Population-Specific Predictors of Immunologic Reconstitution Following Initiation of Combined Antiretroviral Therapy in Children: A Retrospective Observational Study from a 15-Year Cohort of HIV-Positive Children and Adolescents in Eritrea.

IF 1.5 Q4 INFECTIOUS DISEASES HIV AIDS-Research and Palliative Care Pub Date : 2024-11-06 eCollection Date: 2024-01-01 DOI:10.2147/HIV.S483094
Ghirmay Ghebrekidan Ghebremeskel, Samuel Tekle Mengistu, Misgana Teklehaimanot Tsegai, Awet Ghebreberhan Mehretab, Henok Afewerki Kidane, Yonas Tesfagabr Abraham, Robel Afeworki Habte, Habtemichael Mulugeta Teklemariam
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Abstract

Background: In the landscape of HIV treatment, combined antiretroviral therapy (cART) is a cornerstone in managing viral loads and boosting CD4+ T-cell counts. Nevertheless, disparities in treatment outcomes remain persistent, and a subset of children fail to achieve adequate immunologic reconstitution (IR). This study aims to investigate the demographic and clinical factors associated with inadequate IR in HIV-infected children in Eritrea.

Methodology: A retrospective observational study was conducted on 822 children followed at Orotta National Pediatric Referral Hospital between 2005 and 2020. Two distinct analyses were performed, with univariate and multivariate logistic regression models employed to investigate risk factors contributing to inadequate immunologic reconstitution (IR) at the study endpoints of 6- and 12-months post-cART initiation.

Results: From the initial cohort of 822 patients [53.4% were males, cohort median age at cART initiation was 78 (IQR: 48-101) months and median absolute CD4 count 270 (151-441) cells/µL]. Two separate analyses were conducted on two cohort subsets with complete data, including 456 children at the 6-month mark and 495 children at 12 months of follow-up. Following 6 months on cART, Immunologic reconstitution was achieved in 87.8% (95% CI: 84.3-91.2) and increased to 90.4% (95% CI: 87.3-93.5) after 12 months of treatment. Independent predictors of inadequate IR after 6 months of cART were higher baseline absolute CD4 counts (aOR = 1.003, (95% CI: 1.002-1.005); p-value <0.001) and NNRTI (EFV: aOR = 3.9, (95% CI: 1.3-11.9); p-value = 0.01). Meanwhile, gender (females: aOR = 0.3, (95% CI: 0.1-0.9, p-value = 0.03) and higher baseline absolute CD4 counts (aOR = 1.003, (95% CI: 1.002-1.005); p-value < 0.001) were independent risk factors of inadequate IR after 12 months of treatment.

Conclusion: The study underscores the interplay of baseline CD4 count, gender, and regimen choice in shaping the effectiveness of cART in children. Lower baseline absolute CD4 count was associated with IR after starting cART. Notably, children on EFV had a higher likelihood of inadequate IR after 6 months, and male children were more prone to insufficient IR at 12 months. Targeting these population-specific factors may be pivotal in advancing gender-responsive therapeutic strategies and improving health outcomes for HIV-infected children in sub-optimal clinical settings and resource-constrained environments.

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儿童开始联合抗逆转录病毒疗法后免疫功能恢复的人群特异性预测因素:厄立特里亚艾滋病病毒阳性儿童和青少年 15 年队列的回顾性观察研究》(A Retrospective Observational Study from a 15-Year Cohort of HIV-Positive Children and Adolescents in Eritrea)。
背景:在艾滋病治疗领域,联合抗逆转录病毒疗法(cART)是控制病毒载量和提高 CD4+ T 细胞数量的基石。然而,治疗结果的差异依然存在,一部分儿童未能实现充分的免疫重建(IR)。本研究旨在调查与厄立特里亚艾滋病病毒感染儿童免疫重建不足有关的人口和临床因素:2005年至2020年期间,奥罗塔国家儿科转诊医院对822名儿童进行了回顾性观察研究。研究采用单变量和多变量逻辑回归模型进行了两项不同的分析,以调查在开始接受抗逆转录病毒治疗后 6 个月和 12 个月的研究终点时导致免疫重建(IR)不足的风险因素:初始队列中有 822 名患者[53.4% 为男性,开始接受 cART 治疗时的队列中位年龄为 78(IQR:48-101)个月,CD4 绝对计数中位数为 270(151-441)个细胞/µL]。对数据完整的两个队列子集进行了两项单独分析,包括 456 名随访 6 个月的儿童和 495 名随访 12 个月的儿童。在接受 6 个月的 cART 治疗后,87.8%(95% CI:84.3-91.2)的儿童实现了免疫重建,而在治疗 12 个月后,这一比例上升至 90.4%(95% CI:87.3-93.5)。预测 6 个月 cART 治疗后 IR 不充分的独立因素是较高的基线 CD4 绝对计数(aOR = 1.003,(95% CI:1.002-1.005);p 值 结论:该研究强调了 CD4 绝对计数的相互作用:本研究强调了基线 CD4 细胞数、性别和治疗方案选择在影响儿童 cART 疗效方面的相互作用。基线 CD4 绝对计数较低与开始接受 cART 后的 IR 有关。值得注意的是,服用 EFV 的儿童在 6 个月后出现 IR 不足的可能性更大,而男性儿童在 12 个月后出现 IR 不足的可能性更大。针对这些人群特异性因素可能对推进性别反应治疗策略以及改善次优临床环境和资源有限环境中受艾滋病病毒感染儿童的健康状况至关重要。
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来源期刊
CiteScore
3.00
自引率
6.70%
发文量
61
审稿时长
16 weeks
期刊介绍: About Dove Medical Press Dove Medical Press Ltd is part of Taylor & Francis Group, the Academic Publishing Division of Informa PLC. We specialize in the publication of Open Access peer-reviewed journals across the broad spectrum of science, technology and especially medicine. Dove Medical Press was founded in 2003 with the objective of combining the highest editorial standards with the ''best of breed'' new publishing technologies. We have offices in Manchester and London in the United Kingdom, representatives in Princeton, New Jersey in the United States, and our editorial offices are in Auckland, New Zealand. Dr Scott Fraser is our Medical Director based in the UK. He has been in full time clinical practice for over 20 years as well as having an active research interest.
期刊最新文献
Population-Specific Predictors of Immunologic Reconstitution Following Initiation of Combined Antiretroviral Therapy in Children: A Retrospective Observational Study from a 15-Year Cohort of HIV-Positive Children and Adolescents in Eritrea. Improving Access to PMTCT Through the Involvement of Traditional Birth Attendants in Program Activities in the Far North Region of Cameroon: A Retrospective Cohort Study. Isoniazid Preventive Therapy Adherence and Its Predictors Among Soldiers on HIV Antiretroviral Therapy at a General Military Hospital in Uganda. Study on Univariate Modeling and Prediction Methods Using Monthly HIV Incidence and Mortality Cases in China. Assessment of Health-Related Quality of Life in Adults Living with HIV Attending Antiretroviral Clinics versus Traditional Healers' Offices in Bukavu City, Democratic Republic of the Congo.
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