Systematic review of metabolomic alterations in ulcerative colitis: unveiling key metabolic signatures and pathways

Background: Despite numerous metabolomic studies on ulcerative colitis (UC), the results have been highly variable, making it challenging to identify key metabolic abnormalities in UC. Objectives: This study aims to uncover key metabolites and metabolic pathways in UC by analyzing existing metabolom...
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Autor*in:	Meiling Liu [verfasserIn] Siyi Guo [verfasserIn] Liang Wang [verfasserIn]

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2024

Übergeordnetes Werk:	In: Therapeutic Advances in Gastroenterology - SAGE Publishing, 2018, 17(2024)
Übergeordnetes Werk:	volume:17 ; year:2024

Links:	Link aufrufen Link aufrufen Link aufrufen Journal toc

DOI / URN:	10.1177/17562848241239580

Katalog-ID:	DOAJ097303917

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520			\|a Background: Despite numerous metabolomic studies on ulcerative colitis (UC), the results have been highly variable, making it challenging to identify key metabolic abnormalities in UC. Objectives: This study aims to uncover key metabolites and metabolic pathways in UC by analyzing existing metabolomics data. Design: A systematic review. Data sources and methods: We conducted a comprehensive search in databases (PubMed, Cochrane Library, Embase, and Web of Science) and relevant study references for metabolomic research on UC up to 28 December 2022. Significant metabolite differences between UC patients and controls were identified, followed by an analysis of relevant metabolic pathways. Results: This review incorporated 78 studies, identifying 2868 differentially expressed metabolites between UC patients and controls. The metabolites were predominantly from ‘lipids and lipid-like molecules’ and ‘organic acids and derivatives’ superclasses. We found 101 metabolites consistently altered in multiple datasets within the same sample type and 78 metabolites common across different sample types. Of these, 62 metabolites exhibited consistent regulatory trends across various datasets or sample types. Pathway analysis revealed 22 significantly altered metabolic pathways, with 6 pathways being recurrently enriched across different sample types. Conclusion: This study elucidates key metabolic characteristics in UC, offering insights into molecular mechanisms and biomarker discovery for the disease. Future research could focus on validating these findings and exploring their clinical applications.
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allfields	10.1177/17562848241239580 doi (DE-627)DOAJ097303917 (DE-599)DOAJ5b5f746d077e4f4eb458089a24935aa7 DE-627 ger DE-627 rakwb eng RC799-869 Meiling Liu verfasserin aut Systematic review of metabolomic alterations in ulcerative colitis: unveiling key metabolic signatures and pathways 2024 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Background: Despite numerous metabolomic studies on ulcerative colitis (UC), the results have been highly variable, making it challenging to identify key metabolic abnormalities in UC. Objectives: This study aims to uncover key metabolites and metabolic pathways in UC by analyzing existing metabolomics data. Design: A systematic review. Data sources and methods: We conducted a comprehensive search in databases (PubMed, Cochrane Library, Embase, and Web of Science) and relevant study references for metabolomic research on UC up to 28 December 2022. Significant metabolite differences between UC patients and controls were identified, followed by an analysis of relevant metabolic pathways. Results: This review incorporated 78 studies, identifying 2868 differentially expressed metabolites between UC patients and controls. The metabolites were predominantly from ‘lipids and lipid-like molecules’ and ‘organic acids and derivatives’ superclasses. We found 101 metabolites consistently altered in multiple datasets within the same sample type and 78 metabolites common across different sample types. Of these, 62 metabolites exhibited consistent regulatory trends across various datasets or sample types. Pathway analysis revealed 22 significantly altered metabolic pathways, with 6 pathways being recurrently enriched across different sample types. Conclusion: This study elucidates key metabolic characteristics in UC, offering insights into molecular mechanisms and biomarker discovery for the disease. Future research could focus on validating these findings and exploring their clinical applications. Diseases of the digestive system. Gastroenterology Siyi Guo verfasserin aut Liang Wang verfasserin aut In Therapeutic Advances in Gastroenterology SAGE Publishing, 2018 17(2024) (DE-627)573742669 (DE-600)2440710-0 17562848 nnns volume:17 year:2024 https://doi.org/10.1177/17562848241239580 kostenfrei https://doaj.org/article/5b5f746d077e4f4eb458089a24935aa7 kostenfrei https://doi.org/10.1177/17562848241239580 kostenfrei https://doaj.org/toc/1756-2848 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_374 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_2704 GBV_ILN_2707 GBV_ILN_2889 GBV_ILN_2890 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 17 2024
