Metabolomic analysis suggests thiamine monophosphate as a potential marker for mesenchymal stem cell transplantation outcomes in patients with SLE

Objective The objective of this research is to identify metabolic markers associated with successful treatment by evaluating the effect of mesenchymal stem cell transplantation (MSCT) on the metabolic profiles of patients with SLE.Methods Plasma samples were collected from 20 patients with SLE befor...

Full description

Saved in:
Bibliographic Details
Main Authors: Bin Yang, Xuebing Feng, Lingyun Sun, Xiaojun Tang, Xiaoman Jiang, Zhuoyang Jia
Format: Article
Language:English
Published: BMJ Publishing Group 2025-03-01
Series:Lupus Science and Medicine
Online Access:https://lupus.bmj.com/content/12/1/e001197.full
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1849338221420347392
author Bin Yang
Xuebing Feng
Lingyun Sun
Xiaojun Tang
Xiaoman Jiang
Zhuoyang Jia
author_facet Bin Yang
Xuebing Feng
Lingyun Sun
Xiaojun Tang
Xiaoman Jiang
Zhuoyang Jia
author_sort Bin Yang
collection DOAJ
description Objective The objective of this research is to identify metabolic markers associated with successful treatment by evaluating the effect of mesenchymal stem cell transplantation (MSCT) on the metabolic profiles of patients with SLE.Methods Plasma samples were collected from 20 patients with SLE before and after MSCT. Principal component analysis (PCA) was used to distinguish pretreatment and post-treatment groups and pathway analysis for identifying involved metabolic pathways. Clinical variables were monitored with a median follow-up time of 180 days. Pearson correlation and receiver operating characteristics (ROC) analysis were employed to associate metabolite changes with clinical outcomes and to predict treatment success.Results We detected 18 121 metabolites, with 1152 showing significant changes post-treatment, which could be clearly distinguished between pretreatment and post-treatment groups through PCA. Pathway analysis indicated involvement in riboflavin and thiamine metabolism. Clinical improvements were observed at a median follow-up time of 180 days after MSCT, including decreased SLE Disease Activity Index scores, urine protein/creatinine ratios, and erythrocyte sedimentation rates, along with increased levels of complement C3 and C4, haemoglobin, and platelets. Pearson correlation indicated that specific metabolite changes were associated with clinical improvements, particularly increases in thiamine monophosphate (TMP) and asiaticoside levels. ROC analysis identified TMP level changes as the most predictive of treatment success, with a 35% increase indicating a good response to MSCT.Conclusion This study concludes that TMP is a potential biomarker that can predict the efficacy of MSCT in treating SLE, providing valuable insights for clinical practice and further research.
format Article
id doaj-art-a37ae075a81546278b0e618d896d5d8a
institution Kabale University
issn 2053-8790
language English
publishDate 2025-03-01
publisher BMJ Publishing Group
record_format Article
series Lupus Science and Medicine
spelling doaj-art-a37ae075a81546278b0e618d896d5d8a2025-08-20T03:44:28ZengBMJ Publishing GroupLupus Science and Medicine2053-87902025-03-0112110.1136/lupus-2024-001197Metabolomic analysis suggests thiamine monophosphate as a potential marker for mesenchymal stem cell transplantation outcomes in patients with SLEBin Yang0Xuebing Feng1Lingyun Sun2Xiaojun Tang3Xiaoman Jiang4Zhuoyang Jia5China International Neuroscience Institute (China-INI), Beijing, ChinaDepartment of Neurosurgery, Xuanwu Hospital Capital Medical University, Beijing, China7 Department of Rheumatology and Immunology, Affiliated Nanjing Drum Tower Hospital, Medical School of Nanjing University, Nanjing, ChinaSchool of Public Health, Chongqing Medical University, Chongqing, ChinaDepartment of Rheumatology and Immunology, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, Jiangsu, ChinaDepartment of Rheumatology and Immunology, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, Jiangsu, ChinaObjective