Torque Teno病毒作为肾移植受者感染风险的生物标志物:一项机器学习支持的队列研究。

IF 2.4 Q2 INFECTIOUS DISEASES
Sara Querido, Luís Ramalhete, Perpétua Gomes, André Weigert
{"title":"Torque Teno病毒作为肾移植受者感染风险的生物标志物:一项机器学习支持的队列研究。","authors":"Sara Querido, Luís Ramalhete, Perpétua Gomes, André Weigert","doi":"10.3390/idr17050107","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Torque Teno Virus (TTV) viremia has been proposed as a marker for infection risk in kidney transplant (KT) recipients. This study aimed to evaluate the prognostic value of TTV levels for predicting infections post-KT.</p><p><strong>Methods: </strong>A cohort of 82 KT patients was analyzed. TTV loads were measured before KT and at the time of cutoff analysis (mean time since KT: 20.2 ± 10.3 months). Infections were tracked within six months following the time of cutoff analysis. Univariable analyses and a supervised machine learning approach (logistic regression with leave-one-out cross-validation) were conducted to rigorously assess TTV's predictive ability for post-transplant infection.</p><p><strong>Results: </strong>Seventy-two patients (87.8%) had detectable TTV before KT. Of these, 30.5% developed infections, predominantly viral. TTV loads increased significantly from 3.35 ± 1.67 log<sub>10</sub> cp/mL before KT to 4.53 ± 1.93 log<sub>10</sub> cp/mL at the time of cutoff analysis. Infected patients had significantly higher TTV loads (5.39 ± 1.68 log<sub>10</sub> vs. 4.16 ± 1.94 log<sub>10</sub> cp/mL, <i>p</i> = 0.0057). The optimal TTV threshold for predicting infection at the time of cutoff analysis was 5.16 log<sub>10</sub> cp/mL, with 60% sensitivity and 81% specificity. Machine learning models improved performance, with sensitivity and specificity 0.805 and 0.735, respectively.</p><p><strong>Conclusions: </strong>TTV viremia may serve as a biomarker for infection risk, particularly when used with other clinical variables. The identified TTV threshold of 5.16 log<sub>10</sub> cp/mL offers a practical tool for clinical decision-making, particularly when integrated with a machine learning model. Further studies with larger cohorts are needed to validate these findings and refine clinical applications.</p>","PeriodicalId":13579,"journal":{"name":"Infectious Disease Reports","volume":"17 5","pages":""},"PeriodicalIF":2.4000,"publicationDate":"2025-09-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12452520/pdf/","citationCount":"0","resultStr":"{\"title\":\"Torque Teno Virus as a Biomarker for Infection Risk in Kidney Transplant Recipients: A Machine Learning-Enabled Cohort Study.\",\"authors\":\"Sara Querido, Luís Ramalhete, Perpétua Gomes, André Weigert\",\"doi\":\"10.3390/idr17050107\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Torque Teno Virus (TTV) viremia has been proposed as a marker for infection risk in kidney transplant (KT) recipients. This study aimed to evaluate the prognostic value of TTV levels for predicting infections post-KT.</p><p><strong>Methods: </strong>A cohort of 82 KT patients was analyzed. TTV loads were measured before KT and at the time of cutoff analysis (mean time since KT: 20.2 ± 10.3 months). Infections were tracked within six months following the time of cutoff analysis. Univariable analyses and a supervised machine learning approach (logistic regression with leave-one-out cross-validation) were conducted to rigorously assess TTV's predictive ability for post-transplant infection.</p><p><strong>Results: </strong>Seventy-two patients (87.8%) had detectable TTV before KT. Of these, 30.5% developed infections, predominantly viral. TTV loads increased significantly from 3.35 ± 1.67 log<sub>10</sub> cp/mL before KT to 4.53 ± 1.93 log<sub>10</sub> cp/mL at the time of cutoff analysis. Infected patients had significantly higher TTV loads (5.39 ± 1.68 log<sub>10</sub> vs. 4.16 ± 1.94 log<sub>10</sub> cp/mL, <i>p</i> = 0.0057). The optimal TTV threshold for predicting infection at the time of cutoff analysis was 5.16 log<sub>10</sub> cp/mL, with 60% sensitivity and 81% specificity. Machine learning models improved performance, with sensitivity and specificity 0.805 and 0.735, respectively.</p><p><strong>Conclusions: </strong>TTV viremia may serve as a biomarker for infection risk, particularly when used with other clinical variables. The identified TTV threshold of 5.16 log<sub>10</sub> cp/mL offers a practical tool for clinical decision-making, particularly when integrated with a machine learning model. Further studies with larger cohorts are needed to validate these findings and refine clinical applications.</p>\",\"PeriodicalId\":13579,\"journal\":{\"name\":\"Infectious Disease Reports\",\"volume\":\"17 5\",\"pages\":\"\"},\"PeriodicalIF\":2.4000,\"publicationDate\":\"2025-09-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12452520/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Infectious Disease Reports\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.3390/idr17050107\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"INFECTIOUS DISEASES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Infectious Disease Reports","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3390/idr17050107","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"INFECTIOUS DISEASES","Score":null,"Total":0}
引用次数: 0

