PAI-1 Level Differences in Malignant Plural Effusion, Parapneumonic Pleuritis, and Cardiac Hydrothorax.


Journal

Medicina (Kaunas, Lithuania)
ISSN: 1648-9144
Titre abrégé: Medicina (Kaunas)
Pays: Switzerland
ID NLM: 9425208

Informations de publication

Date de publication:
04 Sep 2019
Historique:
received: 27 06 2019
revised: 08 08 2019
accepted: 30 08 2019
entrez: 7 9 2019
pubmed: 7 9 2019
medline: 24 3 2020
Statut: epublish

Résumé

Plasminogen activator inhibitor-1 (PAI-1) is a fibrinolytic system enzyme whose role in various fibrinolytic processes is currently unknown. In clinical manifestations of pleural liquids of diverse etiology, various levels of fibrinolytic activity can be observed-parapneumonic processes tend to loculate in fibrin septa, while malignant pleural effusion (MPE) does not. The purpose of this study was to determine possible differences in PAI-1 levels in pleural effusions of varied etiology. PAI-1 level in pleural effusion and serum was determined in 144 patients with pleural effusions of various etiology (cardiac hydrothorax-42 patients (29.2%), MPE-67 patients (46.5%), parapneumonic pleuritis-27 (18.8%), tuberculous pleuritis-6 patients (4.1%), pancreatogenic pleuritis-1 patient (0.7%) and pulmonary artery thromboembolism with pleuritis-1 patient (0.7%)). The median PAI-1 level (ng/mL) was the highest in the parapneumonic pleuritis group both in the effusion and the serum, with values of 291 (213-499) ng/mL and 204 (151-412) ng/mL, respectively, resulting in a statistically significant difference (p < 0.001) from the cardiac hydrothorax and MPE groups. However, there was no statistically significant difference between PAI-1 levels in the pleural effusion and serum in the cardiac hydrothorax and MPE groups. The PAI-1 level in MPE and cardiac hydrothorax was statistically significantly lower than in parapneumonic pleuritis.

Sections du résumé

BACKGROUND AND OBJECTIVES OBJECTIVE
Plasminogen activator inhibitor-1 (PAI-1) is a fibrinolytic system enzyme whose role in various fibrinolytic processes is currently unknown. In clinical manifestations of pleural liquids of diverse etiology, various levels of fibrinolytic activity can be observed-parapneumonic processes tend to loculate in fibrin septa, while malignant pleural effusion (MPE) does not. The purpose of this study was to determine possible differences in PAI-1 levels in pleural effusions of varied etiology.
MATERIAL AND METHODS METHODS
PAI-1 level in pleural effusion and serum was determined in 144 patients with pleural effusions of various etiology (cardiac hydrothorax-42 patients (29.2%), MPE-67 patients (46.5%), parapneumonic pleuritis-27 (18.8%), tuberculous pleuritis-6 patients (4.1%), pancreatogenic pleuritis-1 patient (0.7%) and pulmonary artery thromboembolism with pleuritis-1 patient (0.7%)).
RESULTS RESULTS
The median PAI-1 level (ng/mL) was the highest in the parapneumonic pleuritis group both in the effusion and the serum, with values of 291 (213-499) ng/mL and 204 (151-412) ng/mL, respectively, resulting in a statistically significant difference (p < 0.001) from the cardiac hydrothorax and MPE groups. However, there was no statistically significant difference between PAI-1 levels in the pleural effusion and serum in the cardiac hydrothorax and MPE groups.
CONCLUSION CONCLUSIONS
The PAI-1 level in MPE and cardiac hydrothorax was statistically significantly lower than in parapneumonic pleuritis.

Identifiants

pubmed: 31487930
pii: medicina55090567
doi: 10.3390/medicina55090567
pmc: PMC6780168
pii:
doi:

Substances chimiques

Plasminogen Activator Inhibitor 1 0
SERPINE1 protein, human 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Déclaration de conflit d'intérêts

The authors declare no conflicts of interest.

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Auteurs

Dace Zentina (D)

Department of Internal Diseases, Pauls Stradins University Hospital, Pilsonu Street 13, LV 1002 Riga, Latvia. dace.zentina@gmail.com.
Department of Internal Diseases, Riga Stradins University, Dzirciema Street 16, LV 1007 Riga, Latvia. dace.zentina@gmail.com.

Inga Stukena (I)

Department of Internal Diseases, Riga Stradins University, Dzirciema Street 16, LV 1007 Riga, Latvia. inga.stukena@gmail.com.
Department of Internal Diseases, Riga East University Hospital, Hipokrata Street 2, LV 1038 Riga, Latvia. inga.stukena@gmail.com.

Alvils Krams (A)

Centre of Tuberculosis and Lung Disease, Riga East University Hospital, Upeslejas, LV 2118 Stopini region, Latvia. alvils.krams@aslimnica.lv.
Department of Internal Disease, Faculty of Medicine, University of Latvia, Jelgavas Street 3, LV 1004 Riga, Latvia. alvils.krams@aslimnica.lv.

Aivars Lejnieks (A)

Department of Internal Diseases, Riga Stradins University, Dzirciema Street 16, LV 1007 Riga, Latvia. lejnieks@latnet.lv.
Department of Internal Diseases, Riga East University Hospital, Hipokrata Street 2, LV 1038 Riga, Latvia. lejnieks@latnet.lv.

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