A comprehensive characterisation of the metabolic profile of varicose veins; implications in elaborating plausible cellular pathways for disease pathogenesis

Metabolic phenotypes reflect both the genetic and environmental factors which contribute to the development of varicose veins (VV). This study utilises analytical techniques to provide a comprehensive metabolic picture of VV disease, with the aim of identifying putative cellular pathways of disease...

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Published inScientific reports Vol. 7; no. 1; pp. 2989 - 13
Main Authors Anwar, Muzaffar A., Adesina-Georgiadis, Kyrillos N., Spagou, K., Vorkas, P. A., Li, J. V., Shalhoub, Joseph, Holmes, Elaine, Davies, Alun H.
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 07.06.2017
Nature Publishing Group
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ISSN2045-2322
2045-2322
DOI10.1038/s41598-017-02529-y

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Abstract Metabolic phenotypes reflect both the genetic and environmental factors which contribute to the development of varicose veins (VV). This study utilises analytical techniques to provide a comprehensive metabolic picture of VV disease, with the aim of identifying putative cellular pathways of disease pathogenesis. VV (n = 80) and non-VV (n = 35) aqueous and lipid metabolite extracts were analysed using 600 MHz 1 H Nuclear Magnetic Resonance spectroscopy and Ultra-Performance Liquid Chromatography Mass Spectrometry. A subset of tissue samples (8 subjects and 8 controls) were analysed for microRNA expression and the data analysed with mirBase (www.mirbase.org). Using Multivariate statistical analysis, Ingenuity pathway analysis software, DIANALAB database and published literature, the association of significant metabolites with relevant cellular pathways were understood. Higher concentrations of glutamate, taurine, myo-inositol, creatine and inosine were present in aqueous extracts and phosphatidylcholine, phosphatidylethanolamine and sphingomyelin in lipid extracts in the VV group compared with non-VV group. Out of 7 differentially expressed miRNAs, spearman correlation testing highlighted correlation of hsa-miR-642a-3p, hsa-miR-4459 and hsa-miR-135a-3p expression with inosine in the vein tissue, while miR-216a-5p, conversely, was correlated with phosphatidylcholine and phosphatidylethanolamine. Pathway analysis revealed an association of phosphatidylcholine and sphingomyelin with inflammation and myo-inositol with cellular proliferation.
AbstractList Metabolic phenotypes reflect both the genetic and environmental factors which contribute to the development of varicose veins (VV). This study utilises analytical techniques to provide a comprehensive metabolic picture of VV disease, with the aim of identifying putative cellular pathways of disease pathogenesis. VV (n = 80) and non-VV (n = 35) aqueous and lipid metabolite extracts were analysed using 600 MHz 1 H Nuclear Magnetic Resonance spectroscopy and Ultra-Performance Liquid Chromatography Mass Spectrometry. A subset of tissue samples (8 subjects and 8 controls) were analysed for microRNA expression and the data analysed with mirBase (www.mirbase.org). Using Multivariate statistical analysis, Ingenuity pathway analysis software, DIANALAB database and published literature, the association of significant metabolites with relevant cellular pathways were understood. Higher concentrations of glutamate, taurine, myo-inositol, creatine and inosine were present in aqueous extracts and phosphatidylcholine, phosphatidylethanolamine and sphingomyelin in lipid extracts in the VV group compared with non-VV group. Out of 7 differentially expressed miRNAs, spearman correlation testing highlighted correlation of hsa-miR-642a-3p, hsa-miR-4459 and hsa-miR-135a-3p expression with inosine in the vein tissue, while miR-216a-5p, conversely, was correlated with phosphatidylcholine and phosphatidylethanolamine. Pathway analysis revealed an association of phosphatidylcholine and sphingomyelin with inflammation and myo-inositol with cellular proliferation.
