Morimoto Helena K, Simão Andréa N C, de Almeida Elaine R D, Ueda Luiz T, Oliveira Sayonara R, de Oliveira Natalia B, Petenucci Diego L, Panis Carolina, Cecchini Rubens, Dichi Isaias, Reiche Edna M V
Department of Pathology, Clinical Analysis and Toxicology, University of Londrina, Londrina, Paraná, Brazil.
Department of Pathology, Clinical Analysis and Toxicology, University of Londrina, Londrina, Paraná, Brazil.
Nutrition. 2014 Nov-Dec;30(11-12):1324-30. doi: 10.1016/j.nut.2014.03.017. Epub 2014 Mar 30.
HIV-1 infection is accompanied by severe metabolic and immune dysfunction. The aim of this study was to evaluate the role of metabolic syndrome (MetS) and antiretroviral therapy (ART) utilization on the adiponectin levels and oxidative stress in patients infected with HIV-1.
We allocated 285 patients into four groups: group 1: patients without MetS who were not using ART; group 2: patients without MetS using ART; group 3: patients with MetS who were not using ART; and group 4: patients with MetS using ART. Biochemical, immunologic, and oxidative stress parameters were measured.
Group 4 exhibited higher lipoperoxides when compared with group 1 (P < 0.0001) and higher advanced oxidation protein products (AOPP) compared with group 2 or group 1 (P < 0.0001). Group 3 also presented higher AOPP than group 2 (P < 0.05). Group 4 showed lower adiponectin levels compared with groups 1 or 2 (P < 0.0001). Similarly, group 3 presented lower adiponectin levels compared with group 2 (P < 0.05) or group 1 (P < 0.0001). Multivariate analysis showed that both an increase in AOPP and a decrease in total radical-trapping antioxidant parameter/uric acid were independently associated with MetS in HIV-1 patients. Regarding immunologic markers of HIV-1 disease progression and viral replication, group 4 exhibited significantly higher CD45(+), CD3(+), and CD4(+) T cells count compared with group 2 (P < 0.01).
HIV-1-infected patients with MetS exhibited hypoadiponectinemia and increased oxidative stress, and these findings were not influenced by ART use. The findings of the present study allow the suggestion that MetS and inflammation might be mainly responsible for the aforementioned features. More studies are needed to verify whether drugs or food, which yield increased adiponectinemia and decreased oxidative stress, could reduce cardiovascular risk in HIV-infected patients.
HIV-1感染伴有严重的代谢和免疫功能障碍。本研究旨在评估代谢综合征(MetS)和抗逆转录病毒疗法(ART)的使用对HIV-1感染患者脂联素水平和氧化应激的作用。
我们将285例患者分为四组:第1组:未患MetS且未使用ART的患者;第2组:未患MetS但使用ART的患者;第3组:患MetS且未使用ART的患者;第4组:患MetS且使用ART的患者。检测生化、免疫和氧化应激参数。
与第1组相比,第4组的脂质过氧化物水平更高(P < 0.0001),与第2组或第1组相比,晚期氧化蛋白产物(AOPP)水平更高(P < 0.0001)。第3组的AOPP水平也高于第2组(P < 0.05)。与第1组或第2组相比,第4组的脂联素水平更低(P < 0.0001)。同样,与第2组(P < 0.05)或第1组(P < 0.0001)相比,第3组的脂联素水平更低。多变量分析显示,AOPP的增加和总自由基捕获抗氧化参数/尿酸的降低均与HIV-1患者的MetS独立相关。关于HIV-1疾病进展和病毒复制的免疫标志物,与第2组相比,第4组的CD45(+)、CD3(+)和CD4(+) T细胞计数显著更高(P < 0.01)。
患MetS的HIV-1感染患者表现为低脂联素血症和氧化应激增加,且这些发现不受ART使用的影响。本研究结果提示,MetS和炎症可能是上述特征的主要原因。需要更多研究来验证能提高脂联素血症和降低氧化应激的药物或食物是否能降低HIV感染患者的心血管风险。