Matches in SemOpenAlex for { <https://semopenalex.org/work/W2962509579> ?p ?o ?g. }
- W2962509579 abstract "Background and Purpose: Susceptibility-weighted imaging (SWI) has been emerged as a useful clinical tool in many neurological diseases including multiple sclerosis (MS). This study is to investigate the relationship between SWI signal changes including due to iron deposition in MS lesions and tissue blood perfusion and microstructural abnormalities to better understand their underlying histopathologies. Methods: Forty-six patients with relapsing remitting MS were recruited for this study. Conventional FLAIR, pre- and post-contrast T1-weighted imaging, SWI, diffusion tensor imaging (DTI), and dynamic susceptibility contrast (DSC) perfusion MRI were performed in these patients at 3T. The SWI was processed using both magnitude and phase information with one slice minimal intensity projection (mIP) and phase multiplication factor of 4. MS lesions were classified into 3 three groups based on their lesional signal appearance on SWI mIP relative to perilesional normal appearing white matter (peri-NAWM): Type-1: hypointense, Type-2: isointense, and Type-3: hyperintense lesions. The DTI and DSC MRI data were processed offline to generate DTI-derived mean diffusivity (MD) and fractional anisotropy (FA) maps as well as DSC-derived cerebral blood flow (CBF) and cerebral blood volume (CBV) maps. Comparisons of diffusion and perfusion measurements between lesions and peri-NAWM as well between different types of lesions were performed. Results: A total of 137 lesions were identified on FLAIR in these patients that include 40 Type-1, 46 Type-2, and 51 Type-3 lesions according to their SWI signal. All lesion types showed significant higher MD and lower FA compared to their peri-NAWM (P<0.0001). Compared to Type-1 lesions (likely represent iron deposition), Type-2 lesions had significantly higher MD and lower FA (P<0.001) as well as lower perfusion measurements (P < 0.05), while Type 3 lesions had significantly higher perfusion (P<0.001) and lower FA (P < 0.05). Compared to Type-2, Type-3 lesions had higher perfusion (P < 0.0001) and marginally higher MD and lower FA (P<0.05). Conclusion: The significant differences of diffusion and perfusion MRI metrics associated with MS lesions that appear with different signal appearance on SWI may help to identify the underlying destructive pathways of myelin and axons and their evolution related to inflammatory activities." @default.
- W2962509579 created "2019-07-23" @default.
- W2962509579 creator A5046513206 @default.
- W2962509579 creator A5055520789 @default.
- W2962509579 creator A5087349385 @default.
- W2962509579 date "2019-07-11" @default.
- W2962509579 modified "2023-10-03" @default.
- W2962509579 title "Blood Perfusion and Cellular Microstructural Changes Associated With Iron Deposition in Multiple Sclerosis Lesions" @default.
- W2962509579 cites W147290092 @default.
- W2962509579 cites W1742765381 @default.
- W2962509579 cites W1973462954 @default.
- W2962509579 cites W1979911585 @default.
- W2962509579 cites W1981700224 @default.
- W2962509579 cites W2013234597 @default.
- W2962509579 cites W2032074383 @default.
- W2962509579 cites W2039966321 @default.
- W2962509579 cites W2049381107 @default.
- W2962509579 cites W2051831186 @default.
- W2962509579 cites W2052590180 @default.
- W2962509579 cites W2067200113 @default.
- W2962509579 cites W2072718666 @default.
- W2962509579 cites W2072839327 @default.
- W2962509579 cites W2097505016 @default.
- W2962509579 cites W2097528079 @default.
- W2962509579 cites W2106455035 @default.
- W2962509579 cites W2110735777 @default.
- W2962509579 cites W2114553926 @default.
- W2962509579 cites W2118060850 @default.
- W2962509579 cites W2135009525 @default.
- W2962509579 cites W2139158372 @default.
- W2962509579 cites W2146336531 @default.
- W2962509579 cites W2149601652 @default.
