Summary of Study ST003939

This data is available at the NIH Common Fund's National Metabolomics Data Repository (NMDR) website, the Metabolomics Workbench, https://www.metabolomicsworkbench.org, where it has been assigned Project ID PR002469. The data can be accessed directly via it's Project DOI: 10.21228/M8H26H This work is supported by NIH grant, U2C- DK119886.

See: https://www.metabolomicsworkbench.org/about/howtocite.php

This study contains a large results data set and is not available in the mwTab file. It is only available for download via FTP as data file(s) here.

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Study IDST003939
Study TitlePlasma amino acids of treated metabolic syndrome patients with and without mild cognitive impairment
Study SummaryIn this study, we validated mass spectrometry-based quantitation methods and quantified amino acids in plasma of ninety-five treated MetS patients with and without MCI assessed by Montreal cognitive assessment.
Institute
Mahidol University
DepartmentFaculty of Medicine Siriraj Hospital
LaboratorySiCORE-MSB
Last NameJariyasopit
First NameNarumol
Address2 Prannok, Bangkok, Non-US, 10700, Thailand
Emailnarumoljariyasopit@gmail.com
Phone+6624195500
Submit Date2025-05-28
Raw Data AvailableYes
Raw Data File Type(s)mzML
Analysis Type DetailGC-MS
Release Date2025-06-25
Release Version1
Narumol Jariyasopit Narumol Jariyasopit
https://dx.doi.org/10.21228/M8H26H
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

Select appropriate tab below to view additional metadata details:


Project:

Project ID:PR002469
Project DOI:doi: 10.21228/M8H26H
Project Title:Higher Plasma Kynurenine to Tryptophan Correlates with Increased Incidence of Mild Cognitive Impairment in Treated Metabolic Syndrome Patients
Project Type:MS quantitative analysis
Project Summary:An increase in cognitive impairment has been observed in metabolic syndrome (MetS) patients. Although alterations in metabolomic profiles have been identified as potential plasma/serum biomarkers of mild cognitive impairment (MCI) and MetS, findings remain inconsistent— likely due to the heterogeneity among MetS patients and the lack of subsequent validation using targeted analysis after initial untargeted analysis. In this study, we validated mass spectrometry-based quantitation methods and quantified amino acids, fatty acids, and tryptophan metabolites in the kynurenine pathway in plasma of ninety-five treated MetS patients with and without MCI assessed by Montreal cognitive assessment. We found that MCI was positively associated with kynurenine to tryptophan ratio (KTR) after the adjustment for age, gender, and BMI, as well as were negatively associated with C20:3 [all-Z-8,11,14] and lysine. One-unit increase in KTR resulted in increased probability of developing MCI by 371%. In contrast, one-unit increases in C20:3 and lysine were associated with decreased odds of developing MCI by 81% and 78%, respectively. Our finding underscores the prominent neuroinflammation, beyond normal aging, in MetS patients, even under ongoing clinical treatment. It also points to the potential of KTR as a risk marker for MCI, offering a valuable complement to the existing cognitive assessments that may be influenced by educational background. In addition, the validated metabolite data is an useful resource for future research. It can facilitate comparisons across different studies, contribute to large-scale analyses, and be used in machine learning models for discovering and validating new biomarkers.
Institute:Mahidol University
Department:Faculty of Medicine Siriraj Hospital
Laboratory:SiCORE-MSB
Last Name:Jariyasopit
First Name:Narumol
Address:2 Prannok, Bangkok, Non-US, 10700, Thailand
Email:narumoljariyasopit@gmail.com
Phone:662-4195507

Subject:

Subject ID:SU004075
Subject Type:Human
Subject Species:Homo sapiens
Taxonomy ID:9606
Gender:Male and female
Human Ethnicity:Thai

Factors:

