Division of Infectious Diseases, Emory University School of Medicine, Atlanta, Georgia, USA.
Grady Healthcare System, Infectious Diseases Program, Atlanta, Georgia, USA.
Clin Infect Dis. 2021 Oct 5;73(7):e2059-e2069. doi: 10.1093/cid/ciaa1928.
Human immunodeficiency virus (HIV) infection may accelerate development of aging-related non-AIDS comorbidities (NACMs). The incidence of NACMs is poorly characterized among women living with HIV (WLWH).
WLWH and HIV-seronegative participants followed in the Women's Interagency HIV Study (WIHS) through 2009 (when >80% of WLWH used antiretroviral therapy) or onward were included, with outcomes measured through 31 March 2018. Sociodemographics, clinical covariates, and prevalent NACM were determined at enrollment. We used Poisson regression models to determine incident NACM burden (number of NACMs accrued through most recent WIHS visit out of 10 total NACMs assessed) by HIV serostatus and age.
There were 3129 participants (2239 WLWH, 890 HIV seronegative) with 36 589 person-years of follow-up. At enrollment, median age was 37 years, 65% were black, and 47% currently smoked. In fully adjusted analyses, WLWH had a higher incident NACM rate compared with HIV-seronegative women (incidence rate ratio, 1.36 [95% confidence interval (CI), 1.02-1.81]). Incident NACM burden was higher among WLWH vs HIV-seronegative women in most age strata (HIV × age interaction: P = .0438), and women <25 years old had the greatest incidence rate ratio by HIV serostatus at 1.48 (95% CI, 1.19-1.84) compared with those in older age groups. Incident NACM burden was associated with traditional comorbidity risk factors but not HIV-specific indices.
Incident NACM burden was higher among WLWH than HIV-seronegative women. This difference was most dramatic among women aged <25 years, a group for whom routine comorbidity screening is not prioritized. Established non-HIV comorbidity risk factors were significantly associated with incident NACM burden. More data are needed to inform best practices for NACM screening, prevention, and management among WLWH, particularly young women.
人类免疫缺陷病毒(HIV)感染可能会加速与衰老相关的非艾滋病合并症(NACMs)的发展。HIV 感染者(WLWH)中 NACMs 的发病率特征描述较差。
在妇女艾滋病研究机构间研究(WIHS)中,将在 2009 年之前(当时超过 80%的 WLWH 使用抗逆转录病毒疗法)或之后接受随访的 HIV 血清阴性参与者纳入研究,结果测量截止至 2018 年 3 月 31 日。在入组时确定社会人口统计学、临床协变量和普遍存在的 NACM。我们使用泊松回归模型来确定 HIV 血清学状态和年龄对 NACM 负担(在最近的 WIHS 就诊中发生的 NACM 数量,占总共评估的 10 种 NACM)的影响。
共有 3129 名参与者(2239 名 WLWH,890 名 HIV 血清阴性),随访 36589 人年。入组时,中位年龄为 37 岁,65%为黑人,47%目前吸烟。在完全调整的分析中,与 HIV 血清阴性女性相比,WLWH 的 NACM 发病率更高(发病率比,1.36[95%置信区间(CI),1.02-1.81])。在大多数年龄组中,WLWH 的 NACM 负担均高于 HIV 血清阴性女性(HIV×年龄交互作用:P=0.0438),与年龄较大的组相比,年龄<25 岁的女性 HIV 血清学状态的发病率比最高,为 1.48(95%CI,1.19-1.84)。NACM 负担与传统的合并症危险因素相关,但与 HIV 特异性指标无关。
与 HIV 血清阴性女性相比,WLWH 的 NACM 负担更高。在年龄<25 岁的女性中,这种差异最为显著,而这一年龄组并未将常规合并症筛查作为优先事项。已建立的非 HIV 合并症危险因素与 NACM 负担的发生显著相关。需要更多的数据来为 WLWH,尤其是年轻女性的 NACM 筛查、预防和管理提供最佳实践。