TY - JOUR
T1 - Histopathology of Cerebral Microinfarcts and Microbleeds in Spontaneous Intracerebral Hemorrhage
AU - Jolink, Wilmar M. T.
AU - van Veluw, Susanne J.
AU - Zwanenburg, Jaco J. M.
AU - Rozemuller, Annemieke J. M.
AU - van Hecke, Wim
AU - Frosch, Matthew P.
AU - Bacskai, Brian J.
AU - Rinkel, Gabriël J. E.
AU - Greenberg, Steven M.
AU - Klijn, Catharina J. M.
N1 - Funding Information:
CJMK is supported by a clinical established investigator grant of the Dutch Heart Foundation (grant no. 2012 T077) and an Aspasia grant from The Netherlands Organization for Health Research and Development (ZonMw grant no. 015.008.048). WMTJ was supported by the Dutch Heart Foundation and the Dr Jan Meerwaldt Foundation. SJvV is supported by the Netherlands Organization for Scientific Research, ZonMW (Veni, grant no. 91619021). AJMR is supported by Alzheimer Nederland (ISAO grant no. NL16054).
Publisher Copyright:
© 2022, The Author(s).
PY - 2022
Y1 - 2022
N2 - In patients with spontaneous intracerebral hemorrhage caused by different vasculopathies, cerebral microinfarcts have the same aspect on MRI and the same applies to cerebral microbleeds. It is unclear what pathological changes underlie these cerebral microinfarcts and cerebral microbleeds. In the current study, we explored the histopathological substrate of these lesions by investigating the brain tissue of 20 patients (median age at death 77 years) who died from ICH (9 lobar, 11 non-lobar) with a combination of post-mortem 7-T MRI and histopathological analysis. We identified 132 CMIs and 204 CMBs in 15 patients on MRI, with higher numbers of CMIs in lobar ICH patients and similar numbers of CMBs. On histopathology, CMIs and CMBs were in lobar ICH more often located in the superficial than in the deep layers of the cortex, and in non-lobar ICH more often in the deeper layers. We found a tendency towards more severe CAA scores in lobar ICH patients. Other histopathological characteristics were comparable between lobar and non-lobar ICH patients. Although CMIs and CMBs were found in different segments of the cortex in lobar ICH compared to non-lobar ICH patients, otherwise similar histopathological features of cortical CMIs and CMBs distant from the ICH suggest shared pathophysiological mechanisms in lobar and non-lobar ICH caused by different vasculopathies.
AB - In patients with spontaneous intracerebral hemorrhage caused by different vasculopathies, cerebral microinfarcts have the same aspect on MRI and the same applies to cerebral microbleeds. It is unclear what pathological changes underlie these cerebral microinfarcts and cerebral microbleeds. In the current study, we explored the histopathological substrate of these lesions by investigating the brain tissue of 20 patients (median age at death 77 years) who died from ICH (9 lobar, 11 non-lobar) with a combination of post-mortem 7-T MRI and histopathological analysis. We identified 132 CMIs and 204 CMBs in 15 patients on MRI, with higher numbers of CMIs in lobar ICH patients and similar numbers of CMBs. On histopathology, CMIs and CMBs were in lobar ICH more often located in the superficial than in the deep layers of the cortex, and in non-lobar ICH more often in the deeper layers. We found a tendency towards more severe CAA scores in lobar ICH patients. Other histopathological characteristics were comparable between lobar and non-lobar ICH patients. Although CMIs and CMBs were found in different segments of the cortex in lobar ICH compared to non-lobar ICH patients, otherwise similar histopathological features of cortical CMIs and CMBs distant from the ICH suggest shared pathophysiological mechanisms in lobar and non-lobar ICH caused by different vasculopathies.
KW - Cerebral amyloid angiopathy
KW - Histopathology
KW - Spontaneous intracerebral hemorrhage
KW - Ultra-high-field MRI
UR - http://www.scopus.com/inward/record.url?scp=85127621408&partnerID=8YFLogxK
U2 - 10.1007/s12975-022-01016-5
DO - 10.1007/s12975-022-01016-5
M3 - Article
C2 - 35384634
SN - 1868-4483
JO - Translational Stroke Research
JF - Translational Stroke Research
ER -