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Plasma mid‐regional pro‐adrenomedullin: A biomarker of the ischemic penumbra in hyperacute stroke

Authors :
Hiroyuki Ishiyama
Tomotaka Tanaka
Satoshi Saito
Teruhide Koyama
Akihiro Kitamura
Manabu Inoue
Naoya Fukushima
Yoshiaki Morita
Masatoshi Koga
Kazunori Toyoda
Nagato Kuriyama
Makoto Urushitani
Masafumi Ihara
Source :
Brain Pathology. 33
Publication Year :
2022
Publisher :
Wiley, 2022.

Abstract

Reperfusion therapy has improved the outcomes of ischemic stroke but also emphasized the importance of ischemic penumbra. However, blood biomarkers are currently unavailable for this region. Adrenomedullin (ADM) is a neuroprotective peptide, secreted in a compensatory response to brain ischemia. We thus investigated whether an increase in mid-regional pro-ADM (MR-proADM), a stable peptide fragment of the ADM precursor, could act as a biomarker by predicting the ischemic penumbra in hyperacute ischemic stroke (HAIS). We prospectively enrolled consecutive HAIS patients (n = 119; median age, 77 years; male, 59.7%) admitted to our institutes from July 2017 to March 2019 and evaluated plasma MR-proADM levels within 4.5 h of onset. MR-proADM levels in HAIS were compared to healthy controls (n = 1298; median age, 58 years; male, 33.2%) in the Japan Multi-Institutional Collaborative Cohort Study from 2013 to 2017. Furthermore, we evaluated whether MR-proADM levels were associated with the penumbra estimated by clinical-diffusion mismatch (CDM) (National Institute of Health Stroke Scale [NIHSS] ≥8, diffusion ischemic core volume ≤25 ml), or magnetic resonance angiography-diffusion-weighted imaging mismatch (MDM) (NIHSS ≥5, a proximal vessel occlusion with core volume ≤25 ml, or a proximal vessel stenosis/distal vessel occlusion with core volume ≤15 ml). In a case-control study, multivariate logistic analysis showed a significant association between HAIS and MR-proADM ≥0.54 nmol/L (adjusted odds ratio, 7.92 [95% CI, 4.17-15.02], p 0.001). Though MR-proADM levels in HAIS did not correlate with the ischemic core volume (r

Details

ISSN :
17503639 and 10156305
Volume :
33
Database :
OpenAIRE
Journal :
Brain Pathology
Accession number :
edsair.doi.dedup.....cf7dcd95ae940389dd6ad052d00c72f3
Full Text :
https://doi.org/10.1111/bpa.13110