Evidence map›Paper›PMID 42121257›Full record

ArticleStem cell research & therapy2026

Serial brain FDG-PET and IMZ-SPECT following intracerebral MSC transplantation in patients with subacute ischemic stroke.

Masahito Kawabori, Kenji Hirata, Hideo Shichinohe, Shiro Watanabe, Arisa Miura, Yoichi M Ito, Kohsuke Kudo, Satoshi Kuroda, Kiyohiro Houkin, Miki Fujimura

Abstract read
In one paragraph

Article in Stem cell research & therapy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Masahito KawaboriDepartment of Neurosurgery, Hokkaido University Graduate School of Medicine, Kita 14, Nishi 5, Kita-ku, Sapporo, 060-8638, Hokkaido, Japan. masahitokawabori@yahoo.co.jp.
Kenji HirataDepartment of Diagnostic Imaging, Hokkaido University Graduate School of Medicine, Sapporo, 060-8638, Japan.
Hideo ShichinoheInstitute of Health Science Innovation for Medical Care, Hokkaido University Hospital, Sapporo, 060-8648, Japan.
Shiro WatanabeDepartment of Diagnostic Imaging, Hokkaido University Graduate School of Medicine, Sapporo, 060-8638, Japan.
Arisa MiuraInstitute of Health Science Innovation for Medical Care, Hokkaido University Hospital, Sapporo, 060-8648, Japan.
Yoichi M ItoInstitute of Health Science Innovation for Medical Care, Hokkaido University Hospital, Sapporo, 060-8648, Japan.
Kohsuke KudoDepartment of Diagnostic Imaging, Hokkaido University Graduate School of Medicine, Sapporo, 060-8638, Japan.
Satoshi KurodaDepartment of Neurosurgery, Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama, Toyama, 930-0194, Japan.
Kiyohiro HoukinDepartment of Neurosurgery, Hokkaido University Graduate School of Medicine, Kita 14, Nishi 5, Kita-ku, Sapporo, 060-8638, Hokkaido, Japan.
Miki FujimuraDepartment of Neurosurgery, Hokkaido University Graduate School of Medicine, Kita 14, Nishi 5, Kita-ku, Sapporo, 060-8638, Hokkaido, Japan.

Funding

Japan Agency for Medical Research and Development JP17bk0104045, JP20bk0104011, JP21bk0104134, JP23ym0126122
6 · The paper itself

Abstract

Ischemic stroke is a leading cause of mortality and long-term neurological disability worldwide, and cell-based therapies represent a promising approach. Although clinical studies have reported favorable outcomes following cell transplantation, the effects on host neuronal integrity remain incompletely understood. This study investigated temporal and spatial changes in fluorodeoxyglucose positron emission tomography (FDG-PET) and 123I-iomazenil single-photon emission computed tomography (IMZ-SPECT) after intracerebral cell transplantation in patients with subacute ischemic stroke and examined their relationship with functional recovery. Seven adults with severe post-stroke disability underwent autologous mesenchymal stromal cell (HUNS001-01) transplantation 47-64 days after stroke onset. Brain FDG-PET and IMZ-SPECT were performed preoperatively and at 1, 3, and 12 months post-transplantation. Regions of interest were first manually set in the ipsilateral cortex where the 12-month postoperative-to-preoperative standard uptake value ratio seems increased, and followed by quantitative measurement. Five of seven patients demonstrated 5% or more increase of FDG-PET and/or IMZ-SPECT uptake in peri-infarct cortical regions, predominantly within the frontal or temporal cortex. Transplanted cells localized either within metabolically enhanced regions or in anatomically remote areas. FDG-PET and IMZ-SPECT changes were strongly interacted in each other and were associated with functional improvement. Overall, improvement of glucose metabolism and synaptic density/viability were observed in patient with subacute ischemic stroke, which may have been attributable to cell transplantation.Trial registration: UMIN000026130.

Indexed as

BrainBrain IschemiaIschemic StrokeMesenchymal Stem CellsMesenchymal Stem Cell TransplantationPositron-Emission TomographyStrokeTomography, Emission-Computed, Single-PhotonAdultAgedFemaleFlumazenilFluorodeoxyglucose F18HumansMaleMiddle AgedFlumazenilFluorodeoxyglucose F18iomazenilAutologous cell therapyBone marrow stromal cellFDGIMZIschemic strokeIsotopeRegenerative medicine

Identifiers

PMID42121257
PMCPMC13335312

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.