Abstract Metabolic phenotypes reflect both the genetic and environmental factors which contribute to the development of varicose veins (VV). This study utilises analytical techniques to provide a comprehensive metabolic picture of VV disease, with the aim of identifying putative cellular pathways of disease pathogenesis. VV (n = 80) and non-VV (n = 35) aqueous and lipid metabolite extracts were analysed using 600 MHz 1H Nuclear Magnetic Resonance spectroscopy and Ultra-Performance Liquid Chromatography Mass Spectrometry. A subset of tissue samples (8 subjects and 8 controls) were analysed for microRNA expression and the data analysed with mirBase (www.mirbase.org). Using Multivariate statistical analysis, Ingenuity pathway analysis software, DIANALAB database and published literature, the association of significant metabolites with relevant cellular pathways were understood. Higher concentrations of glutamate, taurine, myo-inositol, creatine and inosine were present in aqueous extracts and phosphatidylcholine, phosphatidylethanolamine and sphingomyelin in lipid extracts in the VV group compared with non-VV group. Out of 7 differentially expressed miRNAs, spearman correlation testing highlighted correlation of hsa-miR-642a-3p, hsa-miR-4459 and hsa-miR-135a-3p expression with inosine in the vein tissue, while miR-216a-5p, conversely, was correlated with phosphatidylcholine and phosphatidylethanolamine. Pathway analysis revealed an association of phosphatidylcholine and sphingomyelin with inflammation and myo-inositol with cellular proliferation.
Metabolic phenotypes reflect both the genetic and environmental factors which contribute to the development of varicose veins (VV). This study utilises analytical techniques to provide a comprehensive metabolic picture of VV disease, with the aim of identifying putative cellular pathways of disease pathogenesis. VV (n = 80) and non-VV (n = 35) aqueous and lipid metabolite extracts were analysed using 600 MHz H Nuclear Magnetic Resonance spectroscopy and Ultra-Performance Liquid Chromatography Mass Spectrometry. A subset of tissue samples (8 subjects and 8 controls) were analysed for microRNA expression and the data analysed with mirBase (www.mirbase.org). Using Multivariate statistical analysis, Ingenuity pathway analysis software, DIANALAB database and published literature, the association of significant metabolites with relevant cellular pathways were understood. Higher concentrations of glutamate, taurine, myo-inositol, creatine and inosine were present in aqueous extracts and phosphatidylcholine, phosphatidylethanolamine and sphingomyelin in lipid extracts in the VV group compared with non-VV group. Out of 7 differentially expressed miRNAs, spearman correlation testing highlighted correlation of hsa-miR-642a-3p, hsa-miR-4459 and hsa-miR-135a-3p expression with inosine in the vein tissue, while miR-216a-5p, conversely, was correlated with phosphatidylcholine and phosphatidylethanolamine. Pathway analysis revealed an association of phosphatidylcholine and sphingomyelin with inflammation and myo-inositol with cellular proliferation.
Metabolic phenotypes reflect both the genetic and environmental factors which contribute to the development of varicose veins (VV). This study utilises analytical techniques to provide a comprehensive metabolic picture of VV disease, with the aim of identifying putative cellular pathways of disease pathogenesis. VV (n = 80) and non-VV (n = 35) aqueous and lipid metabolite extracts were analysed using 600 MHz 1H Nuclear Magnetic Resonance spectroscopy and Ultra-Performance Liquid Chromatography Mass Spectrometry. A subset of tissue samples (8 subjects and 8 controls) were analysed for microRNA expression and the data analysed with mirBase (www.mirbase.org). Using Multivariate statistical analysis, Ingenuity pathway analysis software, DIANALAB database and published literature, the association of significant metabolites with relevant cellular pathways were understood. Higher concentrations of glutamate, taurine, myo-inositol, creatine and inosine were present in aqueous extracts and phosphatidylcholine, phosphatidylethanolamine and sphingomyelin in lipid extracts in the VV group compared with non-VV group. Out of 7 differentially expressed miRNAs, spearman correlation testing highlighted correlation of hsa-miR-642a-3p, hsa-miR-4459 and hsa-miR-135a-3p expression with inosine in the vein tissue, while miR-216a-5p, conversely, was correlated with phosphatidylcholine and phosphatidylethanolamine. Pathway analysis revealed an association of phosphatidylcholine and sphingomyelin with inflammation and myo-inositol with cellular proliferation.
