Evidence map›Paper›PMID 36751320›Full record

ArticleSkin health and disease2023

Proteomic profiling of sweat in patients with cystic fibrosis provides new insights into epidermal homoeostasis.

Matthieu Cornet, Thao Nguyen-Khoa, Mairead Kelly-Aubert, Vincent Jung, Frédérique Chedevergne, Muriel Le Bourgeois, Laura Aoust, Kévin Roger, Chiara Ida Guerrera, Isabelle Sermet-Gaudelus

Open access · goldAbstract read
In one paragraph

Article in Skin health and disease, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 36% 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

3 citing papers in PubMed, 4 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

10 authors at 3 institutions in 3 countries.

Matthieu CornetInstitut Necker Enfants Malades INSERM U1151 Paris France.ORCID https://orcid.org/0000-0001-5466-9373
Thao Nguyen-KhoaInstitut Necker Enfants Malades INSERM U1151 Paris France.
Mairead Kelly-AubertInstitut Necker Enfants Malades INSERM U1151 Paris France.
Vincent JungProteomics Platform Necker Université Paris Cité Structure Fédérative de Recherche Necker (SFR Necker, INSERM US24/CNRS UAR3633) Paris France.
Frédérique ChedevergneCentre de Référence Maladies Rares Mucoviscidose et Maladies Apparentées Hôpital Necker Enfants Malades AP-HP Centre Paris Cité Paris France.
Muriel Le BourgeoisCentre de Référence Maladies Rares Mucoviscidose et Maladies Apparentées Hôpital Necker Enfants Malades AP-HP Centre Paris Cité Paris France.
Laura AoustCentre de Référence Maladies Rares Mucoviscidose et Maladies Apparentées Hôpital Necker Enfants Malades AP-HP Centre Paris Cité Paris France.
Kévin RogerProteomics Platform Necker Université Paris Cité Structure Fédérative de Recherche Necker (SFR Necker, INSERM US24/CNRS UAR3633) Paris France.
Chiara Ida GuerreraProteomics Platform Necker Université Paris Cité Structure Fédérative de Recherche Necker (SFR Necker, INSERM US24/CNRS UAR3633) Paris France.
Isabelle Sermet-GaudelusInstitut Necker Enfants Malades INSERM U1151 Paris France.
Hôpital Necker-Enfants Malades · FRDélégation Paris 5 · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: A high proportion of patients with Cystic Fibrosis (CF) also present the rare skin disease aquagenic palmoplantar keratoderma. A possible link between this condition and absence of a functional CF Transmembrane conductance Regulator protein in the sweat acinus and collecting duct remains unknown. Methods: In-depth characterization of sweat proteome profiles was performed in 25 CF patients compared to 12 healthy controls. A 20 μL sweat sample was collected after pilocarpine iontophoresis and liquid chromatography tandem mass spectrometry (LC-MS/MS) proteomic analysis was performed. Results: Sweat proteome profile of CF patients was significantly different from that of healthy subjects with 57 differentially expressed proteins. Cystic Fibrosis sweat proteome was characterized by an increase in 25 proteins including proteases (Kallikrein 7 and 13, Phospholipase B domain containing 1, Cathepsin A L2 and B, Lysosomal Pro-X carboxypeptidase); proinflammatory proteins (Annexin A2, Chitinase-3-like protein 1); cytochrome c and transglutaminases. Thirty-two proteins were downregulated in CF sweat including proteases (Elastase 2), antioxidative protein FAM129 B; membrane-bound transporter SLC6A14 and regulator protein Sodium-hydrogen antiporter 3 regulator 1. Conclusion: This study is the first to report in-depth characterization of endogenous peptides in CF sweat and could help understand the complex physiology of the sweat gland. The proteome profile highlights the unbalanced proteolytic and proinflammatory activity of sweat in CF. These results also suggest a defect in pathways involved in skin barrier integrity in CF patients. Sweat proteome profile could prove to be a useful tool in the context of personalized medicine in CF.

Identifiers

PMID36751320
PMCPMC9892418
OpenAlexW4310022304

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.