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10-24 岁青少年和青年中,围生期和非围生期感染 HIV 的特定年龄死亡率比。

Age-specific mortality rate ratios in adolescents and youth aged 10-24 years living with perinatally versus nonperinatally acquired HIV.

机构信息

Inserm U1027, Université Paul Sabatier Toulouse 3, Toulouse, France.

Division of Infectious Diseases, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA.

出版信息

AIDS. 2021 Mar 15;35(4):625-632. doi: 10.1097/QAD.0000000000002765.


DOI:10.1097/QAD.0000000000002765
PMID:33252479
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7904586/
Abstract

OBJECTIVE: To measure mortality incidence rates and incidence rate ratios (IRR) in adolescents and youth living with perinatally acquired HIV (YPHIV) compared with those living with nonperinatally acquired HIV (YNPHIV), by region, by sex, and during the ages of 10-14, 15-19, and 20-24 years in IeDEA. DESIGN AND METHODS: All those with a confirmed HIV diagnosis, antiretroviral therapy (ART)-naive at enrollment, and who have post-ART follow-up while aged 10-24 years between 2004 and 2016 were included. We estimated post-ART mortality incidence rates and 95% confidence intervals (95% CI) per 100 person-years for YPHIV (enrolled into care <10 years of age) and YNPHIV (enrolled ≥10 years and <25 years). We estimate mortality IRRs in a negative binomial regression model, adjusted for sex, region time-varying age, CD4+ cell count at ART initiation (<350 cells/μl, ≥350 cells/μl, unknown), and time on ART (<12 and ≥12 months). RESULTS: Overall, 104 846 adolescents and youth were included: 21 340 (20%) YPHIV (50% women) and 83 506 YNPHIV (80% women). Overall mortality incidence ratios were higher among YNPHIV (incidence ratio: 2.3/100 person-years; 95% CI: 2.2-2.4) compared with YPHIV (incidence ratio: 0.7/100 person-years; 95% CI: 0.7-0.8). Among adolescents aged 10-19 years, mortality was lower among YPHIV compared with YNPHIV (all IRRs <1, ranging from 0.26, 95% CI: 0.13-0.49 in 10-14-year-old boys in the Asia-Pacific to 0.51, 95% CI: 0.30-0.87 in 15-19-year-old boys in West Africa). CONCLUSION: We report substantial amount of deaths occurring during adolescence. Mortality was significantly higher among YNPHIV compared to YPHIV. Specific interventions including HIV testing and early engagement in care are urgently needed to improve survival among YNPHIV.

摘要

目的:通过 IeDEA,按地区、性别和年龄(10-14 岁、15-19 岁和 20-24 岁)测量与先天感染 HIV 的青少年和青年(YPHIV)相比,先天感染 HIV 的青少年和青年(YPHIV)和后天感染 HIV 的青少年和青年(YNPHIV)的死亡率发生率和发病率比(IRR)。

方法和设计:所有在 2004 年至 2016 年期间被诊断为 HIV 阳性、入组时未接受抗逆转录病毒治疗(ART)、并在 10-24 岁时接受 ART 后随访的患者均被纳入研究。我们计算了 YPHIV(入组年龄<10 岁)和 YNPHIV(入组年龄≥10 岁且<25 岁)的每 100 人年的 ART 后死亡率发生率和 95%置信区间(95%CI)。我们在负二项回归模型中估计死亡率 IRR,模型调整了性别、区域时间变化的年龄、ART 起始时的 CD4+细胞计数(<350 个/μl、≥350 个/μl、未知)和 ART 时间(<12 个月和≥12 个月)。

结果:总体而言,共有 104846 名青少年和青年被纳入研究:21340 名(20%)YPHIV(50%为女性)和 83506 名 YNPHIV(80%为女性)。YNPHIV 的总体死亡率发生率高于 YPHIV(发病率比:2.3/100 人年;95%CI:2.2-2.4)。在 10-19 岁的青少年中,YPHIV 的死亡率低于 YNPHIV(所有 IRR<1,范围从 10-14 岁男孩的 0.26(95%CI:0.13-0.49)到西非 15-19 岁男孩的 0.51(95%CI:0.30-0.87)。

结论:我们报告了大量在青春期发生的死亡事件。YNPHIV 的死亡率明显高于 YPHIV。迫切需要包括 HIV 检测和早期参与护理在内的具体干预措施,以提高 YNPHIV 的生存率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dcee/7924975/184905e3caf3/aids-35-625-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dcee/7924975/3bb908b8586f/aids-35-625-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dcee/7924975/184905e3caf3/aids-35-625-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dcee/7924975/3bb908b8586f/aids-35-625-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dcee/7924975/184905e3caf3/aids-35-625-g002.jpg

相似文献

[1]
Age-specific mortality rate ratios in adolescents and youth aged 10-24 years living with perinatally versus nonperinatally acquired HIV.

AIDS. 2021-3-15

[2]
Age-specific all-cause mortality rates among adolescents and youth living with and without HIV: Evidence from a cohort study in South Africa.

J Int AIDS Soc. 2025-6

[3]
Projecting the Clinical and Economic Impacts of Changes to HIV Care Among Adolescents and Young Adults in the United States: Lessons From the COVID-19 Pandemic.

J Pediatric Infect Dis Soc. 2024-1-29

[4]
Antiretroviral therapy (ART) for treating HIV infection in ART-eligible pregnant women.

Cochrane Database Syst Rev. 2010-3-17

[5]
Optimisation of antiretroviral therapy in HIV-infected children under 3 years of age.

Cochrane Database Syst Rev. 2014-5-22

[6]
Global HIV mortality trends among children on antiretroviral treatment corrected for under-reported deaths: an updated analysis of the International epidemiology Databases to Evaluate AIDS collaboration.

J Int AIDS Soc. 2021-9

[7]
Incidence of unintended pregnancies and pregnancy experience among adolescents living with perinatally-acquired HIV in West Africa: a mixed-method study.

BMC Public Health. 2025-1-30

[8]
Differences in clinical characteristics between adolescents and young adults with perinatally and sexually acquired HIV in the Asia-Pacific region.

J Int AIDS Soc. 2025-4

[9]
HIV-related mortality time trends among children and young adolescents on antiretroviral therapy by age, treatment duration, and region: a systematic review and meta-regression analysis.

Lancet HIV. 2025-9-2

[10]
Observed CD4 counts at entry into HIV care and at antiretroviral therapy prescription by age in the USA, 2004-18: a cohort study.

Lancet HIV. 2022-3

引用本文的文献

[1]
Age-specific all-cause mortality rates among adolescents and youth living with and without HIV: Evidence from a cohort study in South Africa.

J Int AIDS Soc. 2025-6

[2]
Adults with perinatally acquired HIV in low- and middle-income settings: time for a generational shift in HIV care and global guidance.

J Int AIDS Soc. 2024-7

[3]
High mortality in adolescents and young adults with perinatally-acquired HIV in Thailand during the transition to adulthood.

AIDS Care. 2024-7

[4]
Mortality and Loss to Follow-Up Among Adolescents and Young Adults Attending HIV Care Programs in Kenya.

AIDS Patient Care STDS. 2023-7

[5]
Incidence and predictors of mortality among adolescents on antiretroviral therapy in Amhara Region, Ethiopia: a retrospective cohort analysis.

BMJ Open. 2022-11-9

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