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Munsch, F.

Publications and source records attributed to Munsch, F..

2 recordsLinked to original sources

Dynamic evolution of infarct volumes at MRI in ischemic stroke due to large vessel occlusion

Background and ObjectivesThe typical infarct volume trajectories in stroke patients, categorized as slow or fast progressors, remain largely unknown. This study aimed to reveal the characteristic spatiotemporal evolutions of infarct volumes caused by large vessel occlusion (LVO) and show that such growth charts help anticipate clinical outcomes. MethodsWe conducted a secondary analysis from prospectively collected databases (FRAME, 2017- 2019; ETIS, 2015-2022). We selected acute MRI data from anterior LVO stroke patients with witnessed onset which were divided into training- and independent validation-datasets. In the training-dataset, using Gaussian mixture analysis, we classified the patients into three growth groups based on their rate of infarct growth (diffusion volume / time-to-imaging). Subsequently, we extrapolated pseudo-longitudinal models of infarct growth for each group and generated sequential frequency maps to highlight the spatial distribution of infarct growth. We used these charts to attribute a growth group to the independent patients from the validation-dataset. We compared their 3-month modified Rankin scale (mRS) with the predicted values based on a multivariable regression model from the training-dataset that used growth group as independent variable. ResultsWe included 804 patients (median age, 73.0 years [IQR, 61.2-82.0 years]; 409 men). The training-dataset revealed non-supervised clustering into 11% (74/703) slow, 62% (437/703) intermediate, and 27% (192/703) fast progressors. Infarct volume evolutions were best fitted with a linear (r=0.809; P<.001), cubic (r=0.471; P<.001), and power (r=0.63; P<.001) functions for the slow, intermediate and fast progressors, respectively. Notably, the deep nuclei and insular cortex were rapidly affected in the intermediate and fast groups with further cortical involvement in the fast group. The variable "growth group" significantly predicted 3-month mRS (multivariate OR, 0.51; 95% CI: 0.37-0.72, P<.0001) in the training-dataset, yielding a mean AUC of 0.78 (95% CI: 0.66-0.88) in the independent validation-dataset. ConclusionsWe revealed spatiotemporal archetype dynamic evolutions following large vessel occlusion stroke according to three growth phenotypes called slow, intermediate and fast progressors, providing insight into anticipating clinical outcome. We expect this could help in designing neuroprotective trials aiming at modulating infarct growth prior EVT.

pathology↗

Effects of tDCS Dose and Electrode Montage on regional cerebral blood flow and motor behavior

We used three dose levels (Sham, 2mA, and 4mA) and two different electrode montages (unihemispheric or bihemispheric) to examine DOSE and MONTAGE effects on regional cerebral blood flow (rCBF) as a surrogate marker of neural activity, and on a finger sequence task, as a surrogate behavioral measure drawing on brain regions targeted by transcranial direct current stimulation (tDCS). We placed the anodal electrode over the right motor region (C4) while the cathodal or return electrode was placed either over a left supraorbital region (unihemispheric montage) or over the left motor region (C3 in the bihemispheric montage). Performance changes in the finger sequence task for both hands (left hand: p = 0.0026, and right hand: p = 0.0002) showed a linear tDCS dose response but no montage effect. rCBF in the right hemispheric perirolandic area increased with dose under the anodal electrode (p = 0.027). In contrast, in the perirolandic ROI in the left hemisphere, rCBF showed a trend to increase with dose (p = 0.053) and a significant effect of montage (p = 0.00004). The bihemispheric montage showed additional rCBF increases in frontomesial regions in the 4mA condition but not in the 2mA condition. Furthermore, we found correlations between rCBF changes in the right perirolandic region and improvements in the finger sequence task performance (FSP) for the left and right hand. Our data support not only a strong direct tDCS dose effect for rCBF and FSP as surrogate measures of targeted brain regions but also indirect effects on rCBF in functionally connected regions (e.g., frontomesial regions), particularly in the higher dose condition and on FSP of the ipsilateral hand (to the anodal electrode). At a higher dose and irrespective of polarity, a wider network of sensorimotor regions is positively affected by tDCS. HighlightsO_LItDCS-DOSE had a linear effect on finger sequence performance for both hands C_LIO_LIrCBF changes in both perirolandic ROIs demonstrated tDCS-DOSE effects, and left perirolandic ROI demonstrated tDCS-MONTAGE effects. C_LIO_LISimulated current intensity in the left and right perirolandic ROI strongly correlated with the contralateral hands finger sequence performance. C_LIO_LItDCS-Tolerability scores did not correlate with change in rCBF or finger sequence performance of the left hand. C_LI Graphical Abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=99 SRC="FIGDIR/small/429369v2_ufig1.gif" ALT="Figure 1"> View larger version (53K): org.highwire.dtl.DTLVardef@763dc5org.highwire.dtl.DTLVardef@d158f4org.highwire.dtl.DTLVardef@271d71org.highwire.dtl.DTLVardef@1fe0597_HPS_FORMAT_FIGEXP M_FIG C_FIG

neuroscience↗