Subject type: Human; Subject species: Homo sapiens (Factor headings shown in green)

mb_sample_id local_sample_id Sample source Factor
SA448822NC-087plasma MetS
SA448823NC-098plasma MetS
SA448824NC-040plasma MetS
SA448825NC-042plasma MetS
SA448826NC-046plasma MetS
SA448827NC-047plasma MetS
SA448828NC-089plasma MetS
SA448829NC-055plasma MetS
SA448830NC-034plasma MetS
SA448831NC-056plasma MetS
SA448832NC-057plasma MetS
SA448833NC-079plasma MetS
SA448834NC-078plasma MetS
SA448835NC-061plasma MetS
SA448836NC-067plasma MetS
SA448837NC-100plasma MetS
SA448838NC-041plasma MetS
SA448839NC-113plasma MetS
SA448840NC-110plasma MetS
SA448841NC-029plasma MetS
SA448842NC-020plasma MetS
SA448843NC-012plasma MetS
SA448844NC-011plasma MetS
SA448845NC-010plasma MetS
SA448846NC-115plasma MetS
SA448847NC-080plasma MetS-MCI
SA448848NC-114plasma MetS-MCI
SA448849NC-116plasma MetS-MCI
SA448850NC-084plasma MetS-MCI
SA448851NC-077plasma MetS-MCI
SA448852NC-076plasma MetS-MCI
SA448853NC-075plasma MetS-MCI
SA448854NC-074plasma MetS-MCI
SA448855NC-073plasma MetS-MCI
SA448856NC-126plasma MetS-MCI
SA448857NC-081plasma MetS-MCI
SA448858NC-104plasma MetS-MCI
SA448859NC-085plasma MetS-MCI
SA448860NC-071plasma MetS-MCI
SA448861NC-102plasma MetS-MCI
SA448862NC-101plasma MetS-MCI
SA448863NC-106plasma MetS-MCI
SA448864NC-099plasma MetS-MCI
SA448865NC-107plasma MetS-MCI
SA448866NC-108plasma MetS-MCI
SA448867NC-095plasma MetS-MCI
SA448868NC-086plasma MetS-MCI
SA448869NC-094plasma MetS-MCI
SA448870NC-093plasma MetS-MCI
SA448871NC-111plasma MetS-MCI
SA448872NC-112plasma MetS-MCI
SA448873NC-092plasma MetS-MCI
SA448874NC-103plasma MetS-MCI
SA448875NC-072plasma MetS-MCI
SA448876NC-001plasma MetS-MCI
SA448877NC-070plasma MetS-MCI
SA448878NC-024plasma MetS-MCI
SA448879NC-037plasma MetS-MCI
SA448880NC-036plasma MetS-MCI
SA448881NC-035plasma MetS-MCI
SA448882NC-033plasma MetS-MCI
SA448883NC-031plasma MetS-MCI
SA448884NC-026plasma MetS-MCI
SA448885NC-025plasma MetS-MCI
SA448886NC-023plasma MetS-MCI
SA448887NC-039plasma MetS-MCI
SA448888NC-022plasma MetS-MCI
SA448889NC-021plasma MetS-MCI
SA448890NC-013plasma MetS-MCI
SA448891NC-009plasma MetS-MCI
SA448892NC-008plasma MetS-MCI
SA448893NC-005plasma MetS-MCI
SA448894NC-003plasma MetS-MCI
SA448895NC-038plasma MetS-MCI
SA448896NC-043plasma MetS-MCI
SA448897NC-069plasma MetS-MCI
SA448898NC-059plasma MetS-MCI
SA448899NC-068plasma MetS-MCI
SA448900NC-066plasma MetS-MCI
SA448901NC-065plasma MetS-MCI
SA448902NC-064plasma MetS-MCI
SA448903NC-063plasma MetS-MCI
SA448904NC-002plasma MetS-MCI
SA448905NC-060plasma MetS-MCI
SA448906NC-058plasma MetS-MCI
SA448907NC-044plasma MetS-MCI
SA448908NC-054plasma MetS-MCI
SA448909NC-053plasma MetS-MCI
SA448910NC-052plasma MetS-MCI
SA448911NC-051plasma MetS-MCI
SA448912NC-050plasma MetS-MCI
SA448913NC-049plasma MetS-MCI
SA448914NC-048plasma MetS-MCI
SA448915NC-045plasma MetS-MCI
SA448916NC-062plasma MetS-MCI
Showing results 1 to 95 of 95

