4.7 Article

Higher Anti-Cytomegalovirus Immunoglobulin G Concentrations Are Associated With Worse Neurocognitive Performance During Suppressive Antiretroviral Therapy

Journal

CLINICAL INFECTIOUS DISEASES
Volume 67, Issue 5, Pages 770-777

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/cid/ciy170

Keywords

HIV; cytomegalovirus; neurocognitive disorders; cerebrospinal fluid

Funding

  1. National Institutes of Health [N01 AI35172, N01 MH22005, HHSN271201000036C]
  2. ACTG Immunology Specialty Laboratory [AI 06701]
  3. [K24 MH097673]
  4. EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT [R21HD094646] Funding Source: NIH RePORTER
  5. FOGARTY INTERNATIONAL CENTER [D43TW000237] Funding Source: NIH RePORTER
  6. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [P30AI036214, R21AI134295, P01AI131385] Funding Source: NIH RePORTER
  7. NATIONAL INSTITUTE OF MENTAL HEALTH [R01MH107345, P30MH062512, U24MH100928, K24MH097673] Funding Source: NIH RePORTER

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Background. Cytomegalovirus (CMV) has been linked to higher risk of cardiovascular disease and mortality. We aimed to determine if CMV is associated with neurocognitive performance in adults infected with human immunodeficiency virus (HIV). Methods. In this cross-sectional analysis, anti-CMV immunoglobulin G (IgG) concentrations in blood and CMV DNA copies in blood and cerebrospinal fluid (CSF) were measured in stored specimens of 80 HIV-infected adults who were previously assessed with a comprehensive neurocognitive test battery. Thirty-eight were taking suppressive antiretroviral therapy (ART) and 42 were not taking ART. A panel of 7 soluble biomarkers was measured by immunoassay in CSF. Results. Anti-CMV IgG concentrations ranged from 5.2 to 46.1 IU/mL. CMV DNA was detected in 7 (8.8%) plasma specimens but in no CSF specimens. Higher anti-CMV IgG levels were associated with older age (P = .0017), lower nadir CD4+ T-cell count (P<.001), AIDS (P < .001), and higher soluble CD163 (P =.009). Higher anti-CMV IgG levels trended toward an association with worse neurocognitive performance overall (P = .059). This correlation was only present in those taking suppressive ART (P = .0049). Worse neurocognitive performance remained associated with higher anti-CMV IgG levels after accounting for other covariates in multivariate models (model P = .0038). Detectable plasma CMV DNA was associated with AIDS (P = .05) but not with neurocognitive performance. Conclusions. CMV may influence neurocognitive performance in HIV-infected adults taking suppressive ART. Future clinical trials of anti-CMV therapy should help to determine whether the observed relationships are causal.

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