Your browser doesn't support javascript.
loading
Cytomegalovirus Immunoglobulin G (IgG) Titer and Coronary Artery Disease in People With Human Immunodeficiency Virus (HIV).
Schnittman, Samuel R; Lu, Michael T; Mayrhofer, Thomas; Burdo, Tricia H; Fitch, Kathleen V; McCallum, Sara; Fulda, Evelynne S; Zanni, Markella V; Foldyna, Borek; Malvestutto, Carlos; Fichtenbaum, Carl J; Aberg, Judith A; Bloomfield, Gerald S; Overton, Edgar T; Currier, Judith; Tebas, Pablo; Sha, Beverly E; Ribaudo, Heather J; Flynn, Jacqueline M; Douglas, Pamela S; Erlandson, Kristine M; Grinspoon, Steven K.
  • Schnittman SR; Division of Infectious Diseases, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Lu MT; Cardiovascular Imaging Research Center, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Mayrhofer T; Cardiovascular Imaging Research Center, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Burdo TH; School of Business Studies, Stralsund University of Applied Sciences, Stralsund, Germany.
  • Fitch KV; Department of Microbiology, Immunology, and Inflammation and Center for Neuro-Virology and Gene Editing, Temple University Lewis Katz School of Medicine, Philadelphia, Pennsylvania, USA.
  • McCallum S; Metabolism Unit, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Fulda ES; Metabolism Unit, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Zanni MV; Metabolism Unit, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Foldyna B; Metabolism Unit, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Malvestutto C; Cardiovascular Imaging Research Center, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Fichtenbaum CJ; Division of Infectious Diseases, The Ohio State University Wexner Medical Center, Columbus, Ohio, USA.
  • Aberg JA; Division of Infectious Diseases, Department of Medicine, University of Cincinnati, Cincinnati, Ohio, USA.
  • Bloomfield GS; Division of Infectious Diseases, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
  • Overton ET; Division of Cardiology, Department of Medicine and Duke Clinical Research Institute, Duke University, Durham, North Carolina, USA.
  • Currier J; Division of Infectious Diseases, University of Alabama at Birmingham, Birmingham, Alabama, USA.
  • Tebas P; Division of Infectious Diseases, University of California at Los Angeles, Los Angeles, California, USA.
  • Sha BE; Department of Medicine, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, USA.
  • Ribaudo HJ; Division of Infectious Diseases, Department of Internal Medicine, Rush University Medical Center, Chicago, Illinois, USA.
  • Flynn JM; Center for Biostatistics in AIDS Research, Harvard T.H. Chan School of Public Health, Boston, Massachusetts, USA.
  • Douglas PS; Department of Microbiology, Immunology, and Inflammation and Center for Neuro-Virology and Gene Editing, Temple University Lewis Katz School of Medicine, Philadelphia, Pennsylvania, USA.
  • Erlandson KM; Duke Clinical Research Institute, Duke University School of Medicine, Durham, North Carolina, USA.
  • Grinspoon SK; Division of Infectious Diseases, Department of Medicine, University of Colorado, Aurora, Colorado, USA.
Clin Infect Dis ; 76(3): e613-e621, 2023 02 08.
Article en En | MEDLINE | ID: mdl-35975297
ABSTRACT

BACKGROUND:

Cytomegalovirus (CMV) infection is thought to result in increased immune activation in people with human immunodeficiency virus (HIV, PWH). Although some data have linked asymptomatic CMV infection to cardiovascular disease among PWH, it remains unknown whether CMV is associated with increased or high-risk coronary plaque.

METHODS:

The Randomized Trial to Prevent Vascular Events in HIV (REPRIEVE) enrolled PWH aged 40-75 years on stable antiretroviral therapy (ART) with low-to-moderate atherosclerotic cardiovascular disease (ASCVD) risk. Among a subset of US REPRIEVE participants, coronary plaque was assessed by coronary computed tomography angiography. Here, we assessed the relationship between CMV immunoglobulin G (IgG) titer and (1) levels of immune activation, (2) inflammatory biomarkers, and (3) coronary plaque phenotypes at study entry.

RESULTS:

Of 672 participants, mean age was 51 years, 83% were men, median ASCVD risk score was 4.5%, and 66% had current CD4+ T-cell count ≥500 cells/mm3. Higher CMV IgG quartile group was associated with older age and lower current and nadir CD4+ T-cell counts. CMV IgG titer was associated with specific inflammatory biomarkers (sCD163, MCP-1, interleukin [IL]-6, hsCRP) in univariate analysis, but not after controlling for HIV-specific factors. In contrast, CMV IgG titer was not associated with coronary artery disease indexes, including presence of plaque, coronary artery calcium (CAC) score >0, vulnerable plaque presence, or Leaman score >5.

CONCLUSIONS:

No meaningful association was seen between CMV IgG titer and coronary artery disease indexes among ART-treated PWH at study enrollment. Longitudinal assessments in REPRIEVE will determine the relationship of CMV IgG titer to plaque progression and cardiovascular events. CLINICAL TRIALS REGISTRATION NCT02344290.
Asunto(s)
Palabras clave

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedad de la Arteria Coronaria / Enfermedades Cardiovasculares / Infecciones por VIH / Infecciones por Citomegalovirus Tipo de estudio: Clinical_trials Límite: Female / Humans / Male / Middle aged Idioma: En Año: 2023 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedad de la Arteria Coronaria / Enfermedades Cardiovasculares / Infecciones por VIH / Infecciones por Citomegalovirus Tipo de estudio: Clinical_trials Límite: Female / Humans / Male / Middle aged Idioma: En Año: 2023 Tipo del documento: Article