BEVITAL AS

Methods & Platforms

Key data of our analytical platforms are described below and include PubChem numbers, reported biomarker concentrations, LODs, CVs, ICCs, sample matrix and method description for most of our analytes.*

Analytical platforms

Short-chain fatty acids.

Sample volume required: 50 µL
GC-MS/MS

All concentrations are reported in µmol/L.

MetabolitesAbbrClassPubChem CIDReported conc.LODCV WtnCV BtwMatrixMethod
AcetateAceShort-chain fatty acid175-1765-3005.03-53-7s, pAce 1
ButyrateButShort-chain fatty acid2641-300.23-63-6s, pBut 1
FormateFrmShort-chain fatty acid2848-1007.03-63-6s, p, csfFrm 1
IsobutyrateiButShort-chain fatty acid65900.7-60.053-63-8s, p, csfiBut 1
IsovalerateiVlrShort-chain fatty acid104300.3-30.023-63-8s, piVlr 1
PropionateProShort-chain fatty acid10421-130.062-63-6s, pPro 1
ValerateVlrShort-chain fatty acid79910.2-10.053-64-8s, pVlr 1
α-MethylbutyrateaMBShort-chain fatty acid83140.3-30.053-74-7s, paMB 1
β-Hydroxy β-methylbutyrateHMBLeu metabolite693620.1-10, 2-6 (csf)s, p, csfHMB 1

Amino- and carboxylic acids. TCA metabolites and intermediates.

Sample volume required: 50 µL
GC-MS/MS

All concentrations are reported in µmol/L.

MetabolitesAbbrClassPubChem CIDReported conc.LODCV WtnCV BtwICCMatrixMethod
2-Aminoadipic acid2AAALys metabolite4690.3-2.00.24.86.9s, p2 Aminoadipic Acid 1
2-HydroxybutyrateaHBα-Hydroxy acid1126610-6011.72.3s, p2 Hydroxybutyrate 1
3-HydroxybutyratebHBKetone body44120-70011.93.4s, p3 Hydroxybutyrate 1
3-Hydroxyisobutyrate3HIBVal metabolite44087315-2512.42.9s, p3 Hydroxyisobutyrate 1
AcetoacetateAcAcKetone body9610-200555s, pAcetoAcetate 1
AlanineAlaHydrophobic amino acid5950230-51011.21.40.43as, pmidttun 2016 ac 88 10427
AsparagineAsnPolar amino acid626720-1300.6330.40as, pmidttun 2016 ac 88 10427
Aspartic acidAspCharged amino acid59600-260.51.84s, pmidttun 2016 ac 88 10427
CarboxyethyllysineCELan AGE***234007790.05-0.40.034.14.4s, pCarboxyethyllysine 1
CarboxymethyllysineCMLan AGE***1238000.05-0.30.034.34.5s, pCarboxymethyllysine 1
CitrateCitTricarboxylic acid31190-200433.1s, pCitrate 1
CystathionineCystaThioether4392580.07-0.550.022.32.90.63s, pmidttun 2016 ac 88 10427
FumarateFumDicarboxylic acid4449720.5-40.21.75.2s, p, csfFumarate 1
Glutamic acidGluCharged amino acid3303220-1400.51.72.7s, pmidttun 2016 ac 88 10427
GlutamineGlnPolar amino acid5961390-700102.12.70.42as, pmidttun 2016 ac 88 10427
GlycineGlyHydrophobic amino acid750150-35031.31.70.81s, pmidttun 2016 ac 88 10427
HistidineHisEssential amino acid627440-1501230.44as, pmidttun 2016 ac 88 10427
IsocitrateiCitTricarboxylic acid11982-220.32.83s, p, csfIsoCitrate 1
IsoleucineIleEssential BCAA**630640-1400.51.51.80.53as, pmidttun 2016 ac 88 10427
KynurenineKynTrp metabolite1611661.0-3.30.121.92.30.68s, pmidttun 2016 ac 88 10427
LactateLacα-Hydroxy acid612500-1600104.64.8s, p, csfLactate 1
LeucineLeuEssential BCAA**610670-1700.53.440.52as, pmidttun 2016 ac 88 10427
LysineLysEssential amino acid5962120-2901.21.41.90.54as, pmidttun 2016 ac 88 10427
MalateMalβ-Hydroxy acid5252-210.42.62.6s, p, csfMalate 1
MethionineMetEssential amino acid613718-5012.24.10.33s, pmidttun 2016 ac 88 10427
Methylmalonic acidMMACarboxylic acid487<0.260.032.430.81s, pmidttun 2016 ac 88 10427
OrnithineOrnCharged amino acid626230-9012.22.70.55as, pmidttun 2016 ac 88 10427
PhenylacetylglutaminePAGlnn-acyl-alpha amino acid922582-1000.65-66-7s, pPhenylActylGlutamine 1
PhenylalaninePheEssential aromatic amino acid614026-850.51.530.44as, pmidttun 2016 ac 88 10427
ProlineProHydrophobic amino acid145742110-3600.52.83.70.71as, pmidttun 2016 ac 88 10427
PyruvatePyrα-Keto acid106080-160566.5s, p, csfPyruvate 1
Sarcosine*SarcMethylated amino acid10880.7-2.30.0351.31.60.68s, pmidttun 2016 ac 88 10427
SerineSerPolar amino acid595195-20051.31.70.71s, pmidttun 2016 ac 88 10427
ThreonineThrEssential amino acid628870-2401.22.43.30.44as, pmidttun 2016 ac 88 10427
Total cysteinetCysSulfur amino acid5862150-35050120.62s, pmidttun 2016 ac 88 10427
Total homocysteinetHcySulfur amino acid915525-150.11.42.70.72s, pmidttun 2016 ac 88 10427
TryptophanTrpEssential aromatic amino acid630540-900.51.62.60.51s, pmidttun 2016 ac 88 10427
TyrosineTyrAromatic amino acid605740-1100.52.12.80.55as, pmidttun 2016 ac 88 10427
ValineValEssential BCAA**6287150-3500.52.22.70.38as, pmidttun 2016 ac 88 10427
α-Hydroxyglutaric acidaHGα-Hydroxy acid430.15-20.104.27.0s, pAlfa Hydroxyglutaric Acdi 1
α-KetoglutarateaKGKeto acid512-400.53.73.7s, p, csfmidttun 2016 ac 88 10427
β-AlaninebAlaβ-Amino acid2390.5-100.334.3s, pBeta Alanine 1
β-AminoisobutyrateBAIBAVal metabolite649560.3-2.00.22.53.7s, pBAIBA 1

