Department of Biostatistics, Epidemiology, and Informatics, Center for Clinical Epidemiology and Biostatistics, Perelman School of Medicine at the University of Pennsylvania, 832 Blockley Hall, 423 Guardian Drive, Philadelphia, PA, 19104-6021, USA.
The Aurum Institute, Johannesburg, South Africa.
BMC Pulm Med. 2023 Feb 3;23(1):53. doi: 10.1186/s12890-023-02325-7.
Patients with tuberculosis (TB) and HIV often present with impairments in lung function and exercise capacity after treatment. We evaluated clinical and immunologic variables associated with a minimum clinically important difference (MCID) in the change in the 6 min walk test distance during the first 24 weeks of antiretroviral (ART) and anti-tubercular therapy.
Adults initiating ART and anti-TB treatment in the setting of newly-diagnosed HIV and pulmonary TB were enrolled in a prospective cohort study in South Africa. Patients underwent 6 min walk tests and spirometry at weeks 0, 4, 12, and 24 and biomarker level measurements early during treatment, at weeks 0, 4, and 12, when inflammation levels are typically elevated. Biomarkers included matrix metalloproteinases-1 (MMP-1), tissue inhibitor of MMP (TIMP)-1, collagen 1a, IL-6, IL-8, vascular cell adhesion molecule 1 (VCAM-1), C-X-C motif chemokine 10 (CXCL-10), CXCL-11, macrophage colony-stimulating factor (M-CSF), plasminogen activator, vascular endothelial growth factor, and chemokine (C-C) motif-2 (CCL-2). An MCID was derived statistically, and achievement of an MCID was modeled as the outcome using logistic regression model.
Eighty-nine patients walked an average of 393 (± standard deviation = 69) meters at baseline, which increased by an average of 9% (430 ± 70 m) at week 24. The MCID for change in walk distance was estimated as 41 m. Patients experiencing an MCID on treatment had worse lung function, lower 6 min walk test distance, higher levels of proinflammatory biomarkers including TIMP-1 and M-CSF, and lower levels of collagen 1a at baseline. Experiencing an MCID during treatment was associated with increases in forced expiratory volume in 1-s [odds ratio (OR) = 1.17, 95% confidence interval (CI) = 1.05-1.33] and increases in blood collagen 1a levels (OR = 1.31, 95%CI 1.06-1.62).
ART and TB treatment are associated with substantial improvements in 6 min walk test distance over time. Achievement of an MCID in the 6 min walk test in this study was associated with more severe disease at baseline and increases in collagen 1a levels and lung function during therapy.
结核病 (TB) 和人类免疫缺陷病毒 (HIV) 患者在治疗后常出现肺功能和运动能力受损。我们评估了与抗逆转录病毒 (ART) 和抗结核治疗最初 24 周内 6 分钟步行试验 (6MWT) 距离变化的最小临床重要差异 (MCID) 相关的临床和免疫变量。
在南非新诊断为 HIV 和肺结核的患者中,开始接受 ART 和抗结核治疗的成年人被纳入前瞻性队列研究。患者在 0 周、4 周、12 周和 24 周进行 6 分钟步行测试和肺活量测试,并在治疗早期,即炎症水平通常升高时,在 0 周、4 周和 12 周进行生物标志物水平测量。生物标志物包括基质金属蛋白酶-1 (MMP-1)、基质金属蛋白酶抑制剂 (TIMP)-1、胶原 1a、白细胞介素 6 (IL-6)、白细胞介素 8 (IL-8)、血管细胞黏附分子 1 (VCAM-1)、C-X-C 基序趋化因子 10 (CXCL-10)、C-X-C 基序趋化因子 11 (CXCL-11)、巨噬细胞集落刺激因子 (M-CSF)、纤溶酶原激活物、血管内皮生长因子和趋化因子 (C-C) 基序-2 (CCL-2)。通过统计学方法得出 MCID,并使用逻辑回归模型将达到 MCID 作为结果进行建模。
89 名患者在基线时平均行走 393(±标准偏差=69)米,在 24 周时平均增加 9%(430±70 m)。步行距离变化的 MCID 估计为 41 m。在治疗过程中经历 MCID 的患者肺功能更差,6 分钟步行测试距离更短,包括 TIMP-1 和 M-CSF 在内的促炎生物标志物水平更高,基线时胶原 1a 水平更低。在治疗过程中经历 MCID 与用力呼气量的增加有关[比值比 (OR) = 1.17,95%置信区间 (CI) = 1.05-1.33]和血液中胶原 1a 水平的增加 (OR = 1.31,95%CI 1.06-1.62)。
ART 和抗结核治疗随时间推移与 6 分钟步行测试距离的显著改善相关。在本研究中,6 分钟步行测试中达到 MCID 与基线时更严重的疾病以及治疗过程中胶原 1a 水平和肺功能的增加有关。