Evidence map›Paper›PMID 32380702›Full record

ArticleInternational journal of molecular sciences2020

Cholinergic Markers and Cytokines in OSA Patients.

Marcella Reale, Lucia Velluto, Marta Di Nicola, Chiara D'Angelo, Erica Costantini, Michele Marchioni, Gianluigi Cerroni, Biancamaria Guarnieri

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed, 15 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

8 authors at 1 institution in 1 country.

Marcella RealeDepartment of Medical, Oral and Biotechnological Science, University "G. d'Annunzio" Chieti- Pescara, 66100 Chieti, Italy.ORCID 0000-0002-4164-8781
Lucia VellutoCenter of Sleep Medicine, Department of Neurology, Villa Serena Hospital, Città S. Angelo, 65013 Pescara, Italy.
Marta Di NicolaDepartment of Medical, Oral and Biotechnological Science, University "G. d'Annunzio" Chieti- Pescara, 66100 Chieti, Italy.ORCID 0000-0003-1748-1931
Chiara D'AngeloDepartment of Medical, Oral and Biotechnological Science, University "G. d'Annunzio" Chieti- Pescara, 66100 Chieti, Italy.ORCID 0000-0002-1477-0706
Erica CostantiniDepartment of Medical, Oral and Biotechnological Science, University "G. d'Annunzio" Chieti- Pescara, 66100 Chieti, Italy.ORCID 0000-0003-2175-4226
Michele MarchioniDepartment of Medical, Oral and Biotechnological Science, University "G. d'Annunzio" Chieti- Pescara, 66100 Chieti, Italy.
Gianluigi CerroniCenter of Sleep Medicine, Department of Neurology, Villa Serena Hospital, Città S. Angelo, 65013 Pescara, Italy.
Biancamaria GuarnieriCenter of Sleep Medicine, Department of Neurology, Villa Serena Hospital, Città S. Angelo, 65013 Pescara, Italy.
University of Chieti-Pescara · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The role of inflammation and dysfunction of the cholinergic system in obstructive sleep apnea (OSA) has not exhaustively clarified. Thus, in this study, we explore the non-neuronal cholinergic system and the balance of T helper (Th) 17- and T regulatory (Treg)-related cytokines in OSA patients. The study includes 33 subjects with obstructive sleep apnea and 10 healthy controls (HC). The expression levels of cholinergic system component, RAR-related orphan receptor (RORc), transcription factor forkhead box protein 3 (Foxp3) and cytokines were evaluated. Th17- and Treg-related cytokines, choline levels and acetylcholinesterase (AChE), butyrylcholinesterase (BuChE) activity were quantified in OSA and control subjects. AChE and nicotinic receptor α 7 subunit (α7nAChR) gene expression and serum levels of choline, AChE and BuChE were lower in OSA patients than in the HC group. Compared with the HC group, OSA patients exhibited an increased expression, secretion and serum levels of pro-inflammatory cytokines, a reduced expression, secretion and serum levels of transforming growth factor (TGF)β and reduced Foxp3 mRNA levels. The Th17/Treg-related cytokine ratio was higher in the OSA group. Our results confirm and reinforce the hypothesis that OSA may be considered a systemic inflammatory disease, and that an imbalance of non-neuronal cholinergic and pro/anti-inflammatory cytokines may contribute to development and progression of comorbidities in OSA subjects. The evaluation of Th17/Treg-related cytokine may provide an additional explanation for OSA pathogenesis and clinical features, opening new directions for the OSA management.

Indexed as

AdultBiomarkersCase-Control StudiesCholineCytokinesDisease SusceptibilityFemaleGene ExpressionHumansInflammation MediatorsMaleSleep Apnea, ObstructiveT-Lymphocyte SubsetsBiomarkersCholineCytokinesInflammation Mediatorscholinergic systemcytokinesinflammationobstructive sleep apneapolysomnographysleepiness

Identifiers

PMID32380702
PMCPMC7246903
OpenAlexW3023902049

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.