*Sarcosine cannot be measured in EDTA-tubes from some suppliers because of the presence of sarcosine in these tubes; **BCAA, Branched chain amino acid; ***AGE, Advanced glycation end product.
aXiaofei Yin, Orla Prendiville, Aoife E. McNamara, and Lorraine Brennan. Targeted Metabolomic Approach to Assess the Reproducibility of
Plasma Metabolites over a Four Month Period in a Free-Living Population. J. Proteome Res. 2022, 21, 683−690.

Choline derivatives. Charged, methylated or sulfur amino acids.

Sample volume required: 35 µL
LC-MS/MS

All concentrations are reported in µmol/L.

MetabolitesAbbrClassPubChem CIDReported conc.LODCV WtnCV BtwICCMatrixMethod
1-Methylhistidine1-MHAmino acid649690.5–150.253.73.9s, p, um1His
3-Methylhistidine3-MHAmino acid921052.7–100.64.44.9s, p, um3His
ArginineArgCharged amino acid632210–1000.252.630.53s, pMidttun 13 ABC 405 2009
Asymmetric dimethylarginineADMAGuanidinated amino acid1238310.4–10.085.25.50.53s, pMidttun 13 ABC 405 2009
BetaineBetMethylated amino acid24715–600.53.84.50.65s, p, uMidttun 13 ABC 405 2009
CarnitineC0Carnitine28820–800.50.69as, pC0
Carnitine, totalbtC0Carnitines30–900.5s, p
CholineCholQuarternary ammonium3055–150.52.83.20.36s, p, uMidttun 13 ABC 405 2009
CitrullineCtnAmino acid975010–6047-86-90.62cs, pCit
CreatineCrnα-Amino acid58610–10013.94s, p, uCrn
CreatinineCreatα-Amino acid58850–1000.252.63.10.79s, p, uMidttun 13 ABC 405 2009
DimethylglycineDMGMethylated amino acid6731.5–50.255.55.90.64s, p, uMidttun 13 ABC 405 2009
HistidineHisEssential amino acid627440–2000.253.53.8s, pHis
HomoargininehArgGuanidinated amino acid90851–60.15.860.65s, pMidttun 13 ABC 405 2009
MethionineMetEssential amino acid613718–5014.14.50.33s, pMidttun 13 ABC 405 2009
Methionine sulfoxideMetSoPolar amino acid1589800.5–50.067.17.90.36s, pMidttun 13 ABC 405 2009
Symmetric dimethylarginineSDMAGuanidinated amino acid1691480.3–0.90.084.85.20.62s, pMidttun 13 ABC 405 2009
Total cysteinetCysSulfur amino acid5862150–4000.1260.56s, pMidttun 13 ABC 405 2009
Total homocysteinetHcyAmino acid91552<150.1120.72s, p, umidttun 2016 ac 88 10427
Trimethylamine N-oxideTMAOAmine oxide11450.5–600.144.1<0.38s, p, uTMAO
TrimethyllysineTMLMethylated amino acid4401210.3–20.244.40.15s, pMidttun 13 ABC 405 2009

