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ArticleFrontiers in neurology2024

Plasma symmetric dimethylarginine as a metabolite biomarker of severe acute ischemic stroke.

Saana Pihlasviita, Olli S Mattila, Tiina Nukarinen, Markku Kuisma, Heini Harve-Rytsälä, Juhani Ritvonen, Gerli Sibolt, Sami Curtze, Daniel Strbian, Mikko Pystynen and 2 more

Abstract read
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Article in Frontiers in neurology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

12 authors.

Saana PihlasviitaNeurology and Clinical Neurosciences, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Olli S MattilaNeurology and Clinical Neurosciences, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Tiina NukarinenNeurology and Clinical Neurosciences, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Markku KuismaEmergency Medicine and Services, Department of Emergency Care, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Heini Harve-RytsäläEmergency Medicine and Services, Department of Emergency Care, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Juhani RitvonenNeurology and Clinical Neurosciences, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Gerli SiboltNeurology and Clinical Neurosciences, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Sami CurtzeNeurology and Clinical Neurosciences, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Daniel StrbianNeurology and Clinical Neurosciences, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Mikko PystynenEmergency Medicine and Services, Department of Emergency Care, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Turgut TatlisumakDepartment of Clinical Neuroscience/Neurology, Institute of Neuroscience and Physiology, Sahlgrenska Academy at University of Gothenburg, Gothenburg, Sweden.
Perttu J LindsbergNeurology and Clinical Neurosciences, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: After severe ischemic stroke (IS), circulating levels of symmetric dimethylarginine (SDMA) increase. We investigated the early dynamics of SDMA in stroke to potentially aid with prehospital identification of severe IS from hemorrhagic stroke (HS). Methods: We performed targeted mass spectrometry (MS) measurements of SDMA in two sequential acute plasma samples (early and secondary) of 50 IS patients with LVO and 49 HS patients. Secondary samples of 227 IS and 84 HS patients with moderate to severe symptoms (NIHSS ≥ 7) subsequently underwent ELISA validation. Results: The median (IQR) last-known-well (LKW) to sampling times were 43 min (35-67) for early samples in the MS analysis, and 83 min (65-113) for secondary samples in MS and ELISA analyses. No inter-group differences existed in early samples, but IS patients had significantly higher mean (IQR) SDMA levels in secondary samples in both analyses: 5.8 (5.3-6.9) vs. 5.1 (4.2-5.8) A.U. for HS, Conclusion: In a large clinical cohort of stroke patients with moderate to severe symptoms, our data suggest that SDMA can assist in differentiation of IS and HS patients already 1 h and a half after symptom onset. SDMA may prove to have future value in a diagnostic stroke biomarker panel.

Indexed as

acute managementbiomarkersdiagnosisSDMAstroke

Identifiers

PMID39574509
PMCPMC11578963

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