spelling	10.1177/17562848241239580 doi (DE-627)DOAJ097303917 (DE-599)DOAJ5b5f746d077e4f4eb458089a24935aa7 DE-627 ger DE-627 rakwb eng RC799-869 Meiling Liu verfasserin aut Systematic review of metabolomic alterations in ulcerative colitis: unveiling key metabolic signatures and pathways 2024 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Background: Despite numerous metabolomic studies on ulcerative colitis (UC), the results have been highly variable, making it challenging to identify key metabolic abnormalities in UC. Objectives: This study aims to uncover key metabolites and metabolic pathways in UC by analyzing existing metabolomics data. Design: A systematic review. Data sources and methods: We conducted a comprehensive search in databases (PubMed, Cochrane Library, Embase, and Web of Science) and relevant study references for metabolomic research on UC up to 28 December 2022. Significant metabolite differences between UC patients and controls were identified, followed by an analysis of relevant metabolic pathways. Results: This review incorporated 78 studies, identifying 2868 differentially expressed metabolites between UC patients and controls. The metabolites were predominantly from ‘lipids and lipid-like molecules’ and ‘organic acids and derivatives’ superclasses. We found 101 metabolites consistently altered in multiple datasets within the same sample type and 78 metabolites common across different sample types. Of these, 62 metabolites exhibited consistent regulatory trends across various datasets or sample types. Pathway analysis revealed 22 significantly altered metabolic pathways, with 6 pathways being recurrently enriched across different sample types. Conclusion: This study elucidates key metabolic characteristics in UC, offering insights into molecular mechanisms and biomarker discovery for the disease. Future research could focus on validating these findings and exploring their clinical applications. Diseases of the digestive system. Gastroenterology Siyi Guo verfasserin aut Liang Wang verfasserin aut In Therapeutic Advances in Gastroenterology SAGE Publishing, 2018 17(2024) (DE-627)573742669 (DE-600)2440710-0 17562848 nnns volume:17 year:2024 https://doi.org/10.1177/17562848241239580 kostenfrei https://doaj.org/article/5b5f746d077e4f4eb458089a24935aa7 kostenfrei https://doi.org/10.1177/17562848241239580 kostenfrei https://doaj.org/toc/1756-2848 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_374 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_2704 GBV_ILN_2707 GBV_ILN_2889 GBV_ILN_2890 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 17 2024
allfields_unstemmed	10.1177/17562848241239580 doi (DE-627)DOAJ097303917 (DE-599)DOAJ5b5f746d077e4f4eb458089a24935aa7 DE-627 ger DE-627 rakwb eng RC799-869 Meiling Liu verfasserin aut Systematic review of metabolomic alterations in ulcerative colitis: unveiling key metabolic signatures and pathways 2024 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Background: Despite numerous metabolomic studies on ulcerative colitis (UC), the results have been highly variable, making it challenging to identify key metabolic abnormalities in UC. Objectives: This study aims to uncover key metabolites and metabolic pathways in UC by analyzing existing metabolomics data. Design: A systematic review. Data sources and methods: We conducted a comprehensive search in databases (PubMed, Cochrane Library, Embase, and Web of Science) and relevant study references for metabolomic research on UC up to 28 December 2022. Significant metabolite differences between UC patients and controls were identified, followed by an analysis of relevant metabolic pathways. Results: This review incorporated 78 studies, identifying 2868 differentially expressed metabolites between UC patients and controls. The metabolites were predominantly from ‘lipids and lipid-like molecules’ and ‘organic acids and derivatives’ superclasses. We found 101 metabolites consistently altered in multiple datasets within the same sample type and 78 metabolites common across different sample types. Of these, 62 metabolites exhibited consistent regulatory trends across various datasets or sample types. Pathway analysis revealed 22 significantly altered metabolic pathways, with 6 pathways being recurrently enriched across different sample types. Conclusion: This study elucidates key metabolic characteristics in UC, offering insights into molecular mechanisms and biomarker discovery for the disease. Future research could focus on validating these findings and exploring their clinical applications. Diseases of the digestive system. Gastroenterology Siyi Guo verfasserin aut Liang Wang verfasserin aut In Therapeutic Advances in Gastroenterology SAGE Publishing, 2018 17(2024) (DE-627)573742669 (DE-600)2440710-0 17562848 nnns volume:17 year:2024 https://doi.org/10.1177/17562848241239580 kostenfrei https://doaj.org/article/5b5f746d077e4f4eb458089a24935aa7 kostenfrei https://doi.org/10.1177/17562848241239580 kostenfrei https://doaj.org/toc/1756-2848 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_374 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_2704 GBV_ILN_2707 GBV_ILN_2889 GBV_ILN_2890 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 17 2024
