FRINK Linked Data Fragments server

Matches in SemOpenAlex for { <https://semopenalex.org/work/W2731876108> ?p ?o ?g. }

• W2731876108 endingPage "67" @default.
• W2731876108 startingPage "64" @default.
• W2731876108 abstract "Introduction An MRI-based score of total small vessel disease burden (CAA-SVD-Score) in cerebral amyloid angiopathy (CAA) has been demonstrated to correlate with severity of pathologic changes. Evidence suggests that CAA-related intracerebral hemorrhage (ICH) recurrence risk is associated with specific disease imaging manifestations rather than overall severity. We compared the correlation between the CAA-SVD-Score with the risk of recurrent CAA-related lobar ICH versus the predictive role of each of its components. Methods Consecutive patients with CAA-related ICH from a single-center prospective cohort were analyzed. Radiological markers of CAA related SVD damage were quantified and categorized according to the CAA-SVD-Score (0–6 points). Subjects were followed prospectively for recurrent symptomatic ICH. Adjusted Cox proportional hazards models were used to investigate associations between the CAA-SVD-Score as well as each of the individual MRI signatures of CAA and the risk of recurrent ICH. Results In 229 CAA patients with ICH, a total of 56 recurrent ICH events occurred during a median follow-up of 2.8 years [IQR 0.9–5.4 years, 781 person-years). Higher CAA-SVD-Score (HR = 1.26 per additional point, 95%CI [1.04–1.52], p = 0.015) and older age were independently associated with higher ICH recurrence risk. Analysis of individual markers of CAA showed that CAA-SVD-Score findings were due to the independent effect of disseminated superficial siderosis (HR for disseminated cSS vs none: 2.89, 95%CI [1.47–5.5], p = 0.002) and high degree of perivascular spaces enlargement (RR = 3.50–95%CI [1.04–21], p = 0.042). Conclusion In lobar CAA-ICH patients, higher CAA-SVD-Score does predict recurrent ICH. Amongst individual elements of the score, superficial siderosis and dilated perivascular spaces are the only markers independently associated with ICH recurrence, contributing to the evidence for distinct CAA phenotypes singled out by neuro-imaging manifestations." @default.
• W2731876108 created "2017-07-14" @default.
• W2731876108 creator A5001703565 @default.
• W2731876108 creator A5001824484 @default.
• W2731876108 creator A5001829677 @default.
• W2731876108 creator A5006664647 @default.
• W2731876108 creator A5016635966 @default.
• W2731876108 creator A5021123257 @default.
• W2731876108 creator A5045439266 @default.
• W2731876108 creator A5053787562 @default.
• W2731876108 creator A5055117066 @default.
• W2731876108 creator A5056733365 @default.
• W2731876108 creator A5061174828 @default.
• W2731876108 creator A5062339766 @default.
• W2731876108 creator A5063509357 @default.
• W2731876108 creator A5071237195 @default.
• W2731876108 creator A5072737556 @default.
• W2731876108 creator A5082820300 @default.
• W2731876108 date "2017-09-01" @default.
• W2731876108 modified "2023-10-17" @default.
• W2731876108 title "Hemorrhage recurrence risk factors in cerebral amyloid angiopathy: Comparative analysis of the overall small vessel disease severity score versus individual neuroimaging markers" @default.
• W2731876108 cites W1827025186 @default.
• W2731876108 cites W2014889602 @default.
• W2731876108 cites W2017302232 @default.
• W2731876108 cites W2023092313 @default.
• W2731876108 cites W2030827970 @default.
• W2731876108 cites W2076779801 @default.
• W2731876108 cites W2135148614 @default.
• W2731876108 cites W2157032372 @default.
• W2731876108 cites W2158742097 @default.
• W2731876108 cites W2275737843 @default.