The objective of this research is to identify metabolic markers associated with successful treatment by evaluating the effect of mesenchymal stem cell transplantation (MSCT) on the metabolic profiles of patients with SLE.Methods Plasma samples were collected from 20 patients with SLE before and after MSCT. Principal component analysis (PCA) was used to distinguish pretreatment and post-treatment groups and pathway analysis for identifying involved metabolic pathways. Clinical variables were monitored with a median follow-up time of 180 days. Pearson correlation and receiver operating characteristics (ROC) analysis were employed to associate metabolite changes with clinical outcomes and to predict treatment success.Results We detected 18 121 metabolites, with 1152 showing significant changes post-treatment, which could be clearly distinguished between pretreatment and post-treatment groups through PCA. Pathway analysis indicated involvement in riboflavin and thiamine metabolism. Clinical improvements were observed at a median follow-up time of 180 days after MSCT, including decreased SLE Disease Activity Index scores, urine protein/creatinine ratios, and erythrocyte sedimentation rates, along with increased levels of complement C3 and C4, haemoglobin, and platelets. Pearson correlation indicated that specific metabolite changes were associated with clinical improvements, particularly increases in thiamine monophosphate (TMP) and asiaticoside levels. ROC analysis identified TMP level changes as the most predictive of treatment success, with a 35% increase indicating a good response to MSCT.Conclusion This study concludes that TMP is a potential biomarker that can predict the efficacy of MSCT in treating SLE, providing valuable insights for clinical practice and further research.https://lupus.bmj.com/content/12/1/e001197.full
spellingShingle Bin Yang
Xuebing Feng
Lingyun Sun
Xiaojun Tang
Xiaoman Jiang
Zhuoyang Jia
Metabolomic analysis suggests thiamine monophosphate as a potential marker for mesenchymal stem cell transplantation outcomes in patients with SLE
Lupus Science and Medicine
title Metabolomic analysis suggests thiamine monophosphate as a potential marker for mesenchymal stem cell transplantation outcomes in patients with SLE
title_full Metabolomic analysis suggests thiamine monophosphate as a potential marker for mesenchymal stem cell transplantation outcomes in patients with SLE
title_fullStr Metabolomic analysis suggests thiamine monophosphate as a potential marker for mesenchymal stem cell transplantation outcomes in patients with SLE
title_full_unstemmed Metabolomic analysis suggests thiamine monophosphate as a potential marker for mesenchymal stem cell transplantation outcomes in patients with SLE
title_short Metabolomic analysis suggests thiamine monophosphate as a potential marker for mesenchymal stem cell transplantation outcomes in patients with SLE
title_sort metabolomic analysis suggests thiamine monophosphate as a potential marker for mesenchymal stem cell transplantation outcomes in patients with sle
url https://lupus.bmj.com/content/12/1/e001197.full
work_keys_str_mv AT binyang metabolomicanalysissuggeststhiaminemonophosphateasapotentialmarkerformesenchymalstemcelltransplantationoutcomesinpatientswithsle
AT xuebingfeng metabolomicanalysissuggeststhiaminemonophosphateasapotentialmarkerformesenchymalstemcelltransplantationoutcomesinpatientswithsle
AT lingyunsun metabolomicanalysissuggeststhiaminemonophosphateasapotentialmarkerformesenchymalstemcelltransplantationoutcomesinpatientswithsle
AT xiaojuntang metabolomicanalysissuggeststhiaminemonophosphateasapotentialmarkerformesenchymalstemcelltransplantationoutcomesinpatientswithsle
AT xiaomanjiang metabolomicanalysissuggeststhiaminemonophosphateasapotentialmarkerformesenchymalstemcelltransplantationoutcomesinpatientswithsle
AT zhuoyangjia metabolomicanalysissuggeststhiaminemonophosphateasapotentialmarkerformesenchymalstemcelltransplantationoutcomesinpatientswithsle