aFloegel A, Drogan D, Wang-Sattler R, Prehn C, Illig T, et al. (2011) Reliability of Serum Metabolite Concentrations over a 4-Month Period Using a
Targeted Metabolomic Approach. PLoS ONE 6(6): e21103. doi:10.1371/journal.pone.0021103.
bMeasured in a separate assay involving alkaline hydrolysis of acylcarnitines.
cXiaofei Yin, Orla Prendiville, Aoife E. McNamara, and Lorraine Brennan. Targeted Metabolomic Approach to Assess the Reproducibility of
Plasma Metabolites over a Four Month Period in a Free-Living Population. J. Proteome Res. 2022, 21, 683−690.

Kynurenine pathway and B vitamins (B1, B2, B3, B6), indoles, nicotin, coffee markers, and inflammation markers.

Sample volume required: 60 µL
LC-MS/MS

All concentrations are reported in µmol/L or nmol/L.

MetabolitesAbbrClassPubChem CIDReported conc.LODUnitCV WtnCV BtwICCMatrixMethod
3-Hydroxyanthranilic acidHAATrp metabolite8610–80/0–7 nmol/L2nmol/L4.660.54s, p, csfMidttun 09 rcms 23 1371
3-HydroxykynurenineHKTrp metabolite1181125–80/0.1–25 nmol/L2nmol/L3.24.50.62s, p, csfMidttun 09 rcms 23 1371
3-Indoxyl sulfate3ISIndole, Trp metabolite102580.9–30 µmol/L0.2µmol/L4–54–6s, p, csf3IS 1
4-Pyridoxic acidPAB6 vitamer672310–200/0–15 nmol/L0.5µmol/L3.65.80.58s, p, csfMidttun 09 rcms 23 1371
Anthranilic acidAATrp metabolite2277–30/3–14 nmol/L2nmol/L7.49.50.64s, p, csfMidttun 09 rcms 23 1371
CotinineCotNicotine metabolite854019Non-smokers < ~5 nmol/L;
passive smokers 5 – 85 nmol/L;
smokers > 85nmol/L;
heavy smokers (>25 cigarettes/day) > 1700 nmol/L
134.20.92s, p,csfMidttun 09 rcms 23 1371
CystathionineCystaThioether43925870–550 nmol/L20nmol/L3.44.50.63s, p, csfMidttun 09 rcms 23 1371
Flavin mononucleotideFMNB2 vitamer6439763–30/1–2 nmol/L0.4nmol/L5.78.10.69s, p, csfMidttun 09 rcms 23 1371
Imidazole propionateImPHistidine metabolite706303–500 nmol/L2nmol/L55.4s, pImP.png
Indole-3-acetamideIAMIndole, Trp metabolite3970–10 nmol/L1nmol/L8–98–10s, pIAM 1
Indole-3-acetateIAAIndole, Trp metabolite8020.3–23 µmol/L0.05µmol/L4–54–6s, pIAA 1
Indole-3-aldehydeIAldIndole, Trp metabolite1025610–200 nmol/L4nmol/L5–85–9s, pIAld 1
Indole-3-lactateILAIndole, Trp metabolite929040.08–5 µmol/L0.025µmol/L4–54–6s, pILA 1
Indole-3-propionateIPAIndole, Trp metabolite37440.5–12 µmol/L0.04µmol/L4–54–6s, pIPA 1
Kynurenic acidKATrp metabolite384520–100/0.5–15 nmol/L0.4nmol/L4.45.40.68s, p, csfMidttun 09 rcms 23 1371
KynurenineKynTrp metabolite1611661.0–3.3/0.02–0.12 µmol/L0.12µmol/L3.65.10.68s, p, csfMidttun 09 rcms 23 1371
N1-methylnicotinamidemNAMB3 vitamer45720–250/5–100 nmol/L5nmol/L45.5s, p, csfMidttun FASEB 2012
