Your browser doesn't support javascript.
loading
Association of HIV infection with clinical and laboratory characteristics of sickle cell disease.
Belisário, André Rolim; Blatyta, Paula F; Vivanco, Diana; Oliveira, Claudia Di Lorenzo; Carneiro-Proietti, Anna Bárbara; Sabino, Ester Cerdeira; de Almeida-Neto, Cesar; Loureiro, Paula; Máximo, Cláudia; de Oliveira Garcia Mateos, Sheila; Flor-Park, Miriam V; de Oliveira Werneck Rodrigues, Daniela; Afonso Mota, Rosimere; Gonçalez, Thelma T; Hoffmann, Thomas J; Kelly, Shannon; Custer, Brian.
Affiliation
  • Belisário AR; Fundação Hemominas, Alameda Ezequiel Dias, 321, Belo Horizonte, Minas Gerais, 30130-110, Brazil. andrebelisario@yahoo.com.br.
  • Blatyta PF; Disciplina de Ciências Médicas, Faculdade de Medicina da Universidade de São Paulo, São Paulo, SP, Brazil.
  • Vivanco D; University of California, San Francisco (UCSF), San Francisco, CA, USA.
  • Oliveira CDL; Universidade Federal de São João Del Rei, São João del Rei, Minas Gerais, Brazil.
  • Carneiro-Proietti AB; Fundação Hemominas, Alameda Ezequiel Dias, 321, Belo Horizonte, Minas Gerais, 30130-110, Brazil.
  • Sabino EC; Faculdade de Medicina (FMUSP) and Instituto de Medicina Tropical, Universidade de São Paulo, São Paulo, Brazil.
  • de Almeida-Neto C; Disciplina de Ciências Médicas, Faculdade de Medicina da Universidade de São Paulo, São Paulo, SP, Brazil.
  • Loureiro P; Fundação Pró-Sangue Hemocentro de São Paulo, São Paulo, SP, Brazil.
  • Máximo C; Fundação Hemope, Recife, Pernambuco, Brazil.
  • de Oliveira Garcia Mateos S; Universidade de Pernambuco, Recife, Pernambuco, Brazil.
  • Flor-Park MV; Fundação Hemorio, Rio de Janeiro, Brazil.
  • de Oliveira Werneck Rodrigues D; Faculdade de Medicina (FMUSP) and Instituto de Medicina Tropical, Universidade de São Paulo, São Paulo, Brazil.
  • Afonso Mota R; Fundação Hemorio, Rio de Janeiro, Brazil.
  • Gonçalez TT; ITACI, Unidade de Onco-hematologia, Instituto da Criança, HCFMUSP, São Paulo, Brazil.
  • Hoffmann TJ; Fundação Hemominas, Alameda Ezequiel Dias, 321, Belo Horizonte, Minas Gerais, 30130-110, Brazil.
  • Kelly S; Fundação Hemominas, Alameda Ezequiel Dias, 321, Belo Horizonte, Minas Gerais, 30130-110, Brazil.
  • Custer B; Vitalant Research Institute, San Francisco, USA.
BMC Infect Dis ; 20(1): 638, 2020 Aug 27.
Article in En | MEDLINE | ID: mdl-32854639
BACKGROUND: Sickle cell disease (SCD) is a multisystem disorder characterized by a wide spectrum of clinical manifestations and severity. Studies investigating potential effects of co-morbid human immunodeficiency virus (HIV) and SCD have produced conflicting results, and additional investigations are needed to elucidate whether the interaction between the two disease states might impact both HIV and SCD clinical outcomes. The association of HIV infection with clinical and laboratory characteristics of patients with SCD was assessed. METHODS: This nested case-control study included individuals with SCD with HIV treated at six Brazilian SCD centers. Clinical and laboratory data were abstracted from medical records. HIV positive participants were compared to age, gender, center, and SCD genotype matched HIV negative participants (ratio 1:4). Individual clinical outcomes as well as a composite outcome of any SCD complication and a composite outcome of any HIV-related complication were compared between the two groups. RESULTS: Fifteen HIV positive participants were included, 12 (80%) alive and 3 (20%) deceased. Most of the HIV positive patients had HbSS (60%; n = 9), 53% (n = 8) were female, and mean age was 30 ± 13 years. The frequency of individual SCD complications of acute chest syndrome/pneumonia, sepsis/bacteremia, pyelonephritis, ischemic stroke, hemorrhagic stroke, abnormal transcranial Doppler (TCD), and pulmonary hypertension was higher in HIV positive participants when compared to HIV negative, although analyzed individually none were statistically significant. HIV positive participants had significantly higher risk of any SCD complication and of a composite HIV-related complication compared to the HIV negative group (HR = 4.6; 95%CI 1.1-19.6; P = 0.04 and HR = 7.7; 95%CI 1.5-40.2; P = 0.02, respectively). There was a non-significant trend towards higher risk of any infections in participants with HIV positive (HR = 3.5; 95%CI 0.92-13.4; P = 0.07). Laboratory parameters levels were not significantly different in individuals with and without HIV. CONCLUSIONS: In summary, our study in SCD patients shows that those with HIV have an increased risk of any SCD complication and HIV-related complications, as well as a suggestive but not significantly increased risk of infections.
Subject(s)
Key words

Full text: 1 Database: MEDLINE Main subject: HIV Infections / Anemia, Sickle Cell Type of study: Observational_studies Limits: Adolescent / Adult / Female / Humans / Male Country/Region as subject: America do sul / Brasil Language: En Year: 2020 Type: Article

Full text: 1 Database: MEDLINE Main subject: HIV Infections / Anemia, Sickle Cell Type of study: Observational_studies Limits: Adolescent / Adult / Female / Humans / Male Country/Region as subject: America do sul / Brasil Language: En Year: 2020 Type: Article