Summary of Study ST002250

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 PR001438. The data can be accessed directly via it's Project DOI: 10.21228/M8V71F This work is supported by NIH grant, U2C- DK119886.

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Study IDST002250
Study TitleRamadan diurnal intermittent fasting is associated with significant plasma metabolomics changes in overweight and obese subjects: A prospective cohort study
Study SummaryDuring the holy month of Ramadan, adult healthy Muslims are mandated to abstain from dawn to sunset, with free eating night hours that may extend up to 12 hours. The current work was designed to investigate the metabolomics changes incurred upon the observance of Ramadan diurnal intermittent fasting (RDIF). Twenty-five metabolically healthy participants with overweight and obesity (7 females and 18 males, with a mean age of 39.48±10.0 years) were recruited for the study and were followed before and at the end of RDIF month. Dietary, anthropometric, biochemical, and physical activity assessments were performed before and at the end of the fasting month. The metabolomic assay was performed using liquid chromatography-mass spectrometry for the two-time points. Metabolomics assay revealed a significant reduction in a few metabolites. The analysis revealed that 27 metabolites differed significantly (P<0.05) between pre-and post-RDIF. Among the differentially abundant metabolites, 23 showed a decrease with fasting, these included several amino acids such as aspartame, tryptophan, phenylalanine, histidine, and other metabolites including valeric acid, and cortisol. On the other hand, only four metabolites showed increased levels with RDIF including traumatic acid, 2-pyrrolidinone, PC(18:1(9Z)/18:1(9Z)), and L-sorbose. The MetaboAnalyst® platform reported that the top enriched metabolic pathways included: (1) histidine metabolism; (2) folate biosynthesis (3) phenylalanine, tyrosine, and tryptophan biosynthesis; (3) aminoacyl-tRNA biosynthesis; (3) caffeine metabolism (4) vitamin B6 metabolism; and several other pathways relating to lipid metabolisms such as arachidonic acid metabolism, glycerophospholipid metabolism, and linoleic acid metabolism. In conclusion, RDIF entails significant changes in various metabolic pathways that reflect different dietary and lifestyle behaviors practiced during the fasting month.
Institute
University of Sharjah
DepartmentSharjah Institute for Medical Research
LaboratoryBiomarker Discovery Group
Last NameSoares
First NameNelson
AddressSharjah
Emailnsoares@sharjah.ac.ae
Phone+971501594048
Submit Date2022-07-24
Raw Data AvailableYes
Raw Data File Type(s)d
Analysis Type DetailLC-MS
Release Date2022-12-22
Release Version1
Nelson Soares Nelson Soares
https://dx.doi.org/10.21228/M8V71F
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Project:

Project ID:PR001438
Project DOI:doi: 10.21228/M8V71F
Project Title:Ramadan diurnal intermittent fasting is associated with significant plasma metabolomics changes in overweight and obese subjects: A prospective cohort study
Project Type:LC-MS/MS
Project Summary:During the holy month of Ramadan, adult healthy Muslims are mandated to abstain from dawn to sunset, with free eating night hours that may extend up to 12 hours. The current work was designed to investigate the metabolomics changes incurred upon the observance of Ramadan diurnal intermittent fasting (RDIF). Twenty-five metabolically healthy participants with overweight and obesity (7 females and 18 males, with a mean age of 39.48±10.0 years) were recruited for the study and were followed before and at the end of RDIF month. Dietary, anthropometric, biochemical, and physical activity assessments were performed before and at the end of the fasting month. The metabolomic assay was performed using liquid chromatography-mass spectrometry for the two-time points. Metabolomics assay revealed a significant reduction in a few metabolites. The analysis revealed that 27 metabolites differed significantly (P<0.05) between pre-and post-RDIF. Among the differentially abundant metabolites, 23 showed a decrease with fasting, these included several amino acids such as aspartame, tryptophan, phenylalanine, histidine, and other metabolites including valeric acid, and cortisol. On the other hand, only four metabolites showed increased levels with RDIF including traumatic acid, 2-pyrrolidinone, PC(18:1(9Z)/18:1(9Z)), and L-sorbose. The MetaboAnalyst® platform reported that the top enriched metabolic pathways included: (1) histidine metabolism; (2) folate biosynthesis (3) phenylalanine, tyrosine, and tryptophan biosynthesis; (3) aminoacyl-tRNA biosynthesis; (3) caffeine metabolism (4) vitamin B6 metabolism; and several other pathways relating to lipid metabolisms such as arachidonic acid metabolism, glycerophospholipid metabolism, and linoleic acid metabolism. In conclusion, RDIF entails significant changes in various metabolic pathways that reflect different dietary and lifestyle behaviors practiced during the fasting month.
Institute:University of Sharjah
Department:Sharjah Institute for Medical Research
Laboratory:Biomarker Discovery Group
Last Name:Soares
First Name:Nelson
Address:Sharjah
Email:nsoares@sharjah.ac.ae
Phone:+971501594048

