{"title":"尿代谢物作为前列腺癌放疗患者早期放射性膀胱炎的生物标志物","authors":"Sachika Shiraishi, Masahiro Sugimoto, Koichi Tokuuye","doi":"10.21873/invivo.14004","DOIUrl":null,"url":null,"abstract":"<p><strong>Background/aim: </strong>Treatment-related bladder toxicities are a primary concern in the management of prostate cancer radiotherapy. This study aimed to identify urinary metabolites that can predict early radiation cystitis-related toxicities in patients undergoing radiotherapy for prostate cancer.</p><p><strong>Patients and methods: </strong>Patients' clinical characteristics and urine samples were collected before, two weeks after, at the end, and three months after the initiation of radiotherapy and subsequently analyzed. Capillary electrophoresis-mass spectrometry and liquid chromatography-mass spectrometry were used for comprehensive quantification of urinary metabolites. Multivariate analysis was conducted to identify potential protective factors against the early toxicities of radiation cystitis.</p><p><strong>Results: </strong>A total of 176 samples were obtained from 44 patients. Betaine, tartrate, N,N-dimethylglycine, and homocarnosine were identified as independent protective factors against early toxicities of radiation cystitis among various potential confounding metabolic factors. Comorbid diabetes mellitus was also identified as a protective factor.</p><p><strong>Conclusion: </strong>Betaine, tartrate, N,N-dimethylglycine, and homocarnosine were identified as protective urinary metabolites against early radiation cystitis. Urinary metabolomic profiling may be a useful tool for investigating disease metabolism in metabolic disorders and cancers. Its ease of use and repeatability make it an optimal method for patient follow-up.</p>","PeriodicalId":13364,"journal":{"name":"In vivo","volume":"39 4","pages":"2091-2100"},"PeriodicalIF":1.8000,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12223610/pdf/","citationCount":"0","resultStr":"{\"title\":\"Urinary Metabolites as Biomarkers of Early Radiation Cystitis in Patients With Prostate Cancer Undergoing Radiotherapy.\",\"authors\":\"Sachika Shiraishi, Masahiro Sugimoto, Koichi Tokuuye\",\"doi\":\"10.21873/invivo.14004\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background/aim: </strong>Treatment-related bladder toxicities are a primary concern in the management of prostate cancer radiotherapy. This study aimed to identify urinary metabolites that can predict early radiation cystitis-related toxicities in patients undergoing radiotherapy for prostate cancer.</p><p><strong>Patients and methods: </strong>Patients' clinical characteristics and urine samples were collected before, two weeks after, at the end, and three months after the initiation of radiotherapy and subsequently analyzed. Capillary electrophoresis-mass spectrometry and liquid chromatography-mass spectrometry were used for comprehensive quantification of urinary metabolites. Multivariate analysis was conducted to identify potential protective factors against the early toxicities of radiation cystitis.</p><p><strong>Results: </strong>A total of 176 samples were obtained from 44 patients. Betaine, tartrate, N,N-dimethylglycine, and homocarnosine were identified as independent protective factors against early toxicities of radiation cystitis among various potential confounding metabolic factors. Comorbid diabetes mellitus was also identified as a protective factor.</p><p><strong>Conclusion: </strong>Betaine, tartrate, N,N-dimethylglycine, and homocarnosine were identified as protective urinary metabolites against early radiation cystitis. Urinary metabolomic profiling may be a useful tool for investigating disease metabolism in metabolic disorders and cancers. Its ease of use and repeatability make it an optimal method for patient follow-up.</p>\",\"PeriodicalId\":13364,\"journal\":{\"name\":\"In vivo\",\"volume\":\"39 4\",\"pages\":\"2091-2100\"},\"PeriodicalIF\":1.8000,\"publicationDate\":\"2025-07-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12223610/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"In vivo\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.21873/invivo.14004\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"MEDICINE, RESEARCH & EXPERIMENTAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"In vivo","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.21873/invivo.14004","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"MEDICINE, RESEARCH & EXPERIMENTAL","Score":null,"Total":0}
Urinary Metabolites as Biomarkers of Early Radiation Cystitis in Patients With Prostate Cancer Undergoing Radiotherapy.
Background/aim: Treatment-related bladder toxicities are a primary concern in the management of prostate cancer radiotherapy. This study aimed to identify urinary metabolites that can predict early radiation cystitis-related toxicities in patients undergoing radiotherapy for prostate cancer.
Patients and methods: Patients' clinical characteristics and urine samples were collected before, two weeks after, at the end, and three months after the initiation of radiotherapy and subsequently analyzed. Capillary electrophoresis-mass spectrometry and liquid chromatography-mass spectrometry were used for comprehensive quantification of urinary metabolites. Multivariate analysis was conducted to identify potential protective factors against the early toxicities of radiation cystitis.
Results: A total of 176 samples were obtained from 44 patients. Betaine, tartrate, N,N-dimethylglycine, and homocarnosine were identified as independent protective factors against early toxicities of radiation cystitis among various potential confounding metabolic factors. Comorbid diabetes mellitus was also identified as a protective factor.
Conclusion: Betaine, tartrate, N,N-dimethylglycine, and homocarnosine were identified as protective urinary metabolites against early radiation cystitis. Urinary metabolomic profiling may be a useful tool for investigating disease metabolism in metabolic disorders and cancers. Its ease of use and repeatability make it an optimal method for patient follow-up.
期刊介绍:
IN VIVO is an international peer-reviewed journal designed to bring together original high quality works and reviews on experimental and clinical biomedical research within the frames of physiology, pathology and disease management.
The topics of IN VIVO include: 1. Experimental development and application of new diagnostic and therapeutic procedures; 2. Pharmacological and toxicological evaluation of new drugs, drug combinations and drug delivery systems; 3. Clinical trials; 4. Development and characterization of models of biomedical research; 5. Cancer diagnosis and treatment; 6. Immunotherapy and vaccines; 7. Radiotherapy, Imaging; 8. Tissue engineering, Regenerative medicine; 9. Carcinogenesis.