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. 2024 Oct:147:107199.
doi: 10.1016/j.ijid.2024.107199. Epub 2024 Aug 13.

Risk of tuberculosis after initiation of antiretroviral therapy among persons with HIV in Europe

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Free article

Risk of tuberculosis after initiation of antiretroviral therapy among persons with HIV in Europe

Isik S Johansen et al. Int J Infect Dis. 2024 Oct.
Free article

Abstract

Objectives: Tuberculosis (TB) risk after initiation of antiretroviral treatment (ART) is not well described in a European setting, with an average TB incidence of 25/105 in the background population.

Methods: We included all adult persons with HIV starting ART in the RESPOND cohort between 2012 and 2020. TB incidence rates (IR) were assessed for consecutive time intervals post-ART initiation. Risk factors for TB within 6 months from ART initiation were evaluated using Poisson regression models.

Results: Among 8441 persons with HIV, who started ART, 66 developed TB during 34,239 person-years of follow-up (PYFU), corresponding to 1.87/1000 PYFU (95% confidence interval [CI]: 1.47-2.37). TB IR was highest in the first 3 months after ART initiation (14.41/1000 PY (95%CI 10.08-20.61]) and declined at 3-6, 6-12, and >12 months post-ART initiation (5.89 [95%CI 3.35-10.37], 2.54 [95%CI 1.36-4.73] and 0.51 [95%CI 0.30-0.86]), respectively. Independent risk factors for TB within the first 6 months after ART initiation included follow-up in Northern or Eastern Europe region, African origin, baseline CD4 count <200 cells/mm3, HIV RNA >100,000 copies/mL, injecting drug use and heterosexual transmission.

Conclusions: TB IR was highest in the first 3 months post-ART initiation and was associated with baseline risk factors, highlighting the importance of thorough TB risk assessment at ART initiation.

Keywords: AIDS; ART; TB/HIV; incidence.

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Conflict of interest statement

Declarations of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: JN received honoraria for presentations from Oxford Immunotec and ViiV and working on the advisory board of Gilead Sciences and ViiV. OK received honoraria for presentations at meetings supported by Merck, unconditional research grants from Gilead and travel support from Gilead and Viiv. HG, JR are employees of ViiV Healthcare, Gilead Sciences, respectively. The remaining authors declared no conflicts of interests.

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