NeopterinNeoptPteridine44555–50/5–50 nmol/L0.7nmol/L5.36.60.6s, p, csfMidttun 09 rcms 23 1371
NicotinamideNAMB3 vitamer936100–600/5–200 nmol/L20nmol/L4.26.1s, p, csfMidttun FASEB 2012
Nicotinic acidNAB3 vitamer938<20 nmol/L10nmol/L45.4s, p, csfMidttun FASEB 2012
Picolinic acidPicTrp metabolite101820–100/5–100 nmol/L8nmol/L6-75-8s, p, csfPic
PyridoxalPLB6 vitamer10505–150/10–50 nmol/L0.2nmol/L3.55.10.62s, p, csfMidttun 09 rcms 23 1371
Pyridoxal 5-phosphatePLPB6 vitamer105115–150/7–70 nmol//L0.2nmol/L3.55.70.7s, p, csfMidttun 09 rcms 23 1371
PyridoxinePNB6 vitamer1054Exogenous metabolite,
reflecting B vitamin supplement use
0.5nmol/L4.55.2s, pMidttun 09 rcms 23 1371
Quinaldic acidQldTrp (KA) metabolite71240.2–100/0.1–10 nmol/L0.5nmol/L6-76-8s, pQld
Quinolinic acidQATrp metabolite1066150–700/10–150 nmol/L1.6nmol/L7-87-10s, p, csfMidttun FASEB 2012
RiboflavinRiboB2 vitamer4935705–100/5–25 nmol/L0.2nmol/L67.10.79s, p, csfMidttun 09 rcms 23 1371
ThiamineThiB1 vitamer11302–50/5–40 nmol/L0.5nmol/L3.54.9s, p, csfmccann 2017 n 9 676
Thiamine monophosphateTMPB1 vitamer11312–15/25–75 nmol/L0.5nmol/L7.111.6s, p, csfmccann 2017 n 9 676
Trans-3-hydroxycotinineOHCotNicotine metabolite107963Concentrations relative to cotinine,
with OHCot/cotinine ratio ranging from 0.02-0.90 nmol/L
2nmol/L3.64.50.85s, p, csfbenowitz 2009 hep 192 29
TrigonellineTrigAlkaloid55700.4–25 µmol/L0.01µmol/L2.93.80.66s, p, csfTrig
Trimethylamine N-oxideTMAOAmine oxide11450.5–60/0.2–12 µmol/L0.1µmol/L4.26.9<0.38s, p, csf
TryptophanTrpEssential aromatic amino acid630540–90/2–7 µmol/L0.5µmol/L3.13.90.51s, p, csfMidttun 09 rcms 23 1371
Xanthurenic acidXATrp metabolite56992–35/<0.5 nmol/L0.5nmol/L4.85.70.58s, p, csfMidttun 09 rcms 23 1371
Folate species and catabolites.

Sample volume required: 60 µL
LC-MS/MS

All concentrations are reported in nmol/L.

MetabolitesAbbrClassPubChem CIDReported conc.LODCV WtnCV BtwMatrixMethod
5-Methyl-tetrahydrofolatemTHFFolate135398561
>7.50.075-94-5s, phannisdal 09 cc 55 1147
5-Formyl-tetrahydrofolatefTHFFolate135403648
0-20.528-96-11s, phannisdal 09 cc 55 1147
Folic acidFAFolate60370-20.277-86-12s, phannisdal 09 cc 55 1147
Serum folate as pABG equivalentsS pABGFolate>7.5s, p
RBC folate as pABG equivalentsE pABGFolate>340e
Para-aminobenzoylglutamatepABGFolate catabolite1964730-0.50.086-93-10s, phannisdal 09 cc 55 1147
AcetamidobenzoylglutamateapABGFolate catabolite30808680.1-10.135-65-9s, phannisdal 09 cc 55 1147
4-α-hydroxy-5-methyl-THFhmTHFOxidized folate0.26-106-7s, phannisdal 09 cc 55 1147

Folate (B9) and cobalamin (B12).

Sample volume required: 15-35 µL
Microbiological assay

All concentrations are reported in nmol/L or pmol/L.

