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The clinical application of 5.0 T 3D TOF MRA in the imaging of AChA and related cerebrovascular diseases
Zhangzhu Li1, Mingyan Shang2, Min Fu3, Zhensong Wang3, Jianxian Liu3, Liang Yin3, Dan Yu4, and Jie Gan2
1Shandong Provincial Third Hospital, Cheeloo College of Medicine, Shandong University, JINAN, China, 2Department of Radiology, Shandong Provincial Third Hospital, Cheeloo College of Medicine, Shandong University, Jinan, China, 3Department of Radiology, Shandong Provincial Third Hospital, Cheeloo College of Medicine, Shandong University, JINAN, China, 4United Imaging Research Institute of Intelligent Imaging, Beijing, People’s Republic of China, Beijing, China

Synopsis

Keywords: Vascular, Brain, magnetic resonance imaging; TOF MRA; Anterior choroidal artery AChA; 5.0 T

Motivation: Improved cerebrovascular disease diagnosis requires enhanced imaging of the anterior choroidal artery (AChA).

Goal(s): To evaluate the effectiveness of a 5.0T ultra-high-field MR scanner for cerebrovascular imaging compared to traditional 3.0T scanners.

Approach: Retrospective analysis using 5.0T MR imaging to assess AChA visualization in patients with cerebrovascular complaints.

Results: The 5.0T scanner significantly outperformed the 3.0T in image quality and detail, providing superior AChA delineation, which is essential for diagnosing related cerebrovascular diseases.

Impact: The 5.0T MR imaging's superior visualization of AChA paves the way for better diagnosis and management of deep brain vascular diseases, potentially influencing treatment outcomes and advancing neurovascular research.

Introduction

The anterior choroidal artery (AChA), despite its small size, is integral for brain motor and sensory functions. Infarcts in the AChA territory, particularly affecting the internal capsule, can cause the AChA syndrome - leading to severe motor and sensory deficits. Traditional magnetic resonance angiography (MRA) techniques often fail to depict the AChA clearly due to its size and complex location. Time-of-flight (TOF) MRA, however, offers a non-invasive, higher resolution alternative without the use of contrast agents. Although 7.0T MR provides even greater detail, its high cost and limited scope of application restrict its clinical use. This study aims to assess the effectiveness of 5.0T TOF MRA for depicting the AChA to aid in the diagnosis and treatment of cerebrovascular diseases, addressing a previously unexplored area of research.

Method

This retrospective study included 80 patients who presented with headache, dizziness, hemisensory disturbances, or focal epilepsy between May 15 and August 1, 2023. They were divided into two groups for imaging: 42 underwent 3.0T MR (Ingenia, Philips), and 38 underwent 5.0T MR (uMR Jupiter, United Imaging Healthcare), with two patients receiving both scans within 24 hours. Exclusions were made for those with aneurysm surgery, cerebral hemorrhage, heart surgery, or those pregnant, planning pregnancy, lactating, or with claustrophobia. TOF MRA was conducted with parameters detailed in Table 1, differing slightly between the 3.0T and 5.0T MR groups to optimize image quality. Images underwent 3D reconstruction, and cerebral arteries were analyzed through maximum intensity projections. Two experienced radiologists, blinded to field strength, evaluated image quality using the Likert 5 scale and counted visible branches. SNR and CNR were calculated for quantitative analysis. Statistical analysis employed SPSS 25.0, utilizing T-tests or Mann-Whitney U tests for parametric and non-parametric data, respectively, with chi-square tests for categorical data. Inter- and intra-observer reliability was determined using the intraclass correlation coefficient (ICC), with a threshold of 0.75 for good consistency. Statistical significance was defined at p<0.05.

