Sortilin levels correlate with major cardiovascular events of diabetic patients with peripheral artery disease following revascularization: a prospective study.
Adaptor Proteins, Vesicular Transport
/ blood
Aged
Aged, 80 and over
Amputation, Surgical
/ statistics & numerical data
Cardiovascular Diseases
/ mortality
Diabetes Mellitus, Type 2
/ blood
Diabetic Angiopathies
/ blood
Endovascular Procedures
Female
Humans
Incidence
Ischemia
/ epidemiology
Male
Middle Aged
Myocardial Infarction
/ epidemiology
Peripheral Arterial Disease
/ blood
Prognosis
Prospective Studies
Stroke
/ epidemiology
Treatment Outcome
Diabetes mellitus
Peripheral artery disease (PAD)
Sortilin
Journal
Cardiovascular diabetology
ISSN: 1475-2840
Titre abrégé: Cardiovasc Diabetol
Pays: England
ID NLM: 101147637
Informations de publication
Date de publication:
25 09 2020
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
147Références
Eur Heart J. 2018 Mar 1;39(9):763-816
pubmed: 28886620
J Lipid Res. 2013 Oct;54(10):2754-62
pubmed: 23904453
Cardiovasc Diabetol. 2016 Sep 02;15(1):129
pubmed: 27590190
J Clin Invest. 2012 Aug;122(8):2807-16
pubmed: 22751103
Circ Res. 2015 Feb 27;116(5):789-96
pubmed: 25593281
Immunity. 2012 Nov 16;37(5):854-66
pubmed: 23084031
Cardiovasc Diabetol. 2019 Nov 15;18(1):155
pubmed: 31730004
Cell Metab. 2010 Sep 8;12(3):213-23
pubmed: 20816088
J Vasc Surg. 1986 Jul;4(1):80-94
pubmed: 3723692
Nature. 2010 Aug 5;466(7307):714-9
pubmed: 20686566
Biochem Biophys Res Commun. 2013 Jan 4;430(1):66-71
pubmed: 23159624
J Biol Chem. 1997 Feb 7;272(6):3599-605
pubmed: 9013611
J Biol Chem. 2015 May 1;290(18):11526-36
pubmed: 25805502
Diabetes Care. 2020 Jan;43(Suppl 1):S111-S134
pubmed: 31862753
Am J Med Sci. 2020 Jan;359(1):8-16
pubmed: 31902442
Atherosclerosis. 2010 Jan;208(1):183-9
pubmed: 19660754
Diabetes Care. 2019 Oct;42(10):1939-1945
pubmed: 31371431
J Clin Invest. 2016 Apr 1;126(4):1323-36
pubmed: 26950419
Intern Emerg Med. 2020 Apr;15(3):381-393
pubmed: 31919781
Sci Rep. 2016 May 25;6:26566
pubmed: 27220277
Transl Psychiatry. 2015 Nov 10;5:e677
pubmed: 26556286
J Atheroscler Thromb. 2017 May 1;24(5):462-472
pubmed: 28302950
J Vasc Interv Radiol. 2003 Sep;14(9 Pt 2):S395-404
pubmed: 14514855
Cardiovasc Diabetol. 2019 Jan 11;18(1):5
pubmed: 30634965
J Am Coll Cardiol. 2018 May 22;71(20):2306-2315
pubmed: 29540326
Curr Atheroscler Rep. 2012 Jun;14(3):211-8
pubmed: 22538429
Curr Opin Lipidol. 2019 Jun;30(3):198-204
pubmed: 30946050
PLoS One. 2017 Oct 26;12(10):e0186220
pubmed: 29073236
Mol Biol Cell. 2017 Jun 15;28(12):1667-1675
pubmed: 28450454
J Clin Invest. 2014 Dec;124(12):5317-22
pubmed: 25401472
Cardiovasc Diabetol. 2017 Jul 20;16(1):92
pubmed: 28728579
Eur J Vasc Endovasc Surg. 2019 Jul;58(1S):S1-S109.e33
pubmed: 31182334
Int J Cardiol. 2017 Jan 15;227:61-65
pubmed: 27846466
Atherosclerosis. 2016 Jun;249:110-5
pubmed: 27085161