004) when controlling for age and sex.Discussion and Conclusion
Increasing arterial
stiffness measured by aPWV was associated with increasing body weight and
inflammatory status in overweight and obese adolescents without hypertension or
metabolic dysfunction. Importantly, poor time resolution has a significant
effect on PWV estimation, and can affect experimental interpretation.
Interpolated methods (integral and time to half peak) of measuring aPWV show
the greatest agreement in our adolescent cohort, with significant bias between
foot-to-foot and the other three methods of estimation. The method used to
calculate Δt in the estimation of aPWV should be carefully considered given
these differences.Acknowledgements
No acknowledgement found.References
[1]
Rider, OJ et al. (2010). Obesity, 18(12),
2311-2316.
[2]
Dogui, A et al. (2011). JMRI, 33(6), 1321-1329.