• W2731876108 cites W2289333406 @default.
• W2731876108 cites W2321488910 @default.
• W2731876108 cites W2403831753 @default.
• W2731876108 cites W2469367031 @default.
• W2731876108 cites W2582964272 @default.
• W2731876108 cites W2596892842 @default.
• W2731876108 doi "https://doi.org/10.1016/j.jns.2017.07.015" @default.
• W2731876108 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/5678990" @default.
• W2731876108 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/28870591" @default.
• W2731876108 hasPublicationYear "2017" @default.
• W2731876108 type Work @default.
• W2731876108 sameAs 2731876108 @default.
• W2731876108 citedByCount "34" @default.
• W2731876108 countsByYear W27318761082017 @default.
• W2731876108 countsByYear W27318761082018 @default.
• W2731876108 countsByYear W27318761082019 @default.
• W2731876108 countsByYear W27318761082020 @default.
• W2731876108 countsByYear W27318761082021 @default.
• W2731876108 countsByYear W27318761082022 @default.
• W2731876108 countsByYear W27318761082023 @default.
• W2731876108 crossrefType "journal-article" @default.
• W2731876108 hasAuthorship W2731876108A5001703565 @default.
• W2731876108 hasAuthorship W2731876108A5001824484 @default.
• W2731876108 hasAuthorship W2731876108A5001829677 @default.
• W2731876108 hasAuthorship W2731876108A5006664647 @default.
• W2731876108 hasAuthorship W2731876108A5016635966 @default.
• W2731876108 hasAuthorship W2731876108A5021123257 @default.
• W2731876108 hasAuthorship W2731876108A5045439266 @default.
• W2731876108 hasAuthorship W2731876108A5053787562 @default.
• W2731876108 hasAuthorship W2731876108A5055117066 @default.
• W2731876108 hasAuthorship W2731876108A5056733365 @default.
• W2731876108 hasAuthorship W2731876108A5061174828 @default.
• W2731876108 hasAuthorship W2731876108A5062339766 @default.
• W2731876108 hasAuthorship W2731876108A5063509357 @default.
• W2731876108 hasAuthorship W2731876108A5071237195 @default.
• W2731876108 hasAuthorship W2731876108A5072737556 @default.
• W2731876108 hasAuthorship W2731876108A5082820300 @default.
• W2731876108 hasBestOaLocation W27318761082 @default.
• W2731876108 hasConcept C126322002 @default.
• W2731876108 hasConcept C188816634 @default.
• W2731876108 hasConcept C207103383 @default.
• W2731876108 hasConcept C207886595 @default.
• W2731876108 hasConcept C2777094939 @default.
• W2731876108 hasConcept C2777736543 @default.
• W2731876108 hasConcept C2777790613 @default.
• W2731876108 hasConcept C2779134260 @default.
• W2731876108 hasConcept C2779483572 @default.
• W2731876108 hasConcept C2780860705 @default.
• W2731876108 hasConcept C44249647 @default.
• W2731876108 hasConcept C50382708 @default.
• W2731876108 hasConcept C71924100 @default.
• W2731876108 hasConcept C72563966 @default.
• W2731876108 hasConcept C90924648 @default.
• W2731876108 hasConceptScore W2731876108C126322002 @default.
• W2731876108 hasConceptScore W2731876108C188816634 @default.
• W2731876108 hasConceptScore W2731876108C207103383 @default.
• W2731876108 hasConceptScore W2731876108C207886595 @default.
• W2731876108 hasConceptScore W2731876108C2777094939 @default.
• W2731876108 hasConceptScore W2731876108C2777736543 @default.
• W2731876108 hasConceptScore W2731876108C2777790613 @default.
• W2731876108 hasConceptScore W2731876108C2779134260 @default.
• W2731876108 hasConceptScore W2731876108C2779483572 @default.
• W2731876108 hasConceptScore W2731876108C2780860705 @default.
• W2731876108 hasConceptScore W2731876108C44249647 @default.
• W2731876108 hasConceptScore W2731876108C50382708 @default.
• W2731876108 hasConceptScore W2731876108C71924100 @default.
• W2731876108 hasConceptScore W2731876108C72563966 @default.

• next