Subject:

Subject ID:SU002336
Subject Type:Human
Subject Species:Homo sapiens
Taxonomy ID:9606
Age Or Age Range:39.48 +-10.0
Weight Or Weight Range:29.09 +-4.76
Gender:Male and female
Human Inclusion Criteria:Overweight (BMI>=25), otherwise healthy, between 18 and 60 years, no chronic disease, willingness to observe Ramadan Fasting
Human Exclusion Criteria:Medication use within 1 week, bariatric surgery within 6 months, or any weight reduction regimen within 1 month of the commencement of Ramadan

Factors:

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

mb_sample_id local_sample_id Treatment
SA216263Plasma33-02_39_1_2899Post-Fasting
SA216264Plasma34-01_40_1_2900Post-Fasting
SA216265Plasma33-01_39_1_2898Post-Fasting
SA216266Plasma32-02_34_1_2889Post-Fasting
SA216267Plasma32-01_34_1_2888Post-Fasting
SA216268Plasma34-02_40_1_2901Post-Fasting
SA216269Plasma35-01_41_1_2902Post-Fasting
SA216270Plasma37-01_43_1_2906Post-Fasting
SA216271Plasma36-02_42_1_2905Post-Fasting
SA216272Plasma36-01_42_1_2904Post-Fasting
SA216273Plasma35-02_41_1_2903Post-Fasting
SA216274Plasma31-02_33_1_2887Post-Fasting
SA216275Plasma31-01_33_1_2886Post-Fasting
SA216276Plasma27-02_31_1_2883Post-Fasting
SA216277Plasma27-01_31_1_2882Post-Fasting
SA216278Plasma26-02_30_1_2881Post-Fasting
SA216279Plasma26-01_30_1_2880Post-Fasting
SA216280Plasma28-01_37_1_2894Post-Fasting
SA216281Plasma28-02_37_1_2895Post-Fasting
SA216282Plasma30-02_32_1_2885Post-Fasting
SA216283Plasma30-01_32_1_2884Post-Fasting
SA216284Plasma29-02_38_1_2897Post-Fasting
SA216285Plasma29-01_38_1_2896Post-Fasting
SA216286Plasma37-02_43_1_2907Post-Fasting
SA216287Plasma38-02_44_1_2909Post-Fasting
SA216288Plasma46-01_52_1_2924Post-Fasting
SA216289Plasma46-02_52_1_2925Post-Fasting
SA216290Plasma45-02_51_1_2923Post-Fasting
SA216291Plasma45-01_51_1_2922Post-Fasting
SA216292Plasma44-02_50_1_2921Post-Fasting
SA216293Plasma47-01_53_1_2926Post-Fasting
SA216294Plasma47-02_53_1_2927Post-Fasting
SA216295Plasma49-02_55_1_2931Post-Fasting
SA216296Plasma49-01_55_1_2930Post-Fasting
SA216297Plasma48-02_54_1_2929Post-Fasting
SA216298Plasma48-01_54_1_2928Post-Fasting
SA216299Plasma44-01_50_1_2920Post-Fasting
SA216300Plasma43-02_49_1_2919Post-Fasting
SA216301Plasma40-01_46_1_2912Post-Fasting
SA216302Plasma39-02_45_1_2911Post-Fasting
SA216303Plasma39-01_45_1_2910Post-Fasting
SA216304Plasma25-02_29_1_2879Post-Fasting