MetabolitesAbbrClassReported conc.LODUnitCV WtnCV BtwICCMatrixMethod
Serum folates-FolateB vitamin>7.5 nmol/L2nmol/L450.56s, pMolloy 97 ME 281 43
Erythrocyte folatee-FolateB vitamin>340 nmol/Lnmol/Le
Serum cobalamins-B12B vitamin>150 pmol/L30pmol/L450.82s, pKelleher 91 JCP 44 592
Protein markers.

This platform has been discontinued and will be replaced soon.

All concentrations are reported in µg/ml or %.

ProteinsAbbrClassUniProtProteoformsReported conc.LODCV WtnCV BtwICC**MatrixMethod
C-reactive proteinCRPProteinP0274110-10 µg/mL***0.14-57-90.5-0.7s, pgao 2018 ac 90 3366meyer 2014 ac 86 5807
Serum amyloid ASAAProteinP0DJI8, P0DJI9180-20 µg/mL0.054-58-100.4-0.7s, pgao 2018 ac 90 3366
CalprotectinS100AProteinP05109, P067026*0-30 µg/mL0.024-77-80.3-0.5s, p, csfgao 2018 ac 90 3366
Cystatin CCnCProteinP010345*0-8 µg/mL0.014-54-50.7s, p, csfgao 2018 ac 90 3366meyer 2014 ac 86 5807
Glycated hemoglobinHbA1cProteinP69905, F8W6P54-14 %2-6wBiroccio 05 AB 336 279

*Mass interference of S100A and CnC proteoforms; **ICCs of proteoforms are reported here; *** high sensitive CRP (hs-CRP)

Lipid-soluble vitamins.

Sample volume required: 50-100 µL
LC-MS/MS

All concentrations are reported in µmol/L or nmol/L.

MetabolitesAbbrClassPubChem CIDReported conc.LODUnitCV WtnCV BtwICCMatrixMethod
All-trans retinolVit. AA vitamer4453540.3-8 µmol/L 0.1µmol/L2.93.60.87s, pMidttun 11 rcms 25 1942presse 2012 jn 142 1910midttun 2016 ac 88 10427
25-hydroxy vitamin D225OH-D2D vitamer57101480-60 nmol/L5nmol/L6.68.1s, pMidttun 11 rcms 25 1942presse 2012 jn 142 1910midttun 2016 ac 88 10427
25-hydroxy vitamin D325OH-D3D vitamer528373110-280 nmol/L3.3nmol/L5.16.10.71s, pMidttun 11 rcms 25 1942presse 2012 jn 142 1910midttun 2016 ac 88 10427
α-tocopherolaTocE vitamer1498511-106 µmol/L 2µmol/L4.35.80.86s, pMidttun 11 rcms 25 1942presse 2012 jn 142 1910midttun 2016 ac 88 10427
γ-tocopherolgTocE vitamer927290.5-11 µmol/L 0.1µmol/L3.75s, pMidttun 11 rcms 25 1942presse 2012 jn 142 1910midttun 2016 ac 88 10427
PhylloquinoneVit. K1K vitamer52846070.5-20 nmol/L0.5nmol/L4.87.40.49s, pMidttun 11 rcms 25 1942presse 2012 jn 142 1910midttun 2016 ac 88 10427
Short-, medium- and long-chain acylcarnitines.

Sample volume required: 60 µL
LC (HILIC)-MS/MS

All concentrations are reported in µmol/L. Read more about acylcarnitines here.