Metabolic phenotypes reflect both the genetic and environmental factors which contribute to the development of varicose veins (VV). This study utilises analytical techniques to provide a comprehensive metabolic picture of VV disease, with the aim of identifying putative cellular pathways of disease pathogenesis. VV (n = 80) and non-VV (n = 35) aqueous and lipid metabolite extracts were analysed using 600 MHz 1H Nuclear Magnetic Resonance spectroscopy and Ultra-Performance Liquid Chromatography Mass Spectrometry. A subset of tissue samples (8 subjects and 8 controls) were analysed for microRNA expression and the data analysed with mirBase (www.mirbase.org). Using Multivariate statistical analysis, Ingenuity pathway analysis software, DIANALAB database and published literature, the association of significant metabolites with relevant cellular pathways were understood. Higher concentrations of glutamate, taurine, myo-inositol, creatine and inosine were present in aqueous extracts and phosphatidylcholine, phosphatidylethanolamine and sphingomyelin in lipid extracts in the VV group compared with non-VV group. Out of 7 differentially expressed miRNAs, spearman correlation testing highlighted correlation of hsa-miR-642a-3p, hsa-miR-4459 and hsa-miR-135a-3p expression with inosine in the vein tissue, while miR-216a-5p, conversely, was correlated with phosphatidylcholine and phosphatidylethanolamine. Pathway analysis revealed an association of phosphatidylcholine and sphingomyelin with inflammation and myo-inositol with cellular proliferation.Metabolic phenotypes reflect both the genetic and environmental factors which contribute to the development of varicose veins (VV). This study utilises analytical techniques to provide a comprehensive metabolic picture of VV disease, with the aim of identifying putative cellular pathways of disease pathogenesis. VV (n = 80) and non-VV (n = 35) aqueous and lipid metabolite extracts were analysed using 600 MHz 1H Nuclear Magnetic Resonance spectroscopy and Ultra-Performance Liquid Chromatography Mass Spectrometry. A subset of tissue samples (8 subjects and 8 controls) were analysed for microRNA expression and the data analysed with mirBase (www.mirbase.org). Using Multivariate statistical analysis, Ingenuity pathway analysis software, DIANALAB database and published literature, the association of significant metabolites with relevant cellular pathways were understood. Higher concentrations of glutamate, taurine, myo-inositol, creatine and inosine were present in aqueous extracts and phosphatidylcholine, phosphatidylethanolamine and sphingomyelin in lipid extracts in the VV group compared with non-VV group. Out of 7 differentially expressed miRNAs, spearman correlation testing highlighted correlation of hsa-miR-642a-3p, hsa-miR-4459 and hsa-miR-135a-3p expression with inosine in the vein tissue, while miR-216a-5p, conversely, was correlated with phosphatidylcholine and phosphatidylethanolamine. Pathway analysis revealed an association of phosphatidylcholine and sphingomyelin with inflammation and myo-inositol with cellular proliferation.
ArticleNumber 2989
Author Li, J. V.
Spagou, K.
Vorkas, P. A.
Holmes, Elaine
Adesina-Georgiadis, Kyrillos N.
Davies, Alun H.
Anwar, Muzaffar A.