allfieldsGer	10.1177/17562848241239580 doi (DE-627)DOAJ097303917 (DE-599)DOAJ5b5f746d077e4f4eb458089a24935aa7 DE-627 ger DE-627 rakwb eng RC799-869 Meiling Liu verfasserin aut Systematic review of metabolomic alterations in ulcerative colitis: unveiling key metabolic signatures and pathways 2024 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Background: Despite numerous metabolomic studies on ulcerative colitis (UC), the results have been highly variable, making it challenging to identify key metabolic abnormalities in UC. Objectives: This study aims to uncover key metabolites and metabolic pathways in UC by analyzing existing metabolomics data. Design: A systematic review. Data sources and methods: We conducted a comprehensive search in databases (PubMed, Cochrane Library, Embase, and Web of Science) and relevant study references for metabolomic research on UC up to 28 December 2022. Significant metabolite differences between UC patients and controls were identified, followed by an analysis of relevant metabolic pathways. Results: This review incorporated 78 studies, identifying 2868 differentially expressed metabolites between UC patients and controls. The metabolites were predominantly from ‘lipids and lipid-like molecules’ and ‘organic acids and derivatives’ superclasses. We found 101 metabolites consistently altered in multiple datasets within the same sample type and 78 metabolites common across different sample types. Of these, 62 metabolites exhibited consistent regulatory trends across various datasets or sample types. Pathway analysis revealed 22 significantly altered metabolic pathways, with 6 pathways being recurrently enriched across different sample types. Conclusion: This study elucidates key metabolic characteristics in UC, offering insights into molecular mechanisms and biomarker discovery for the disease. Future research could focus on validating these findings and exploring their clinical applications. Diseases of the digestive system. Gastroenterology Siyi Guo verfasserin aut Liang Wang verfasserin aut In Therapeutic Advances in Gastroenterology SAGE Publishing, 2018 17(2024) (DE-627)573742669 (DE-600)2440710-0 17562848 nnns volume:17 year:2024 https://doi.org/10.1177/17562848241239580 kostenfrei https://doaj.org/article/5b5f746d077e4f4eb458089a24935aa7 kostenfrei https://doi.org/10.1177/17562848241239580 kostenfrei https://doaj.org/toc/1756-2848 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_374 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_2704 GBV_ILN_2707 GBV_ILN_2889 GBV_ILN_2890 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 17 2024
allfieldsSound	10.1177/17562848241239580 doi (DE-627)DOAJ097303917 (DE-599)DOAJ5b5f746d077e4f4eb458089a24935aa7 DE-627 ger DE-627 rakwb eng RC799-869 Meiling Liu verfasserin aut Systematic review of metabolomic alterations in ulcerative colitis: unveiling key metabolic signatures and pathways 2024 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Background: Despite numerous metabolomic studies on ulcerative colitis (UC), the results have been highly variable, making it challenging to identify key metabolic abnormalities in UC. Objectives: This study aims to uncover key metabolites and metabolic pathways in UC by analyzing existing metabolomics data. Design: A systematic review. Data sources and methods: We conducted a comprehensive search in databases (PubMed, Cochrane Library, Embase, and Web of Science) and relevant study references for metabolomic research on UC up to 28 December 2022. Significant metabolite differences between UC patients and controls were identified, followed by an analysis of relevant metabolic pathways. Results: This review incorporated 78 studies, identifying 2868 differentially expressed metabolites between UC patients and controls. The metabolites were predominantly from ‘lipids and lipid-like molecules’ and ‘organic acids and derivatives’ superclasses. We found 101 metabolites consistently altered in multiple datasets within the same sample type and 78 metabolites common across different sample types. Of these, 62 metabolites exhibited consistent regulatory trends across various datasets or sample types. Pathway analysis revealed 22 significantly altered metabolic pathways, with 6 pathways being recurrently enriched across different sample types. Conclusion: This study elucidates key metabolic characteristics in UC, offering insights