NMR and MS urinary metabolic phenotyping in kidney diseases is fit-for-purpose in the presence of a protease inhibitor
Nephrotic syndrome with idiopathic membranous nephropathy as a major contributor, is characterized by proteinuria, hypoalbuminemia and oedema. Diagnosis is based on renal biopsy and the condition is treated using immunosuppressive drugs; however nephrotic syndrome treatment efficacy varies among patients. Multi-omic urine analyses can discover new markers of nephrotic syndrome that can be used to develop personalized treatments. For proteomics, a protease inhibitor (PI) is sometimes added at sample collection to conserve proteins but its impact on urine metabolic phenotyping needs to be evaluated. Urine from controls (n = 4) and idiopathic membranous nephropathy (iMN) patients (n = 6) were collected with and without PI addition and analysed using 1H NMR spectroscopy and UPLC-MS. PI-related data features were observed in the 1H NMR spectra but their removal followed by a median fold change normalisation, eliminated the PI contribution. PI-related metabolites in UPLC-MS data had limited effect on metabolic patterns specific to iMN. When using an appropriate data processing pipeline, PI-containing urine samples are appropriate for 1H NMR and MS metabolic profiling of patients with nephrotic syndrome.
Medienart: |
E-Artikel |
---|
Erscheinungsjahr: |
2019 |
---|---|
Erschienen: |
2019 |
Enthalten in: |
Zur Gesamtaufnahme - volume:15 |
---|---|
Enthalten in: |
Molecular omics - 15(2019), 1 vom: 11. Feb., Seite 39-49 |
Sprache: |
Englisch |
---|
Beteiligte Personen: |
Boulangé, Claire L [VerfasserIn] |
---|
Links: |
---|
Themen: |
Biomarkers |
---|
Anmerkungen: |
Date Completed 07.06.2019 Date Revised 07.06.2019 published: Print Citation Status MEDLINE |
---|
doi: |
10.1039/c8mo00190a |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
NLM293001014 |
---|
LEADER | 01000naa a22002652 4500 | ||
---|---|---|---|
001 | NLM293001014 | ||
003 | DE-627 | ||
005 | 20231225074346.0 | ||
007 | cr uuu---uuuuu | ||
008 | 231225s2019 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.1039/c8mo00190a |2 doi | |
028 | 5 | 2 | |a pubmed24n0976.xml |
035 | |a (DE-627)NLM293001014 | ||
035 | |a (NLM)30672550 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
100 | 1 | |a Boulangé, Claire L |e verfasserin |4 aut | |
245 | 1 | 0 | |a NMR and MS urinary metabolic phenotyping in kidney diseases is fit-for-purpose in the presence of a protease inhibitor |
264 | 1 | |c 2019 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a ƒaComputermedien |b c |2 rdamedia | ||
338 | |a ƒa Online-Ressource |b cr |2 rdacarrier | ||
500 | |a Date Completed 07.06.2019 | ||
500 | |a Date Revised 07.06.2019 | ||
500 | |a published: Print | ||
500 | |a Citation Status MEDLINE | ||
520 | |a Nephrotic syndrome with idiopathic membranous nephropathy as a major contributor, is characterized by proteinuria, hypoalbuminemia and oedema. Diagnosis is based on renal biopsy and the condition is treated using immunosuppressive drugs; however nephrotic syndrome treatment efficacy varies among patients. Multi-omic urine analyses can discover new markers of nephrotic syndrome that can be used to develop personalized treatments. For proteomics, a protease inhibitor (PI) is sometimes added at sample collection to conserve proteins but its impact on urine metabolic phenotyping needs to be evaluated. Urine from controls (n = 4) and idiopathic membranous nephropathy (iMN) patients (n = 6) were collected with and without PI addition and analysed using 1H NMR spectroscopy and UPLC-MS. PI-related data features were observed in the 1H NMR spectra but their removal followed by a median fold change normalisation, eliminated the PI contribution. PI-related metabolites in UPLC-MS data had limited effect on metabolic patterns specific to iMN. When using an appropriate data processing pipeline, PI-containing urine samples are appropriate for 1H NMR and MS metabolic profiling of patients with nephrotic syndrome | ||
650 | 4 | |a Journal Article | |
650 | 4 | |a Research Support, Non-U.S. Gov't | |
650 | 7 | |a Biomarkers |2 NLM | |
650 | 7 | |a Protease Inhibitors |2 NLM | |
700 | 1 | |a Rood, Ilse M |e verfasserin |4 aut | |
700 | 1 | |a Posma, Joram M |e verfasserin |4 aut | |
700 | 1 | |a Lindon, John C |e verfasserin |4 aut | |
700 | 1 | |a Holmes, Elaine |e verfasserin |4 aut | |
700 | 1 | |a Wetzels, Jack F M |e verfasserin |4 aut | |
700 | 1 | |a Deegens, Jeroen K J |e verfasserin |4 aut | |
700 | 1 | |a Kaluarachchi, Manuja R |e verfasserin |4 aut | |
773 | 0 | 8 | |i Enthalten in |t Molecular omics |d 2018 |g 15(2019), 1 vom: 11. Feb., Seite 39-49 |w (DE-627)NLM282256393 |x 2515-4184 |7 nnns |
773 | 1 | 8 | |g volume:15 |g year:2019 |g number:1 |g day:11 |g month:02 |g pages:39-49 |
856 | 4 | 0 | |u http://dx.doi.org/10.1039/c8mo00190a |3 Volltext |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_NLM | ||
951 | |a AR | ||
952 | |d 15 |j 2019 |e 1 |b 11 |c 02 |h 39-49 |