Evidence map›Paper›PMID 38050358›Full record

ArticleAsian spine journal2023

Inhibition of Neurogenic Inflammatory Pathways Associated with the Reduction in Discogenic Back Pain.

Jose A Canseco, Hannah A Levy, Brian A Karamian, Olivia Blaber, Michael Chang, Neil Patel, John Curran, Alan S Hilibrand, Gregory D Schroeder, Alexander R Vaccaro and 3 more

Open access · diamondAbstract read
In one paragraph

Article in Asian spine journal, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

9 citing papers in PubMed, 8 citations in OpenAlex.

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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

13 authors at 2 institutions in 1 country.

Jose A CansecoDepartment of Orthopaedic Surgery, Rothman Institute, Philadelphia, PA, USA.
Hannah A LevyDepartment of Orthopaedic Surgery, Thomas Jefferson University, Philadelphia, PA, USA.
Brian A KaramianDepartment of Orthopaedic Surgery, Rothman Institute, Philadelphia, PA, USA.
Olivia BlaberDepartment of Orthopaedic Surgery, Thomas Jefferson University, Philadelphia, PA, USA.
Michael ChangDepartment of Orthopaedic Surgery, Thomas Jefferson University, Philadelphia, PA, USA.
Neil PatelDepartment of Orthopaedic Surgery, Thomas Jefferson University, Philadelphia, PA, USA.
John CurranDepartment of Orthopaedic Surgery, Thomas Jefferson University, Philadelphia, PA, USA.
Alan S HilibrandDepartment of Orthopaedic Surgery, Rothman Institute, Philadelphia, PA, USA.
Gregory D SchroederDepartment of Orthopaedic Surgery, Rothman Institute, Philadelphia, PA, USA.
Alexander R VaccaroDepartment of Orthopaedic Surgery, Rothman Institute, Philadelphia, PA, USA.
Dessislava Z MarkovaDepartment of Orthopaedic Surgery, Thomas Jefferson University, Philadelphia, PA, USA.
David E SurreyDepartment of Physical and Rehabilitative Medicine, Rothman Institute, Philadelphia, PA, USA.
Christopher K KeplerDepartment of Orthopaedic Surgery, Rothman Institute, Philadelphia, PA, USA.
Thomas Jefferson University · USRothman Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

STUDY

designRetrospective cohort study. PURPOSE: This study aimed to determine whether the initiation of anti-calcitonin gene-related peptide (CGRP inhibitor) medication therapy for migraines was also associated with improvements in back/neck pain, mobility, and function in a patient population with comorbid degenerative spinal disease and migraine. OVERVIEW OF LITERATURE: CGRP upregulates pro-inflammatory cytokines such as tumor necrosis factor-α, interleukin-6, brain-derived neurotrophic factor, and nerve growth factor in spinal spondylotic disease, which results in disc degeneration and sensitization of nociceptive neurons. Although CGRP inhibitors can quell neurogenic inflammation in migraines, their off-site efficacy as a therapeutic target for discogenic back/neck pain conditions remains unknown.

methodsAll adult patients diagnosed with spinal spondylosis and migraine treated with CGRP inhibitors at a single academic institution between 2017 and 2020 were retrospectively identified. Patient demographic and medical data, follow-up duration, migraine severity and frequency, spinal pain, functional status, and mobility before and after the administration of CGRP inhibitors were collected. Paired univariate analysis was conducted to determine significant changes in spinal pain, headache severity, and headache frequency before and after the administration of CGRP inhibitors. The correlation between changes in the spinal pain score and functional or mobility improvement was assessed with Spearman's rho.

resultsIn total, 56 patients were included. The mean follow-up time after the administration of CGRP inhibitors was 123 days for spinal pain visits and 129 days for migraine visits. Back/neck pain decreased significantly (p <0.001) from 6.30 to 4.36 after starting CGRP inhibitor therapy for migraine control. As recorded in the spine follow-up notes, 25% of patients experienced a functional improvement in the activities of daily living, and 17.5% experienced mobility improvement while taking CGRP inhibitors. Change in back/ neck pain moderately correlated (ρ=-0.430) with functional improvement but was not correlated with mobility improvement (ρ=-0.052).

conclusionsPatients taking CGRP inhibitors for chronic migraines with comorbid degenerative spinal conditions experienced significant off-target reduction of back/neck pain.

Indexed as

Anti-calcitonin gene-related peptideBiologicsClinical outcomesDegenerative disc disease

Identifiers

PMID38050358
PMCPMC10764143
OpenAlexW4389342660

What OpenQuestion holds

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Registered trials

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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.