Freimane Lauma, Kivrāne Agnija, Ulanova Viktorija, Vīksna Anda, Sevostjanovs Eduards, Grīnberga Solveiga, Cīrule Andra, Krams Alvils, Ranka Renāte
Latvian Biomedical Research and Study Centre, Ratsupites street 1, k-1, Riga, LV-1067, Latvia.
Riga Stradiņš University, Pharmacogenetic and Precision Medicine Laboratory, Konsula street 21, Riga, LV-1007, Latvia.
Tuberculosis (Edinb). 2025 Mar;151:102611. doi: 10.1016/j.tube.2025.102611. Epub 2025 Jan 21.
Biomarker research characterising the effect of anti-tuberculosis (TB) chemotherapy on systemic body response is still limited. In this study, we aimed to investigate fluctuations in circulating cell-free mitochondrial DNA (ccf-mtDNA) and circulating cell-free nuclear DNA (ccf-nDNA) copy number (CN) in blood plasma of patients with drug-susceptible TB (DS-TB) and to decipher factors related to these fluctuations. The results showed considerable changes in ccf-mtDNA CN in plasma samples before drug intake and 2 and 6 h afterwards, with high inter patient variability at each time point. Multivariate linear regression revealed that the dynamics of ccf-mtDNA CN was influenced by patients' age, ethambutol pharmacokinetics, and body-mass index (BMI); ethambutol exposure emerged as the most significant factor. Very low ccf-nDNA CN in all three time points with little variation was observed; none factors were strongly associated with ccf-nDNA. In conclusion, our study revealed the effect of anti-TB chemotherapy, age and BMI on acute changes in circulating ccf-mtDNA CN in blood plasma and highlighted the systemic, mitochondria-related effects of ethambutol in patients with TB. Further studies with larger cohorts are needed to understand the biological relevance of ccf-DNA in patients with TB and to validate its application in TB treatment monitoring.
表征抗结核化疗对全身机体反应影响的生物标志物研究仍然有限。在本研究中,我们旨在调查药物敏感型结核病(DS-TB)患者血浆中循环游离线粒体DNA(ccf-mtDNA)和循环游离核DNA(ccf-nDNA)拷贝数(CN)的波动情况,并解读与这些波动相关的因素。结果显示,服药前以及服药后2小时和6小时血浆样本中的ccf-mtDNA CN有显著变化,每个时间点患者间的变异性都很高。多变量线性回归显示,ccf-mtDNA CN的动态变化受患者年龄、乙胺丁醇药代动力学和体重指数(BMI)影响;乙胺丁醇暴露是最显著的因素。在所有三个时间点均观察到ccf-nDNA CN极低且变化很小;没有因素与ccf-nDNA密切相关。总之,我们的研究揭示了抗结核化疗、年龄和BMI对血浆中循环ccf-mtDNA CN急性变化的影响,并突出了乙胺丁醇在结核病患者中的全身线粒体相关效应。需要开展更大样本队列的进一步研究,以了解ccf-DNA在结核病患者中的生物学相关性,并验证其在结核病治疗监测中的应用。