Validation of Mycobacterium tuberculosis real-time polymerase chain reaction for diagnosis of tuberculous meningitis using cerebrospinal fluid samples: a pilot study

Background Timely diagnosis of tuberculous meningitis (TBM) remains challenging. Molecular diagnostic tools are necessary, particularly in low- and middle-income countries. There is no approved commercial polymerase chain reaction (PCR) assay that can be used to detect Mycobacterium tuberculosis in...

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Veröffentlicht in:Clinical chemistry and laboratory medicine 2019-04, Vol.57 (4), p.556-564
Hauptverfasser: de Almeida, Sérgio M., Borges, Conrado M., Santana, Lucas B., Golin, Gilberto, Correa, Lísia, Kussen, Gislene B., Nogueira, Keite
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container_end_page 564
container_issue 4
container_start_page 556
container_title Clinical chemistry and laboratory medicine
container_volume 57
creator de Almeida, Sérgio M.
Borges, Conrado M.
Santana, Lucas B.
Golin, Gilberto
Correa, Lísia
Kussen, Gislene B.
Nogueira, Keite
description Background Timely diagnosis of tuberculous meningitis (TBM) remains challenging. Molecular diagnostic tools are necessary, particularly in low- and middle-income countries. There is no approved commercial polymerase chain reaction (PCR) assay that can be used to detect Mycobacterium tuberculosis in non-respiratory samples, such as the cerebrospinal fluid (CSF). We aimed to validate the threshold cycle (Ct) cut-off points; calculate the operational characteristics of real-time PCR for detection of M. tuberculosis (MTb qPCR) in the CSF; and the inhibitory affect of CSF red blood cells (RBC) and total proteins on MTb qPCR. Methods A total of 334 consecutive participants were enrolled. Based on clinical, laboratory and imaging data, cases of suspected TBM were categorized as definite, probable, possible or not TBM cases. Receiver operating characteristic curve analysis was used to select the best discriminating Ct value. Results For TBM cases categorized as definite or probable (n=21), the Ct validated for CSF (≤39.5) improved the diagnostic performance of MTb qPCR on CSF samples. The sensitivity was 29%, specificity was 95%, positive predictive value was 26%, negative predictive value was 95%, efficiency was 90% and positive likelihood was 5.3. The CSF RBC and total protein did not affect the positivity of the MTb qPCR. Conclusions These data support the validation of a highly specific but low sensitive MTb qPCR assay for the TBM diagnosis using CSF samples. MTb qPCR contributes significantly to the diagnosis, mainly when associated with conventional microbiology tests and clinical algorithms.
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Molecular diagnostic tools are necessary, particularly in low- and middle-income countries. There is no approved commercial polymerase chain reaction (PCR) assay that can be used to detect Mycobacterium tuberculosis in non-respiratory samples, such as the cerebrospinal fluid (CSF). We aimed to validate the threshold cycle (Ct) cut-off points; calculate the operational characteristics of real-time PCR for detection of M. tuberculosis (MTb qPCR) in the CSF; and the inhibitory affect of CSF red blood cells (RBC) and total proteins on MTb qPCR. Methods A total of 334 consecutive participants were enrolled. Based on clinical, laboratory and imaging data, cases of suspected TBM were categorized as definite, probable, possible or not TBM cases. Receiver operating characteristic curve analysis was used to select the best discriminating Ct value. Results For TBM cases categorized as definite or probable (n=21), the Ct validated for CSF (≤39.5) improved the diagnostic performance of MTb qPCR on CSF samples. The sensitivity was 29%, specificity was 95%, positive predictive value was 26%, negative predictive value was 95%, efficiency was 90% and positive likelihood was 5.3. The CSF RBC and total protein did not affect the positivity of the MTb qPCR. Conclusions These data support the validation of a highly specific but low sensitive MTb qPCR assay for the TBM diagnosis using CSF samples. MTb qPCR contributes significantly to the diagnosis, mainly when associated with conventional microbiology tests and clinical algorithms.</description><identifier>ISSN: 1434-6621</identifier><identifier>EISSN: 1437-4331</identifier><identifier>DOI: 10.1515/cclm-2018-0524</identifier><identifier>PMID: 30267625</identifier><language>eng</language><publisher>Germany: De Gruyter</publisher><subject>Adolescent ; Adult ; Algorithms ; central nervous system ; Cerebrospinal fluid ; Cerebrospinal Fluid - microbiology ; Computed tomography ; Diagnosis ; Diagnostic software ; Diagnostic systems ; Erythrocytes ; Female ; Humans ; inhibition ; Male ; meningeal tuberculosis ; Meningitis ; Microbiology ; Middle Aged ; Mycobacterium tuberculosis ; Mycobacterium tuberculosis - genetics ; Pilot Projects ; Polymerase chain reaction ; Proteins ; Real time ; Real-Time Polymerase Chain Reaction ; Tuberculosis ; Tuberculosis, Meningeal - diagnosis ; Tuberculosis, Meningeal - microbiology ; tuberculous meningitis (TBM) ; Young Adult</subject><ispartof>Clinical chemistry and laboratory medicine, 2019-04, Vol.57 (4), p.556-564</ispartof><rights>2019 Walter de Gruyter GmbH, Berlin/Boston</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c442t-6853de1d0e586e878a8fc280a7814628aab11a17fbe9d91d84ac92d5eac42a293</citedby><cites>FETCH-LOGICAL-c442t-6853de1d0e586e878a8fc280a7814628aab11a17fbe9d91d84ac92d5eac42a293</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.degruyter.com/document/doi/10.1515/cclm-2018-0524/pdf$$EPDF$$P50$$Gwalterdegruyter$$H</linktopdf><linktohtml>$$Uhttps://www.degruyter.com/document/doi/10.1515/cclm-2018-0524/html$$EHTML$$P50$$Gwalterdegruyter$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,66754,68538</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30267625$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>de Almeida, Sérgio M.