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Circulating naive and memory CD4+ T cells and metabolic syndrome in patients with systemic lupus erythematosus: data from a primarily Mestizo population.
Ugarte-Gil, Manuel F; Sánchez-Zúñiga, César; Gamboa-Cárdenas, Rocío V; Aliaga-Zamudio, Madeley; Zevallos, Francisco; Tineo-Pozo, Giannina; Cucho-Venegas, Jorge M; Mosqueira-Riveros, Ana; Perich-Campos, Risto A; Alfaro-Lozano, José L; Medina, Mariela; Rodríguez-Bellido, Zoila; Alarcón, Graciela S; Pastor-Asurza, Cesar A.
Affiliation
  • Ugarte-Gil MF; Rheumatology Department, Hospital Nacional Guillermo Almenara Irigoyen, EsSalud, School of Medicine, Universidad Científica del Sur, Molecular Biology Department, Hospital Nacional Guillermo Almenara Irigoyen, EsSalud, School of Medicine, Universidad Nacional Mayor de San Marcos, Lima, Perú and Scho
  • Sánchez-Zúñiga C; Rheumatology Department, Hospital Nacional Guillermo Almenara Irigoyen, EsSalud, School of Medicine, Universidad Científica del Sur, Molecular Biology Department, Hospital Nacional Guillermo Almenara Irigoyen, EsSalud, School of Medicine, Universidad Nacional Mayor de San Marcos, Lima, Perú and Scho
  • Gamboa-Cárdenas RV; Rheumatology Department, Hospital Nacional Guillermo Almenara Irigoyen, EsSalud, School of Medicine, Universidad Científica del Sur, Molecular Biology Department, Hospital Nacional Guillermo Almenara Irigoyen, EsSalud, School of Medicine, Universidad Nacional Mayor de San Marcos, Lima, Perú and Scho
  • Aliaga-Zamudio M; Rheumatology Department, Hospital Nacional Guillermo Almenara Irigoyen, EsSalud, School of Medicine, Universidad Científica del Sur, Molecular Biology Department, Hospital Nacional Guillermo Almenara Irigoyen, EsSalud, School of Medicine, Universidad Nacional Mayor de San Marcos, Lima, Perú and Scho
  • Zevallos F; Rheumatology Department, Hospital Nacional Guillermo Almenara Irigoyen, EsSalud, School of Medicine, Universidad Científica del Sur, Molecular Biology Department, Hospital Nacional Guillermo Almenara Irigoyen, EsSalud, School of Medicine, Universidad Nacional Mayor de San Marcos, Lima, Perú and Scho
  • Tineo-Pozo G; Rheumatology Department, Hospital Nacional Guillermo Almenara Irigoyen, EsSalud, School of Medicine, Universidad Científica del Sur, Molecular Biology Department, Hospital Nacional Guillermo Almenara Irigoyen, EsSalud, School of Medicine, Universidad Nacional Mayor de San Marcos, Lima, Perú and Scho
  • Cucho-Venegas JM; Rheumatology Department, Hospital Nacional Guillermo Almenara Irigoyen, EsSalud, School of Medicine, Universidad Científica del Sur, Molecular Biology Department, Hospital Nacional Guillermo Almenara Irigoyen, EsSalud, School of Medicine, Universidad Nacional Mayor de San Marcos, Lima, Perú and Scho
  • Mosqueira-Riveros A; Rheumatology Department, Hospital Nacional Guillermo Almenara Irigoyen, EsSalud, School of Medicine, Universidad Científica del Sur, Molecular Biology Department, Hospital Nacional Guillermo Almenara Irigoyen, EsSalud, School of Medicine, Universidad Nacional Mayor de San Marcos, Lima, Perú and Scho
  • Perich-Campos RA; Rheumatology Department, Hospital Nacional Guillermo Almenara Irigoyen, EsSalud, School of Medicine, Universidad Científica del Sur, Molecular Biology Department, Hospital Nacional Guillermo Almenara Irigoyen, EsSalud, School of Medicine, Universidad Nacional Mayor de San Marcos, Lima, Perú and Scho
  • Alfaro-Lozano JL; Rheumatology Department, Hospital Nacional Guillermo Almenara Irigoyen, EsSalud, School of Medicine, Universidad Científica del Sur, Molecular Biology Department, Hospital Nacional Guillermo Almenara Irigoyen, EsSalud, School of Medicine, Universidad Nacional Mayor de San Marcos, Lima, Perú and Scho
  • Medina M; Rheumatology Department, Hospital Nacional Guillermo Almenara Irigoyen, EsSalud, School of Medicine, Universidad Científica del Sur, Molecular Biology Department, Hospital Nacional Guillermo Almenara Irigoyen, EsSalud, School of Medicine, Universidad Nacional Mayor de San Marcos, Lima, Perú and Scho
  • Rodríguez-Bellido Z; Rheumatology Department, Hospital Nacional Guillermo Almenara Irigoyen, EsSalud, School of Medicine, Universidad Científica del Sur, Molecular Biology Department, Hospital Nacional Guillermo Almenara Irigoyen, EsSalud, School of Medicine, Universidad Nacional Mayor de San Marcos, Lima, Perú and Scho
  • Alarcón GS; Rheumatology Department, Hospital Nacional Guillermo Almenara Irigoyen, EsSalud, School of Medicine, Universidad Científica del Sur, Molecular Biology Department, Hospital Nacional Guillermo Almenara Irigoyen, EsSalud, School of Medicine, Universidad Nacional Mayor de San Marcos, Lima, Perú and Scho
  • Pastor-Asurza CA; Rheumatology Department, Hospital Nacional Guillermo Almenara Irigoyen, EsSalud, School of Medicine, Universidad Científica del Sur, Molecular Biology Department, Hospital Nacional Guillermo Almenara Irigoyen, EsSalud, School of Medicine, Universidad Nacional Mayor de San Marcos, Lima, Perú and Scho
Rheumatology (Oxford) ; 54(7): 1302-7, 2015 Jul.
Article in En | MEDLINE | ID: mdl-25413944
ABSTRACT

