Evidence map›Paper›PMID 35015839›Full record

ArticleClinical infectious diseases : an official publication of the Infectious Diseases Society of America2022

Development and Validation of a Parsimonious Tuberculosis Gene Signature Using the digital NanoString nCounter Platform.

Vaishnavi Kaipilyawar, Yue Zhao, Xutao Wang, Noyal M Joseph, Selby Knudsen, Senbagavalli Prakash Babu, Muthuraj Muthaiah, Natasha S Hochberg, Sonali Sarkar, Charles R Horsburgh and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 26% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 9 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Developing a Predictive Model for Metastatic Potential in Pancreatic Neuroendocrine Tumor.The Journal of clinical endocrinology and metabolism · 2024
    Article
  6. Article
  7. Review
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

13 authors at 5 institutions in 2 countries.

Vaishnavi KaipilyawarDepartment of Medicine, Center for Emerging Pathogens, Rutgers-New Jersey Medical School, Newark, New Jersey, USA.
Yue ZhaoDepartment of Medicine, Division of Computational Biomedicine, Boston University School of Medicine, Boston, Massachusetts, USA.
Xutao WangDepartment of Medicine, Division of Computational Biomedicine, Boston University School of Medicine, Boston, Massachusetts, USA.
Noyal M JosephDepartment of Microbiology, Jawaharlal Institute of Postgraduate Medical Education and Research, Puducherry, India.
Selby KnudsenBoston Medical Center, Boston, Massachusetts, USA.
Senbagavalli Prakash BabuDepartment of Preventive and Social Medicine, Jawaharlal Institute of Postgraduate Medical Education and Research, Puducherry, India.
Muthuraj MuthaiahDepartment of Microbiology, State TB Training and Demonstration Center, Government Hospital for Chest Disease, Gorimedu, Puducherry, India.
Natasha S HochbergBoston Medical Center, Boston, Massachusetts, USA.
Sonali SarkarDepartment of Preventive and Social Medicine, Jawaharlal Institute of Postgraduate Medical Education and Research, Puducherry, India.
Charles R HorsburghDepartment of Epidemiology, Boston University School of Public Health, Boston, Massachusetts, USA.
Jerrold J EllnerDepartment of Medicine, Center for Emerging Pathogens, Rutgers-New Jersey Medical School, Newark, New Jersey, USA.
W Evan JohnsonDepartment of Medicine, Division of Computational Biomedicine, Boston University School of Medicine, Boston, Massachusetts, USA.
Padmini SalgameDepartment of Medicine, Center for Emerging Pathogens, Rutgers-New Jersey Medical School, Newark, New Jersey, USA.
Boston University · USJawaharlal Institute of Post Graduate Medical Education and Research · INBoston Medical Center · USRutgers New Jersey Medical SchoolRutgers, The State University of New Jersey · US

Funding

Validation and Application of a Model for Human-like TB Latency in RabbitsU19AI111276 · NIAID · RBHS-NEW JERSEY MEDICAL SCHOOL · PI ALLAND, DAVID, ALLAND, DAVID · 2014 to 2020
$23.3M
TB-RICC 3.0U01AI174268 · NIAID · RUTGERS BIOMEDICAL AND HEALTH SCIENCES · PI Jerrold J. Ellner, TIMOTHY R STERLING · 2023 to 2026
$15.7M
Systems Biology CoreU19AI162598 · NIAID · RUTGERS BIOMEDICAL AND HEALTH SCIENCES · PI RUSSELL, DAVID G · 2021 to 2025
$13.9M
Bacteria and Host in TB TransmissionR01AI147345 · NIAID · RUTGERS BIOMEDICAL AND HEALTH SCIENCES · PI ALLAND, DAVID, ELLNER, JERROLD J. · 2020 to 2025
$8.7M
Impact of Pregnancy on TuberculosisR01AI124217 · NIAID · RBHS-NEW JERSEY MEDICAL SCHOOL · PI ELLNER, JERROLD J. · 2015 to 2018
$2.6M
Removing batch effects in high-throughput biomedical studiesR01GM127430 · NIGMS · RUTGERS BIOMEDICAL AND HEALTH SCIENCES · PI William Evan Johnson · 2018 to 2026
$2.4M
Signature of profiling and staging the progression of TB from infection to disease.R21AI154387 · NIAID · BOSTON UNIVERSITY MEDICAL CAMPUS · PI JOHNSON, WILLIAM EVAN · 2020 to 2021
$468k
National Science Foundation OISE-9531011NIAID NIH HHS R01 AI124217NIAID NIH HHS R01 AI147345NIAID NIH HHS R21 AI154387NIAID NIH HHS U01 AI174268NIAID NIH HHS U19 AI111276NIAID NIH HHS U19 AI162598NIGMS NIH HHS R01 GM127430
6 · The paper itself

Abstract

backgroundBlood-based biomarkers for diagnosing active tuberculosis (TB), monitoring treatment response, and predicting risk of progression to TB disease have been reported. However, validation of the biomarkers across multiple independent cohorts is scarce. A robust platform to validate TB biomarkers in different populations with clinical end points is essential to the development of a point-of-care clinical test. NanoString nCounter technology is an amplification-free digital detection platform that directly measures mRNA transcripts with high specificity. Here, we determined whether NanoString could serve as a platform for extensive validation of candidate TB biomarkers.

methodsThe NanoString platform was used for performance evaluation of existing TB gene signatures in a cohort in which signatures were previously evaluated on an RNA-seq dataset. A NanoString codeset that probes 107 genes comprising 12 TB signatures and 6 housekeeping genes (NS-TB107) was developed and applied to total RNA derived from whole blood samples of TB patients and individuals with latent TB infection (LTBI) from South India. The TBSignatureProfiler tool was used to score samples for each signature. An ensemble of machine learning algorithms was used to derive a parsimonious biomarker.

resultsGene signatures present in NS-TB107 had statistically significant discriminative power for segregating TB from LTBI. Further analysis of the data yielded a NanoString 6-gene set (NANO6) that when tested on 10 published datasets was highly diagnostic for active TB.

conclusionsThe NanoString nCounter system provides a robust platform for validating existing TB biomarkers and deriving a parsimonious gene signature with enhanced diagnostic performance.

Indexed as

Latent TuberculosisMycobacterium tuberculosisTuberculosisBiomarkersHumansRNA, MessengerBiomarkersRNA, Messengerlatent TB infectionNanoStringTB biomarkerTBSignatureProfiler

Identifiers

PMID35015839
PMCPMC9522394
OpenAlexW4205826012

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.