Wilson Douglas, Moosa Mahomed-Yunus S, Cohen Ted, Cudahy Patrick, Aldous Collen, Maartens Gary
Department of Internal Medicine, Edendale Hospital, University of KwaZulu-Natal, Pietermaritzburg, South Africa.
Division of Medicine, Department of Infectious Diseases, Nelson R Mandela School of Medicine, University of KwaZulu-Natal, Durban, South Africa.
Open Forum Infect Dis. 2018 Oct 10;5(11):ofy253. doi: 10.1093/ofid/ofy253. eCollection 2018 Nov.
Novel biomarkers are needed to assess response to antituberculosis therapy in smear-negative patients.
To evaluate the utility of C-reactive protein (CRP) in monitoring response to antituberculosis therapy, we conducted a post hoc analysis on a cohort of adults with symptoms of tuberculosis and negative sputum smears in a high-tuberculosis and HIV prevalence setting in KwaZulu-Natal, South Africa. Serial changes in CRP, weight, and hemoglobin were evaluated over 8 weeks.
Four hundred twenty-one participants being evaluated for smear-negative tuberculosis were enrolled, and 33 were excluded. Two hundred ninety-five were treated for tuberculosis (137 confirmed, 158 possible), and 93 did not have tuberculosis. One hundred and eighty-three of 213 (86%) participants who agreed to HIV testing were HIV positive. At week 8, the on-treatment median CRP reduction in the tuberculosis group (interquartile range [IQR]) was 79.5% (25.4% to 91.7%), the median weight gain was 2.3% (-1.0% to 5.6%), and the median hemoglobin increase was 7.0% (0.8% to 18.9%); < .0001 for baseline to week 8 comparison of absolute median values. Only CRP changed significantly at week 2 (median reduction [IQR], 75.1% [46.9% to 89.2%]) in the group with confirmed tuberculosis and in the possible tuberculosis group (median reduction [IQR], 49.0% [-0.4% to 80.9%]). Failure of CRP to reduce to ≤55% of the baseline value at week 2 predicted hospitalization or death in both tuberculosis groups, with 99% negative predictive value.
Change in CRP may have utility in early evaluation of response to antituberculosis treatment and to identify those at increased risk of adverse outcomes.
需要新的生物标志物来评估涂片阴性患者对抗结核治疗的反应。
为评估C反应蛋白(CRP)在监测抗结核治疗反应中的作用,我们对南非夸祖鲁 - 纳塔尔省结核病和艾滋病毒高流行地区一组有结核病症状且痰涂片阴性的成年人进行了事后分析。在8周内评估CRP、体重和血红蛋白的系列变化。
纳入421名接受涂片阴性结核病评估的参与者,排除33名。295名接受结核病治疗(137名确诊,158名可能患病),93名未患结核病。213名同意进行艾滋病毒检测的参与者中有183名(86%)为艾滋病毒阳性。在第8周时,结核病组治疗期间CRP的中位数降低(四分位间距[IQR])为79.5%(25.4%至91.7%),体重中位数增加2.3%(-1.0%至5.6%),血红蛋白中位数增加7.0%(0.8%至18.9%);基线至第8周绝对中位数比较P<0.0001。仅在确诊结核病组和可能患结核病组中,CRP在第2周有显著变化(中位数降低[IQR],分别为75.1%[46.9%至89.2%]和49.0%[-0.4%至80.9%])。在两个结核病组中,第2周时CRP未能降至基线值的≤55%可预测住院或死亡,阴性预测值为99%。
CRP变化可能有助于早期评估抗结核治疗反应,并识别不良结局风险增加的患者。