Normalizing Untargeted Periconceptional Urinary Metabolomics Data: A Comparison of Approaches

被引:40
作者
Vollmar, Ana K. Rosen [1 ]
Rattray, Nicholas J. W. [1 ,2 ]
Cai, Yuping [1 ]
Santos-Neto, Alvaro J. [1 ,3 ]
Deziel, Nicole C. [1 ]
Jukic, Anne Marie Z. [4 ]
Johnson, Caroline H. [1 ]
机构
[1] Yale Sch Publ Hlth, Dept Environm Hlth Sci, New Haven, CT 06510 USA
[2] Univ Strathclyde, Strathclyde Inst Pharm & Biomed Sci, Glasgow G4 ORE, Lanark, Scotland
[3] Univ Sao Paulo, Sao Carlos Inst Chem, BR-13566590 Sao Carlos, SP, Brazil
[4] Natl Inst Environm Hlth Sci, Epidemiol Branch, Durham, NC 27709 USA
基金
巴西圣保罗研究基金会;
关键词
urinary dilution; normalization; pregnancy; creatinine; specific gravity; probabilistic quotient normalization; BATCH EFFECT CORRECTION; QUALITY-CONTROL; GRAVITY NORMALIZATION; CREATININE; SAMPLES; ADJUSTMENT; CHALLENGES; STRATEGIES; PHYSIOLOGY; DISCOVERY;
D O I
10.3390/metabo9100198
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Metabolomics studies of the early-life exposome often use maternal urine specimens to investigate critical developmental windows, including the periconceptional period and early pregnancy. During these windows changes in kidney function can impact urine concentration. This makes accounting for differential urinary dilution across samples challenging. Because there is no consensus on the ideal normalization approach for urinary metabolomics data, this study's objective was to determine the optimal post-analytical normalization approach for untargeted metabolomics analysis from a periconceptional cohort of 45 women. Urine samples consisted of 90 paired pre- and post-implantation samples. After untargeted mass spectrometry-based metabolomics analysis, we systematically compared the performance of three common approaches to adjust for urinary dilution-creatinine adjustment, specific gravity adjustment, and probabilistic quotient normalization (PQN)-using unsupervised principal components analysis, relative standard deviation (RSD) of pooled quality control samples, and orthogonal partial least-squares discriminant analysis (OPLS-DA). Results showed that creatinine adjustment is not a reliable approach to normalize urinary periconceptional metabolomics data. Either specific gravity or PQN are more reliable methods to adjust for urinary concentration, with tighter quality control sample clustering, lower RSD, and better OPLS-DA performance compared to creatinine adjustment. These findings have implications for metabolomics analyses on urine samples taken around the time of conception and in contexts where kidney function may be altered.
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页数:15
相关论文
共 53 条
[1]   Anatomical, Physiological and Metabolic Changes with Gestational Age during Normal PregnancyA Database for Parameters Required in Physiologically Based Pharmacokinetic Modelling [J].
Khaled Abduljalil ;
Penny Furness ;
Trevor N. Johnson ;
Amin Rostami-Hodjegan ;
Hora Soltani .
Clinical Pharmacokinetics, 2012, 51 (6) :365-396
[2]   Sources of Variability in Biomarker Concentrations [J].
Aylward, Lesa L. ;
Hays, Sean M. ;
Smolders, Roel ;
Koch, Holger M. ;
Cocker, John ;
Jones, Kate ;
Warren, Nicholas ;
Levy, Len ;
Bevan, Ruth .
JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH-PART B-CRITICAL REVIEWS, 2014, 17 (01) :45-61
[3]   Urinary creatinine concentrations in the US population: Implications for urinary biologic monitoring measurements [J].
Barr, DB ;
Wilder, LC ;
Caudill, SP ;
Gonzalez, AJ ;
Needham, LL ;
Pirkle, JL .
ENVIRONMENTAL HEALTH PERSPECTIVES, 2005, 113 (02) :192-200
[4]   CONTROLLING THE FALSE DISCOVERY RATE - A PRACTICAL AND POWERFUL APPROACH TO MULTIPLE TESTING [J].
BENJAMINI, Y ;
HOCHBERG, Y .
JOURNAL OF THE ROYAL STATISTICAL SOCIETY SERIES B-STATISTICAL METHODOLOGY, 1995, 57 (01) :289-300
[5]   Correction of mass calibration gaps in liquid chromatography-mass spectrometry metabolomics data [J].
Benton, H. Paul ;
Want, Elizabeth J. ;
Ebbels, Timothy M. D. .
BIOINFORMATICS, 2010, 26 (19) :2488-2489
[6]  
Blackburn ST., 2007, MATERNAL FETAL NEONA
[7]  
BOENIGER MF, 1993, AM IND HYG ASSOC J, V54, P615, DOI 10.1202/0002-8894(1993)054<0615:IOURUT>2.0.CO
[8]  
2
[9]  
Cai Y., 2019, Computational Methods and Data Analysis for Metabolomics
[10]  
Carrieri M, 2001, INT ARCH OCC ENV HEA, V74, P63