Evidence map›Paper›PMID 40404300›Full record

ArticleJournal of neurointerventional surgery2026

Role of biliverdin reductase, a heme degradation pathway enzyme, in the development of vasospasm after subarachnoid hemorrhage.

Zahra Hasanpour-Segherlou, Hunter Hutchinson, Haiyan Xu, Shawna Amini, Elizabeth Klaas, Melanie E Martinez, Brandon Lucke-Wold, Koji Hosaka, Brian Hoh

Abstract read
In one paragraph

Article in Journal of neurointerventional surgery, 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

9 authors.

Zahra Hasanpour-SegherlouDepartment of Neurosurgery, University of Florida, Gainesville, Florida, USA.ORCID http://orcid.org/0000-0003-2001-0268
Hunter HutchinsonDepartment of Neurosurgery, University of Florida, Gainesville, Florida, USA.ORCID http://orcid.org/0009-0005-3202-3949
Haiyan XuDepartment of Neurosurgery, University of Florida, Gainesville, Florida, USA.ORCID http://orcid.org/0009-0009-6014-2792
Shawna AminiDepartment of Neurosurgery, University of Florida, Gainesville, Florida, USA.ORCID http://orcid.org/0000-0002-6241-3770
Elizabeth KlaasDepartment of Neurosurgery, University of Florida, Gainesville, Florida, USA.ORCID http://orcid.org/0000-0001-6845-2052
Melanie E MartinezDepartment of Neurosurgery, University of Florida, Gainesville, Florida, USA.ORCID http://orcid.org/0000-0001-8171-8839
Brandon Lucke-WoldDepartment of Neurosurgery, University of Florida, Gainesville, Florida, USA.ORCID http://orcid.org/0000-0001-6577-4080
Koji HosakaDepartment of Neurosurgery, University of Florida, Gainesville, Florida, USA.ORCID http://orcid.org/0000-0003-0106-4586
Brian HohDepartment of Neurosurgery, University of Florida, Gainesville, Florida, USA brian.hoh@neurosurgery.ufl.edu.ORCID http://orcid.org/0000-0002-4997-4469

Funding

Neurovascular protection by adropin in acute neural injury from subarachnoid hemorrhageR01NS124620 · NINDS · UNIVERSITY OF FLORIDA · PI Brian Lim Hoh · 2022 to 2026
$1.9M
NINDS NIH HHS R01 NS124620
6 · The paper itself

Abstract

backgroundSubarachnoid hemorrhage (SAH) is a life-threatening condition with high mortality and significant neurological morbidity, often complicated by delayed cerebral ischemia (DCI) and vasospasm. Heme metabolites such as biliverdin (BV) are implicated in SAH-induced vascular dysfunction, yet the role of biliverdin reductase-A (BVR-A), an enzyme that reduces BV to bilirubin, remains underexplored. This study investigates the contribution of BV and oxidative post-translational modifications of BVR-A to vasospasm development.

methodsWe used a murine model of BV injection into the subarachnoid space and analyzed its effects on vasospasm, microthrombosis, neuronal apoptosis, and microglial activation. Additionally, human plasma and cerebrospinal fluid (CSF) samples from patients with SAH with and without vasospasm were evaluated for BVR-A expression and oxidative modifications using immunoprecipitation and western blot techniques.

resultsBV injection in the murine model induced significant vasospasm, increased microthrombosis, neuronal apoptosis, and a reactive morphological shift in microglia. In human samples, oxidative modifications of BVR-A were significantly raised in plasma from patients with SAH with vasospasm compared with those without, despite similar BVR-A expression levels. No significant differences in oxidative modifications were observed in CSF samples.

conclusionThis study shows a novel role of BV in vasospasm development and identifies oxidative modifications of BVR-A as potential modulators of SAH pathology. These findings suggest that BV and altered BVR-A activity may serve as biomarkers or therapeutic targets for improving outcomes in patients with SAH.

Indexed as

HemeOxidoreductases Acting on CH-CH Group DonorsSubarachnoid HemorrhageVasospasm, IntracranialAnimalsApoptosisBiliverdineDisease Models, AnimalFemaleHumansMaleMiceMice, Inbred C57BLMiddle AgedBiliverdinebiliverdin reductaseHemeOxidoreductases Acting on CH-CH Group DonorsAneurysmbiliverdinCerebral VasospasmSubarachnoid Hemorrhage

Identifiers

PMID40404300
PMCPMC12354163

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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.