TY - JOUR
T1 - Circulating naive and memory CD4+ T cells and metabolic syndrome in patients with systemic lupus erythematosus
T2 - Data from a primarily Mestizo population
AU - Ugarte-Gil, Manuel F.
AU - Sánchez-Zúñiga, César
AU - Gamboa-Cárdenas, Rocío V.
AU - Aliaga-Zamudio, Madeley
AU - Zevallos, Francisco
AU - Tineo-Pozo, Giannina
AU - Cucho-Venegas, Jorge M.
AU - Mosqueira-Riveros, Ana
AU - Perich-Campos, Risto A.
AU - Alfaro-Lozano, José L.
AU - Medina, Mariela
AU - Rodríguez-Bellido, Zoila
AU - Alarcón, Graciela S.
AU - Pastor-Asurza, Cesar A.
N1 - Publisher Copyright:
© The Author 2014. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved.
PY - 2015/7/1
Y1 - 2015/7/1
N2 - 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 memory:naive 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 memory:naive 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 memory:naive 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.
AB - 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 memory:naive 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 memory:naive 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 memory:naive 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.
KW - Cardiovascular disease
KW - Metabolic syndrome
KW - Systemic lupus erythematosus
KW - T lymphocytes
UR - http://www.scopus.com/inward/record.url?scp=84936869900&partnerID=8YFLogxK
U2 - 10.1093/rheumatology/keu434
DO - 10.1093/rheumatology/keu434
M3 - Artículo
C2 - 25413944
AN - SCOPUS:84936869900
SN - 1462-0324
VL - 54
SP - 1302
EP - 1307
JO - Rheumatology
JF - Rheumatology
IS - 7
ER -