Evidence map›Paper›PMID 29925923›Full record

ReviewNature reviews. Neurology2018

Haemoglobin scavenging in intracranial bleeding: biology and clinical implications.

Diederik Bulters, Ben Gaastra, Ardalan Zolnourian, Sheila Alexander, Dianxu Ren, Spiros L Blackburn, Mark Borsody, Sylvain Doré, James Galea, Koji Iihara and 2 more

Open access · bronzeAbstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Neurology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 100 papers, 8 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
100citing papers in PubMed, 8 pooled it
9.5field-weighted citation impact, top 1% of its field
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

100 citing papers in PubMed, 8 syntheses or guidelines pooled it, 147 citations in OpenAlex.

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  7. Genetic determinants of circulating haptoglobin concentration.Clinica chimica acta; international journal of clinical chemistry · 2019
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40 more citing papers are in PubMed but not listed here.

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

12 authors at 8 institutions in 3 countries.

Diederik BultersWessex Neurological Centre, University Hospital Southampton, Southampton, UK.
Ben GaastraWessex Neurological Centre, University Hospital Southampton, Southampton, UK.
Ardalan ZolnourianWessex Neurological Centre, University Hospital Southampton, Southampton, UK.
Sheila AlexanderSchool of Nursing, University of Pittsburgh, Pittsburgh, PA, USA.
Dianxu RenSchool of Nursing, University of Pittsburgh, Pittsburgh, PA, USA.
Spiros L BlackburnDepartment of Neurosurgery, University of Texas Health Science Center at Houston, Houston, TX, USA.
Mark BorsodyNeuroSpring, Dover, DE, USA.
Sylvain DoréDepartment of Anesthesiology, Neurology, Psychiatry, Psychology, Pharmaceutics and Neuroscience, College of Medicine, Center for Translational Research in Neurodegenerative Disease, University of Florida, Gainesville, FL, USA.
James GaleaBrain Injury Research Group, Manchester Academic Health Sciences Centre, University of Manchester, Manchester, UK.
Koji IiharaDepartment of Neurosurgery, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
Paul NyquistDepartment of Anesthesiology and Critical Care Medicine, Neurology, Neurosurgery and General Internal Medicine, Johns Hopkins University, Baltimore, MD, USA.
Ian GaleaClinical Neurosciences, Clinical and Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton, UK. I.Galea@soton.ac.uk.
Essex Cardiothoracic Centre · GBUniversity of Pittsburgh · USJohns Hopkins Medicine · USKyushu University · JPManchester Academic Health Science Centre · GBThe University of Texas Health Science Center at Houston · USUniversity of Florida · USUniversity of Southampton · GB

Funding

Medical Research Council MC_PC_16059
6 · The paper itself

Abstract

Haemoglobin is released into the CNS during the breakdown of red blood cells after intracranial bleeding. Extracellular free haemoglobin is directly neurotoxic. Haemoglobin scavenging mechanisms clear haemoglobin and reduce toxicity; these mechanisms include erythrophagocytosis, haptoglobin binding of haemoglobin, haemopexin binding of haem and haem oxygenase breakdown of haem. However, the capacity of these mechanisms is limited in the CNS, and they easily become overwhelmed. Targeting of haemoglobin toxicity and scavenging is, therefore, a rational therapeutic strategy. In this Review, we summarize the neurotoxic mechanisms of extracellular haemoglobin and the peculiarities of haemoglobin scavenging pathways in the brain. Evidence for a role of haemoglobin toxicity in neurological disorders is discussed, with a focus on subarachnoid haemorrhage and intracerebral haemorrhage, and emerging treatment strategies based on the molecular pathways involved are considered. By focusing on a fundamental biological commonality between diverse neurological conditions, we aim to encourage the application of knowledge of haemoglobin toxicity and scavenging across various conditions. We also hope that the principles highlighted will stimulate research to explore the potential of the pathways discussed. Finally, we present a consensus opinion on the research priorities that will help to bring about clinical benefits.

Indexed as

Brain InjuriesCerebral HemorrhageFibrinolytic AgentsHaptoglobinsHemopexinIron Chelating AgentsSubarachnoid HemorrhageAnimalsHemoglobinsHumansMechanical ThrombolysisFibrinolytic AgentsHaptoglobinsHemoglobinsHemopexinIron Chelating Agents

Identifiers

PMID29925923
OpenAlexW2809481702

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.