Periventricular magnetisation transfer abnormalities in early multiple sclerosis
OBJECTIVE: Recent studies suggested that CSF-mediated factors contribute to periventricular (PV) T2-hyperintense lesion formation in multiple sclerosis (MS) and this in turn correlates with cortical damage. We thus investigated if such PV-changes are observable microstructurally in early-MS and if t...
Elmentve itt :
| Szerzők: | |
|---|---|
| Dokumentumtípus: | Cikk |
| Megjelent: |
2022
|
| Sorozat: | NEUROIMAGE-CLINICAL
34 |
| Tárgyszavak: | |
| doi: | 10.1016/j.nicl.2022.103012 |
| mtmt: | 32805575 |
| Online Access: | http://publicatio.bibl.u-szeged.hu/24279 |
| LEADER | 02632nab a2200325 i 4500 | ||
|---|---|---|---|
| 001 | publ24279 | ||
| 005 | 20220505095707.0 | ||
| 008 | 220505s2022 hu o 0|| Angol d | ||
| 022 | |a 2213-1582 | ||
| 024 | 7 | |a 10.1016/j.nicl.2022.103012 |2 doi | |
| 024 | 7 | |a 32805575 |2 mtmt | |
| 040 | |a SZTE Publicatio Repozitórium |b hun | ||
| 041 | |a Angol | ||
| 100 | 1 | |a Pirpamer Lukas | |
| 245 | 1 | 0 | |a Periventricular magnetisation transfer abnormalities in early multiple sclerosis |h [elektronikus dokumentum] / |c Pirpamer Lukas |
| 260 | |c 2022 | ||
| 300 | |a Azonosító: 103012-Terjedelem: 8 p. | ||
| 490 | 0 | |a NEUROIMAGE-CLINICAL |v 34 | |
| 520 | 3 | |a OBJECTIVE: Recent studies suggested that CSF-mediated factors contribute to periventricular (PV) T2-hyperintense lesion formation in multiple sclerosis (MS) and this in turn correlates with cortical damage. We thus investigated if such PV-changes are observable microstructurally in early-MS and if they correlate with cortical damage. METHODS: We assessed the magnetisation transfer ratio (MTR) in PV normal-appearing white matter (NAWM) and in MS lesions in 44 patients with a clinically isolated syndrome (CIS) suggestive of MS and 73 relapsing-remitting MS (RRMS) patients. Band-wise MTR values were related to cortical mean thickness (CMT) and compared with 49 healthy controls (HCs). For each band, MTR changes were assessed relative to the average MTR values of all HCs. RESULTS: Relative to HCs, PV-MTR was significantly reduced up to 2.63% in CIS and 5.37% in RRMS (p<0.0001). The MTR decreased towards the lateral ventricles with 0.18%/mm in CIS and 0.31%/mm in RRMS patients, relative to HCs. In RRMS, MTR-values adjacent to the ventricle and in PV-lesions correlated positively with CMT and negatively with EDSS. CONCLUSION: PV-MTR gradients are present from the earliest stage of MS, consistent with more pronounced microstructural WM-damage closer to the ventricles. The positive association between reduced CMT and lower MTR in PV-NAWM suggests a common pathophysiologic mechanism. Together, these findings indicate the potential use of multimodal MRI as refined marker for MS-related tissue changes. | |
| 650 | 4 | |a Klinikai neurológia | |
| 700 | 0 | 1 | |a Kincses Bálint |e aut |
| 700 | 0 | 1 | |a Kincses Zsigmond Tamás |e aut |
| 700 | 0 | 1 | |a Kiss Christian |e aut |
| 700 | 0 | 1 | |a Damulina Anna |e aut |
| 700 | 0 | 1 | |a Khalil Michael |e aut |
| 700 | 0 | 1 | |a Stollberger Rudolf |e aut |
| 700 | 0 | 1 | |a Schmidt Reinhold |e aut |
| 700 | 0 | 1 | |a Enzinger Christian |e aut |
| 700 | 0 | 1 | |a Ropele Stefan |e aut |
| 856 | 4 | 0 | |u http://publicatio.bibl.u-szeged.hu/24279/1/328055751-s2.0-S2213158222000778-main.pdf |z Dokumentum-elérés |