The Prognostic Role of ST2L and sST2 in Patients Who Underwent Carotid Plaque Endarterectomy: A Five-Year Follow-Up Study.

ST2L atherosclerosis biomarkers carotid plaque prognosis sST2

Journal

Journal of clinical medicine
ISSN: 2077-0383
Titre abrégé: J Clin Med
Pays: Switzerland
ID NLM: 101606588

Informations de publication

Date de publication:
31 May 2022
Historique:
received: 28 04 2022
revised: 29 05 2022
accepted: 30 05 2022
entrez: 10 6 2022
pubmed: 11 6 2022
medline: 11 6 2022
Statut: epublish

Résumé

Soluble suppressor of tumorigenicity (sST)-2 plasma concentration is related to atherosclerosis. The aim of this study was to assess the prognostic impact of sST2 and its membrane-associated form (ST2L) in patients with carotid atherosclerotic plaque who underwent endarterectomy (CEA). Eighty-two consecutive patients (age range: 48−86 years) who underwent CEA were enrolled. Anthropometric, clinical, instrumental, and laboratory evaluations were gathered. Thirty-seven (45%) patients were symptomatic of cerebrovascular diseases. Patients underwent a five-year follow-up. Phone calls and the analysis of national and regional databases were performed in order to evaluate the occurrence of the primary outcome (all-cause mortality). The population was divided according to survival status. Statins were administered in 81% and 87.5% of survivors and non-survivors, respectively. sST2 levels were higher in non-survivors than in survivors (117.0 ± 103.9 vs. 38.0 ± 30.0 ng/mL, p < 0.001) and in symptomatic individuals, compared with asymptomatic (80.3 ± 92.1 ng/mL vs. 45.4 ± 41.4 ng/mL, p = 0.02). ROC curve analysis identified sST2 cut-off: >98.44 ng/mL as the best predictor for mortality. At the one-year follow-up, the survival rate decreased up to 20% in patients with sST2 higher than the cut-off value. A multivariate regression analysis revealed that only sST2 (HR: 1.012, 95% CI: 1.008−1.016, p < 0.0001) and triglycerides plasma levels (HR: 1.008, 95% CI: 1.002−1.015, p = 0.0135) remained significantly associated with all-cause mortality. ST2L was not associated with all-cause mortality risk. sST2 may act as an independent prognostic determinant of all-cause mortality and symptomatic cerebrovascular diseases in patients with carotid atherosclerotic plaque who underwent CEA.

Identifiants

pubmed: 35683529
pii: jcm11113142
doi: 10.3390/jcm11113142
pmc: PMC9181783
pii:
doi:

Types de publication

Journal Article

Langues

eng

Références

Eur J Neurol. 2020 Nov;27(11):2202-2208
pubmed: 32593220
J Neurosci. 2017 May 3;37(18):4692-4704
pubmed: 28389473
Eur J Vasc Endovasc Surg. 2018 Jan;55(1):3-81
pubmed: 28851594
Sci Rep. 2021 Jul 26;11(1):15203
pubmed: 34312471
PLoS One. 2016 May 25;11(5):e0156315
pubmed: 27223112
Scand J Clin Lab Invest. 2021 Jul;81(4):324-331
pubmed: 33794701
Stroke. 2015 Sep;46(9):2568-75
pubmed: 26219649
Atherosclerosis. 2013 Nov;231(1):48-53
pubmed: 24125409
Clin Chim Acta. 2020 Nov;510:767-771
pubmed: 32926842
Acta Diabetol. 2019 Mar;56(3):273-280
pubmed: 30259114
Eur J Heart Fail. 2020 Nov;22(11):2078-2088
pubmed: 31919929
Cardiovasc Diabetol. 2021 Feb 19;20(1):49
pubmed: 33608010
Eur J Vasc Endovasc Surg. 2018 Mar;55(3):305-368
pubmed: 28851596
Brain Behav Immun. 2015 Oct;49:322-36
pubmed: 26111431
Cardiovasc Drugs Ther. 2017 Apr;31(2):167-177
pubmed: 28283847
Eur Heart J. 2021 Sep 7;42(34):3227-3337
pubmed: 34458905
Clin Lab. 2018 Sep 1;64(9):1349-1356
pubmed: 30274001
JACC Heart Fail. 2017 Apr;5(4):287-296
pubmed: 28189578
J Exp Med. 2008 Feb 18;205(2):339-46
pubmed: 18268038
Int J Stroke. 2021 Aug;16(6):660-668
pubmed: 33167787
Front Cardiovasc Med. 2020 Dec 22;7:605669
pubmed: 33415128
PLoS One. 2020 Sep 4;15(9):e0238775
pubmed: 32886697
Neurocrit Care. 2021 Dec;35(3):887-893
pubmed: 34231185
Brain Res. 2015 Feb 9;1597:86-94
pubmed: 25500143
Cytokine. 2019 Aug;120:242-250
pubmed: 31132589
Molecules. 2013 Dec 11;18(12):15314-28
pubmed: 24335613
JACC Heart Fail. 2017 Apr;5(4):280-286
pubmed: 27816512
Clin Chem. 2014 Mar;60(3):530-40
pubmed: 24401186
Immunity. 2005 Nov;23(5):479-90
pubmed: 16286016
Cardiol Res Pract. 2020 Nov 17;2020:4375651
pubmed: 33282418

Auteurs

Pietro Scicchitano (P)

Cardiology Department, Hospital "F. Perinei", 70022 Altamura, Italy.

Andrea Marzullo (A)

Pathology Division, Department of Emergency and Organ Transplantation, University of Bari, 70121 Bari, Italy.

Annarita Santoro (A)

Section of Cardiovascular Diseases, Department of Emergency and Organ Transplantation, University of Bari, 70121 Bari, Italy.

Annapaola Zito (A)

Section of Cardiovascular Diseases, Department of Emergency and Organ Transplantation, University of Bari, 70121 Bari, Italy.

Francesca Cortese (F)

Section of Cardiovascular Diseases, Department of Emergency and Organ Transplantation, University of Bari, 70121 Bari, Italy.

Cristina Galeandro (C)

Section of Vascular Surgery, Department of Emergency and Organ Transplantation, University of Bari, 70121 Bari, Italy.

Andrea Sebastiano Ciccone (AS)

Pathology Division, Department of Emergency and Organ Transplantation, University of Bari, 70121 Bari, Italy.

Domenico Angiletta (D)

Section of Vascular Surgery, Department of Emergency and Organ Transplantation, University of Bari, 70121 Bari, Italy.

Fabio Manca (F)

Department of Science of Educational Psychology and Communication, University of Bari, 70121 Bari, Italy.

Raffaele Pulli (R)

Section of Vascular Surgery, Department of Emergency and Organ Transplantation, University of Bari, 70121 Bari, Italy.

Eliano Pio Navarese (EP)

Inova Center for Thrombosis Research and Drug Development, Inova Heart and Vascular Institute, Inova Fairfax Medical Center, Falls Church, VA 22042, USA.

Paul A Gurbel (PA)

Inova Center for Thrombosis Research and Drug Development, Inova Heart and Vascular Institute, Inova Fairfax Medical Center, Falls Church, VA 22042, USA.

Marco Matteo Ciccone (MM)

Section of Cardiovascular Diseases, Department of Emergency and Organ Transplantation, University of Bari, 70121 Bari, Italy.

Classifications MeSH