Shalhoub, Joseph
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Cites_doi 10.1097/00024382-200014060-00006
10.1002/bjs.6798
10.1126/science.123.3202.845-a
10.1080/004982599238047
10.1016/j.ejvs.2010.08.001
10.1158/0008-5472.CAN-07-2678
10.1016/j.jvs.2009.11.037
10.1074/jbc.M111.252395
10.1152/ajpheart.00066.2008
10.1002/cbf.1003
10.1038/nature04648
10.1021/ac102523q
10.1038/nprot.2010.45
10.1021/ac051437y
10.1021/ac0713961
10.1006/abbi.1995.9959
10.1214/aos/1013699998
10.1074/jbc.M111.228593
10.1021/ac051632c
10.1016/j.ejvs.2012.05.020
10.1007/BF00580802
10.1039/C5AN01041A
10.1002/cbf.644
10.1007/s00726-012-1225-y
10.1021/ac503775m
10.1038/sj.emboj.7600034
10.1038/ng0795-288
10.1016/j.jvs.2004.09.027
10.1016/S0021-9258(18)51879-2
10.1016/S0021-9258(18)35858-7
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References Chao, Khan, Hannun (CR23) 1992; 267
Anwar (CR5) 2012; 44
Smith, Want, O’Maille, Abagyan, Siuzdak (CR30) 2006; 78
Eagle, Oyama, Levy, Freeman (CR12) 1956; 123
Vorkas (CR28) 2015; 87
Niizeki (CR20) 2008; 295
Anwar (CR26) 2015; 140
Newsholme, Procopio, Lima, Pithon-Curi, Curi (CR7) 2003; 21
Huitema, van den Dikkenberg, Brouwers, Holthuis (CR19) 2004; 23
Eklof (CR25) 2004; 40
O’Neill (CR9) 2000; 14
Raffetto (CR24) 2010; 51
Gatt (CR21) 1963; 238
Newsholme, Costa Rosa, Newsholme, Curi (CR8) 1996; 14
Das, Sil (CR11) 2012; 43
Tanaka (CR13) 2010; 40
Schrader, Haddy, Gerlach (CR17) 1977; 369
Clayton (CR3) 2006; 440
Coen (CR6) 2007; 79
Ripps, Shen (CR10) 2012; 18
Nicholson, Lindon, Holmes (CR2) 1999; 29
Ratnam, Kent (CR15) 1995; 323
Spagou (CR29) 2011; 83
Horinouchi (CR22) 1995; 10
Beckonert (CR4) 2010; 5
Dieterle, Ross, Schlotterbeck, Senn (CR27) 2006; 78
Shakor (CR14) 2011; 286
Lim, Davies (CR1) 2009; 96
Glunde (CR16) 2008; 68
Diguet (CR18) 2011; 286
Benjamini Yoav (CR31) 2001; 29
TA Clayton (2529_CR3) 2006; 440
M Coen (2529_CR6) 2007; 79
H Ripps (2529_CR10) 2012; 18
B Eklof (2529_CR25) 2004; 40
K Horinouchi (2529_CR22) 1995; 10
YD Benjamini Yoav (2529_CR31) 2001; 29
AB Shakor (2529_CR14) 2011; 286
H Tanaka (2529_CR13) 2010; 40
CA Smith (2529_CR30) 2006; 78
K Spagou (2529_CR29) 2011; 83
R Chao (2529_CR23) 1992; 267
S Gatt (2529_CR21) 1963; 238
CS Lim (2529_CR1) 2009; 96
PA Vorkas (2529_CR28) 2015; 87
K Huitema (2529_CR19) 2004; 23
J Das (2529_CR11) 2012; 43
P Newsholme (2529_CR8) 1996; 14
JK Nicholson (2529_CR2) 1999; 29
MA Anwar (2529_CR5) 2012; 44
P Newsholme (2529_CR7) 2003; 21
O Beckonert (2529_CR4) 2010; 5
JD Raffetto (2529_CR24) 2010; 51
K Glunde (2529_CR16) 2008; 68
S Ratnam (2529_CR15) 1995; 323
H Eagle (2529_CR12) 1956; 123
N Diguet (2529_CR18) 2011; 286
F Dieterle (2529_CR27) 2006; 78
T Niizeki (2529_CR20) 2008; 295
AJ O’Neill (2529_CR9) 2000; 14
J Schrader (2529_CR17) 1977; 369
MA Anwar (2529_CR26) 2015; 140
References_xml – volume: 14
  start-page: 605
  year: 2000
  end-page: 609
  ident: CR9
  article-title: Glutathione depletion-induced neutrophil apoptosis is caspase 3 dependent
  publication-title: Shock
  doi: 10.1097/00024382-200014060-00006
– volume: 96
  start-page: 1231
  issue: 11
  year: 2009
  end-page: 1242
  ident: CR1
  article-title: Pathogenesis of primary varicose veins
  publication-title: Br J Surg
  doi: 10.1002/bjs.6798
– volume: 123
  start-page: 845
  year: 1956
  end-page: 847
  ident: CR12
