Evidence map›Paper›PMID 34266288›Full record

ArticleCephalalgia : an international journal of headache2021

CGRP measurements in human plasma - a methodological study.

Karl Messlinger, Birgit Vogler, Annette Kuhn, Julika Sertel-Nakajima, Florian Frank, Gregor Broessner

Registry-linked trialOpen access · hybridAbstract read
In one paragraph

Article in Cephalalgia : an international journal of headache, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05888766 (How to Predict Response to Acute Treatment of Migraine With Rimegepant 75 mg), which is not on this map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
3.4field-weighted citation impact, top 7% 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.

NCT05888766 unknown statusnot on this mapstarted 2023, after this paper: background citation

How to Predict Response to Acute Treatment of Migraine With Rimegepant 75 mg: a Biochemical and Neurophysiological Study.

TypeobservationalSponsorUniversity of Roma La SapienzaRan2023 to 2024Enrolled20ConditionsMigraine DisordersArmsRimegepant 75 milligrams
3 · Its place in the literature

Who cites it

24 citing papers in PubMed, 1 synthesis or guideline pooled it, 39 citations in OpenAlex.

  1. Pooled it
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  16. Serological Biomarkers of Chronic Migraine.Current pain and headache reports · 2023
    Review
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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

6 authors at 2 institutions in 2 countries.

Karl MesslingerInstitute of Physiology and Pathophysiology, Friedrich-Alexander-University Erlangen-Nürnberg, Germany.ORCID 0000-0002-8099-3860
Birgit VoglerInstitute of Physiology and Pathophysiology, Friedrich-Alexander-University Erlangen-Nürnberg, Germany.
Annette KuhnInstitute of Physiology and Pathophysiology, Friedrich-Alexander-University Erlangen-Nürnberg, Germany.
Julika Sertel-NakajimaInstitute of Physiology and Pathophysiology, Friedrich-Alexander-University Erlangen-Nürnberg, Germany.
Florian FrankDepartment of Neurology, Headache Outpatient Clinic, Medical University of Innsbruck, Austria.ORCID 0000-0002-7236-5557
Gregor BroessnerDepartment of Neurology, Headache Outpatient Clinic, Medical University of Innsbruck, Austria.
Friedrich-Alexander-Universität Erlangen-Nürnberg · DEInnsbruck Medical University · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCalcitonin gene-related peptide plasma levels have frequently been determined as a biomarker for primary headaches. However, published data is often inconsistent resulting from different methods that are not precisely described in most studies.

methodsWe applied a well-proven enzyme-linked immunosorbent assay to measure calcitonin gene-related peptide concentrations in human blood plasma, we modified parameters of plasma preparation and protein purification and used calcitonin gene-related peptide-free plasma for standard solutions, which are described in detail.

resultsCalcitonin gene-related peptide levels are stable in plasma with peptidase inhibitors and after deep-freezing. Calcitonin gene-related peptide standard solutions based on synthetic intercellular fluid or pooled plasma with pre-absorbed calcitonin gene-related peptide influenced the measurements but yielded both comprehensible results. In a sample of 56 healthy subjects the calcitonin gene-related peptide plasma levels varied considerably from low (<50 pg/mL) to very high (>500 pg/mL) values. After a 12-hour exposure of these subjects to normobaric hypoxia the individual calcitonin gene-related peptide levels remained stable.

conclusionBuffering with peptidase inhibitors and immediate freezing or processing of plasma samples is essential to achieve reliable measurements. Individuals show considerable differences and partly high calcitonin gene-related peptide plasma levels without detectable pathological reason. Thus plasma measurements are suited particularly to follow calcitonin gene-related peptide levels in longitudinal studies.The use of data for this study was approved by the Ethics Committee of the MedicalUniversity of Innsbruck (https://www.i-med.ac.at/ethikkommission/; EK Nr: 1242/2017).

Indexed as

Calcitonin Gene-Related PeptidePlasmaBiomarkersEnzyme-Linked Immunosorbent AssayHumansBiomarkersCalcitonin Gene-Related Peptideblood plasmaCalcitonin gene-related peptideenzyme-linked immunosorbent assaynormobaric hypoxia

Identifiers

PMID34266288
PMCPMC8592105
OpenAlexW3181551387

What OpenQuestion holds

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Registered trials

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.