Collection:

Collection ID:CO004068
Collection Summary:Blood was collected in EDTA-coated tubes and centrifuged at 3,000 rpm to obtain plasma. The plasma was then transferred into cryovials and stored at –85°C until use.
Sample Type:Blood (plasma)

Treatment:

Treatment ID:TR004084
Treatment Summary:All patients were divided into two groups: 1) MetS patients with MCI and 2) MetS patients with normal cognitive function. MCI was determined when the MoCA score was less than 23.

Sample Preparation:

Sampleprep ID:SP004081
Sampleprep Summary:Sample extraction of amino acids from plasma was modified from a published method. In brief, 30 µL of plasma was extracted with 1 mL of pre-cooled mixture of acetonitrile/isopropanol/water (3:3:2, v/v/v), containing isotopically labeled internal standards that include alanine-d3 and phenylalanine-d5 with final concentrations of ~ 5 ng/µL. The extracts were shaken at 2,000 rpm for 2 min using a vortex mixture (Scientific Industries) before being kept at -20ºC for 1 h. The extracts were then centrifuged for 10 min at 4ºC and 19,600 ×g. A 450-µL aliquot of supernatant was evaporated to dryness using a vacuum concentrator (Labconco, MO, USA) and kept at -20ºC until analysis. Prior to derivatization, the dried aliquot was resuspended in 450 µL acetonitrile/water (50:50, v/v) followed by centrifugation at 14,000 ×g and room temperature for 2 min. The supernatant was transferred to a new Eppendorf tube and dried at 50ºC under vacuum. The dried sample was reconstituted in 450 µL acetonitrile/water (50:50, v/v) before centrifugation at 14,000 ×g for 2 min at room temperature. The supernatant was evaporated to dryness. The dried samples were derivatized with 50 µL N-tert-Butyldimethylsilyl-N-methyltrifluoroacetamide with 1% tert-butyldimethylchlorosilane (MTBSTFA + 1% TBDMSCl) and 50 µL acetonitrile, followed by incubating at 100ºC for 4 h.
Sampleprep Protocol Filename:AA.txt

Chromatography:

Chromatography ID:CH004914
Chromatography Summary:The quantification of amino acids was carried out using a GC-TOFMS (Pegasus HRT+4D, Leco Corp., St.Joseph, MI). The separation was achieved on a nonpolar Rxi-5sil MS column (5% diphenyl-methyl polysiloxane and 95% dimethylpolysiloxane, 30 m × 0.25 mm I.D., 0.25 μM film thickness, Restek). The injection volume was 1 µL, with the injector temperature of 250 ºC. in The samples were analyzed in splitless mode. Helium was used as a carrier gas at a constant flow rate of 1 mL min-1. The GC oven temperature program started at 50 ºC (2 min hold) and ramped to 320ºC at 20 ºC min-1 (3 min hold). Transfer line and electron impact (EI) ion source temperatures were kept at 320ºC and 250ºC, respectively.
Instrument Name:Agilent 7890B
Column Name:Restek Rxi-5Sil MS GC Capillary Column (30 m, 0.25 mm, 0.25 µm)
Column Temperature:programmed
Flow Gradient:n/a
Flow Rate:1 mL/min
Solvent A:n/a
Solvent B:n/a
Chromatography Type:GC

Analysis:

Analysis ID:AN006468
Analysis Type:MS
Chromatography ID:CH004914
Num Factors:2
Num Metabolites:13
Units:µmol/dL plasma
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