  article-title: Myo-inositol as an essential growth factor for normal and malignant human cells in tissue culture
  publication-title: Science
  doi: 10.1126/science.123.3202.845-a
– volume: 29
  start-page: 1181
  year: 1999
  end-page: 1189
  ident: CR2
  article-title: ‘Metabonomics’: understanding the metabolic responses of living systems to pathophysiological stimuli via multivariate statistical analysis of biological NMR spectroscopic data
  publication-title: Xenobiotica
  doi: 10.1080/004982599238047
– volume: 40
  start-page: 657
  year: 2010
  end-page: 663
  ident: CR13
  article-title: Imaging mass spectrometry reveals unique lipid distribution in primary varicose veins
  publication-title: Eur J Vasc Endovasc Surg
  doi: 10.1016/j.ejvs.2010.08.001
– volume: 68
  start-page: 172
  year: 2008
  end-page: 180
  ident: CR16
  article-title: Hypoxia regulates choline kinase expression through hypoxia-inducible factor-1 alpha signaling in a human prostate cancer model
  publication-title: Cancer Res
  doi: 10.1158/0008-5472.CAN-07-2678
– volume: 51
  start-page: 962
  year: 2010
  end-page: 971
  ident: CR24
  article-title: Functional adaptation of venous smooth muscle response to vasoconstriction in proximal, distal, and varix segments of varicose veins
  publication-title: J Vasc Surg
  doi: 10.1016/j.jvs.2009.11.037
– volume: 286
  start-page: 35007
  year: 2011
  end-page: 35019
  ident: CR18
  article-title: Muscle creatine kinase deficiency triggers both actin depolymerization and desmin disorganization by advanced glycation end products in dilated cardiomyopathy
  publication-title: J Biol Chem
  doi: 10.1074/jbc.M111.252395
– volume: 295
  start-page: H245
  year: 2008
  end-page: 255
  ident: CR20
  article-title: Diacylglycerol kinase-epsilon restores cardiac dysfunction under chronic pressure overload: a new specific regulator of Galpha(q) signaling cascade
  publication-title: Am J Physiol Heart Circ Physiol
  doi: 10.1152/ajpheart.00066.2008
– volume: 21
  start-page: 1
  year: 2003
  end-page: 9
  ident: CR7
  article-title: Glutamine and glutamate–their central role in cell metabolism and function
  publication-title: Cell biochemistry and function
  doi: 10.1002/cbf.1003
– volume: 440
  start-page: 1073
  year: 2006
  end-page: 1077
  ident: CR3
  article-title: Pharmaco-metabonomic phenotyping and personalized drug treatment
  publication-title: Nature
  doi: 10.1038/nature04648
– volume: 83
  start-page: 382
  year: 2011
  end-page: 390
  ident: CR29
  article-title: HILIC-UPLC-MS for exploratory urinary metabolic profiling in toxicological studies
  publication-title: Anal Chem
  doi: 10.1021/ac102523q
– volume: 267
  start-page: 23459
  year: 1992
  end-page: 23462
  ident: CR23
  article-title: Retinoblastoma protein dephosphorylation induced by D-erythro-sphingosine
  publication-title: J Biol Chem
– volume: 238
  start-page: 3131
  year: 1963
  end-page: 3133
  ident: CR21
  article-title: Enzymic Hydrolysis and Synthesis of Ceramides
  publication-title: J Biol Chem
– volume: 5
  start-page: 1019
  year: 2010
  end-page: 1032
  ident: CR4
  article-title: High-resolution magic-angle-spinning NMR spectroscopy for metabolic profiling of intact tissues
  publication-title: Nat Protoc
  doi: 10.1038/nprot.2010.45
– volume: 78
  start-page: 779
  year: 2006
  end-page: 787
  ident: CR30
