Department of Infectious Diseases, Amsterdam Infection and Immunity Institute, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, Netherlands; Department of Global Health, Amsterdam Institute for Global Health and Development and Amsterdam Public Health Research Institute, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, Netherlands.
HIV Monitoring Foundation, Amsterdam, Netherlands; Department of Infectious Diseases, Public Health Service of Amsterdam, Amsterdam, Netherlands.
Lancet Healthy Longev. 2021 Apr;2(4):e202-e211. doi: 10.1016/S2666-7568(21)00033-7.
The AGEIV cohort study is a prospective cohort study evaluating the occurrence of age-related comorbidities in people living with and without HIV. We previously reported a lower forced vital capacity (FVC) in HIV-positive compared with HIV-negative participants in those without heavy smoking exposure at time of enrolment in the AGEIV cohort study. In this study we evaluate longitudinal changes in spirometry indices in the same AGEIV cohort accounting for smoking behaviour and other risk factors.
We obtained pre-bronchodilator spirometry measurements in AGEIV cohort participants during biennial visits over a median of 5·9 years (IQR 5·7-6·0). Adjusted declines in forced expiratory volume in 1 s (FEV), FVC, and FEV/FVC ratio were modelled using linear mixed-effects models and compared by HIV status and smoking status. To evaluate whether changes in spirometry measurements could be driven by increased levels of chronic inflammation, we assessed associations between rates of FEV and FVC decline and CD4 and CD8 T-cell counts, and plasma concentrations of C-reactive protein (CRP), interleukin 6, soluble CD14, soluble CD163, and intestinal fatty-acid-binding protein in separate models. The study is registered at ClinicalTrials.gov, NCT01466582.
500 HIV-positive and 481 HIV-negative participants were included with spirometry data from Oct 29, 2010, to Aug 14, 2018. HIV-positive participants were virally suppressed (<40 copies per mL) during 1627 (95%) study visits, and 159 (32%) HIV-positive and 183 (38%) HIV-negative participants had never smoked. Adjusted declines in FEV were 10·0 mL per year faster in HIV-positive non-smokers (95% CI 4·2 to 15·7, p=0·00066) compared with HIV-negative non-smokers, and 11·1 mL per year faster in HIV-positive smokers (95% CI 0·7 to 21·4, p=0·036) compared with HIV-negative smokers. In comparison, smoking was associated with a 16·4 mL per year steeper decline in FEV among HIV-positive participants (95% CI 8·0 to 24·7, p=0·00012), and 15·3 mL per year steeper decline among HIV-negative participants (95% CI 6·7-24·0, p=0·00052) compared with not smoking. Adjusted yearly declines in FEV and FVC, but not FEV/FVC, were significantly greater in HIV-positive than HIV-negative participants overall (additional decline in HIV-positive participants, FEV 10·5 mL per year [95% CI 4·7 to 16·3], p=0·00040; FVC 11·5 mL per year [2·8 to 20·3], p=0·0096; FEV/FVC 0·07% per year [-0·05 to 0·19], p=0·26), with a similar observation for never-smokers (FEV 6·0 mL per year [-1·8 to 13·7], p=0·13; FVC 9·1 mL per year [-3·0 to 21·1], p=0·14; FEV/FVC ratio 0·00% per year [-0·18 to -0·18], p=0·97). Higher CRP concentrations during follow-up were associated with accelerated declines in FEV and FVC among HIV-positive participants but not among HIV-negative participants.
Treated HIV infection was associated with faster declines in both FEV and FVC, but not in the FEV/FVC ratio. These changes were independent of smoking and might have been driven by ongoing interstitial or small airway damage, potentially related to increased inflammation.
ZonMW, Aidsfonds, Gilead Sciences, ViiV Healthcare, Janssen Pharmaceuticals, Merck.
AGEIV 队列研究是一项前瞻性队列研究,评估了患有和不患有 HIV 的人群中与年龄相关的合并症的发生情况。我们之前报道过,在 AGEIV 队列研究中,与 HIV 阴性参与者相比,没有大量吸烟史的 HIV 阳性参与者的用力肺活量(FVC)较低。在这项研究中,我们评估了同一 AGEIV 队列中 spirometry 指标的纵向变化,考虑了吸烟行为和其他危险因素。
我们在中位时间为 5.9 年(IQR 5.7-6.0)的两年一次访视中,在 AGEIV 队列参与者中获得了支气管扩张剂前 spirometry 测量值。使用线性混合效应模型对 1 秒用力呼气量(FEV)、FVC 和 FEV/FVC 比值的调整下降进行建模,并根据 HIV 状态和吸烟状态进行比较。为了评估 spirometry 测量值的变化是否可以由慢性炎症水平的增加驱动,我们评估了 FEV 和 FVC 下降率与 CD4 和 CD8 T 细胞计数以及血浆 C 反应蛋白(CRP)、白细胞介素 6(IL-6)、可溶性 CD14、可溶性 CD163 和肠脂肪酸结合蛋白之间的相关性在单独的模型中。该研究在 ClinicalTrials.gov 注册,NCT01466582。
共有 500 名 HIV 阳性和 481 名 HIV 阴性参与者纳入研究,其中包括 2010 年 10 月 29 日至 2018 年 8 月 14 日的 spirometry 数据。在 1627 次研究访视中(95%),HIV 阳性参与者的病毒得到抑制(<40 拷贝/ml),159 名(32%)HIV 阳性和 183 名(38%)HIV 阴性参与者从未吸烟。与 HIV 阴性非吸烟者相比,HIV 阳性非吸烟者的 FEV 调整后每年下降 10.0ml(95%CI 4.2-15.7,p=0.00066),与 HIV 阴性吸烟者相比,HIV 阳性吸烟者的 FEV 调整后每年下降 11.1ml(95%CI 0.7-21.4,p=0.036)。相比之下,吸烟与 HIV 阳性参与者的 FEV 每年下降 16.4ml(95%CI 8.0-24.7,p=0.00012)和 HIV 阴性参与者的 FEV 每年下降 15.3ml(95%CI 6.7-24.0,p=0.00052)有关,与不吸烟相比。总体而言,与 HIV 阴性参与者相比,HIV 阳性参与者的 FEV 和 FVC 调整后每年下降幅度更大,但 FEV/FVC 无显著差异(HIV 阳性参与者的额外下降,FEV 每年 10.5ml[95%CI 4.7-16.3],p=0.00040;FVC 每年 11.5ml[2.8-20.3],p=0.0096;FEV/FVC 每年增加 0.07%[-0.05-0.19],p=0.26),从未吸烟者也有类似的观察结果(FEV 每年 6.0ml[-1.8-13.7],p=0.13;FVC 每年 9.1ml[-3.0-21.1],p=0.14;FEV/FVC 比值每年增加 0.00%[-0.18-0.18],p=0.97)。在随访期间,更高的 CRP 浓度与 HIV 阳性参与者的 FEV 和 FVC 下降加速有关,但与 HIV 阴性参与者无关。
经治疗的 HIV 感染与 FEV 和 FVC 的下降速度加快有关,但与 FEV/FVC 比值无关。这些变化独立于吸烟,可能是由持续的间质或小气道损伤引起的,可能与炎症增加有关。
ZonMW、Aidsfonds、Gilead Sciences、ViiV Healthcare、Janssen Pharmaceuticals、Merck。