Winje Brita Askeland, White Richard, Syre Heidi, Skutlaberg Dag Harald, Oftung Fredrik, Mengshoel Anne Torunn, Blix Hege Salvesen, Brantsæter Arne Broch, Holter Ellen Kristine, Handal Nina, Simonsen Gunnar Skov, Afset Jan Egil, Bakken Kran Anne Marte
Department of Vaccine Preventable Diseases, Norwegian Institute of Public Health, Oslo, Norway.
Department of Infectious Disease Epidemiology and Modelling, Norwegian Institute of Public Health, Oslo, Norway.
Thorax. 2018 Apr 5. doi: 10.1136/thoraxjnl-2017-211147.
Targeted testing and treatment of latent TB infection (LTBI) are priorities on the global health agenda, but LTBI management remains challenging. We aimed to evaluate the prognostic value of the QuantiFERON TB-Gold (QFT) test for incident TB, focusing on the interferon (IFN)-γ level, when applied in routine practice in a low TB incidence setting.
In this large population-based prospective cohort, we linked QFT results in Norway (1 January 2009-30 June 2014) with national registry data (Norwegian Surveillance System for Infectious Diseases, Norwegian Prescription Database, Norwegian Patient Registry and Statistics Norway) to assess the prognostic value of QFT for incident TB. Participants were followed until 30 June 2016. We used restricted cubic splines to model non-linear relationships between IFN-γ levels and TB, and applied these findings to a competing risk model.
The prospective analyses included 50 389 QFT results from 44 875 individuals, of whom 257 developed TB. Overall, 22% (n=9878) of QFT results were positive. TB risk increased with the IFN-γ level until a plateau level, above which further increase was not associated with additional prognostic information. The HRs for TB were 8.8 (95% CI 4.7 to 16.5), 19.2 (95% CI 11.6 to 31.6) and 31.3 (95% CI 19.8 to 49.5) times higher with IFN-γ levels of 0.35 to <1.00, 1.00 to <4.00 and >4.00 IU/mL, respectively, compared with negative tests (<0.35 IU/mL).
Consistently, QFT demonstrates increased risk of incident TB with rising IFN-γ concentrations, indicating that IFN-γ levels may be used to guide targeted treatment of LTBI.
潜伏性结核感染(LTBI)的靶向检测和治疗是全球卫生议程的重点,但LTBI的管理仍然具有挑战性。我们旨在评估结核感染T细胞检测(QFT)试验对结核病发病的预后价值,重点关注干扰素(IFN)-γ水平,该试验应用于结核病低发病率地区的常规实践中。
在这个基于人群的大型前瞻性队列研究中,我们将挪威(2009年1月1日至2014年6月30日)的QFT结果与国家登记数据(挪威传染病监测系统、挪威处方数据库、挪威患者登记处和挪威统计局)相联系,以评估QFT对结核病发病的预后价值。对参与者进行随访至2016年6月30日。我们使用受限立方样条来模拟IFN-γ水平与结核病之间的非线性关系,并将这些结果应用于竞争风险模型。
前瞻性分析纳入了来自44875人的50389份QFT结果,其中257人发生了结核病。总体而言,22%(n = 9878)的QFT结果为阳性。结核病风险随着IFN-γ水平的升高而增加,直至达到一个平台水平,超过该水平后进一步升高与额外的预后信息无关。与阴性检测结果(< 0.35 IU/mL)相比,IFN-γ水平分别为0.35至<1.00、1.00至<4.00和>4.00 IU/mL时,结核病的风险比分别高8.8倍(95%CI 4.7至16.5)、19.2倍(95%CI 11.6至31.6)和31.3倍(95%CI 19.8至49.5)。
一致地,QFT显示随着IFN-γ浓度升高,结核病发病风险增加,表明IFN-γ水平可用于指导LTBI的靶向治疗。