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Severe infection increases cardiovascular risk among HIV-infected individuals
Emersom Cicilini Mesquita1, Lara Esteves Coelho2, Rodrigo Teixeira Amancio1
1Laboratório de Pesquisa Clínica em Medicina Intensiva, Instituto Nacional de Infectologia Evandro Chagas (INI), Fundação Oswaldo Cruz (FIOCRUZ), Rio de Janeiro, Brazil.
Insights
Severe infections significantly increase cardiovascular disease risk in HIV-positive individuals, especially within the first year post-hospitalization. Effective combination antiretroviral therapy (cART) and high CD4 counts reduce this risk.
Area of Science:
- Infectious Diseases
- Cardiology
- Public Health
Background:
- Cardiovascular risk factor management is crucial for HIV-infected individuals in the post-combination antiretroviral therapy (cART) era.
- The association between severe infections and cardiovascular diseases (CVDs) warrants investigation in the HIV-infected population.
Purpose of the Study:
- To investigate the role of severe infections in the incidence of cardiovascular diseases (CVDs) among HIV-infected individuals.
- To analyze the time-dependent association between severe infections and incident CVDs.
Main Methods:
- A cohort of HIV-infected individuals (≥18 years) without prior CVD was followed from 2000 to 2013.
- Extended Cox regression models were used to analyze the risk of CVD events, stratifying follow-up time post-hospitalization (<3 months, 3-12 months, >12 months).
Main Results:
- The incidence rate of CVD among HIV-infected individuals was 11.10 per 1000 person-years.
- Severe infections increased CVD risk significantly within 3 months (aHR 4.52) and up to 1 year (aHR 2.39) post-hospitalization.
- Non-white race/ethnicity, age ≥60, and hypertension were associated with increased CVD risk, while high CD4 count and cART use were associated with reduced risk.
Conclusions:
- A time-dependent association exists between severe infections and incident CVD in HIV-infected individuals.
- Combination antiretroviral therapy (cART) use and high CD4 counts are associated with significantly reduced CVD hazards.
Background:
The identification and management of cardiovascular risk factors became a major clinical issue among HIV-infected individuals in the post-cART era. As in the past decades the link between acute infections and cardiovascular diseases became clear in the general population, we sorted to investigate the role of severe infections on incident cardiovascular diseases (CVDs) among HIV-infected individuals.
Methods:
HIV-infected individuals aged ≥18 years, with no history of CVD were followed from January 2000 to December 2013 until the occurrence of the first CVD event, death or end of study, whichever occurred first. To explore the effect of severe infections on the incidence of CVD we used extended Cox regression models and stratified post-hospitalization follow-up time into three periods: < 3 months, 3-12 months and > 12 months post discharge.
Results:
One hundred-eighty four persons from 3384 HIV-infected individuals developed incident CVD events during the follow-up (incidence rate = 11.10/1000 PY (95%CI: 9.60-12.82)). Risk of an incident CVD was 4-fold higher at < 3 months post-hospitalization for severe infections (adjusted hazard ratio [aHR], 4.52; 95% confidence interval [CI] 2.46-8.30), after adjusting for sociodemographic and clinical factors as well as comorbidities. This risk remained significant up to one year (3-12 months post hospital discharge aHR 2.39, 95% CI 1.30-4.38). Additionally, non-white race/ethnicity (aHR 1.49, 95% CI 1.10-2.02), age ≥ 60 years (aHR 2.01, 95% CI 1.01-3.97) and hypertension (aHR 1.90, 95% CI 1.38-2.60) were associated with an increased risk of CVD events. High CD4 (≥ 500 cells/mm3: aHR 0.41, 95% CI 0.27-0.62) and cART use (aHR 0.21, 95% CI 0.14-0.31) reduced the risk of CVD events.
Conclusions:
We provide evidence for a time-dependent association between severe infection and incident cardiovascular disease in HIV-infected individuals. cART use, and high CD4 count were significantly associated with reduced hazards of CVD.
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