Han Minkyung, Ha Jang Woo, Jung Inkyung, Kim Chi Young, Ahn Sung Soo
Biostatistics Collaboration Unit, Department of Biomedical Systems Informatics, Yonsei University College of Medicine, Seoul, Republic of Korea.
Division of Rheumatology, Department of Internal Medicine, Yongin Severance Hospital, Yonsei University College of Medicine, Yongin, Gyeonggi-do, Republic of Korea.
Clin Exp Rheumatol. 2024 Sep;42(9):1812-1819. doi: 10.55563/clinexprheumatol/cccp8o. Epub 2024 May 1.
Tuberculosis is a highly contagious disease that has a significant impact on global health. Emerging evidence suggests that tuberculosis can lead to an altered immune response. We investigated the association between tuberculosis and the onset of inflammatory arthritides (IA).
Patients with incident tuberculosis in the South Korean National Claims database from 2010 to 2021 were included, and those who had undergone appendectomy during 2010-2011 served as controls. The onset of IA (including seropositive rheumatoid arthritis [SPRA], ankylosing spondylitis [AS], and psoriatic arthritis [PsA]) after tuberculosis was compared between patients with tuberculosis and the control group. Sensitivity analysis was performed using stabilised inverse probability of treatment weighting (sIPTW).
A total of 408,685 patients with tuberculosis and 159,675 controls were included. During the mean follow-up of 7.5 years, a total of 1,957 (0.3%) were diagnosed with IA (SPRA, 1,397; AS, 481; and PsA, 79). Multivariable Cox hazard analysis indicated that the overall risk of IA was elevated in the tuberculosis group (hazard ratio [HR], 1.71; 95% confidence interval [CI], 1.51-1.93) compared with controls. This increased incidence in patients with tuberculosis was identical among IA subgroups even after adjustment (SPRA [HR, 1.72; 95% CI, 1.49-2.00], AS [HR, 1.64; 95% CI, 1.30-2.06], and PsA [HR, 2.59; 95% CI, 1.32-5.07]) and was replicated in the sIPTW.
The increased overall risk of developing IA after tuberculosis corroborates the hypothesis that tuberculosis can trigger dysregulated immunity. This necessitates an increased awareness of autoimmunity in this patient group.
结核病是一种具有高度传染性的疾病,对全球健康有重大影响。新出现的证据表明,结核病可导致免疫反应改变。我们调查了结核病与炎性关节炎(IA)发病之间的关联。
纳入2010年至2021年韩国国家索赔数据库中初发结核病患者,并将2010 - 2011年期间接受阑尾切除术的患者作为对照。比较结核病患者和对照组在患结核病后IA(包括血清阳性类风湿关节炎[SPRA]、强直性脊柱炎[AS]和银屑病关节炎[PsA])的发病情况。使用稳定化逆概率治疗加权法(sIPTW)进行敏感性分析。
共纳入408,685例结核病患者和159,675例对照。在平均7.5年的随访期间,共有1957例(0.3%)被诊断为IA(SPRA 1397例、AS 481例、PsA 79例)。多变量Cox风险分析表明,与对照组相比,结核病组IA的总体风险升高(风险比[HR],1.71;95%置信区间[CI],1.51 - 1.93)。即使在调整后,结核病患者中这种发病率增加在IA亚组中也是相同的(SPRA[HR,1.72;95% CI,1.49 - 2.00]、AS[HR,1.64;95% CI,1.30 - 2.06]、PsA[HR,2.59;95% CI,1.32 - 5.07]),并且在sIPTW中得到了重复验证。
结核病后发生IA的总体风险增加证实了结核病可引发免疫失调的假说。这需要提高对该患者群体自身免疫性的认识。