John-Olabode Sarah O, Akintan Patricia, Okunade Kehinde S, Ajie Iwuchukwu
Haematology and Blood Transfusion, College of Medicine, University of Lagos, Lagos, NGA.
Paediatrics, College of Medicine, University of Lagos, Lagos, NGA.
Cureus. 2023 May 29;15(5):e39626. doi: 10.7759/cureus.39626. eCollection 2023 May.
Background Selenium is an essential micronutrient that plays a crucial role in a wide range of physiological processes, including immune responses. Selenium deficiency has been recognized as an associated factor in the progression of HIV to advanced HIV disease and/or mortality. Although selenium supplementation has been shown to reduce hospitalizations and improve cellular immunity, the evidence remains mixed. This study aimed to determine the prevalence of selenium deficiency and its relationship with HIV disease markers in HIV-infected children at the Lagos University Teaching Hospital. Methodology This is a cross-sectional, comparative, pilot study of plasma concentrations of selenium in HIV-infected (n = 30) and non-infected (n = 20) children enrolled in the pediatric HIV clinic of the Lagos University Teaching Hospital, Lagos, Nigeria, from May 2019 to May 2021. HIV-infected children were on stable antiretroviral therapy (ART) with an undetectable viral load. The serum concentration of selenium was measured using the automated atomic absorption spectrophotometer (hydride generation method). Logistic regression was used to study the effect of selenium status on the levels of HIV disease markers (CD4 count, viral load, weight, opportunistic infections) in the study participants. Results The median age of all participants was nine (4-12) years, with 74% being boys. The mean selenium concentrations were lower in HIV-infected children (91.1 ± 12.0 µg/L) compared to the comparison group without HIV (147.8 ± 4.9 µg/L) (p = 0.001). After controlling for age, ART duration, markers of HIV infection, and other potentially confounding variables, participants with selenium deficiency had approximately 11-fold odds of increased hospital admissions (adjusted odds ratio = 10.57, 95% confidence interval = 1.58 to 70.99; p = 0.015). Conclusions In this study, selenium concentrations were significantly lower in HIV-infected children than in the HIV-negative comparison group. Lower serum selenium concentrations were associated with increased hospitalizations. Although our findings suggest the potential need for selenium supplementation for children living with HIV in Nigeria, further studies are warranted to determine the safety and efficacy of selenium supplementation in this key population.
背景 硒是一种必需的微量营养素,在包括免疫反应在内的广泛生理过程中发挥着关键作用。硒缺乏已被认为是HIV进展为晚期HIV疾病和/或导致死亡的一个相关因素。尽管补充硒已被证明可减少住院次数并改善细胞免疫,但证据仍不一致。本研究旨在确定拉各斯大学教学医院中感染HIV儿童的硒缺乏患病率及其与HIV疾病标志物的关系。方法 这是一项横断面、对比性的试点研究,对2019年5月至2021年5月在尼日利亚拉各斯拉各斯大学教学医院儿科HIV诊所登记的感染HIV儿童(n = 30)和未感染儿童(n = 20)的血浆硒浓度进行研究。感染HIV的儿童接受稳定的抗逆转录病毒治疗(ART),病毒载量不可检测。使用自动原子吸收分光光度计(氢化物发生法)测量血清硒浓度。采用逻辑回归研究硒状态对研究参与者中HIV疾病标志物(CD4计数、病毒载量、体重、机会性感染)水平的影响。结果 所有参与者的中位年龄为9岁(4 - 12岁),其中74%为男孩。与未感染HIV的对照组(147.8 ± 4.9 µg/L)相比,感染HIV的儿童平均硒浓度较低(91.1 ± 12.0 µg/L)(p = 0.001)。在控制年龄、ART持续时间、HIV感染标志物和其他潜在混杂变量后,硒缺乏的参与者住院次数增加的几率约为11倍(调整后的优势比 = 10.57,95%置信区间 = 1.58至70.99;p = 0.015)。结论 在本研究中,感染HIV的儿童硒浓度显著低于HIV阴性对照组。较低的血清硒浓度与住院次数增加有关。尽管我们的研究结果表明尼日利亚感染HIV儿童可能需要补充硒,但仍需进一步研究以确定在这一关键人群中补充硒的安全性和有效性。