MetabolitesAbbrClassPubChem CIDReported conc.LODCV WtnCV BtwICCMatrix
ButyrobetaineBBQuarternary ammonium7250.2–20.014.32.5s, p
CarnitineC0Carnitine2887–900.502.72.40.69s, p
AcetylcarnitineC2Acylcarnitine70457671–350.063.02.10.63s, p
PropionylcarnitineC3Acylcarnitine1077380.1–1.50.013.81.60.62s, p
MalonylcarnitineC3DCAcylcarnitine918256060–0.50.052.82.4s, p
ButyrylcarnitineC4Acylcarnitine2131440.04–1.20.0053.43.1s, p
HydroxybutyrylcarnitineC4OHAcylcarnitine906598850.01–0.50.015.31.6s, p
Succinylcarnitine / MethylmalonylcarnitineC4DCAcylcarnitine1318020750.01–10.018.412.7s, p
IsovalerylcarnitineiC5Acylcarnitine64268510.04–0.50.012.71.80.68s, p
GlutarylcarnitineC5DCAcylcarnitine714644880.01–0.30.018.08.2s, p
Methylcrotonylcarnitine / TiglylcarnitineC5:1Acylcarnitine717502540.005–0.10.0055.03.7s, p
HexanoylcarnitineC6Acylcarnitine64268530.005–2.10.0055.63.8s, p
OctanoylcarnitineC8Acylcarnitine1237010.03–1.10.0053.53.70.41s, p
DecanoylcarnitineC10Acylcarnitine102451900.03–2.10.0053.21.7s, p
DodecanoylcarnitineC12Acylcarnitine1683810.01–0.50.012.31.4s, p
Tetradecanoylcarnitine (Myristoylcarnitine)C14Acylcarnitine64268540.015–0.30.0155.42.70.38s, p
HydroxytetradecanoylcarnitineC14OHAcylcarnitine714645410.005–0.080.0057.64.1s, p
Hexadecanoylcarnitine (Palmitoylcarnitine)C16Acylcarnitine4610.04–1.30.013.12.60.49s, p
HydroxyhexadecanoylcarnitineC16OHAcylcarnitine1264562280–0.050.0055.24.1s, p
Octadecanoylcarnitine (Stearoylcarnitine)C18Acylcarnitine529220560.01–0.50.0065.06.60.4s, p
HydroxyoctadecanoylcarnitineC18OHAcylcarnitine714645600.019.94.6s, p
Octadecenoylcarnitine (Oleylcarnitine)C18:1Acylcarnitine469079330.02–10.013.42.20.66s, p
Octadecadienylcarnitine (Linoleylcarnitine)C18:2Acylcarnitine64500150.02–0.30.013.52.4s, p

NAD metabolome.

Sample volume required: 50 µL
LC (HILIC)-MS/MS

All concentrations are reported in µmol/L. Read more about NAD here.

MetabolitesAbbrClassPubChem CIDReported conc.LODCV WtnCV BtwMatrix
N1-methylnicotinamidemNAMNAD catabolite4570.1-30.010.91.5w
NicotinamideNAMNAD precursor9365-250.10 (0.04 csf)3.55.6w
Nicotinamide adenine dinucleotide (oxidized)NADNAD oxidized589310-500.252.62.4w
Nicotinamide adenine dinucleotide (reduced)NADHNAD reduced4391530.5-30.152.13.1w
Nicotinamide adenine dinucleotide phosphate (oxidized)NADPNADP oxidized588610-400.2510.210.9w
Nicotinamide adenine dinucleotide phosphate (reduced)NADPHNADP reduced58851-40.128.010.1w
Nicotinamide mononucleotideNMNNAD biosynthesis intermediate141802-100.22.95.4w
Nicotinamide N-oxideNAMONAD catabolite726610.005-1.50.01 (0.005 csf)2.34.5w
Nicotinamide ribosideNRNAD precursor, supplement4399240-95.62.9w
Nicotinic acidNANAD precursor9380-0.60.0251.52.5w
Nicotinic acid adenine dinucleotideNAADNAD biosynthesis intermediate1654910.005-10.00758.311.4w
Nicotinic acid ribosideNARNAD precursor1612333-150.0022.42.7w
N-methyl-2-pyridone-5-carboxamidem2PYNAD catabolite696980-200.0101.72.7w
N-methyl-4-pyridone-3-carboxamidem4PYNAD catabolite4408100.00251.82.8w

Bile acids.

Sample volume required: 50 µL
LC-MS/MS

All concentrations are reported in µmol/L. Read more about bile acids here.

