Evidence map›Paper›PMID 33611777›Full record

ArticleClinical and experimental medicine2021

Impact of cathepsin D activity and C224T polymorphism (rs17571) on chronic obstructive pulmonary disease: correlations with oxidative and inflammatory markers.

Sarra Bchir, Soumaya Boumiza, Hela Ben Nasr, Abdelhamid Garrouch, Imen Kallel, Zouhair Tabka, Karim Chahed

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Article in Clinical and experimental medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.6field-weighted citation impact, top 41% 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

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3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 8 citations in OpenAlex.

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4 · The record

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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

7 authors at 3 institutions in 1 country.

Sarra BchirLaboratoire de Recherche LR19ES09, Physiologie de L'Exercice Et Physiopathologie : de L'Intégré Au Moléculaire Biologie, Médecine Et Santé, Faculté de Médecine de Sousse, Université de Sousse, Sousse, Tunisia. sarra.bchir@yahoo.fr.ORCID http://orcid.org/0000-0001-6861-2191
Soumaya BoumizaLaboratoire de Recherche LR19ES09, Physiologie de L'Exercice Et Physiopathologie : de L'Intégré Au Moléculaire Biologie, Médecine Et Santé, Faculté de Médecine de Sousse, Université de Sousse, Sousse, Tunisia.
Hela Ben NasrLaboratoire de Recherche LR19ES09, Physiologie de L'Exercice Et Physiopathologie : de L'Intégré Au Moléculaire Biologie, Médecine Et Santé, Faculté de Médecine de Sousse, Université de Sousse, Sousse, Tunisia.
Abdelhamid GarrouchService de Pneumo-Allergologie, CHU Farhat Hached, Sousse, Tunisia.
Imen KallelLaboratoire de Recherche Toxicologie Microbiologie Environnementale Et Santé LR17ES06, Faculté Des Sciences de Sfax, Université de Sfax, Sfax, Tunisia.
Zouhair TabkaLaboratoire de Recherche LR19ES09, Physiologie de L'Exercice Et Physiopathologie : de L'Intégré Au Moléculaire Biologie, Médecine Et Santé, Faculté de Médecine de Sousse, Université de Sousse, Sousse, Tunisia.
Karim ChahedLaboratoire de Recherche LR19ES09, Physiologie de L'Exercice Et Physiopathologie : de L'Intégré Au Moléculaire Biologie, Médecine Et Santé, Faculté de Médecine de Sousse, Université de Sousse, Sousse, Tunisia.
University of Sousse · TNUniversity of Sfax · TNHôpital Farhat Hached · TN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCathepsin D (CTSD) is an aspartyl proteinase that plays an important role in protein degradation, antigen processing and apoptosis. It has been associated with several pathologies such as cancer, Alzheimer's disease and inflammatory disorders. Its function in lung diseases remains, however, controversial. In the current study, we determined CTSD activity in serum of patients with chronic obstructive pulmonary disease (COPD) and evaluated the correlations between this proteinase and inflammatory and oxidative parameters. We also investigated the impact of a CTSD C224T polymorphism on enzyme activity and clinicopathological parameters.

methodsOur population included 211 healthy controls and 138 patients with COPD. CTSD activity, MMPs (-1/-7/-12), cytokines (IL-6, TNF-α), malondialdehyde (MDA), nitric oxide and peroxynitrite levels were measured in patients and controls using standard methods. Genotyping of CTSD C224T polymorphism was determined using PCR-RFLP.

resultsOur results showed an increased CTSD activity in COPD patients compared to healthy controls (4.87 [3.99-6.07] vs. 3.94 [2.91-5.84], respectively, p < 0.001). COPD smokers presented also a higher CTSD activity when compared to nonsmokers (4.91[3.98-6.18] vs. 4.65[4.16-5.82], respectively, p = 0.01), while no differences were found when subjects were compared according to their GOLD stages. The activity of this proteinase was not dependent on the C224T polymorphism because we did not found any influence of this SNP on proteinase activity among patients and controls. Furthermore, our data provide the first evidence of the interrelationships between CTSD activity and both MMPs and TNF-α levels (MMP-1[r = - 0.4; p = 0.02], MMP-7[r = 0.37; p = 0.04], MMP-12[r = 0.43; p = 0.02], TNF-α [r = 0.89, p = 0.001]) in COPD smokers. There were no correlations, however, between CTSD activity and oxidative stress parameters in controls and patients.

conclusionOur findings suggest that CTSD could be a relevant marker for COPD disease. Alteration of CTSD activity may be related to increased MMPs and TNF-α levels, particularly in COPD smokers.

Indexed as

Polymorphism, GeneticAgedCase-Control StudiesCathepsin DCytokinesFemaleGenetic Predisposition to DiseaseHumansMaleMatrix MetalloproteinasesMiddle AgedOxidative StressPulmonary Disease, Chronic ObstructiveTobacco SmokingCathepsin DCTSD protein, humanCytokinesMatrix MetalloproteinasesCathepsin DChronic obstructive pulmonary diseasePolymorphismSmoking

Identifiers

PMID33611777
OpenAlexW3129786355

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.