  article-title: XCMS: processing mass spectrometry data for metabolite profiling using nonlinear peak alignment, matching, and identification
  publication-title: Anal Chem
  doi: 10.1021/ac051437y
– volume: 79
  start-page: 8956
  year: 2007
  end-page: 8966
  ident: CR6
  article-title: Heteronuclear 1H-31P statistical total correlation NMR spectroscopy of intact liver for metabolic biomarker assignment: application to galactosamine-induced hepatotoxicity
  publication-title: Anal Chem
  doi: 10.1021/ac0713961
– volume: 323
  start-page: 313
  year: 1995
  end-page: 322
  ident: CR15
  article-title: Early increase in choline kinase activity upon induction of the H-ras oncogene in mouse fibroblast cell lines
  publication-title: Archives of biochemistry and biophysics
  doi: 10.1006/abbi.1995.9959
– volume: 29
  start-page: 1165
  year: 2001
  end-page: 1188
  ident: CR31
  article-title: The control of the false discovery rate in multiple testing under dependency
  publication-title: Ann. Statist
  doi: 10.1214/aos/1013699998
– volume: 286
  start-page: 36053
  year: 2011
  end-page: 36062
  ident: CR14
  article-title: Sphingomyelin synthase 1-generated sphingomyelin plays an important role in transferrin trafficking and cell proliferation
  publication-title: J Biol Chem
  doi: 10.1074/jbc.M111.228593
– volume: 78
  start-page: 4281
  year: 2006
  end-page: 4290
  ident: CR27
  article-title: Probabilistic quotient normalization as robust method to account for dilution of complex biological mixtures. Application in 1H NMR metabonomics
  publication-title: Anal Chem
  doi: 10.1021/ac051632c
– volume: 44
  start-page: 442
  year: 2012
  end-page: 450
  ident: CR5
  article-title: Identification of Distinctive Metabolic Signatures of Intact Varicose Vein Tissue via Magic Angle Spinning Nuclear Magnetic Resonance Spectroscopy
  publication-title: Eur J Vasc Endovasc Surg
  doi: 10.1016/j.ejvs.2012.05.020
– volume: 18
  start-page: 2673
  year: 2012
  end-page: 2686
  ident: CR10
  article-title: Review: taurine: a “very essential” amino acid
  publication-title: Molecular vision
– volume: 369
  start-page: 1
  year: 1977
  end-page: 6
  ident: CR17
  article-title: Release of adenosine, inosine and hypoxanthine from the isolated guinea pig heart during hypoxia, flow-autoregulation and reactive hyperemia
  publication-title: Pflugers Archiv: European journal of physiology
  doi: 10.1007/BF00580802
– volume: 140
  start-page: 7586
  year: 2015
  end-page: 7597
  ident: CR26
  article-title: Optimization of metabolite extraction of human vein tissue for ultra performance liquid chromatography-mass spectrometry and nuclear magnetic resonance-based untargeted metabolic profiling
  publication-title: The Analyst
  doi: 10.1039/C5AN01041A
– volume: 14
  start-page: 1
  year: 1996
  end-page: 10
  ident: CR8
  article-title: The importance of fuel metabolism to macrophage function
  publication-title: Cell biochemistry and function
  doi: 10.1002/cbf.644
– volume: 43
  start-page: 1509
  year: 2012
  end-page: 1523
  ident: CR11
  article-title: Taurine ameliorates alloxan-induced diabetic renal injury, oxidative stress-related signaling pathways and apoptosis in rats
  publication-title: Amino Acids
  doi: 10.1007/s00726-012-1225-y
– volume: 87
  start-page: 4184
  year: 2015
  end-page: 4193
  ident: CR28