into molecular mechanisms and biomarker discovery for the disease. Future research could focus on validating these findings and exploring their clinical applications. Diseases of the digestive system. Gastroenterology Siyi Guo verfasserin aut Liang Wang verfasserin aut In Therapeutic Advances in Gastroenterology SAGE Publishing, 2018 17(2024) (DE-627)573742669 (DE-600)2440710-0 17562848 nnns volume:17 year:2024 https://doi.org/10.1177/17562848241239580 kostenfrei https://doaj.org/article/5b5f746d077e4f4eb458089a24935aa7 kostenfrei https://doi.org/10.1177/17562848241239580 kostenfrei https://doaj.org/toc/1756-2848 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_374 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_2704 GBV_ILN_2707 GBV_ILN_2889 GBV_ILN_2890 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 17 2024
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authorswithroles_txt_mv	Meiling Liu @@aut@@ Siyi Guo @@aut@@ Liang Wang @@aut@@
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Objectives: This study aims to uncover key metabolites and metabolic pathways in UC by analyzing existing metabolomics data. Design: A systematic review. Data sources and methods: We conducted a comprehensive search in databases (PubMed, Cochrane Library, Embase, and Web of Science) and relevant study references for metabolomic research on UC up to 28 December 2022. Significant metabolite differences between UC patients and controls were identified, followed by an analysis of relevant metabolic pathways. Results: This review incorporated 78 studies, identifying 2868 differentially expressed metabolites between UC patients and controls. The metabolites were predominantly from ‘lipids and lipid-like molecules’ and ‘organic acids and derivatives’ superclasses. We found 101 metabolites consistently altered in multiple datasets within the same sample type and 78 metabolites common across different sample types. 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callnumber-first	R - Medicine
author	Meiling Liu
spellingShingle	Meiling Liu misc RC799-869 misc Diseases of the digestive system. Gastroenterology Systematic review of metabolomic alterations in ulcerative colitis: unveiling key metabolic signatures and pathways
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topic_title	RC799-869 Systematic review of metabolomic alterations in ulcerative colitis: unveiling key metabolic signatures and pathways
topic	misc RC799-869 misc Diseases of the digestive system. Gastroenterology
topic_unstemmed	misc RC799-869 misc Diseases of the digestive system. Gastroenterology
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title	Systematic review of metabolomic alterations in ulcerative colitis: unveiling key metabolic signatures and pathways
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title_full	Systematic review of metabolomic alterations in ulcerative colitis: unveiling key metabolic signatures and pathways
author_sort	Meiling Liu
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title_sort	systematic review of metabolomic alterations in ulcerative colitis: unveiling key metabolic signatures and pathways
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title_auth	Systematic review of metabolomic alterations in ulcerative colitis: unveiling key metabolic signatures and pathways
abstract	Background: Despite numerous metabolomic studies on ulcerative colitis (UC), the results have been highly variable, making it challenging to identify key metabolic abnormalities in UC. Objectives: This study aims to uncover key metabolites and metabolic pathways in UC by analyzing existing metabolomics data. Design: A systematic review. Data sources and methods: We conducted a comprehensive search in databases (PubMed, Cochrane Library, Embase, and Web of Science) and relevant study references for metabolomic research on UC up to 28 December 2022. Significant metabolite differences between UC patients and controls were identified, followed by an analysis of relevant metabolic pathways. Results: This review incorporated 78 studies, identifying 2868 differentially expressed metabolites between UC patients and controls. The metabolites were predominantly from ‘lipids and lipid-like molecules’ and ‘organic acids and derivatives’ superclasses. We found 101 metabolites consistently altered in multiple datasets within the same sample type and 78 metabolites common across different sample types. Of these, 62 metabolites exhibited consistent regulatory trends across various datasets or sample types. Pathway analysis revealed 22 significantly altered metabolic pathways, with 6 pathways being recurrently enriched across different sample types. Conclusion: This study elucidates key metabolic characteristics in UC, offering insights into molecular mechanisms and biomarker discovery for the disease. Future research could focus on validating these findings and exploring their clinical applications.
