Evidence map›Paper›PMID 33435197›Full record

ArticleCells2021

Herpesvirus Antibodies, Vitamin D and Short-Chain Fatty Acids: Their Correlation with Cell Subsets in Multiple Sclerosis Patients and Healthy Controls.

Maria Inmaculada Dominguez-Mozo, Silvia Perez-Perez, Noelia Villarrubia, Lucienne Costa-Frossard, Jose Ignacio Fernandez-Velasco, Isabel Ortega-Madueño, Maria Angel Garcia-Martinez, Estefania Garcia-Calvo, Hector Estevez, Jose Luis Luque Garcia and 4 more

Open access · goldAbstract read
In one paragraph

Article in Cells, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

12 citing papers in PubMed, 17 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

14 authors at 3 institutions in 1 country.

Maria Inmaculada Dominguez-MozoGrupo de Investigación de Factores Ambientales en Enfermedades Degenerativas, Instituto de Investigación Sanitaria del Hospital Clínico San Carlos (IdISSC)/Red Española de Esclerosis Múltiple (REEM), 28040 Madrid, Spain.
Silvia Perez-PerezGrupo de Investigación de Factores Ambientales en Enfermedades Degenerativas, Instituto de Investigación Sanitaria del Hospital Clínico San Carlos (IdISSC)/Red Española de Esclerosis Múltiple (REEM), 28040 Madrid, Spain.ORCID 0000-0002-3899-8932
Noelia VillarrubiaServicio de Inmunología, Hospital Universitario Ramón y Cajal/Instituto Ramón y Cajal de Investigación Sanitaria (IRYCIS), Red Española de Esclerosis Múltiple (REEM), 28040 Madrid, Spain.
Lucienne Costa-FrossardServicio de Neurología, Hospital Universitario Ramón y Cajal/Instituto Ramón y Cajal de Investigación Sanitaria (IRYCIS), Red Española de Esclerosis Múltiple (REEM), 28040 Madrid, Spain.
Jose Ignacio Fernandez-VelascoServicio de Inmunología, Hospital Universitario Ramón y Cajal/Instituto Ramón y Cajal de Investigación Sanitaria (IRYCIS), Red Española de Esclerosis Múltiple (REEM), 28040 Madrid, Spain.
Isabel Ortega-MadueñoGrupo de Investigación de Factores Ambientales en Enfermedades Degenerativas, Instituto de Investigación Sanitaria del Hospital Clínico San Carlos (IdISSC)/Red Española de Esclerosis Múltiple (REEM), 28040 Madrid, Spain.
Maria Angel Garcia-MartinezGrupo de Investigación de Factores Ambientales en Enfermedades Degenerativas, Instituto de Investigación Sanitaria del Hospital Clínico San Carlos (IdISSC)/Red Española de Esclerosis Múltiple (REEM), 28040 Madrid, Spain.
Estefania Garcia-CalvoDepartment of Analytical Chemistry, Faculty of Chemical Sciences, Universidad Complutense de Madrid, 28040 Madrid, Spain.
Hector EstevezDepartment of Analytical Chemistry, Faculty of Chemical Sciences, Universidad Complutense de Madrid, 28040 Madrid, Spain.
Jose Luis Luque GarciaDepartment of Analytical Chemistry, Faculty of Chemical Sciences, Universidad Complutense de Madrid, 28040 Madrid, Spain.
Maria Josefa TorrejonServicio de Análisis Clínicos, Hospital Clínico San Carlos, 28040 Madrid, Spain.
Rafael ArroyoDepartamento de Neurología, Hospital Universitario Quironsalud Madrid, Red Española de Esclerosis Múltiple (REEM), 28040 Madrid, Spain.
Luisa Maria VillarServicio de Inmunología, Hospital Universitario Ramón y Cajal/Instituto Ramón y Cajal de Investigación Sanitaria (IRYCIS), Red Española de Esclerosis Múltiple (REEM), 28040 Madrid, Spain.
Roberto Alvarez-LafuenteGrupo de Investigación de Factores Ambientales en Enfermedades Degenerativas, Instituto de Investigación Sanitaria del Hospital Clínico San Carlos (IdISSC)/Red Española de Esclerosis Múltiple (REEM), 28040 Madrid, Spain.ORCID 0000-0002-3132-1486
Hospital Clínico San Carlos · ESSpanish Multiple Sclerosis Network · ESUniversidad Complutense de Madrid · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although the etiology of multiple sclerosis (MS) is still unknown, it is commonly accepted that environmental factors could contribute to the disease. The objective of this study was to analyze the humoral response to Epstein-Barr virus, human herpesvirus 6A/B and cytomegalovirus, and the levels of 25-hydroxyvitamin D (25(OH)D) and the three main short-chain fatty acids (SCFA), propionate (PA), butyrate (BA) and acetate (AA), in MS patients and healthy controls (HC) to understand how they could contribute to the pathogenesis of the disease. With this purpose, we analyzed the correlations among them and with different clinical variables and a wide panel of cell subsets. We found statistically significant differences for most of the environmental factors analyzed when we compared MS patients and HC, supporting their possible involvement in the disease. The strongest correlations with the clinical variables and the cell subsets analyzed were found for 25(OH)D and SCFAs levels. A correlation was also found between 25(OH)D and PA/AA ratio, and the interaction between these factors negatively correlated with interleukin 17 (IL-17)-producing CD4+ and CD8+ T cells in untreated MS patients. Therapies that simultaneously increase vitamin D levels and modify the proportion of SCFA could be evaluated in the future.

Indexed as

AdultAntibodies, ViralCase-Control StudiesEnvironmentFatty Acids, VolatileFemaleHerpesvirus 4, HumanHumansImmunoglobulin GImmunoglobulin MMaleMiddle AgedMultiple SclerosisVitamin D25-hydroxyvitamin DAntibodies, ViralFatty Acids, VolatileImmunoglobulin GImmunoglobulin MVitamin DELISAflow-cytometryhuman herpesvirusmultiple sclerosisvitamin D

Identifiers

PMID33435197
PMCPMC7826528
OpenAlexW3118591439

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.