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1 H NMR Signals from Urine Excreted Protein Are a Source of Bias in Probabilistic Quotient Normalization.

Authors :
Correia GDS
Takis PG
Sands CJ
Kowalka AM
Tan T
Turtle L
Ho A
Semple MG
Openshaw PJM
Baillie JK
Takáts Z
Lewis MR
Source :
Analytical chemistry [Anal Chem] 2022 May 17; Vol. 94 (19), pp. 6919-6923. Date of Electronic Publication: 2022 May 03.
Publication Year :
2022

Abstract

Normalization to account for variation in urinary dilution is crucial for interpretation of urine metabolic profiles. Probabilistic quotient normalization (PQN) is used routinely in metabolomics but is sensitive to systematic variation shared across a large proportion of the spectral profile (>50%). Where <superscript>1</superscript> H nuclear magnetic resonance (NMR) spectroscopy is employed, the presence of urinary protein can elevate the spectral baseline and substantially impact the resulting profile. Using <superscript>1</superscript> H NMR profile measurements of spot urine samples collected from hospitalized COVID-19 patients in the ISARIC 4C study, we determined that PQN coefficients are significantly correlated with observed protein levels ( r <superscript>2</superscript> = 0.423, p < 2.2 × 10 <superscript>-16</superscript> ). This correlation was significantly reduced ( r <superscript>2</superscript> = 0.163, p < 2.2 × 10 <superscript>-16</superscript> ) when using a computational method for suppression of macromolecular signals known as small molecule enhancement spectroscopy (SMolESY) for proteinic baseline removal prior to PQN. These results highlight proteinuria as a common yet overlooked source of bias in <superscript>1</superscript> H NMR metabolic profiling studies which can be effectively mitigated using SMolESY or other macromolecular signal suppression methods before estimation of normalization coefficients.

Details

Language :
English
ISSN :
1520-6882
Volume :
94
Issue :
19
Database :
MEDLINE
Journal :
Analytical chemistry
Publication Type :
Academic Journal
Accession number :
35503092
Full Text :
https://doi.org/10.1021/acs.analchem.2c00466