Chee Wai Ku, Yu Bin Tan, Kuan Yang Chew, Chee Onn Ku, Shi Tong Carissa Ng, Thiam Chye Tan, Yie Hou Lee
{"title":"Untargeted metabolomics reveals key pathways in miscarriage: steroid, folate, fatty acid & glycosaminoglycan metabolism.","authors":"Chee Wai Ku, Yu Bin Tan, Kuan Yang Chew, Chee Onn Ku, Shi Tong Carissa Ng, Thiam Chye Tan, Yie Hou Lee","doi":"10.1038/s44294-025-00085-9","DOIUrl":null,"url":null,"abstract":"<p><p>Metabolites influencing miscarriage outcomes remain understudied. We hypothesized that aberrant metabolism impacts threatened miscarriage outcomes and that understanding these pathways could offer new management strategies. This case-control study analyzed serum metabolomics from 80 women between 5 and 12 weeks' gestation at KK Women's and Children's Hospital, Singapore, comparing three groups: women with threatened miscarriage who miscarried (TM<sub>MC</sub>), those with ongoing pregnancies (TM<sub>O</sub>), and women with normal pregnancies (NP). Using untargeted liquid chromatography-mass spectrometry and pathway analysis through MetaboAnalyst 5.0 and the Kyoto Encyclopedia of Genes and Genomes, 267 metabolites across 12 enriched pathways were identified. Dysregulations in steroid (AUC 0.82), folate (AUC 0.59), fatty acid (AUC 0.70), and glucosaminoglycan (AUC 0.64) pathways distinguished women who miscarried from those with ongoing pregnancies (TM<sub>MC</sub> vs TM<sub>O</sub>). We provide initial insights into the metabolic profile associated with miscarriage, highlighting disruptions in steroid hormone, fatty acid, folate, and glucosaminoglycan biosynthesis. Further validation may support biomarker development for prognostication.</p>","PeriodicalId":520241,"journal":{"name":"npj women's health","volume":"3 1","pages":"35"},"PeriodicalIF":0.0000,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12165837/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"npj women's health","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1038/s44294-025-00085-9","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/6/13 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Metabolites influencing miscarriage outcomes remain understudied. We hypothesized that aberrant metabolism impacts threatened miscarriage outcomes and that understanding these pathways could offer new management strategies. This case-control study analyzed serum metabolomics from 80 women between 5 and 12 weeks' gestation at KK Women's and Children's Hospital, Singapore, comparing three groups: women with threatened miscarriage who miscarried (TMMC), those with ongoing pregnancies (TMO), and women with normal pregnancies (NP). Using untargeted liquid chromatography-mass spectrometry and pathway analysis through MetaboAnalyst 5.0 and the Kyoto Encyclopedia of Genes and Genomes, 267 metabolites across 12 enriched pathways were identified. Dysregulations in steroid (AUC 0.82), folate (AUC 0.59), fatty acid (AUC 0.70), and glucosaminoglycan (AUC 0.64) pathways distinguished women who miscarried from those with ongoing pregnancies (TMMC vs TMO). We provide initial insights into the metabolic profile associated with miscarriage, highlighting disruptions in steroid hormone, fatty acid, folate, and glucosaminoglycan biosynthesis. Further validation may support biomarker development for prognostication.
影响流产结果的代谢物仍未得到充分研究。我们假设异常代谢影响威胁流产结果,了解这些途径可以提供新的管理策略。本病例对照研究分析了新加坡KK妇女儿童医院80名妊娠5至12周妇女的血清代谢组学,比较了三组:流产的先兆流产妇女(TMMC)、持续妊娠妇女(TMO)和正常妊娠妇女(NP)。采用非靶向液相色谱-质谱联用技术,通过MetaboAnalyst 5.0和京都基因与基因组百科全书(Kyoto Encyclopedia of Genes and Genomes)进行通路分析,鉴定出12条富集通路中的267种代谢物。类固醇(AUC 0.82)、叶酸(AUC 0.59)、脂肪酸(AUC 0.70)和葡萄糖氨基聚糖(AUC 0.64)通路的失调将流产妇女与妊娠妇女区分开来(TMMC vs TMO)。我们提供了与流产相关的代谢谱的初步见解,强调了类固醇激素、脂肪酸、叶酸和葡萄糖氨基聚糖生物合成的破坏。进一步的验证可能支持用于预测的生物标志物的开发。