Determinants and Outcomes of Accelerated Arteriosclerosis: Major Impact of Circulating Antibodies.

Circ Res

From the Paris Translational Research Center for Organ Transplantation and Cardiovascular Disease, INSERM, UMR-S970, Paris, France (A.L., D. Viglietti, O.A., J.-P.D.V.H., J.-P.E., P.B., D.G., C. Legendre, X.J., C. Lefaucheur); Paris Descartes University, Sorbonne Paris Cité and Necker Hospital (A.L., J.-P.D.V.H., C. Legendre) and Department of Transplantation, Saint-Louis Hospital (D. Viglietti, D.G., C. Lefaucheur), Assistance Publique - Hôpitaux de Paris, Paris, France; Methodology Unit (EA 3181) CHRU de Besançon, Besançon, France (D. Vernerey); Department of Pathology, Necker Hospital, Paris, France (J.-P.D.V.H.); and Department of Pathology (P.B.) and Department of Cardiology (X.J.), Georges Pompidou European Hospital, Paris, France.

Published: August 2015

Rationale: The role of circulating antibodies in addition to traditional cardiovascular risk factors in the development of accelerated arteriosclerosis and their long-term clinical consequences have not been demonstrated.

Objective: We investigated the role of circulating antibodies in accelerated arteriosclerosis and the role of immune-associated arteriosclerosis in graft and patient survival and the occurrence of major adverse cardiovascular events.

Methods And Results: This was an observational prospective cohort study that included 1065 kidney transplant patients (principal cohort, n=744; validation cohort, n=321) between 2004 and 2010. Participants were assessed for traditional cardiovascular risk factors and circulating anti-human leukocyte antigen (HLA) antibodies. All patients underwent allograft biopsies to assess arteriosclerotic lesions and endothelial activation, endarteritis, and complement deposition. In the principal cohort, 250 (33.6%) patients had severe arteriosclerosis (luminal narrowing >25% via fibrointimal arterial thickening). Circulating donor-specific anti-HLA antibodies were significantly associated with severe allograft arteriosclerosis (hazard ratio, 2.9; P<0.0001), independently of traditional risk factors. Patients with severe arteriosclerosis and anti-HLA antibodies (n=91, 12.2%) demonstrated allograft endothelial activation, endarteritis, and complement deposition. High levels of anti-HLA antibodies and their complement binding capacity were associated with increased severity of arteriosclerosis. Patients with antibody-associated severe arteriosclerosis had decreased allograft survival and increased mortality (P<0.0001); they exhibited a 2.5- and 4.1-fold increased risk of major adverse cardiovascular events compared with patients who had severe arteriosclerosis without antibodies and patients with minimal arteriosclerosis, respectively (P<0.0005). Circulating donor-specific anti-HLA antibodies were significantly associated with occurrence of major adverse cardiovascular events (hazard ratio, 2.4; P=0.0004), independently of traditional risk factors.

Conclusions: Circulating antibodies are major determinants of severe arteriosclerosis and major adverse cardiovascular events, independent of traditional cardiovascular risk factors.

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Source
http://dx.doi.org/10.1161/CIRCRESAHA.117.306340DOI Listing

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