MetabolitesAbbrClassPubChem CIDReported conc.LODCV WtnCV BtwMatrixMethods
7α-hydroxy-cholesten-3-oneC4Bile acid precursor123743206.856.84s, pScreenshot 2025 06 30 at 13 58 17 supplementaryData method BAs withCVs toKlaus 250630.pdf
Cholic acidCAPrimary bile acid2214935.76–2951.50502.311.82s, pScreenshot 2025 06 30 at 13 58 17 supplementaryData method BAs withCVs toKlaus 250630.pdf
Chenodeoxycholic acidCDCAPrimary bile acid101338.05–3432.25254.463.76s, pScreenshot 2025 06 30 at 13 58 17 supplementaryData method BAs withCVs toKlaus 250630.pdf
Deoxycholic acidDCASecondary bile acid2225288.72–1854.50254.752.16s, pScreenshot 2025 06 30 at 13 58 17 supplementaryData method BAs withCVs toKlaus 250630.pdf
Glycocholic acidGCAConjugated bile acid1014022.32–4567.25252.472.61s, pScreenshot 2025 06 30 at 13 58 17 supplementaryData method BAs withCVs toKlaus 250630.pdf
Glycochenodeoxycholic acidGCDCAConjugated bile acid12544172.85–80523003.734.19s, pScreenshot 2025 06 30 at 13 58 17 supplementaryData method BAs withCVs toKlaus 250630.pdf
Glycodeoxycholic acidGDCAConjugated bile acid303502614.96–2752.25205.868.25s, pScreenshot 2025 06 30 at 13 58 17 supplementaryData method BAs withCVs toKlaus 250630.pdf
Glycohyocholic acidGHCAConjugated bile acid713614621.19–20623.332.89s, pScreenshot 2025 06 30 at 13 58 17 supplementaryData method BAs withCVs toKlaus 250630.pdf
Glycohyodeoxycholic acidGHDCAConjugated bile acid114611153.293.58s, pScreenshot 2025 06 30 at 13 58 17 supplementaryData method BAs withCVs toKlaus 250630.pdf
Glycolithocholic acidGLCAConjugated bile acid1152451.19–16123.263.75s, pScreenshot 2025 06 30 at 13 58 17 supplementaryData method BAs withCVs toKlaus 250630.pdf
Glycoursodeoxycholic acidGUDCAConjugated bile acid1231028813.23–1511.25104.473.92s, pScreenshot 2025 06 30 at 13 58 17 supplementaryData method BAs withCVs toKlaus 250630.pdf
Hyocholic acidHCAPrimary bile acid1317503241.19–85.6754.682.92s, pScreenshot 2025 06 30 at 13 58 17 supplementaryData method BAs withCVs toKlaus 250630.pdf
Hyodeoxycholic acidHDCASecondary bile acid5283820<160155.85.9s, pScreenshot 2025 06 30 at 13 58 17 supplementaryData method BAs withCVs toKlaus 250630.pdf
Iso-litocholic acidiLCASecondary bile acid1648535Under optimizationUnder optimizations, pScreenshot 2025 06 30 at 13 58 17 supplementaryData method BAs withCVs toKlaus 250630.pdf
Lithocholic acidLCASecondary bile acid99032.5–7873.336.25s, pScreenshot 2025 06 30 at 13 58 17 supplementaryData method BAs withCVs toKlaus 250630.pdf
Lithocholic acid sulfateLCAsSecondary bile acid45148954.286.97s, pScreenshot 2025 06 30 at 13 58 17 supplementaryData method BAs withCVs toKlaus 250630.pdf
Tauro-alfa-muricholic acidTaMCAConjugated bile acid1016575661.19–66300.756.384.44s, pScreenshot 2025 06 30 at 13 58 17 supplementaryData method BAs withCVs toKlaus 250630.pdf
Taurocholic acidTCAConjugated bile acid66751.85–3163154.145.31s, pScreenshot 2025 06 30 at 13 58 17 supplementaryData method BAs withCVs toKlaus 250630.pdf
Taurochenodeoxycholic acidTCDCAConjugated bile acid38731619.16–1730.25304.62.32s, pScreenshot 2025 06 30 at 13 58 17 supplementaryData method BAs withCVs toKlaus 250630.pdf
Taurodeoxycholic acidTDCAConjugated bile acid27337681.85–2384107.634.46s, pScreenshot 2025 06 30 at 13 58 17 supplementaryData method BAs withCVs toKlaus 250630.pdf
Taurohyocholic acidTHCAConjugated bile acid119541950.753.944.15s, pScreenshot 2025 06 30 at 13 58 17 supplementaryData method BAs withCVs toKlaus 250630.pdf
Taurohyodeoxycholic acidTHDCAConjugated bile acid119046<4554.766.68s, pScreenshot 2025 06 30 at 13 58 17 supplementaryData method BAs withCVs toKlaus 250630.pdf
Taurolithocholic acidTLCAConjugated bile acid439763<6525.44.2s, pScreenshot 2025 06 30 at 13 58 17 supplementaryData method BAs withCVs toKlaus 250630.pdf
Tauroursodeoxycholic acidTUDCAConjugated bile acid98488181.19–195104.392.41s, pScreenshot 2025 06 30 at 13 58 17 supplementaryData method BAs withCVs toKlaus 250630.pdf
Ursodeoxycholic acidUDCASecondary bile acid314015.75–741.33104.335.18s, pScreenshot 2025 06 30 at 13 58 17 supplementaryData method BAs withCVs toKlaus 250630.pdf

*Multianalyte determination is carried out in a single aliquot. Volume requirement is independent of the number of metabolites. Reported concentrations are not strictly normal reference range, which depends on the population, and several factors, including age, gender, ethnicity and procedures for sample handling and analytical technology. Reported concentrations are values that we and others have observed or reported in various cohorts of healthy subjects. For some biomarkers the assay performance may be different from those given in published articles. This is due to continuous improvements of the methods. LODs, CVs, and ICCs are not available for all biomarkers.

