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Toxoplasmic retinochoroiditis: The influence of age, number of retinochoroidal lesions and genetic polymorphism for IFN-γ +874 T/A as risk factors for recurrence in a survival analysis.
Aleixo, Ana Luisa Quintella do Couto; Vasconcelos C de Oliveira, Raquel; Cavalcanti Albuquerque, Maíra; Biancardi, Ana Luiza; Land Curi, André Luiz; Israel Benchimol, Eliezer; Reis Amendoeira, Maria Regina.
Afiliação
  • Aleixo ALQDC; Infectious Ophthalmology Laboratory, Evandro Chagas National Institute of Infectious Diseases-FIOCRUZ, Rio de Janeiro, Brazil.
  • Vasconcelos C de Oliveira R; Evandro Chagas National Institute of Infectious Diseases-FIOCRUZ, Rio de Janeiro, Brazil.
  • Cavalcanti Albuquerque M; Laboratory, Oswaldo Cruz Institute -FIOCRUZ, Rio de Janeiro, Brazil.
  • Biancardi AL; Universidade Federal do Rio de Janeiro -UFRJ, Rio de Janeiro, Brazil.
  • Land Curi AL; Infectious Ophthalmology Laboratory, Evandro Chagas National Institute of Infectious Diseases-FIOCRUZ, Rio de Janeiro, Brazil.
  • Israel Benchimol E; Infectious Ophthalmology Laboratory, Evandro Chagas National Institute of Infectious Diseases-FIOCRUZ, Rio de Janeiro, Brazil.
  • Reis Amendoeira MR; Laboratory, Oswaldo Cruz Institute -FIOCRUZ, Rio de Janeiro, Brazil.
PLoS One ; 14(2): e0211627, 2019.
Article em En | MEDLINE | ID: mdl-30753197
ABSTRACT

PURPOSE:

To analyze risk factors for recurrent toxoplasmic retinochoroiditis.

DESIGN:

Single center prospective case series. POPULATION AND

METHODS:

A total of 230 patients with toxoplasmic retinochoroiditis were prospectively followed to assess recurrences. All patients were treated with a specific drug regime for toxoplasmosis in each episode of active retinochoroiditis. Individuals with chronic diseases and pregnant women were excluded. Survival analysis by extended Cox regression model (Prentice-Williams-Peterson counting process model) was performed to evaluate the time between recurrences according to some potential risk factors age, number of retinochoroidal lesions at initial evaluation, sex and interferon gamma +874 T/A gene polymorphism. Hazard Ratios (HR) and 95% confidence intervals (CI) were provided to interpret the risk effects.

RESULTS:

One hundred sixty-two recurrence episodes were observed in 104 (45.2%) patients during follow-up that lasted from 269 to 1976 days. Mean age at presentation was 32.8 years (Standard deviation = 11.38). The risk of recurrence during follow up was influenced by age (HR = 1.02, 95% CI = 1.01-1.04) and number of retinochoroidal lesions at the beginning of the study (HR = 1.60, 95% CI = 1.07-2.40). Heterozygosis for IFN-γ gene polymorphism at position +874 T/A was also associated with recurrence (HR = 1.49, 95% CI = 1.04-2.14).

CONCLUSION:

The risk of ocular toxoplasmosis recurrence after an active episode increased with age and was significantly higher in individuals with primary lesions, which suggests that individuals with this characteristic and the elderly could benefit from recurrence prophylactic strategies with antimicrobials. Results suggest an association between IFN-γ gene polymorphism at position +874T/A and recurrence.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polimorfismo Genético / Toxoplasmose Ocular / Coriorretinite / Interferon gama Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Female / Humans / Male Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polimorfismo Genético / Toxoplasmose Ocular / Coriorretinite / Interferon gama Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Female / Humans / Male Idioma: En Ano de publicação: 2019 Tipo de documento: Article