OBJECTIVE:

The aim of this study was to determine whether the proportions of naive and memory CD4(+) T cell are independently associated with the metabolic syndrome (MetS) in patients with SLE.

METHODS:

This cross-sectional study was conducted in SLE patients seen at our rheumatology department between September 2013 and April 2014. CD4(+) T cell subpopulations were examined by flow cytometry. The association of MetS and CD4(+) T cell subpopulations was examined by Mann-Whitney U-test and by multivariable analysis, adjusting for all possible confounding variables.

RESULTS:

One hundred and seventeen patients were evaluated. Their mean age was 44.6 years (S.D. 12.6), 109 (93.2%) were female and all patients were Mestizo (mixed Caucasian and Amerindian ancestry). Fifty-two patients (44.4%) presented with MetS. Disease duration was 7.6 years (S.D. 6.8). The percentage of naive CD4(+) T cells was 25.0 (S.D. 12.7) and memory CD4(+) T cells was 66.7 (S.D. 13.2) and the memorynaive CD4(+) T cell ratio was 4.3 (S.D. 5.6). In multivariable analysis, the percentage of naive CD4(+) T cells was negatively associated with the presence of MetS [odds ratio (OR) 0.959 (95% CI 0.923, 0.997), P = 0.033], whereas the percentage of memory CD4(+)T cells and the memorynaive CD4(+) T cell ratio were positively associated with its presence [OR 1.040 (95% CI 1.003, 1.078), P = 0.031 and OR 1.238 (95% CI 1.041, 1.472), P = 0.016, respectively].

CONCLUSION:

In the SLE patients studied, a lower percentage of naive CD4(+) T cells, a higher percentage of memory CD4(+) T cells and the memorynaive CD4(+) T cell ratio were independently associated with the presence of MetS. This association could reflect the impact of immunosenescence among SLE patients with cardiovascular morbidity.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: CD4-Positive T-Lymphocytes / Indians, South American / T-Lymphocyte Subsets / Metabolic Syndrome / White People / Lupus Erythematosus, Systemic Type of study: Incidence_studies / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Female / Humans / Male / Middle aged Country/Region as subject: America do sul / Peru Language: En Journal: Rheumatology (Oxford) Journal subject: REUMATOLOGIA Year: 2015 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: CD4-Positive T-Lymphocytes / Indians, South American / T-Lymphocyte Subsets / Metabolic Syndrome / White People / Lupus Erythematosus, Systemic Type of study: Incidence_studies / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Female / Humans / Male / Middle aged Country/Region as subject: America do sul / Peru Language: En Journal: Rheumatology (Oxford) Journal subject: REUMATOLOGIA Year: 2015 Document type: Article