Evidence map›Paper›PMID 36336706›Full record

ArticleScientific reports2022

Functional connectivity response to acute pain assessed by fNIRS is associated with BDNF genotype in fibromyalgia: an exploratory study.

Álvaro de Oliveira Franco, Guilherme de Oliveira Venturini, Camila Fernanda da Silveira Alves, Rael Lopes Alves, Paul Vicuña, Leticia Ramalho, Rafaela Tomedi, Samara Machado Bruck, Iraci L S Torres, Felipe Fregni and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

7 citing papers in PubMed, 11 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

11 authors at 4 institutions in 2 countries.

Álvaro de Oliveira FrancoLaboratory of Pain and Neuromodulation, Hospital de Clínicas de Porto Alegre (HCPA), 2400 Rua Ramiro Barcelos, Porto Alegre, RS, 90035-003, Brazil.
Guilherme de Oliveira VenturiniLaboratory of Pain and Neuromodulation, Hospital de Clínicas de Porto Alegre (HCPA), 2400 Rua Ramiro Barcelos, Porto Alegre, RS, 90035-003, Brazil.
Camila Fernanda da Silveira AlvesLaboratory of Pain and Neuromodulation, Hospital de Clínicas de Porto Alegre (HCPA), 2400 Rua Ramiro Barcelos, Porto Alegre, RS, 90035-003, Brazil.
Rael Lopes AlvesLaboratory of Pain and Neuromodulation, Hospital de Clínicas de Porto Alegre (HCPA), 2400 Rua Ramiro Barcelos, Porto Alegre, RS, 90035-003, Brazil.
Paul VicuñaLaboratory of Pain and Neuromodulation, Hospital de Clínicas de Porto Alegre (HCPA), 2400 Rua Ramiro Barcelos, Porto Alegre, RS, 90035-003, Brazil.
Leticia RamalhoLaboratory of Pain and Neuromodulation, Hospital de Clínicas de Porto Alegre (HCPA), 2400 Rua Ramiro Barcelos, Porto Alegre, RS, 90035-003, Brazil.
Rafaela TomediLaboratory of Pain and Neuromodulation, Hospital de Clínicas de Porto Alegre (HCPA), 2400 Rua Ramiro Barcelos, Porto Alegre, RS, 90035-003, Brazil.
Samara Machado BruckLaboratory of Pain and Neuromodulation, Hospital de Clínicas de Porto Alegre (HCPA), 2400 Rua Ramiro Barcelos, Porto Alegre, RS, 90035-003, Brazil.
Iraci L S TorresPost-Graduate Program in Medical Sciences, School of Medicine, Universidade Federal Do Rio Grande Do Sul (UFRGS), Porto Alegre, Brazil.
Felipe FregniLaboratory of Neuromodulation and Center for Clinical Research Learning, Physics and Rehabilitation Department, Spaulding Rehabilitation Hospital, Boston, MA, USA.
Wolnei CaumoLaboratory of Pain and Neuromodulation, Hospital de Clínicas de Porto Alegre (HCPA), 2400 Rua Ramiro Barcelos, Porto Alegre, RS, 90035-003, Brazil. wcaumo@hcpa.edu.br.
Universidade Federal do Rio Grande do Sul · BRHospital de Clínicas de Porto Alegre · BRUniversidade Federal do Rio Grande · BRSpaulding Rehabilitation Hospital · US

Funding

Brazilian Innovation Agency (Financiadora de Estudos e Projetos (FINEP)) process number 1245/13Conselho Nacional de Desenvolvimento Científico e Tecnológico 302688/2017-0Coordenação de Aperfeiçoamento de Pessoal de Nível Superior 2018Fundação de Amparo à Pesquisa do Estado do Rio Grande do Sul 17/2551-0001 087-6Fundação de Amparo à Pesquisa do Estado do Rio Grande do Sul (FAPERGS) 17/2551-0001 476-6Fundo de Incentivo à Pesquisa e Eventos (FIPE) from the Postgraduate Research Group at the Hospital de Clínicas de Porto Alegre Project No. 2017-0329
6 · The paper itself

Abstract

Fibromyalgia is a heterogenous primary pain syndrome whose severity has been associated with descending pain modulatory system (DPMS) function and functional connectivity (FC) between pain processing areas. The brain-derived neurotrophic factor (BDNF) Val66Met single nucleotide polymorphism has been linked to vulnerability to chronic pain. In this cross-sectional imaging genetics study, we investigated fibromyalgia, the relationship between BDNF Val66Met heterozygous genotypes (Val/Met), and the functional connectivity (FC) response pattern to acute pain stimulus in the motor (MC) and prefrontal (PFC) cortex assessed by near-infrared spectroscopy (fNIRS) before and after a cold pressor test utilizing water (0-1 °C). Also, we assessed the relationship between this genotype with the DPMS function and quality of life. We included 42 women (Val/Val = 30; Val/Met = 12) with fibromyalgia, ages 18-65. The MANCOVA comparing Val/Met to Val/Val genotypes showed higher ΔFC between left(l)-PFC-l-MC (β = 0.357, p = 0.048), l-PFC-right(r)-PFC (β = 0.249, p = 0.012), l-PFC-r-MC (β = 0.226, p = 0.022), and l-MC-r-PFC (β = 0.260, p = 0.016). Val/Met genotypes showed higher efficiency of the DPMS and lower disability due to pain. Here we show that fibromyalgia patients carrying the Val/Met BDNF genotype presented an increased ΔFC across MC and PFC in response to acute pain associated with differences in acute pain perception and fibromyalgia symptoms.

Indexed as

Acute PainFibromyalgiaAdolescentAdultAgedBrain-Derived Neurotrophic FactorFemaleGenotypeHumansMiddle AgedPolymorphism, Single NucleotideQuality of LifeSuccinimidesYoung Adult3-(3,5-dichlorophenyl)-1-methyl-2,5-pyrrolidinedioneBrain-Derived Neurotrophic FactorSuccinimides

Identifiers

PMID36336706
PMCPMC9637689
OpenAlexW4308451501

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LicenceCC BY
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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.