6 research outputs found

    Assessing the Prognostic Significance of CD8+ T-Cell Counts in Determining the Risk of Myocardial Infarction in the Setting of HIV Infection

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    There is a growing body of research to suggest that Human Immunodeficiency Virus (HIV) infection is associated with an increased risk for myocardial infarction (MI) although the underlying processes remain unclear. An assessment of MI risk using a commonly-available measure of the immune status is therefore of Public Health importance. CD8+ and CD4+ T-cell counts are periodically measured in the routine management of HIV-infected patients. However, CD8+ T-cell counts are often not reported or are simply incorporated into the calculation of a CD4+/CD8+ ratio. Total CD8+ T-cell counts have been shown to be associated with an increased risk for MI in at least one recent study. A few other studies have examined this association indirectly by using the CD4+/CD8+ ratio, but only considered MI surrogates (e.g. subclinical coronary atherosclerosis) as an outcome. Also, measuring cell-surface markers of CD8+ T-cell activation and HIV-specific CD8+ T cell counts is costly and often not requested in the routine management of HIV infection. This study investigated the association between total CD8+ T-cell counts and MI risk among a large cohort of HIV-uninfected and HIV-infected Veterans. Using Cox proportional hazard regression models, the results suggest that MI risk is associated with a high CD8+ T-cell count of ≥1066 cells/ mm3 (Adjusted HR = 1.82, P <0.001, 95% CI: 1.46 to 2.28). They also suggest that the risk for MI posed by total CD8+ T-cell counts should be interpreted in the context of CD4+ T-cell clinical cut-points, or the overall immune status. The degree of MI risk in the cohort differed depending on the level of the immunosuppression. Total CD8+ T cell-counts seemed to modestly improve the risk stratification provided by CD4+ T-cell clinical cut-points, though the mechanisms are still unclear. Future studies will be instrumental in understanding the role of the immune system in MI risk prediction

    CD8+ T-cells count in acute myocardial infarction in HIV diseases in a predominantly male cohort

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    Human Immunodeficiency Virus- (HIV-) infected persons have a higher risk for acute myocardial infarction (AMI) than HIV-uninfected persons. Earlier studies suggest that HIV viral load, CD4+ T-cell count, and antiretroviral therapy are associated with cardiovascular disease (CVD) risk. Whether CD8+ T-cell count is associated with CVD risk is not clear. We investigated the association between CD8+ T-cell count and incident AMI in a cohort of 73,398 people (of which 97.3% were men) enrolled in the U.S. Veterans Aging Cohort Study-Virtual Cohort (VACS-VC). Compared to uninfected people, HIV-infected people with high baseline CD8+ T-cell counts (\u3e1065 cells/mm3) had increased AMI risk (adjusted , 95% CI: 1.46 to 2.28). There was evidence that the effect of CD8+ T-cell tertiles on AMI risk differed by CD4+ T-cell level: compared to uninfected people, HIV-infected people with CD4+ T-cell counts ≥200 cells/mm3 had increased AMI risk with high CD8+ T-cell count, while those with CD4+ T-cell counts \u3c200 cells/mm3 had increased AMI risk with low CD8+ T-cell count. CD8+ T-cell counts may add additional AMI risk stratification information beyond that provided by CD4+ T-cell counts alone

    CD8+ T-cells count in acute myocardial infarction in HIV disease in a predominantly male cohort.

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    Human Immunodeficiency Virus- (HIV-) infected persons have a higher risk for acute myocardial infarction (AMI) than HIV-uninfected persons. Earlier studies suggest that HIV viral load, CD4+ T-cell count, and antiretroviral therapy are associated with cardiovascular disease (CVD) risk. Whether CD8+ T-cell count is associated with CVD risk is not clear. We investigated the association between CD8+ T-cell count and incident AMI in a cohort of 73,398 people (of which 97.3% were men) enrolled in the U.S. Veterans Aging Cohort Study-Virtual Cohort (VACS-VC). Compared to uninfected people, HIV-infected people with high baseline CD8+ T-cell counts (\u3e1065 cells/mm3) had increased AMI risk (adjusted HR=1.82,

    CD8 + T-Cells Count in Acute Myocardial Infarction in HIV Disease in a Predominantly Male Cohort

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    Human Immunodeficiency Virus-(HIV-) infected persons have a higher risk for acute myocardial infarction (AMI) than HIVuninfected persons. Earlier studies suggest that HIV viral load, CD4 + T-cell count, and antiretroviral therapy are associated with cardiovascular disease (CVD) risk. Whether CD8 + T-cell count is associated with CVD risk is not clear. We investigated the association between CD8 + T-cell count and incident AMI in a cohort of 73,398 people (of which 97.3% were men) enrolled in the U.S. Veterans Aging Cohort Study-Virtual Cohort (VACS-VC). Compared to uninfected people, HIV-infected people with high baseline CD8 + T-cell counts (&gt;1065 cells/mm 3 ) had increased AMI risk (adjusted HR = 1.82, &lt; 0.001, 95% CI: 1.46 to 2.28). There was evidence that the effect of CD8 + T-cell tertiles on AMI risk differed by CD4 + T-cell level: compared to uninfected people, HIVinfected people with CD4 + T-cell counts ≥200 cells/mm 3 had increased AMI risk with high CD8 + T-cell count, while those with CD4 + T-cell counts &lt;200 cells/mm 3 had increased AMI risk with low CD8 + T-cell count. CD8 + T-cell counts may add additional AMI risk stratification information beyond that provided by CD4 + T-cell counts alone

    CD8+ T-Cells Count in Acute Myocardial Infarction in HIV Disease in a Predominantly Male Cohort

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    Human Immunodeficiency Virus- (HIV-) infected persons have a higher risk for acute myocardial infarction (AMI) than HIV-uninfected persons. Earlier studies suggest that HIV viral load, CD4+ T-cell count, and antiretroviral therapy are associated with cardiovascular disease (CVD) risk. Whether CD8+ T-cell count is associated with CVD risk is not clear. We investigated the association between CD8+ T-cell count and incident AMI in a cohort of 73,398 people (of which 97.3% were men) enrolled in the U.S. Veterans Aging Cohort Study-Virtual Cohort (VACS-VC). Compared to uninfected people, HIV-infected people with high baseline CD8+ T-cell counts (>1065 cells/mm3) had increased AMI risk (adjusted HR=1.82, P<0.001, 95% CI: 1.46 to 2.28). There was evidence that the effect of CD8+ T-cell tertiles on AMI risk differed by CD4+ T-cell level: compared to uninfected people, HIV-infected people with CD4+ T-cell counts ≥200 cells/mm3 had increased AMI risk with high CD8+ T-cell count, while those with CD4+ T-cell counts <200 cells/mm3 had increased AMI risk with low CD8+ T-cell count. CD8+ T-cell counts may add additional AMI risk stratification information beyond that provided by CD4+ T-cell counts alone
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