Sortilin levels correlate with major cardiovascular events of diabetic patients with peripheral artery disease following revascularization: a prospective study.


Journal

Cardiovascular diabetology
ISSN: 1475-2840
Titre abrégé: Cardiovasc Diabetol
Pays: England
ID NLM: 101147637

Informations de publication

Date de publication:
25 09 2020
Historique:
received: 26 05 2020
accepted: 12 09 2020
entrez: 26 9 2020
pubmed: 27 9 2020
medline: 7 9 2021
Statut: epublish

Résumé

Peripheral artery disease (PAD) represents one of the most relevant vascular complications of type 2 diabetes mellitus (T2DM). Moreover, T2DM patients suffering from PAD have an increased risk of major adverse cardiovascular events (MACE) and major adverse limb events (MALE). Sortilin, a protein involved in apolipoproteins trafficking, is associated with lower limb PAD in T2DM patients. To evaluate the relationship between baseline serum levels of sortilin, MACE and MALE occurrence after revascularization of T2DM patients with PAD and chronic limb-threatening ischemia (CLTI). We performed a prospective non-randomized study including 230 statin-free T2DM patients with PAD and CLTI. Sortilin levels were measured before the endovascular intervention and incident outcomes were assessed during a 12 month follow-up. Sortilin levels were significantly increased in individuals with more aggressive PAD (2.25 ± 0.51 ng/mL vs 1.44 ± 0.47 ng/mL, p < 0.001). During follow-up, 83 MACE and 116 MALE occurred. In patients, who then developed MACE and MALE, sortilin was higher. In particular, 2.46 ± 0.53 ng/mL vs 1.55 ± 0.42 ng/mL, p < 0.001 for MACE and 2.10 ± 0.54 ng/mL vs 1.65 ± 0.65 ng/mL, p < 0.001 for MALE. After adjusting for traditional atherosclerosis risk factors, the association between sortilin and vascular outcomes remained significant in a multivariate analysis. In our receiver operating characteristics (ROC) curve analysis using sortilin levels the prediction of MACE incidence improved (area under the curve [AUC] = 0.94) and MALE (AUC = 0.72). This study demonstrates that sortilin correlates with incidence of MACE and MALE after endovascular revascularization in a diabetic population with PAD and CLTI.

Sections du résumé

BACKGROUND
Peripheral artery disease (PAD) represents one of the most relevant vascular complications of type 2 diabetes mellitus (T2DM). Moreover, T2DM patients suffering from PAD have an increased risk of major adverse cardiovascular events (MACE) and major adverse limb events (MALE). Sortilin, a protein involved in apolipoproteins trafficking, is associated with lower limb PAD in T2DM patients.
OBJECTIVE
To evaluate the relationship between baseline serum levels of sortilin, MACE and MALE occurrence after revascularization of T2DM patients with PAD and chronic limb-threatening ischemia (CLTI).
RESEARCH DESIGN AND METHODS
We performed a prospective non-randomized study including 230 statin-free T2DM patients with PAD and CLTI. Sortilin levels were measured before the endovascular intervention and incident outcomes were assessed during a 12 month follow-up.
RESULTS
Sortilin levels were significantly increased in individuals with more aggressive PAD (2.25 ± 0.51 ng/mL vs 1.44 ± 0.47 ng/mL, p < 0.001). During follow-up, 83 MACE and 116 MALE occurred. In patients, who then developed MACE and MALE, sortilin was higher. In particular, 2.46 ± 0.53 ng/mL vs 1.55 ± 0.42 ng/mL, p < 0.001 for MACE and 2.10 ± 0.54 ng/mL vs 1.65 ± 0.65 ng/mL, p < 0.001 for MALE. After adjusting for traditional atherosclerosis risk factors, the association between sortilin and vascular outcomes remained significant in a multivariate analysis. In our receiver operating characteristics (ROC) curve analysis using sortilin levels the prediction of MACE incidence improved (area under the curve [AUC] = 0.94) and MALE (AUC = 0.72).
CONCLUSIONS
This study demonstrates that sortilin correlates with incidence of MACE and MALE after endovascular revascularization in a diabetic population with PAD and CLTI.

Identifiants

pubmed: 32977814
doi: 10.1186/s12933-020-01123-3
pii: 10.1186/s12933-020-01123-3
pmc: PMC7519536
doi:

Substances chimiques

Adaptor Proteins, Vesicular Transport 0
sortilin Z020Y8WIJ4

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

147

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Auteurs

Federico Biscetti (F)

Department of Internal Medicine, Fondazione Policlinico Universitario A. Gemelli IRCCS, Largo Agostino Gemelli 8, Roma, 00168, Italia. f.biscetti@gmail.com.
Internal Medicine and Vascular Diseases Unit, Roma, Italia. f.biscetti@gmail.com.
Laboratory of Vascular Biology and Genetics, Department of Translational Medicine and Surgery, Roma, Italia. f.biscetti@gmail.com.

Elisabetta Nardella (E)

Internal Medicine and Vascular Diseases Unit, Roma, Italia.

Maria Margherita Rando (MM)

Internal Medicine and Vascular Diseases Unit, Roma, Italia.

Andrea Leonardo Cecchini (AL)

Internal Medicine and Vascular Diseases Unit, Roma, Italia.

Nicola Bonadia (N)

Department of Internal Medicine, Fondazione Policlinico Universitario A. Gemelli IRCCS, Largo Agostino Gemelli 8, Roma, 00168, Italia.
Emergency Medicine, Roma, Italia.

Piergiorgio Bruno (P)

Department of Internal Medicine, Fondazione Policlinico Universitario A. Gemelli IRCCS, Largo Agostino Gemelli 8, Roma, 00168, Italia.
Cardiac Surgery Unit, Roma, Italia.

Flavia Angelini (F)

Laboratory of Vascular Biology and Genetics, Department of Translational Medicine and Surgery, Roma, Italia.

Carmine Di Stasi (C)

Department of Radiology, Roma, Italia.

Andrea Contegiacomo (A)

Department of Radiology, Roma, Italia.

Angelo Santoliquido (A)

Department of Internal Medicine, Fondazione Policlinico Universitario A. Gemelli IRCCS, Largo Agostino Gemelli 8, Roma, 00168, Italia.
Università Cattolica del Sacro Cuore, Roma, Italia.
Angiology Unit, Roma, Italia.

Dario Pitocco (D)

Department of Internal Medicine, Fondazione Policlinico Universitario A. Gemelli IRCCS, Largo Agostino Gemelli 8, Roma, 00168, Italia.
Università Cattolica del Sacro Cuore, Roma, Italia.
Diabetology Unit, Roma, Italia.

Raffaele Landolfi (R)

Department of Internal Medicine, Fondazione Policlinico Universitario A. Gemelli IRCCS, Largo Agostino Gemelli 8, Roma, 00168, Italia.
Internal Medicine and Vascular Diseases Unit, Roma, Italia.
Università Cattolica del Sacro Cuore, Roma, Italia.

Andrea Flex (A)

Department of Internal Medicine, Fondazione Policlinico Universitario A. Gemelli IRCCS, Largo Agostino Gemelli 8, Roma, 00168, Italia.
Internal Medicine and Vascular Diseases Unit, Roma, Italia.
Laboratory of Vascular Biology and Genetics, Department of Translational Medicine and Surgery, Roma, Italia.
Università Cattolica del Sacro Cuore, Roma, Italia.

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