Development of a Nomogram Based on Transcriptional Signatures, IFN-γ Response and Neutrophils for Diagnosis of Tuberculosis.

IF 4.2 2区 医学 Q2 IMMUNOLOGY Journal of Inflammation Research Pub Date : 2024-11-13 eCollection Date: 2024-01-01 DOI:10.2147/JIR.S480173
Yan-Hua Liu, Jin-Wen Su, Jing Jiang, Bing-Fen Yang, Zhi-Hong Cao, Fei Zhai, Wen-Na Sun, Ling-Xia Zhang, Xiao-Xing Cheng
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Abstract

Purpose: Tuberculosis (TB) is a major global health threat and its diagnosis remains challenging. This study aimed to develop a nomogram that incorporated peripheral blood transcriptional signatures and other blood tests for the diagnosis of tuberculosis.

Patients and methods: Patients with TB, patients with other definite pulmonary diseases (OPD), individuals with latent tuberculosis infection (LTBI), and healthy controls (HC) were retrospectively enrolled between May 2017 and April 2018. The results of the interferon-γ release assay (IGRA) and blood counts were obtained from medical records, and the transcripts of 10 genes were detected using reverse transcription polymerase chain reaction (RT-PCR). Variable selection was performed using least absolute shrinkage and selection operator regression (LASSO) and multivariate logistic regression was performed for the optimal prediction model with backward direction. The model was displayed as a nomogram, and its performance was evaluated for discrimination ability, calibration ability, and clinical usefulness. Internal validation of the prediction model was conducted using bootstrap resampling.

Results: A total of 185 participants were enrolled, including 84 patients with TB and 101 controls. A prediction nomogram composed of IGRA, percentage of neutrophils, and expression levels of CD64, granzyme A (GZMA), and PR/SET domain 1 (PRDM1) was established. The nomogram demonstrated good discrimination, with an unadjusted area under the curve (AUC) of 0.914 (95% CI: 0.875-0.954) and a bootstrap-corrected AUC of 0.914 (95% CI: 0.874-0.947). With a cutoff value of 0.519, the sensitivity and specificity for discriminating PTB from controls were 0.81 and 0.871, respectively. The nomogram also showed good calibration with the Hosmer-Lemeshow test (P=0.58) and good clinical practicality displayed by the decision curve analysis.

Conclusion: A nomogram composed of IGRA, percentage of neutrophils, and expression of CD64, GZMA, and PRDM1 was established. The nomogram demonstrated a sensitivity and specificity of 81% and 87%, respectively, for differentiating TB from controls.

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基于转录特征、IFN-γ 反应和中性粒细胞的结核病诊断提名图的开发。
目的:结核病(TB)是威胁全球健康的一大疾病,其诊断仍然具有挑战性。本研究旨在开发一种结合外周血转录特征和其他血液检验的提名图,用于肺结核的诊断:2017年5月至2018年4月期间,回顾性招募了肺结核患者、其他明确肺部疾病(OPD)患者、潜伏肺结核感染者(LTBI)和健康对照组(HC)。干扰素-γ释放测定(IGRA)结果和血细胞计数均来自病历,并使用反转录聚合酶链反应(RT-PCR)检测了10个基因的转录本。使用最小绝对缩减和选择算子回归(LASSO)进行变量选择,并通过多变量逻辑回归(multivariate logistic regression)建立反向最优预测模型。该模型以提名图的形式显示,并对其辨别能力、校准能力和临床实用性进行了评估。采用引导重采样法对预测模型进行了内部验证:结果:共招募了 185 名参与者,包括 84 名肺结核患者和 101 名对照者。建立了一个由 IGRA、中性粒细胞百分比以及 CD64、粒酶 A (GZMA) 和 PR/SET domain 1 (PRDM1) 表达水平组成的预测提名图。该提名图显示出良好的区分度,未经调整的曲线下面积(AUC)为 0.914(95% CI:0.875-0.954),自举校正后的 AUC 为 0.914(95% CI:0.874-0.947)。以 0.519 为临界值,区分 PTB 和对照组的灵敏度和特异度分别为 0.81 和 0.871。通过 Hosmer-Lemeshow 检验(P=0.58),提名图也显示出良好的校准性,决策曲线分析也显示出良好的临床实用性:由 IGRA、中性粒细胞百分比以及 CD64、GZMA 和 PRDM1 表达组成的提名图已经建立。该提名图在区分肺结核与对照组方面的灵敏度和特异度分别为 81% 和 87%。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Inflammation Research
Journal of Inflammation Research Immunology and Microbiology-Immunology
CiteScore
6.10
自引率
2.20%
发文量
658
审稿时长
16 weeks
期刊介绍: An international, peer-reviewed, open access, online journal that welcomes laboratory and clinical findings on the molecular basis, cell biology and pharmacology of inflammation.
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