  article-title: Untargeted UPLC-MS profiling pipeline to expand tissue metabolome coverage: application to cardiovascular disease
  publication-title: Anal Chem
  doi: 10.1021/ac503775m
– volume: 23
  start-page: 33
  year: 2004
  end-page: 44
  ident: CR19
  article-title: Identification of a family of animal sphingomyelin synthases
  publication-title: The EMBO journal
  doi: 10.1038/sj.emboj.7600034
– volume: 10
  start-page: 288
  year: 1995
  end-page: 293
  ident: CR22
  article-title: Acid sphingomyelinase deficient mice: a model of types A and B Niemann-Pick disease
  publication-title: Nat Genet
  doi: 10.1038/ng0795-288
– volume: 40
  start-page: 1248
  year: 2004
  end-page: 1252
  ident: CR25
  article-title: Revision of the CEAP classification for chronic venous disorders: consensus statement
  publication-title: J Vasc Surg
  doi: 10.1016/j.jvs.2004.09.027
– volume: 238
  start-page: 3131
  year: 1963
  ident: 2529_CR21
  publication-title: J Biol Chem
  doi: 10.1016/S0021-9258(18)51879-2
– volume: 43
  start-page: 1509
  year: 2012
  ident: 2529_CR11
  publication-title: Amino Acids
  doi: 10.1007/s00726-012-1225-y
– volume: 18
  start-page: 2673
  year: 2012
  ident: 2529_CR10
  publication-title: Molecular vision
– volume: 140
  start-page: 7586
  year: 2015
  ident: 2529_CR26
  publication-title: The Analyst
  doi: 10.1039/C5AN01041A
– volume: 78
  start-page: 779
  year: 2006
  ident: 2529_CR30
  publication-title: Anal Chem
  doi: 10.1021/ac051437y
– volume: 14
  start-page: 605
  year: 2000
  ident: 2529_CR9
  publication-title: Shock
  doi: 10.1097/00024382-200014060-00006
– volume: 286
  start-page: 36053
  year: 2011
  ident: 2529_CR14
  publication-title: J Biol Chem
  doi: 10.1074/jbc.M111.228593
– volume: 29
  start-page: 1165
  year: 2001
  ident: 2529_CR31
  publication-title: Ann. Statist
  doi: 10.1214/aos/1013699998
– volume: 286
  start-page: 35007
  year: 2011
  ident: 2529_CR18
  publication-title: J Biol Chem
  doi: 10.1074/jbc.M111.252395
– volume: 5
  start-page: 1019
  year: 2010
  ident: 2529_CR4
  publication-title: Nat Protoc
  doi: 10.1038/nprot.2010.45
– volume: 323
  start-page: 313
  year: 1995
  ident: 2529_CR15
  publication-title: Archives of biochemistry and biophysics
  doi: 10.1006/abbi.1995.9959
– volume: 123
  start-page: 845
  year: 1956
  ident: 2529_CR12
  publication-title: Science
  doi: 10.1126/science.123.3202.845-a
– volume: 40
  start-page: 1248
  year: 2004
  ident: 2529_CR25
  publication-title: J Vasc Surg
  doi: 10.1016/j.jvs.2004.09.027
– volume: 267
  start-page: 23459
  year: 1992
  ident: 2529_CR23
  publication-title: J Biol Chem
  doi: 10.1016/S0021-9258(18)35858-7
– volume: 295
  start-page: H245
  year: 2008
  ident: 2529_CR20
  publication-title: Am J Physiol Heart Circ Physiol
  doi: 10.1152/ajpheart.00066.2008
– volume: 79
  start-page: 8956
  year: 2007
  ident: 2529_CR6
  publication-title: Anal Chem
  doi: 10.1021/ac0713961
– volume: 40
  start-page: 657
  year: 2010
  ident: 2529_CR13
  publication-title: Eur J Vasc Endovasc Surg
  doi: 10.1016/j.ejvs.2010.08.001
– volume: 68
  start-page: 172
  year: 2008
  ident: 2529_CR16
  publication-title: Cancer Res
  doi: 10.1158/0008-5472.CAN-07-2678
– volume: 51
  start-page: 962
  year: 2010
  ident: 2529_CR24
  publication-title: J Vasc Surg
  doi: 10.1016/j.jvs.2009.11.037
– volume: 87
  start-page: 4184
