Home > Publications Database > Detection of Cerebral Microbleeds With Venous Connection at 7-Tesla MRI. > print |
001 | 157814 | ||
005 | 20240305154120.0 | ||
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024 | 7 | _ | |a 1526-632X |2 ISSN |
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041 | _ | _ | |a English |
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100 | 1 | _ | |a Rotta, Johanna |b 0 |
245 | _ | _ | |a Detection of Cerebral Microbleeds With Venous Connection at 7-Tesla MRI. |
260 | _ | _ | |a [S.l.] |c 2021 |b Ovid |
336 | 7 | _ | |a article |2 DRIVER |
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336 | 7 | _ | |a Journal Article |b journal |m journal |0 PUB:(DE-HGF)16 |s 1709649657_29110 |2 PUB:(DE-HGF) |
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336 | 7 | _ | |a Journal Article |0 0 |2 EndNote |
520 | _ | _ | |a Cerebral microbleeds (MBs) are a common finding in patients with cerebral small vessel disease (CSVD) and Alzheimer disease as well as in healthy elderly people, but their pathophysiology remains unclear. To investigate a possible role of veins in the development of MBs, we performed an exploratory study, assessing in vivo presence of MBs with a direct connection to a vein.7-Tesla (7T) MRI was conducted and MBs were counted on quantitative susceptibility mapping (QSM). A submillimeter resolution QSM-based venogram allowed identification of MBs with a direct spatial connection to a vein.A total of 51 people (mean age [SD] 70.5 [8.6] years, 37% female) participated in the study: 20 had CSVD (cerebral amyloid angiopathy [CAA] with strictly lobar MBs [n = 8], hypertensive arteriopathy [HA] with strictly deep MBs [n = 5], or mixed lobar and deep MBs [n = 7], 72.4 [6.1] years, 30% female) and 31 were healthy controls (69.4 [9.9] years, 42% female). In our cohort, we counted a total of 96 MBs with a venous connection, representing 14% of all detected MBs on 7T QSM. Most venous MBs (86%, n = 83) were observed in lobar locations and all of these were cortical. Patients with CAA showed the highest ratio of venous to total MBs (19%) (HA = 9%, mixed = 18%, controls = 5%).Our findings establish a link between cerebral MBs and the venous vasculature, pointing towards a possible contribution of veins to CSVD in general and to CAA in particular. Pathologic studies are needed to confirm our observations. |
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650 | _ | 2 | |a Aged |2 MeSH |
650 | _ | 2 | |a Cerebral Hemorrhage: diagnostic imaging |2 MeSH |
650 | _ | 2 | |a Cerebral Hemorrhage: etiology |2 MeSH |
650 | _ | 2 | |a Cerebral Hemorrhage: pathology |2 MeSH |
650 | _ | 2 | |a Cerebral Small Vessel Diseases: complications |2 MeSH |
650 | _ | 2 | |a Cerebral Small Vessel Diseases: pathology |2 MeSH |
650 | _ | 2 | |a Female |2 MeSH |
650 | _ | 2 | |a Humans |2 MeSH |
650 | _ | 2 | |a Image Interpretation, Computer-Assisted |2 MeSH |
650 | _ | 2 | |a Magnetic Resonance Imaging |2 MeSH |
650 | _ | 2 | |a Male |2 MeSH |
650 | _ | 2 | |a Middle Aged |2 MeSH |
650 | _ | 2 | |a Neuroimaging: methods |2 MeSH |
650 | _ | 2 | |a Veins: diagnostic imaging |2 MeSH |
650 | _ | 2 | |a Veins: pathology |2 MeSH |
700 | 1 | _ | |a Perosa, Valentina |0 P:(DE-2719)9000985 |b 1 |u dzne |
700 | 1 | _ | |a Yakupov, Renat |0 P:(DE-2719)2812398 |b 2 |u dzne |
700 | 1 | _ | |a Kuijf, Hugo J |0 0000-0001-6997-9059 |b 3 |
700 | 1 | _ | |a Schreiber, Frank |0 P:(DE-2719)9000986 |b 4 |u dzne |
700 | 1 | _ | |a Dobisch, Laura |0 P:(DE-2719)2811611 |b 5 |u dzne |
700 | 1 | _ | |a Oltmer, Jan |0 P:(DE-2719)2811736 |b 6 |u dzne |
700 | 1 | _ | |a Assmann, Anne |0 P:(DE-2719)2812914 |b 7 |u dzne |
700 | 1 | _ | |a Speck, Oliver |0 P:(DE-2719)2810706 |b 8 |u dzne |
700 | 1 | _ | |a Heinze, Hans-Jochen |0 P:(DE-2719)2260426 |b 9 |u dzne |
700 | 1 | _ | |a Acosta-Cabronero, Julio |0 P:(DE-2719)2810751 |b 10 |u dzne |
700 | 1 | _ | |a Düzel, Emrah |0 P:(DE-2719)2000005 |b 11 |u dzne |
700 | 1 | _ | |a Schreiber, Stefanie |0 P:(DE-2719)2812631 |b 12 |e Last author |u dzne |
773 | _ | _ | |a 10.1212/WNL.0000000000011790 |g Vol. 96, no. 16, p. e2048 - e2057 |0 PERI:(DE-600)1491874-2 |n 16 |p e2048 - e2057 |t Neurology |v 96 |y 2021 |x 1526-632X |
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