Evidence map›Paper›PMID 39298089›Full record

ArticleIrish journal of medical science2024

Clinical diagnostic value of CRISPR-Cas13a-based molecular technology for tuberculosis.

Kai Wu, Zhenyao Wu, Xiongjie Li

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Article in Irish journal of medical science, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Kai WuDepartment of Thoracic Surgery, Jianghan Oilfield General Hospital, No. T32 Ankang Road, Qianjiang, 433124, Hubei, China.
Zhenyao WuDepartment of Thoracic Surgery, Jianghan Oilfield General Hospital, No. T32 Ankang Road, Qianjiang, 433124, Hubei, China.
Xiongjie LiDepartment of Thoracic Surgery, Jianghan Oilfield General Hospital, No. T32 Ankang Road, Qianjiang, 433124, Hubei, China. Lixiongjie6049@163.com.ORCID http://orcid.org/0009-0009-2377-124X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo address the clinical diagnostic value of CRISPR-Cas13a-based molecular technology for tuberculosis (TB).

methodsThe 189 suspected TB patients were simultaneously sent for acid-fast staining smear of bronchoalveolar lavage fluid, MGIT 960 cultures, Xpert MTB/RIF assay, and CRISPR-Cas13a assay. Using the final clinical diagnosis as the gold standard, the TB and non-TB groups were determined, and the diagnostic values of the four assays and the combined test in TB were compared. Using MGIT 960 culture as the gold standard, the diagnostic value of CRISPR-Cas13a assay was explored in TB, and the concordance between the CRISPR-Cas13a assay and MGIT 960 culture was compared.

resultsThe 189 preliminary diagnosed patients with suspected TB were diagnosed, with 147 in the TB group and 42 in the non-TB group. Taking the final clinical diagnosis as the gold standard, the sensitivity, negative predictive value, and accuracy of CRISPR-Cas13a assay, MGIT 960 culture, and XpertMTB/RIF assay were higher than those of acid-fast staining smear; by comparing the area under the ROC curve, the diagnostic value of the CRISPR-Cas13a assay, MGIT 960 culture, and XpertMTB/RIF assay was superior to that of acid-fast staining smear (all P < 0.05). Using the MGIT 960 culture results as the gold standard, there was a moderate concordance between the CRISPR-Cas13a assay and the MGIT 960 culture (kappa = 0.666).

conclusionBronchoalveolar lavage fluid CRISPR-Cas13a assay has high application value in the clinical diagnosis of TB and can be recommended for the initial screening of patients with suspected TB.

Indexed as

CRISPR-Cas SystemsAdultAgedBronchoalveolar Lavage FluidFemaleHumansMaleMiddle AgedMycobacterium tuberculosisSensitivity and SpecificityTuberculosisTuberculosis, PulmonaryBronchoalveolar lavage fluidCRISPR-Cas13aDiagnostic valueSensitivitySpecificityTuberculosis

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.