Abdulmajeed Alotaibi1
1King Saud University for Health Sciences, Riyadh, Saudi Arabia
Synopsis
Motivation: We want to confirm MK's ability in MS by a meta-analysis because different research have reported contradicting outcomes of MK value (that can indicate axon and myelin microstructural complexity).
Goal(s): To compare DKI in WMLs and NAWM
Approach: Tabular pairwise comparison estimates for each category. Mean ranks, 95% confidence intervals, and cumulative ranking curve were shown.
Results: 3 studies evaluated MK in NAWM and WM among MS patients; 4 compared MK in WM among control and MS patients; and 5 compared MK in WM and NAWM as well.
Impact: The study found that MS WMLs and NAWM have lower MKs. The findings may help physicians evaluate MS WMLs using MK consistency.
Multiple sclerosis (MS) is a chronic inflammatory demyelinated disease characterised by oedema, inflammation, demyelination, and axonal loss in the central nervous system. Magnetic resonance imaging (MRI) can provide information and track disease progression to improve MS diagnosis and evaluation in clinical practice. However, conventional MRI cannot capture microstructural damage information. Diffusion tensor imaging (DTI) is widely used in clinical practice and research to evaluate microstructural changes in white matter lesions (WMLs) and normal-appearing white matter (NAWM), which provides more sensitive measures for clinically relevant brain abnormalities. However, the diffusion of water molecules in brain tissue follows a non-Gaussian distribution, which DTI does not entirely characterise. Diffusion kurtosis imaging (DKI) is an extension of DTI that can quantify the non-Gaussian diffusion properties of water molecules in tissues and provides more accurate tissue microstructure information than DTI. The primary objective is to assess the primary DKI parameter known as Mean Kurtosis (MK) used to quantify microstructural abnormalities in neuroaxonal pathology in WMLs and NAWM in MS subjects compared with the WM in healthy controls. It was measured as standardised mean difference (SMD), where MK's lower values will equal more advanced axonal pathology. Three reviewers conducted the literature search of four electronic databases (Medline, Embase, Scopus, and PubMed) according to the updated PRISMA guidelines. We performed a random-effect network meta-analysis. Pairwise comparison estimates for each category were in tabular format, and rankings represented the probability of each node producing the best outcome. The rankings were presented with mean ranks, 95% confidence intervals, and the surface under the cumulative ranking curve. Analyses were conducted using MetaInsight Software and an open-source web interface to perform analysis in an intuitive ‘point and click’ manner. We included 6 studies and a total of 239 participants with three comparison groups in our network meta-analysis. 3 studies compared MK in NAWM and WM among MS subjects; 4 studies compared MK in WM among control subjects and patients with MS, 5 studies compared MK in WM and NAWM among control and MS subjects. We identified more reduced MK values in MS WMLs compared to NAWM and healthy WM. Also, less reduced MK values were seen in NAWM than in MS WMLs. There was a statistically significant difference in standardised mean difference among groups. The key finding is that MK had been proven to be closely linked to structural abnormalities seen on conventional MRI. The reduction of MK values in WMLs, compared to NAWM and WM in healthy controls, may be caused by severe axonal loss, myelin sheath damage, and the destruction of cellular components. Likewise, similar neuroaxonal pathology trends with less severity are seen within NAWM. This network meta-analysis confirmed that the MK is reduced in MS WMLs and NAWM from WM in healthy participants, which may correspond to axonal loss or myelin sheath damage. Acknowledgements
No acknowledgement found.References
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