December 8, 2025
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Per Christian Eriksen

Øivind

Per Magne Ueland has been Professor at the University of Bergen 1987-2018. He is one of the founders of Bevital AS and the scientific advisor in Bevital since 2023. His interests includes biomarkers related to nutrition, inflammation, ageing and life-style related chronic diseases. Per is committed to the development of precise, high-throughput mass spectrometry methods, tailored for metabolic profiling of biobank specimens from large cohorts.

Marit holds a degree in chemical engineering from Bergen Ingeniørhøyskole, which is now part of the Western Norway University of Applied Sciences. She works with quantitative analysis and method development on LC-MS/MS at the laboratory of Bevital AS.

Ove completed a bachelor’s degree in Biomedical Laboratory Sciences at the Western Norway University of Applied Sciences in Bergen. With extensive experience in method development and expertise in GC-MS/MS, he specializes in optimizing analytical techniques for research-focused studies. At Bevital, Ove is dedicated to advancing laboratory methods and workflows, contributing to innovative research through precise and reliable analytical solutions.

Lene holds a bachelor’s degree in Biomedical Laboratory Science from the Western Norway University of Applied Sciences, where she is also completing her master’s degree in Medical Laboratory Technology. At Bevital, she works with GC-MS/MS analyses, focusing on accurate and reliable testing of biological samples. With her strong laboratory background, Lene is committed to delivering high-quality results that support medical research.

Klaus holds a PhD in physics from the University of Münster in Germany. He has over three decades of experience in Time-of-Flight mass spectrometry. He leverages his extensive expertise to provide customers with cutting-edge MALDI-MS analysis and the newest Olink Proteomics services.

Adrian holds a PhD in diabetes research, along with bachelor’s and master’s degrees in biomedical science and public health, respectively. With over 20 years of experience in laboratory science, he leads high-precision metabolite analyses and method development at Bevital. His expertise centers on quantifying biomarkers, metabolite classes, and metabolic pathways related to nutrition, cardiovascular and neurodegenerative diseases, and cancer. Adrian is committed to advancing research quality and actively collaborates nationally and internationally, leveraging targeted metabolomics to support innovative, multidisciplinary research.

Statistical power is the probability that a statistical test will correctly reject a false null hypothesis (H0​) when a specific alternative hypothesis (H1​) is true. H0​ is the null hypothesis, which states there is no effect or no difference. H1​ is the alternative hypothesis, which states there is a real effect or difference. Alpha (α) is the probability of a Type I error (a false positive), which is the risk of incorrectly rejecting the H0​ when it is actually true. You set this value before the experiment, commonly at 0.05. Beta (β) is the probability of a Type II error (a false negative), which is the risk of failing to reject the H0​ when it is actually false.

Power is calculated as 1−β. Increasing power means you are decreasing the probability of making a Type II error.

Several factors can be adjusted to increase the power of a statistical test:

  • Effect Size: This is the magnitude of the difference you are trying to detect. A larger effect size is easier to detect, thus increasing power. 

  • Sample Size: The number of observations in a study. A larger sample size provides more information about the population, reducing the margin of error and increasing the power to detect a true effect.

  • Variation: Refers to the spread or standard deviation of the data within the population. Less variation makes it easier to distinguish a real effect from random noise, thereby increasing power.

  • Alpha (): Increasing the alpha level (e.g., from 0.05 to 0.10) also increases power, but at the cost of a higher risk of a Type I error. This trade-off is often undesirable.

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561.

Vollset, S E; Nygârd, O; Refsum, H; Ueland, P M

Coffee and homocysteine Miscellaneous

2000, ISSN: 0002-9165.

Links | BibTeX

562.

Schneede, J; Refsum, H; Ueland, P M

Biological and environmental determinants of plasma homocysteine Journal Article

In: Semin Thromb Hemost, vol. 26, no. 3, pp. 263–279, 2000, ISSN: 0094-6176.

Abstract | Links | BibTeX

562 entries « 29 of 29 »

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