SA216305Plasma40-02_46_1_2913Post-Fasting
SA216306Plasma41-01_47_1_2914Post-Fasting
SA216307Plasma43-01_49_1_2918Post-Fasting
SA216308Plasma42-02_48_1_2917Post-Fasting
SA216309Plasma42-01_48_1_2916Post-Fasting
SA216310Plasma41-02_47_1_2915Post-Fasting
SA216311Plasma38-01_44_1_2908Post-Fasting
SA216312Plasma25-01_29_1_2878Post-Fasting
SA216313Plasma09-02_14_1_2849Pre-Fasting
SA216314Plasma10-01_15_1_2850Pre-Fasting
SA216315Plasma09-01_14_1_2848Pre-Fasting
SA216316Plasma08-02_13_1_2847Pre-Fasting
SA216317Plasma08-01_13_1_2846Pre-Fasting
SA216318Plasma10-02_15_1_2851Pre-Fasting
SA216319Plasma11-01_16_1_2852Pre-Fasting
SA216320Plasma13-01_18_1_2856Pre-Fasting
SA216321Plasma12-02_17_1_2855Pre-Fasting
SA216322Plasma12-01_17_1_2854Pre-Fasting
SA216323Plasma11-02_16_1_2853Pre-Fasting
SA216324Plasma07-02_12_1_2845Pre-Fasting
SA216325Plasma07-01_12_1_2844Pre-Fasting
SA216326Plasma03-01_8_1_2836Pre-Fasting
SA216327Plasma03-02_8_1_2837Pre-Fasting
SA216328Plasma02-02_35_1_2891Pre-Fasting
SA216329Plasma02-01_35_1_2890Pre-Fasting
SA216330Plasma01-02_7_1_2835Pre-Fasting
SA216331Plasma04-01_9_1_2838Pre-Fasting
SA216332Plasma04-02_9_1_2839Pre-Fasting
SA216333Plasma06-02_11_1_2843Pre-Fasting
SA216334Plasma06-01_11_1_2842Pre-Fasting
SA216335Plasma05-02_10_1_2841Pre-Fasting
SA216336Plasma05-01_10_1_2840Pre-Fasting
SA216337Plasma13-02_18_1_2857Pre-Fasting
SA216338Plasma14-01_19_1_2858Pre-Fasting
SA216339Plasma22-01_27_1_2874Pre-Fasting
SA216340Plasma22-02_27_1_2875Pre-Fasting
SA216341Plasma21-02_26_1_2873Pre-Fasting
SA216342Plasma21-01_26_1_2872Pre-Fasting
SA216343Plasma20-02_25_1_2871Pre-Fasting
SA216344Plasma23-01_36_1_2892Pre-Fasting
SA216345Plasma23-02_36_1_2893Pre-Fasting
SA216346Plasma50-02_56_1_2933Pre-Fasting
SA216347Plasma50-01_56_1_2932Pre-Fasting
SA216348Plasma24-02_28_1_2877Pre-Fasting
SA216349Plasma24-01_28_1_2876Pre-Fasting
SA216350Plasma20-01_25_1_2870Pre-Fasting
SA216351Plasma19-02_24_1_2869Pre-Fasting
SA216352Plasma16-01_21_1_2862Pre-Fasting
SA216353Plasma15-02_20_1_2861Pre-Fasting
SA216354Plasma15-01_20_1_2860Pre-Fasting
SA216355Plasma14-02_19_1_2859Pre-Fasting
SA216356Plasma16-02_21_1_2863Pre-Fasting
SA216357Plasma17-01_22_1_2864Pre-Fasting
SA216358Plasma19-01_24_1_2868Pre-Fasting
SA216359Plasma18-02_23_1_2867Pre-Fasting
SA216360Plasma18-01_23_1_2866Pre-Fasting
SA216361Plasma17-02_22_1_2865Pre-Fasting
SA216362Plasma01-01_7_1_2834Pre-Fasting
Showing results 1 to 100 of 100

