Evidence map›Paper›PMID 25867946›Full record

ArticlePloS one2015

Diagnostic values of the QuantiFERON-TB Gold In-tube assay carried out in China for diagnosing pulmonary tuberculosis.

Hui Xia, Xiaomen Wang, Fabin Li, Christophe Longuet, Guy Vernet, Delia Goletti, Yanlin Zhao, Philippe H Lagrange

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 25% of its field
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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 18 citations in OpenAlex.

  1. Pooled it
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4 · The record

Corrections and comments

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

8 authors at 6 institutions in 3 countries.

Hui XiaNational Tuberculosis Reference Laboratory, Chinese Center for Disease Control and Prevention, Beijing, People's Republic of China.
Xiaomen WangTuberculosis Control Center of Heilongjiang Province, Harbin, Heilongjiang, People's Republic of China.
Fabin LiZhejiang Provincial Center for Disease Control and Prevention, Binjiang District, Hangzhou, Zhejiang, People's Republic of China.
Christophe LonguetFondation Mérieux, Lyon, France.
Guy VernetFondation Mérieux, Lyon, France.
Delia GolettiDepartment of Epidemiology and Preclinical Research, L. Spallanzani National Institute for Infectious Diseases (INMI), Rome, Italy.
Yanlin ZhaoNational Tuberculosis Reference Laboratory, Chinese Center for Disease Control and Prevention, Beijing, People's Republic of China.
Philippe H LagrangeService de Microbiologie, Hôpital Saint Louis, Assistance Publique-Hôpitaux de Paris, Paris VII Denis Diderot University, Paris, France.
Chinese Center For Disease Control and Prevention · CNFondation Mérieux · FRAssistance Publique – Hôpitaux de Paris · FRHeilongjiang Center for Tuberculosis Control and Prevention · CNIstituto Nazionale per le Malattie Infettive Lazzaro Spallanzani · ITZhejiang Center for Disease Control and Prevention · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundInterferon-release assays (IGRAs) for diagnosing active pulmonary tuberculosis (PTB) are not yet fully validated, particularly in high TB-endemic areas as the People's Republic of China (PRC). The aim of this report was to assess the performance of the QuantiFERON-TB Gold In-tube (QFT-GIT) and tuberculin skin test (TST), in addition to microbiological results, as contributors for diagnosing active PTB in the PRC. METHODS/PRINCIPAL

findingsA total of 300 PTB patients, 41 disease controls (DC) and 59 healthy community controls (HCC) were included prospectively between May 2010 and April 2011 from two provinces of the PRC (Heilongjiang and Zhejiang). The QFT-GIT and TST yielded an overall sensitivity for active TB of 80.9% and 86.2%, and a specificity of 36.6% and 26.8%, respectively. The province of origin and smear microscopy status did not significantly impact the diagnostic values for PTB. However, using the TST with a 10 mm cut-off point, a significantly higher proportion of LTBI was observed in the DC than the HCC (p=0.01). Discordant results between the QFT-GIT and TST were found among 1/3 of the PTB, HCC and DC. Two-thirds of the individuals presented TST-positive/QFT-GIT-negative discordant results. The TST-negative/QFT-GIT-positive result was not associated with age or bacillary load. Cumulative QFT-GIT and TST positive results increased the overall sensitivity (95.9%), but it was associated with a dramatic decrease of the overall specificity (24.8%) leading to a suboptimal PPV (80.1%) and a low NPV (61.1%). CONCLUSIONS/SIGNIFICANCE: The usefulness of the QFT-GIT to diagnose active TB in high TB-endemic countries remains doubtful because like the TST, the QFT-GIT cannot distinguish between LTBI and active TB. Used as single stand-alone tests, both the QFT-GIT and TST have very limited roles in the diagnosis of active PTB. However, the combined use of SM, the TST and QFT-GIT may allow for the exclusion of ATB.

Indexed as

Reagent Kits, DiagnosticAdultCase-Control StudiesChinaFemaleHumansMaleMiddle AgedSensitivity and SpecificityTuberculosis, PulmonaryYoung AdultReagent Kits, Diagnostic

Identifiers

PMID25867946
PMCPMC4395092
OpenAlexW2103600898

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Registered trials

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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.