Subclinical atherosclerosis in asymptomatic carriers of persistent antiphospholipid antibodies positivity: A cross-sectional study.


Journal

International journal of cardiology
ISSN: 1874-1754
Titre abrégé: Int J Cardiol
Pays: Netherlands
ID NLM: 8200291

Informations de publication

Date de publication:
01 Jan 2019
Historique:
received: 20 12 2017
revised: 20 04 2018
accepted: 04 06 2018
entrez: 21 11 2018
pubmed: 21 11 2018
medline: 23 7 2019
Statut: ppublish

Résumé

Whereas the relationship between subclinical atherosclerosis and antiphospholipid syndrome (APS) has been widely investigated, little is known about subclinical atherosclerosis in asymptomatic carriers with isolated antiphospholipid antibodies positivity (APP). Consecutive APP carriers, APS subjects and matched controls were enrolled. Intima-media thickness of the common carotid artery (CCA-IMT) and of the Bulb (Bulb-IMT) and the prevalence of carotid plaques were assessed in all enrolled subjects. A total of 104 APP carriers, 221 APS subjects, and 325 matched controls were recruited. As compared with controls, APP carriers and APS subjects showed a higher CCA-IMT (0.90 ± 0.24 vs 0.82 ± 0.12, p = 0.014 and 0.93 ± 0.42 vs 0.82 ± 0.12, p < 0.001, respectively), Bulb-IMT (1.10 ± 0.44 vs 0.95 ± 0.18, p = 0.006 and 1.22 ± 0.68 vs 0.95 ± 0.18, p < 0.001, respectively) and an increased prevalence of carotid plaques (33.7% vs 10.2%, p < 0.001 and 38.5% vs 10.2%, p < 0.001, respectively). These results were confirmed stratifying for antibody isotype, after excluding subjects with systemic lupus erythematosus or other autoimmune diseases and after adjusting for major clinical and demographic variables. CCA-IMT, Bulb-IMT and the prevalence of carotid plaques were higher in subjects with high-titer antibodies and progressively increased for an increasing number of positive antibodies. Similar to APS subjects, APP carriers have enhanced subclinical atherosclerosis, a more severe disease being observed in the presence of high-titer antibodies and multiple antibodies positivity. These data argue for a strict monitoring of subclinical signs of atherosclerosis and of cardiovascular risk factors in asymptomatic APP carriers.

Sections du résumé

BACKGROUND BACKGROUND
Whereas the relationship between subclinical atherosclerosis and antiphospholipid syndrome (APS) has been widely investigated, little is known about subclinical atherosclerosis in asymptomatic carriers with isolated antiphospholipid antibodies positivity (APP).
METHODS METHODS
Consecutive APP carriers, APS subjects and matched controls were enrolled. Intima-media thickness of the common carotid artery (CCA-IMT) and of the Bulb (Bulb-IMT) and the prevalence of carotid plaques were assessed in all enrolled subjects.
RESULTS RESULTS
A total of 104 APP carriers, 221 APS subjects, and 325 matched controls were recruited. As compared with controls, APP carriers and APS subjects showed a higher CCA-IMT (0.90 ± 0.24 vs 0.82 ± 0.12, p = 0.014 and 0.93 ± 0.42 vs 0.82 ± 0.12, p < 0.001, respectively), Bulb-IMT (1.10 ± 0.44 vs 0.95 ± 0.18, p = 0.006 and 1.22 ± 0.68 vs 0.95 ± 0.18, p < 0.001, respectively) and an increased prevalence of carotid plaques (33.7% vs 10.2%, p < 0.001 and 38.5% vs 10.2%, p < 0.001, respectively). These results were confirmed stratifying for antibody isotype, after excluding subjects with systemic lupus erythematosus or other autoimmune diseases and after adjusting for major clinical and demographic variables. CCA-IMT, Bulb-IMT and the prevalence of carotid plaques were higher in subjects with high-titer antibodies and progressively increased for an increasing number of positive antibodies.
CONCLUSIONS CONCLUSIONS
Similar to APS subjects, APP carriers have enhanced subclinical atherosclerosis, a more severe disease being observed in the presence of high-titer antibodies and multiple antibodies positivity. These data argue for a strict monitoring of subclinical signs of atherosclerosis and of cardiovascular risk factors in asymptomatic APP carriers.

Identifiants

pubmed: 30454720
pii: S0167-5273(17)37794-X
doi: 10.1016/j.ijcard.2018.06.010
pii:
doi:

Substances chimiques

Antibodies, Antiphospholipid 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1-6

Informations de copyright

Copyright © 2017 Elsevier B.V. All rights reserved.

Auteurs

Matteo Nicola Dario Di Minno (MND)

Department of Translational Medical Sciences, Federico II University, Naples, Italy. Electronic address: dario.diminno@hotmail.it.

Giacomo Emmi (G)

Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy.

Pasquale Ambrosino (P)

Department of Clinical Medicine and Surgery, Federico II University, Naples, Italy.

Antonella Scalera (A)

Department of Clinical Medicine and Surgery, Federico II University, Naples, Italy.

Antonella Tufano (A)

Department of Clinical Medicine and Surgery, Federico II University, Naples, Italy.

Giovanni Cafaro (G)

Department of Clinical Medicine and Surgery, Federico II University, Naples, Italy.

Rosario Peluso (R)

Department of Clinical Medicine and Surgery, Federico II University, Naples, Italy.

Alessandra Bettiol (A)

Department of Neurosciences, Psychology, Pharmacology and Child Health (NEUROFARBA), University of Florence, Florence, Italy.

Gerardo Di Scala (G)

Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy.

Elena Silvestri (E)

Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy.

Domenico Prisco (D)

Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy.

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