C反应蛋白作为一种分型测试,指导谁应该接受成人肺结核诊断的确证测试:来自坦桑尼亚城市的病例对照概念验证研究

E. Chiweka, Thomas Maroa, Hosiana Temba, Joseph Ponera, S. Athumani, L. Kamwela, M. Sasamalo, Rastard Naftari, M.D.L.Q. Tito, F. Mhimbira, J. Hella
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Blood was collected from cases and controls for measuring CRP levels during recruitment. We compared socio-demographic characteristics, clinical and laboratory parameters obtained during recruitment and performed diagnostic accuracy analyses for CRP. Results: Out of all 193 study participants who were involved in final analysis, 147 (76.2%) were males. Pulmonary TB cases had significantly lower median BMI than controls (median 17.4 kg/m2 [IQR: 15.8–19.2 kg/m2] vs., 24.9 kg/m2 [IQR: 22.1–28.5 kg/m2), p < 0.001). There was no statistical difference in prevalence of HIV between PTB cases and controls i.e., 13.33% vs., 11.7%, p = 0.48. CRP was significantly higher in PTB cases vs., controls (median 67.8 mg/L, [IQR: 36.5– 116.9 mg/L] vs., 1.55 mg/L, [IQR: 0.59–6.0mg/L], p = 0.003). 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引用次数: 0

摘要

背景:目前的结核病筛查工具不足,导致结核病病例检测不足,结核病继续在社区传播。随着全世界都在努力寻找遗漏的结核病病例,需要制定新的战略来帮助快速识别结核病病例。本研究旨在评估C反应蛋白(CRP)在坦桑尼亚城市活动性肺结核诊断中的作用。方法:在肺结核(PTB)患者和无活动性PTB的接触者中进行病例对照研究。PTB的诊断采用GeneXpert MTB/RIF检测和培养。从病例和对照组中采集血液,用于在招募期间测量CRP水平。我们比较了招募期间获得的社会人口学特征、临床和实验室参数,并对CRP进行了诊断准确性分析。结果:在参与最终分析的193名研究参与者中,147名(76.2%)为男性。肺结核病例的中位BMI显著低于对照组(中位17.4 kg/m2[IQR:15.8–19.2 kg/m2]vs.24.9 kg/m2[IRR:22.1–28.5 kg/m2),p<0.001)。肺结核病例和对照组之间的HIV流行率没有统计学差异,即13.33%vs.11.7%,p=0.48。PTB患者的CRP显著高于对照组(中位数67.8 mg/L,[IQR:36.5–116.9 mg/L]vs.1.55 mg/L,[ICR:0.59–6.0mg/L],p=0.003)。此外,临界值≥10mg/L的CRP与敏感性、特异性和曲线下面积的最佳组合相关,分别为89.9%、95%CI:82.2-95.0、80.9%、71.4-88.2和0.85,95%CI:0.80-0.90。经发热、盗汗和体重指数校正后的多元逻辑回归模型显示,CRP高于10mg/L与PTB显著相关,aOR 5.2,95%CI 1.2-22.8。结论:临界CRP≥10mg/L可用于肺结核的筛查。这些发现可用于改进结核病筛查算法,将CRP与结核病症状结合起来,以确定需要进一步确认结核病检测的患者。然而,还需要更多的前瞻性研究来支持我们的发现,并为在肺结核筛查算法中使用CRP的政策建议做出贡献。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
C-Reactive Protein As a Triage Test in Guiding Who Should Get a Confirmatory Test For Pulmonary Tuberculosis Diagnosis Among Adults: A Case-Control Proof-of-Concept Study From Urban Tanzania
Background: The current screening tools for tuberculosis (TB) are inadequate resulting in insufficient TB case detection and continued community transmission of TB.As the world in geared into finding missing TB cases, new strategies are called for to aid in rapid identification of TB cases. This study aimed to evaluate the role C-reactive protein (CRP)in triaging for who to get a definitive test for active pulmonary TB diagnosis in urban Tanzania.Methods: A case–control study was conducted among pulmonary TB (PTB) patients and contacts without active PTB. The diagnosis of PTB was performed using GeneXpert MTB/RIF assay and culture. Blood was collected from cases and controls for measuring CRP levels during recruitment. We compared socio-demographic characteristics, clinical and laboratory parameters obtained during recruitment and performed diagnostic accuracy analyses for CRP. Results: Out of all 193 study participants who were involved in final analysis, 147 (76.2%) were males. Pulmonary TB cases had significantly lower median BMI than controls (median 17.4 kg/m2 [IQR: 15.8–19.2 kg/m2] vs., 24.9 kg/m2 [IQR: 22.1–28.5 kg/m2), p < 0.001). There was no statistical difference in prevalence of HIV between PTB cases and controls i.e., 13.33% vs., 11.7%, p = 0.48. CRP was significantly higher in PTB cases vs., controls (median 67.8 mg/L, [IQR: 36.5– 116.9 mg/L] vs., 1.55 mg/L, [IQR: 0.59–6.0mg/L], p = 0.003). Furthermore, CRP at cut-off ≥ 10mg/L were associated with best combination of sensitivity, specificity and area under the curve of 89.9%, 95% CI: 82.2-95.0, 80.9%, CI: 71.4-88.2 and 0.85, 95%CI: 0.80-0.90 respectively. A multivariate logistic regression model adjusted for fever, night sweats and body mass index showed that CRP above 10mg/L was significantly associated with PTB, aOR 5.2, 95% CI 1.2-22.8. Conclusions: CRP at cut-off ≥ 10mg/L can be used to screen pulmonary TB. These findings can be used to improve TB screening algorithm by incorporating CRP in combination with TB symptoms to identify patients who need further confirmatory TB tests. However, additional prospective studies are required to support our findings and contribute into policy recommendations on use of CRP in a screening algorithm for pulmonary TB.
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