Department of Internal Medicine, Faculty of Medicine, Black Lion University Hospital, Addis Ababa University, Addis Ababa, Ethiopia.
Center for Infectious Medicine (CIM), F59, Department of Medicine, Karolinska University Hospital Huddinge, Karolinska Institutet, Stockholm, Sweden.
J Intern Med. 2018 Sep;284(3):292-306. doi: 10.1111/joim.12767. Epub 2018 May 23.
Immunotherapy using vitamin D (vitD ) and phenylbutyrate (PBA) may support standard drug regimens used to treat infectious diseases. We investigated if vitD + PBA enhanced clinical recovery from pulmonary tuberculosis (TB).
A randomized controlled trial was conducted in Addis Ababa, Ethiopia. Patients with smear-positive or smear-negative TB received daily oral supplementation with 5000 IU vitD and 2 × 500 mg PBA or placebo for 16 weeks, together with 6-month chemotherapy. Primary end-point: reduction of a clinical composite TB score at week 8 compared with baseline using modified intention-to-treat (mITT, n = 348) and per-protocol (n = 296) analyses. Secondary end-points: primary and modified TB scores (week 0, 4, 8, 16, 24), sputum conversion, radiological findings and plasma 25(OH)D concentrations.
Most subjects had low baseline plasma 25(OH)D levels that increased gradually in the vitD + PBA group compared with placebo (P < 0.0001) from week 0 to 16 (mean 34.7 vs. 127.4 nmol L ). In the adjusted mITT analysis, the primary TB score was significantly reduced in the intervention group at week 8 (-0.52, 95% CI -0.93, -0.10; P = 0.015) while the modified TB score was reduced at week 8 (-0.58, 95% CI -1.02, -0.14; P = 0.01) and 16 (-0.34, 95% CI -0.64, -0.03; P = 0.03). VitD + PBA had no effect on longitudinal sputum-smear conversion (P = 0.98). Clinical adverse events were more common in the placebo group (24.3%) compared with the vitD + PBA group (12.6%).
Daily supplementation with vitD + PBA may ameliorate clinical TB symptoms and disease-specific complications, while the intervention had no effect on bacterial clearance in sputum.
使用维生素 D(vitD)和苯丁酸钠(PBA)进行免疫疗法可能有助于支持用于治疗传染病的标准药物方案。我们研究了 vitD+PBA 是否能促进肺结核(TB)的临床康复。
在埃塞俄比亚亚的斯亚贝巴进行了一项随机对照试验。患有痰涂片阳性或痰涂片阴性 TB 的患者每天口服补充 5000IU vitD 和 2×500mg PBA 或安慰剂,共 16 周,同时接受 6 个月的化疗。主要终点:使用改良意向治疗(mITT,n=348)和方案治疗(n=296)分析,与基线相比,第 8 周临床复合 TB 评分的降低。次要终点:主要和改良 TB 评分(第 0、4、8、16、24 周)、痰培养转化、影像学发现和血浆 25(OH)D 浓度。
大多数患者的基线血浆 25(OH)D 水平较低,与安慰剂相比,vitD+PBA 组从第 0 周到第 16 周逐渐升高(P<0.0001)(均值 34.7 vs. 127.4 nmol/L)。在调整后的 mITT 分析中,干预组在第 8 周时主要 TB 评分显著降低(-0.52,95%CI-0.93,-0.10;P=0.015),而改良 TB 评分在第 8 周(-0.58,95%CI-1.02,-0.14;P=0.01)和第 16 周(-0.34,95%CI-0.64,-0.03;P=0.03)时降低。vitD+PBA 对纵向痰涂片转化无影响(P=0.98)。安慰剂组(24.3%)比 vitD+PBA 组(12.6%)更常见临床不良事件。
每日补充 vitD+PBA 可能改善 TB 症状和疾病特异性并发症,但干预对痰中细菌清除无影响。