Result

This study comprised 80 participants (37 males and 43 females, age range 12-87 years, mean age 59). It included 42 patients in the 3.0T group (23 males, 19 females, mean age 59.4) and 38 in the 5.0T group (16 males, 24 females, mean age 60.5). Age and gender distributions between groups were statistically comparable (P > 0.05). Inter- and intra-physician assessments demonstrated strong consistency in image and vascular quality evaluations (ICC between 0.93 and 0.99). In the 3.0T group, observations included 84 AChA-A1 segments, 56 AChA-A2, and 20 AChA-A3. The 5.0T group had 80 AChA-A1, 80 AChA-A2, and 60 AChA-A3 segments observed. SNR and CNR values were significantly higher in the 5.0T group compared to the 3.0T group (P < 0.05), and the subjective image quality rating also significantly differed between groups (P < 0.05). TOF MRA images from both groups showed significantly improved visualization of the anterior choroidal artery's length and diameter compared to standard 3.0T MR imaging (P < 0.05). These findings are detailed in Table 4 and illustrated in Figure 1 and Figure 2.

Discussion

This retrospective study compared the image quality and vessel delineation of TOF MRAs between 3.0T and 5.0T MR imaging, revealing that the 5.0T provided significantly higher SNR and CNR. Particularly, the 5.0T system offered superior visualization of the anterior choroidal artery, enhancing the detail of intracranial vessels, and thereby improving non-invasive vascular imaging for cerebrovascular disease assessment. The anterior choroidal artery is vital for supplying various brain regions; thus, its clear imaging is crucial for diagnosing related infarcts, which may lead to severe neurological symptoms. The 5.0T MR's enhanced capabilities not only yield better image quality but also facilitate more accurate diagnosis of small vessel diseases, aiding in the management of conditions like moyamoya syndrome and potentially improving outcomes for neurodegenerative diseases and stroke. Despite these advancements, this study's limitations include its single-center nature and the absence of a 7.0T control group, indicating a need for more comprehensive, multi-center studies to validate these findings.

Conclusion

This study showcases the application of a 5.0T ultra-high-field MR scanner for comprehensive cerebrovascular assessment, marking a significant stride in the diagnosis and differentiation of cerebrovascular conditions. It underscores the clinical value of detailed AChA visualization, which is crucial for diagnosing conditions like moyamoya disease, hippocampal sclerosis, and Parkinson's disease. The 5.0T system surpasses the limitations of 7.0T scanners for whole-body scans and outperforms 3.0T in visualizing deep brain vascular structures, offering substantial support for clinical diagnosis and management of cerebrovascular diseases.

Acknowledgements

Conflict of interest The authors state no conflict of interest.

References

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Figures

Figure 1.Comparison flow chart of 3.0T and 5.0TMR anterior choroidal artery imaging.


Figure 2 shows the same inspector. a1and c1 is 3.0T MIP image, b1and d1 is 5.0T MIP image, c1 is 3.0T MIP image corrected and straightened after right AChA measurement, showing that the measured length is about 2.7cm and the maximum diameter is about 1.1cm.d1 is the correction and straightening image after 5.0T MIP image is measured against the right AChA, showing that the measured length is 3.6cm and the maximum diameter is about 1.2cm. The AChA length measured by 5.0T MIP is significantly better than that measured by 3.0T MIP.

Figure3 shows the reverse color imaging of the brain MRA of the same subject. a2 and b2 are MRA images obtained by 3.0T MR Scan, c2 and d2 are MRA images obtained by 5.0T MR Scan, indicating that the quality of 5.0T brain MRA images is significantly better than 3.0T imaging. The red arrow indicates 3.0T MR AChA imaging and the blue arrow indicates 5.0T Mr AChA imaging.

Table 1. Acquisition parameters for the acquired MRA at 3T and 5T.

Table 2 Quantitative comparison of image quality between 3.0T group and 5.0T group

Table 3 Qualitative comparison between 3.0T group and 5.0T group

Table 4 Comparison of AChA length and diameter between 3.0T group and 5.0T group

Proc. Intl. Soc. Mag. Reson. Med. 32 (2024)
4917
DOI: https://doi.org/10.58530/2024/4917