</creatorcontrib><creatorcontrib>Borges, Conrado M.</creatorcontrib><creatorcontrib>Santana, Lucas B.</creatorcontrib><creatorcontrib>Golin, Gilberto</creatorcontrib><creatorcontrib>Correa, Lísia</creatorcontrib><creatorcontrib>Kussen, Gislene B.</creatorcontrib><creatorcontrib>Nogueira, Keite</creatorcontrib><title>Validation of Mycobacterium tuberculosis real-time polymerase chain reaction for diagnosis of tuberculous meningitis using cerebrospinal fluid samples: a pilot study</title><title>Clinical chemistry and laboratory medicine</title><addtitle>Clin Chem Lab Med</addtitle><description>Background Timely diagnosis of tuberculous meningitis (TBM) remains challenging. Molecular diagnostic tools are necessary, particularly in low- and middle-income countries. There is no approved commercial polymerase chain reaction (PCR) assay that can be used to detect Mycobacterium tuberculosis in non-respiratory samples, such as the cerebrospinal fluid (CSF). We aimed to validate the threshold cycle (Ct) cut-off points; calculate the operational characteristics of real-time PCR for detection of M. tuberculosis (MTb qPCR) in the CSF; and the inhibitory affect of CSF red blood cells (RBC) and total proteins on MTb qPCR. Methods A total of 334 consecutive participants were enrolled. Based on clinical, laboratory and imaging data, cases of suspected TBM were categorized as definite, probable, possible or not TBM cases. Receiver operating characteristic curve analysis was used to select the best discriminating Ct value. Results For TBM cases categorized as definite or probable (n=21), the Ct validated for CSF (≤39.5) improved the diagnostic performance of MTb qPCR on CSF samples. The sensitivity was 29%, specificity was 95%, positive predictive value was 26%, negative predictive value was 95%, efficiency was 90% and positive likelihood was 5.3. The CSF RBC and total protein did not affect the positivity of the MTb qPCR. Conclusions These data support the validation of a highly specific but low sensitive MTb qPCR assay for the TBM diagnosis using CSF samples. 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Molecular diagnostic tools are necessary, particularly in low- and middle-income countries. There is no approved commercial polymerase chain reaction (PCR) assay that can be used to detect Mycobacterium tuberculosis in non-respiratory samples, such as the cerebrospinal fluid (CSF). We aimed to validate the threshold cycle (Ct) cut-off points; calculate the operational characteristics of real-time PCR for detection of M. tuberculosis (MTb qPCR) in the CSF; and the inhibitory affect of CSF red blood cells (RBC) and total proteins on MTb qPCR. Methods A total of 334 consecutive participants were enrolled. Based on clinical, laboratory and imaging data, cases of suspected TBM were categorized as definite, probable, possible or not TBM cases. Receiver operating characteristic curve analysis was used to select the best discriminating Ct value. Results For TBM cases categorized as definite or probable (n=21), the Ct validated for CSF (≤39.5) improved the diagnostic performance of MTb qPCR on CSF samples. The sensitivity was 29%, specificity was 95%, positive predictive value was 26%, negative predictive value was 95%, efficiency was 90% and positive likelihood was 5.3. The CSF RBC and total protein did not affect the positivity of the MTb qPCR. Conclusions These data support the validation of a highly specific but low sensitive MTb qPCR assay for the TBM diagnosis using CSF samples. MTb qPCR contributes significantly to the diagnosis, mainly when associated with conventional microbiology tests and clinical algorithms.</abstract><cop>Germany</cop><pub>De Gruyter</pub><pmid>30267625</pmid><doi>10.1515/cclm-2018-0524</doi><tpages>9</tpages></addata></record>
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source MEDLINE; De Gruyter journals
subjects Adolescent
Adult
Algorithms
central nervous system
Cerebrospinal fluid
Cerebrospinal Fluid - microbiology
Computed tomography
Diagnosis
Diagnostic software
Diagnostic systems
Erythrocytes
Female
Humans
inhibition
Male
meningeal tuberculosis
Meningitis
Microbiology
Middle Aged
Mycobacterium tuberculosis
Mycobacterium tuberculosis - genetics
Pilot Projects
Polymerase chain reaction
Proteins
Real time
Real-Time Polymerase Chain Reaction
Tuberculosis
Tuberculosis, Meningeal - diagnosis
Tuberculosis, Meningeal - microbiology
tuberculous meningitis (TBM)
Young Adult
title Validation of Mycobacterium tuberculosis real-time polymerase chain reaction for diagnosis of tuberculous meningitis using cerebrospinal fluid samples: a pilot study
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