TY - JOUR
T1 - Discovery and validation of an NMR-based metabolomic profile in urine as TB biomarker
AU - Izquierdo-Garcia, José Luis
AU - Comella-del-Barrio, Patricia
AU - Campos-Olivas, Ramón
AU - Villar-Hernández, Raquel
AU - Prat-Aymerich, Cristina
AU - De Souza-Galvão, Maria Luiza
AU - Jiménez-Fuentes, Maria Angeles
AU - Ruiz-Manzano, Juan
AU - Stojanovic, Zoran
AU - González, Adela
AU - Serra-Vidal, Mar
AU - García-García, Esther
AU - Muriel-Moreno, Beatriz
AU - Millet, Joan Pau
AU - Molina-Pinargote, Israel
AU - Casas, Xavier
AU - Santiago, Javier
AU - Sabriá, Fina
AU - Martos, Carmen
AU - Herzmann, Christian
AU - Ruiz-Cabello, Jesús
AU - Domínguez, José
N1 - Funding Information:
Authors would thank Federico Casanova (Magritek GmbH, Aachen, Germany) for providing the Spinsolve 60 Ultra Spectrometer for acquiring the LF urine spectra, and his technical support. This research was supported by: (i) a grant from the Spanish Ministry of Economy, Industry, and Competitiveness (MEIC-AEI) (SAF2017-84494-C2-1-R); (ii) a grant from the Instituto de Salud Carlos III (PI13/01546, PI16/01912, and DTS18/0092), integrated in the Plan Nacional de I+D+I, and cofounded by the ISCIII Subdirec-ción General de Evaluación and the European Reginal Development Fund (ERDF); (iii) a grant from the Socie-dad Española de Neumología y Cirugía Torácica (project 052/2011; SEPAR; Barcelona, Spain); (iv) grants from Fundación para la Innovación y la Prospectiva en Salud en España (FIPSE: 02730-16 and 3307-17); (v) a grant from the Spanish Ministry of Science and Innovation (PID2019-10656RJ-I00); (vi) a grant from the Comunidad de Madrid (B2017/BMD3875); (vii) a grant from the Gobierno Vasco, Dpto. Industria, Innovación, Comercio y Turismo, under the ELKARTEK programme (No. KK-2019/bmG19); and (viii) CPA received the support of the European Respiratory Society—ERS Short-Term Research Fellowship October 2018. STRTF201810-00467; JRC received a grant from the BBVA Foundation (Ayudas a Equipos de Investigación Científica de Biomedicina 2018). CIC biomaGUNE is supported by the Maria de Maeztu Units of Excellence programme from the Spanish State Research Agency (Grant No. MDM-2017-0720). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Publisher Copyright:
© 2020, The Author(s).
PY - 2020/12/18
Y1 - 2020/12/18
N2 - Despite efforts to improve tuberculosis (TB) detection, limitations in access, quality and timeliness of diagnostic services in low- and middle-income countries are challenging for current TB diagnostics. This study aimed to identify and characterise a metabolic profile of TB in urine by high-field nuclear magnetic resonance (NMR) spectrometry and assess whether the TB metabolic profile is also detected by a low-field benchtop NMR spectrometer. We included 189 patients with tuberculosis, 42 patients with pneumococcal pneumonia, 61 individuals infected with latent tuberculosis and 40 uninfected individuals. We acquired the urine spectra from high and low-field NMR. We characterised a TB metabolic fingerprint from the Principal Component Analysis. We developed a classification model from the Partial Least Squares-Discriminant Analysis and evaluated its performance. We identified a metabolic fingerprint of 31 chemical shift regions assigned to eight metabolites (aminoadipic acid, citrate, creatine, creatinine, glucose, mannitol, phenylalanine, and hippurate). The model developed using low-field NMR urine spectra correctly classified 87.32%, 85.21% and 100% of the TB patients compared to pneumococcal pneumonia patients, LTBI and uninfected individuals, respectively. The model validation correctly classified 84.10% of the TB patients. We have identified and characterised a metabolic profile of TB in urine from a high-field NMR spectrometer and have also detected it using a low-field benchtop NMR spectrometer. The models developed from the metabolic profile of TB identified by both NMR technologies were able to discriminate TB patients from the rest of the study groups and the results were not influenced by anti-TB treatment or TB location. This provides a new approach in the search for possible biomarkers for the diagnosis of TB.
AB - Despite efforts to improve tuberculosis (TB) detection, limitations in access, quality and timeliness of diagnostic services in low- and middle-income countries are challenging for current TB diagnostics. This study aimed to identify and characterise a metabolic profile of TB in urine by high-field nuclear magnetic resonance (NMR) spectrometry and assess whether the TB metabolic profile is also detected by a low-field benchtop NMR spectrometer. We included 189 patients with tuberculosis, 42 patients with pneumococcal pneumonia, 61 individuals infected with latent tuberculosis and 40 uninfected individuals. We acquired the urine spectra from high and low-field NMR. We characterised a TB metabolic fingerprint from the Principal Component Analysis. We developed a classification model from the Partial Least Squares-Discriminant Analysis and evaluated its performance. We identified a metabolic fingerprint of 31 chemical shift regions assigned to eight metabolites (aminoadipic acid, citrate, creatine, creatinine, glucose, mannitol, phenylalanine, and hippurate). The model developed using low-field NMR urine spectra correctly classified 87.32%, 85.21% and 100% of the TB patients compared to pneumococcal pneumonia patients, LTBI and uninfected individuals, respectively. The model validation correctly classified 84.10% of the TB patients. We have identified and characterised a metabolic profile of TB in urine from a high-field NMR spectrometer and have also detected it using a low-field benchtop NMR spectrometer. The models developed from the metabolic profile of TB identified by both NMR technologies were able to discriminate TB patients from the rest of the study groups and the results were not influenced by anti-TB treatment or TB location. This provides a new approach in the search for possible biomarkers for the diagnosis of TB.
UR - https://www.scopus.com/pages/publications/85097798273
U2 - 10.1038/s41598-020-78999-4
DO - 10.1038/s41598-020-78999-4
M3 - Article
C2 - 33339845
AN - SCOPUS:85097798273
SN - 2045-2322
VL - 10
JO - Scientific Reports
JF - Scientific Reports
IS - 1
M1 - 22317
ER -