Xiaobin Zhou1, Xiaoyu Wei1, Yingjie Mei2, Qiong Ou3, Zhecheng Du4, and Hui Liu1
1Department of Radiology, Guangdong Provincial People’s Hospital, Guangdong Academy of Medical Sciences, Guangzhou, China, 2Philips Healthcare, Guangzhou, China, 3Sleep Center, Department of Pulmonary and Critical Care Medicine, Guangdong Provincial People’s Hospital, Guangdong Academy of Medical Sciences, Guangdong Provincial Geriatrics Institute, Guangzhou, China, 4Department of Medical Statistics, School of Public Health, Sun Yat-sen University, Guangzhou, China
Synopsis
The comprehensive assessment of left ventricular (LV)
remodeling by cardiac magnetic resonance (CMR) imaging with T1 mapping and feature tracking (FT) technology in obstructive
sleep apnea (OSA) was conducted in this study. Indexed extracellular volume
(iECV) and indexed cellular volume (iCV) of myocardial tissue construction were
derived from T1 mapping. The results show that elevated LV mass index (LVMi) in
OSA was mainly from iCV, while not from iECV, with no LV ejection function
(LVEF) or strain parameters impairment. Cellular hypertrophy accompanied with
normal LV systolic function in patients with OSA may contribute to adaptive LV
remodeling phase.
Purpose and Introduction
Obstructive sleep apnea,
characterized by repetitive partial or complete upper respiratory tract
obstruction during sleep, is a common respiratory disorder affecting more than
39.4% individuals in China1. OSA is associated with cardiac
hypertrophy and have high odds of developing concentric left ventricular
hypertrophy2. For
detecting detrimental effect on the heart in OSA patients, echocardiographic
examination is the most widely utilized method. However, CMR, as the gold
standard imaging technology to evaluate
left ventricular function and structure and as the unique tool for
characterizing myocardial tissue changes, is scare, especially in OSA patients
without any other medical disorders. Therefore, we aimed to characterize and
assess myocardial structure, volume, function and tissue characteristic changes
following LV remodeling in first diagnosed OSA patients by CMR method with T1
mapping and feature tracking technology.Materials and Methods
All 41 participants without major
cardiovascular diseases were recruited from the Sleep Center of our hospital
for snoring or sleeping problems. After an overnight polysomnography
examination, all participants underwent standard CMR imaging protocol on a 3.0
T clinical scanner (Ingenia, Philips Medical Systems, Best, the Netherlands),
with a 32-channel coil for signal reception. CMR scans were used to evaluate LV
function, volume, structure, deformation with feature tracking, diffuse
myocardial fibrosis with T1 mapping and focal replacement fibrosis with late
gadolinium enhancement (LGE) in these subjects. iECV obtained as LVMi/1.05×ECV%
and iCV derived as (LVMi/1.05×[1–ECV%]) were recorded. Based on the
apnea-hypopnea index (AHI), participants were divided into the OSA (AHI ≥ 5
events/h) and control (AHI < 5 events/h) groups. Statistical analysis was
performed with SPSS and the GraphPad Prism software. Normally distributed
continuous variables were expressed as mean ± standard deviation (SD), while
skewed ones were expressed as median (interquartile range). Categorical
variables were reported as number and frequency (%). Comparisons between the
OSA and control groups were performed by the Student’s t-test, Mann-Whitney U
test, Fisher’s exact test or Chi-square test as appropriate. Multiple linear
regression analyses were applied to confirm the significant impact of OSA on LVMi
value. Two-sided P values <0.05 was considered statistically significant.Results
24 patients
with OSA (AHI ≥ 5 events/h; age 42.7±11.6 years; 75% male) were compared with
17 controls (AHI < 5 events/h; age 41.2±8.2 years; 58.8% male). The subjects
were predominantly middle-aged males without significant differences between
the two groups. The OSA group had slightly elevated body mass index (26.5±3.6
kg/m2 vs. 24.4±2.5 kg/m2, P=0.04) compared with controls,
and 9 (37.5%) OSA patients also had hypertension. The OSA group had higher LVMi
value than control group (45.4±8.7 g/m2 vs. 36.1±7.7 g/m2,
P = 0.001). Both groups kept preserved LV systolic function as demonstrated by
similar LV ejection fraction, global longitudinal strain, global
circumferential strain and global radial strain values (all P >0.05). Late
gadolinium enhancement was not detected in these two groups, whereas ECV% was
slightly decreased in the OSA group (24.7±2.1 % vs. 26.6±3.0%, P = 0.02).
Compared with controls, iCV was greatly larger (median 32.6 ml/m2,
interquartile range [IQR]: 29.4-37.5 vs. median 23.1 ml/m2, IQR:
21.2-30.8, P = 0.001), while iECV was slightly increased (10.6 ± 1.8 ml/m2
vs. 9.1 ± 1.9 ml/m2, P = 0.01). On multivariate linear regression
analysis, OSA (β =0.358, P =0.021), male gender (β =0.359, P =0.011) and
systolic blood pressure (β =0.340, P =0.014) were the strongest factor
correlated with elevated LVMi. Conclusion
In conclusion, the
presence of OSA is significantly associated with elevated LVMi. Elevated LVMi accompanied with
normal LV systolic function in first diagnosed OSA patients may contribute to
adaptive LV remodeling phase, which can be assessed with T1 mapping and feature
tracking technique.Acknowledgements
No acknowledgement found.References
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