Collection:

Collection ID:CO002329
Collection Summary:A total of 4 mL of blood was then collected from each subject into a sterile container. The samples were stored immediately at –80 ºC for long-term storage until further metabolomics analysis.
Sample Type:Blood (plasma)
Storage Conditions:-80℃

Treatment:

Treatment ID:TR002348
Treatment Summary:Our prospective study was executed during Ramadan (from June 2016 to July 2016, corresponding to Ramadan month in the 1438 Hijri of the lunar calendar), where the daily fasting period covered nearly 15 hours. Data were collected 1 week before Ramadan (pre-fasting or baseline) and after completing 28–30 days of Ramadan (at the end of Ramadan). During Ramadan, fasting people abstain from food and drink (including water) and do not smoke from dawn to sunset. We compared the studied variables for each participant before and during Ramadan, meaning each participant served as their control. Participants did not receive any nutritional recommendations or physical activity advice at any stage during this study. The Islamic laws of Ramadan excuse females from fasting during Ramadan while their menstrual period; therefore, the fasting days for female participants were about 23–25 days.
Human Fasting:Ramadan Intermittent Fasting

Sample Preparation:

Sampleprep ID:SP002342
Sampleprep Summary:For analysis, an aliquot of thawed plasma sample was transferred into a microcentrifuge tube and cold methanol added at 3:1 v/v (i.e., 30 μL sample, add 90 μL cold methanol), vortexed and allowed to sit at –20ºC for two hours. Next, samples were centrifuged at 20,817 x g for 15 min at 4ºC and the supernatant transferred to a new microcentrifuge tube. Usually, the transferred volume was three times that of the original sample (i.e., for a 30 μL sample, add 90 μL cold methanol, then transfer 90 μL supernatant). The samples were dried using a Speed vac at 30 – 40°C and the dried sample stored in a –80ºC freezer for further use or dissolved in solvent for LC-MS/MS analysis. Samples were resuspended in the starting solvent (0.1% formic acid) where the volume was three times the original plasma volume, i.e., 90 μL for 30 μL serum/plasma aliquot.
Processing Storage Conditions:Described in summary
Extract Storage:4℃

Combined analysis:

Analysis ID AN003676
Analysis type MS
Chromatography type Reversed phase
Chromatography system Bruker Elute
Column Hamilton Intensity Solo 2 C18
MS Type ESI
MS instrument type QTOF
MS instrument name Bruker timsTOF
Ion Mode POSITIVE
Units AU

Chromatography:

Chromatography ID:CH002726
Chromatography Summary:Samples were chromatographically separated using a Hamilton® Intensity Solo 2 C18 column (100 mm x 2.1 mm x 1.8 µm) and eluted using 0.1% formic acid in water (A) and 0.1% formic acid in ACN (B) using the following gradient: at a flow rate of 0.250 ml/min 1% B from 0-2 min, then gradient elution to 99% B from 2-17 min, held at 99% B from 17-20 min, then re-equilibrated to 1% B from 20-30 min using a flow rate of 0.350 ml/min. The autosampler temperature was set at 8℃ and the column oven temperature at 35℃.
Instrument Name:Bruker Elute
Column Name:Hamilton Intensity Solo 2 C18
Column Temperature:35
Flow Gradient:1%B to 99%B in 15 min
Flow Rate:250 uL/min
Solvent A:100% water; 0.1% formic acid
Solvent B:100% acetonitrile; 0.1% formic acid
Oven Temperature:35C
Chromatography Type:Reversed phase

MS:

MS ID:MS003427
Analysis ID:AN003676
Instrument Name:Bruker timsTOF
Instrument Type:QTOF
MS Type:ESI
MS Comments:Auto MS/MS mode with 0.5 second cycle time. The ESI source with dry nitrogen gas was 10 L/min, and the drying temperature was equal to 220℃ with nebulizer gas pressure set to 2.2 bar. The capillary voltage of the ESI was 4500 V and the Plate Offset 500 V. MS acquisition scan was set from 20-1300 m/z and the collision energy to 7 eV.
Ion Mode:POSITIVE
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