- W2962509579 cites W2154189431 @default.
- W2962509579 cites W2160760506 @default.
- W2962509579 cites W2180194522 @default.
- W2962509579 cites W2235034379 @default.
- W2962509579 cites W2317513491 @default.
- W2962509579 cites W2321572725 @default.
- W2962509579 cites W2332064267 @default.
- W2962509579 cites W2462120210 @default.
- W2962509579 cites W2519028342 @default.
- W2962509579 cites W2524490682 @default.
- W2962509579 cites W2542350582 @default.
- W2962509579 cites W2763429356 @default.
- W2962509579 cites W2767615018 @default.
- W2962509579 cites W2794201194 @default.
- W2962509579 cites W2916380399 @default.
- W2962509579 cites W2921928513 @default.
- W2962509579 cites W4234126893 @default.
- W2962509579 doi "https://doi.org/10.3389/fneur.2019.00747" @default.
- W2962509579 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6637756" @default.
- W2962509579 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/31354613" @default.
- W2962509579 hasPublicationYear "2019" @default.
- W2962509579 type Work @default.
- W2962509579 sameAs 2962509579 @default.
- W2962509579 citedByCount "6" @default.
- W2962509579 countsByYear W29625095792020 @default.
- W2962509579 countsByYear W29625095792021 @default.
- W2962509579 countsByYear W29625095792022 @default.
- W2962509579 countsByYear W29625095792023 @default.
- W2962509579 crossrefType "journal-article" @default.
- W2962509579 hasAuthorship W2962509579A5046513206 @default.
- W2962509579 hasAuthorship W2962509579A5055520789 @default.
- W2962509579 hasAuthorship W2962509579A5087349385 @default.
- W2962509579 hasBestOaLocation W29625095791 @default.
- W2962509579 hasConcept C101070640 @default.
- W2962509579 hasConcept C118552586 @default.
- W2962509579 hasConcept C126322002 @default.
- W2962509579 hasConcept C126838900 @default.
- W2962509579 hasConcept C142724271 @default.
- W2962509579 hasConcept C143409427 @default.
- W2962509579 hasConcept C146957229 @default.
- W2962509579 hasConcept C149550507 @default.
- W2962509579 hasConcept C157767197 @default.
- W2962509579 hasConcept C16246696 @default.
- W2962509579 hasConcept C2780640218 @default.
- W2962509579 hasConcept C2781156865 @default.
- W2962509579 hasConcept C2781192897 @default.
- W2962509579 hasConcept C2989005 @default.
- W2962509579 hasConcept C71924100 @default.
- W2962509579 hasConcept C89916169 @default.
- W2962509579 hasConceptScore W2962509579C101070640 @default.
- W2962509579 hasConceptScore W2962509579C118552586 @default.
- W2962509579 hasConceptScore W2962509579C126322002 @default.
- W2962509579 hasConceptScore W2962509579C126838900 @default.
- W2962509579 hasConceptScore W2962509579C142724271 @default.
- W2962509579 hasConceptScore W2962509579C143409427 @default.
- W2962509579 hasConceptScore W2962509579C146957229 @default.
- W2962509579 hasConceptScore W2962509579C149550507 @default.
- W2962509579 hasConceptScore W2962509579C157767197 @default.
- W2962509579 hasConceptScore W2962509579C16246696 @default.
- W2962509579 hasConceptScore W2962509579C2780640218 @default.
- W2962509579 hasConceptScore W2962509579C2781156865 @default.
- W2962509579 hasConceptScore W2962509579C2781192897 @default.
- W2962509579 hasConceptScore W2962509579C2989005 @default.
- W2962509579 hasConceptScore W2962509579C71924100 @default.
- W2962509579 hasConceptScore W2962509579C89916169 @default.
- W2962509579 hasLocation W29625095791 @default.
- W2962509579 hasLocation W29625095792 @default.
- W2962509579 hasLocation W29625095793 @default.