abstractGer	Background: Despite numerous metabolomic studies on ulcerative colitis (UC), the results have been highly variable, making it challenging to identify key metabolic abnormalities in UC. Objectives: This study aims to uncover key metabolites and metabolic pathways in UC by analyzing existing metabolomics data. Design: A systematic review. Data sources and methods: We conducted a comprehensive search in databases (PubMed, Cochrane Library, Embase, and Web of Science) and relevant study references for metabolomic research on UC up to 28 December 2022. Significant metabolite differences between UC patients and controls were identified, followed by an analysis of relevant metabolic pathways. Results: This review incorporated 78 studies, identifying 2868 differentially expressed metabolites between UC patients and controls. The metabolites were predominantly from ‘lipids and lipid-like molecules’ and ‘organic acids and derivatives’ superclasses. We found 101 metabolites consistently altered in multiple datasets within the same sample type and 78 metabolites common across different sample types. Of these, 62 metabolites exhibited consistent regulatory trends across various datasets or sample types. Pathway analysis revealed 22 significantly altered metabolic pathways, with 6 pathways being recurrently enriched across different sample types. Conclusion: This study elucidates key metabolic characteristics in UC, offering insights into molecular mechanisms and biomarker discovery for the disease. Future research could focus on validating these findings and exploring their clinical applications.
abstract_unstemmed	Background: Despite numerous metabolomic studies on ulcerative colitis (UC), the results have been highly variable, making it challenging to identify key metabolic abnormalities in UC. Objectives: This study aims to uncover key metabolites and metabolic pathways in UC by analyzing existing metabolomics data. Design: A systematic review. Data sources and methods: We conducted a comprehensive search in databases (PubMed, Cochrane Library, Embase, and Web of Science) and relevant study references for metabolomic research on UC up to 28 December 2022. Significant metabolite differences between UC patients and controls were identified, followed by an analysis of relevant metabolic pathways. Results: This review incorporated 78 studies, identifying 2868 differentially expressed metabolites between UC patients and controls. The metabolites were predominantly from ‘lipids and lipid-like molecules’ and ‘organic acids and derivatives’ superclasses. We found 101 metabolites consistently altered in multiple datasets within the same sample type and 78 metabolites common across different sample types. Of these, 62 metabolites exhibited consistent regulatory trends across various datasets or sample types. Pathway analysis revealed 22 significantly altered metabolic pathways, with 6 pathways being recurrently enriched across different sample types. Conclusion: This study elucidates key metabolic characteristics in UC, offering insights into molecular mechanisms and biomarker discovery for the disease. Future research could focus on validating these findings and exploring their clinical applications.
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title_short	Systematic review of metabolomic alterations in ulcerative colitis: unveiling key metabolic signatures and pathways
url	https://doi.org/10.1177/17562848241239580 https://doaj.org/article/5b5f746d077e4f4eb458089a24935aa7 https://doaj.org/toc/1756-2848
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Systematic review of metabolomic alterations in ulcerative colitis: unveiling key metabolic signatures and pathways

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