  year: 2015
  ident: 2529_CR28
  publication-title: Anal Chem
  doi: 10.1021/ac503775m
– volume: 44
  start-page: 442
  year: 2012
  ident: 2529_CR5
  publication-title: Eur J Vasc Endovasc Surg
  doi: 10.1016/j.ejvs.2012.05.020
– volume: 83
  start-page: 382
  year: 2011
  ident: 2529_CR29
  publication-title: Anal Chem
  doi: 10.1021/ac102523q
– volume: 10
  start-page: 288
  year: 1995
  ident: 2529_CR22
  publication-title: Nat Genet
  doi: 10.1038/ng0795-288
– volume: 369
  start-page: 1
  year: 1977
  ident: 2529_CR17
  publication-title: Pflugers Archiv: European journal of physiology
  doi: 10.1007/BF00580802
– volume: 23
  start-page: 33
  year: 2004
  ident: 2529_CR19
  publication-title: The EMBO journal
  doi: 10.1038/sj.emboj.7600034
– volume: 96
  start-page: 1231
  issue: 11
  year: 2009
  ident: 2529_CR1
  publication-title: Br J Surg
  doi: 10.1002/bjs.6798
– volume: 78
  start-page: 4281
  year: 2006
  ident: 2529_CR27
  publication-title: Anal Chem
  doi: 10.1021/ac051632c
– volume: 29
  start-page: 1181
  year: 1999
  ident: 2529_CR2
  publication-title: Xenobiotica
  doi: 10.1080/004982599238047
– volume: 440
  start-page: 1073
  year: 2006
  ident: 2529_CR3
  publication-title: Nature
  doi: 10.1038/nature04648
– volume: 21
  start-page: 1
  year: 2003
  ident: 2529_CR7
  publication-title: Cell biochemistry and function
  doi: 10.1002/cbf.1003
– volume: 14
  start-page: 1
  year: 1996
  ident: 2529_CR8
  publication-title: Cell biochemistry and function
  doi: 10.1002/cbf.644
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Snippet Metabolic phenotypes reflect both the genetic and environmental factors which contribute to the development of varicose veins (VV). This study utilises...
Abstract Metabolic phenotypes reflect both the genetic and environmental factors which contribute to the development of varicose veins (VV). This study...
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pubmedcentral
proquest
pubmed
crossref
springer
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Open Access Repository
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Index Database
Enrichment Source
Publisher
StartPage 2989
SubjectTerms 101/58
101/6
38/61
631/92/320
692/420/256/2515
Chromatography, High Pressure Liquid
Creatine
Data processing
Environmental factors
Female
Gene Expression Profiling
Humanities and Social Sciences
Humans
Inositol
Lecithin
Liquid chromatography
Magnetic Resonance Spectroscopy
Male
Mass Spectrometry
Mass spectroscopy
Metabolism
Metabolites
Metabolome
miRNA
multidisciplinary
NMR
Nuclear magnetic resonance
Pathogenesis
Phosphatidylcholine
Phosphatidylethanolamine
RNA, Messenger - analysis
Science
Science (multidisciplinary)
Spectroscopy
Sphingomyelin
Statistical analysis
Taurine
Varicose veins
Varicose Veins - pathology
Veins
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Title A comprehensive characterisation of the metabolic profile of varicose veins; implications in elaborating plausible cellular pathways for disease pathogenesis
URI https://link.springer.com/article/10.1038/s41598-017-02529-y
https://www.ncbi.nlm.nih.gov/pubmed/28592827
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https://pubmed.ncbi.nlm.nih.gov/PMC5462754
https://doaj.org/article/d4c7e59691b340f18eb5f2eab7477b93
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