Department of Clinical Research, Indian Council of Medical Research-National Institute for Research in Tuberculosis, Chennai, India.
Division of Data Management, Biostatistics and IT, Department of Clinical Research, Indian Council of Medical Research-National AIDS Research Institute, Pune, India.
Clin Infect Dis. 2022 Aug 31;75(3):425-434. doi: 10.1093/cid/ciab964.
Metformin, by reducing intracellular Mycobacterium tuberculosis growth, can be considered an adjunctive therapy to anti-tuberculosis treatment (ATT). We determined whether metformin with standard ATT reduces time to sputum culture conversion and tissue inflammation in adults with pulmonary tuberculosis (PTB).
In a randomized, 8-week, clinical trial, newly diagnosed, culture-positive PTB patients were randomized to standard ATT (HREZ = control arm) or standard ATT plus daily 1000 mg metformin (MET-HREZ = Metformin with Rifampicin [METRIF] arm) for 8 weeks during 2018-2020 at 5 sites in India. The primary end point was time to sputum culture conversion by liquid culture during 8 weeks of ATT. Plasma inflammatory markers were estimated in a subset. A Cox proportional hazard model was used to estimate time and predictors of culture conversion.
Of the 322 patients randomized, 239 (74%) were male, and 212 (66%) had bilateral disease on chest radiograph with 54 (18%) showing cavitation. The median time to sputum culture conversion by liquid culture was 42 days in the METRIF arm and 41 days in the control arm (hazard ratio, 0.8; 95% confidence interval [CI], .624-1.019). After 8 weeks of ATT, cavitary lesions on X-ray (7, 5.3% vs 18, 12.9%; relative risk, 0.42; 95% CI, .18-.96; P = .041) and inflammatory markers were significantly lower in the METRIF arm. Higher body mass index and lower sputum smear grading were associated with faster sputum culture conversion.
The addition of metformin to standard ATT did not hasten sputum culture conversion but diminished excess inflammation, thus reducing lung tissue damage as seen by faster clearance on X-ray and reduced inflammatory markers.
Clinical Trial Registry of India (CTRI/2018/01/011176).
二甲双胍通过抑制细胞内结核分枝杆菌的生长,可被视为抗结核治疗(ATT)的辅助治疗。我们旨在确定在患有肺结核(PTB)的成年人中,二甲双胍联合标准 ATT 是否会缩短痰培养转为阴性的时间,并减轻组织炎症。
在一项随机的 8 周临床试验中,于 2018 年至 2020 年期间在印度的 5 个地点,对新诊断的、培养阳性的 PTB 患者进行了随机分组,分别接受标准 ATT(HREZ=对照组)或标准 ATT 加每日 1000mg 二甲双胍(MET-HREZ=二甲双胍联合利福平[METRIF]组)治疗 8 周。主要终点是在 ATT 的 8 周内通过液体培养达到痰培养转为阴性的时间。在亚组中估计了血浆炎症标志物。使用 Cox 比例风险模型来估计文化转变的时间和预测因素。
在 322 名随机分组的患者中,239 名(74%)为男性,212 名(66%)胸部 X 线片显示双侧病变,54 名(18%)显示空洞。在 METRIF 组中,通过液体培养达到痰培养转为阴性的中位时间为 42 天,在对照组中为 41 天(风险比,0.8;95%置信区间[CI],0.624-1.019)。在 ATT 治疗 8 周后,METRIF 组的 X 射线空洞病变(7 例,5.3% vs. 18 例,12.9%;相对风险,0.42;95%CI,0.18-0.96;P=0.041)和炎症标志物显著降低。更高的体重指数和更低的痰涂片分级与痰培养转为阴性的速度更快相关。
在标准 ATT 中添加二甲双胍并未加速痰培养转为阴性,但减轻了过度的炎症,从而通过更快地清除 X 射线和降低炎症标志物来减少肺组织损伤。
印度临床试验注册处(CTRI/2018/01/011176)。