摘要

背景:扭矩Teno病毒(TTV)病毒血症被认为是肾移植(KT)受者感染风险的标志。本研究旨在评估TTV水平对预测kt后感染的预后价值。方法:对82例KT患者进行队列分析。在KT前和截止分析时测量TTV负荷(KT后平均时间:20.2±10.3个月)。在截止分析时间后的六个月内追踪感染情况。采用单变量分析和监督机器学习方法(留一交叉验证的逻辑回归)严格评估TTV对移植后感染的预测能力。结果:72例患者(87.8%)在KT前检出TTV。其中,30.5%发生了感染,主要是病毒性感染。TTV负荷从KT前的3.35±1.67 log10 cp/mL显著增加到截止分析时的4.53±1.93 log10 cp/mL。感染患者TTV载量显著高于对照组(5.39±1.68 log10 vs. 4.16±1.94 log10 cp/mL, p = 0.0057)。切断分析时预测感染的最佳TTV阈值为5.16 log10 cp/mL,灵敏度为60%,特异性为81%。机器学习模型提高了性能,灵敏度和特异性分别为0.805和0.735。结论:TTV病毒血症可以作为感染风险的生物标志物,特别是当与其他临床变量一起使用时。确定的TTV阈值为5.16 log10 cp/mL,为临床决策提供了实用的工具,特别是与机器学习模型相结合时。需要更大规模的进一步研究来验证这些发现并完善临床应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Torque Teno Virus as a Biomarker for Infection Risk in Kidney Transplant Recipients: A Machine Learning-Enabled Cohort Study.

Background: Torque Teno Virus (TTV) viremia has been proposed as a marker for infection risk in kidney transplant (KT) recipients. This study aimed to evaluate the prognostic value of TTV levels for predicting infections post-KT.

Methods: A cohort of 82 KT patients was analyzed. TTV loads were measured before KT and at the time of cutoff analysis (mean time since KT: 20.2 ± 10.3 months). Infections were tracked within six months following the time of cutoff analysis. Univariable analyses and a supervised machine learning approach (logistic regression with leave-one-out cross-validation) were conducted to rigorously assess TTV's predictive ability for post-transplant infection.

Results: Seventy-two patients (87.8%) had detectable TTV before KT. Of these, 30.5% developed infections, predominantly viral. TTV loads increased significantly from 3.35 ± 1.67 log10 cp/mL before KT to 4.53 ± 1.93 log10 cp/mL at the time of cutoff analysis. Infected patients had significantly higher TTV loads (5.39 ± 1.68 log10 vs. 4.16 ± 1.94 log10 cp/mL, p = 0.0057). The optimal TTV threshold for predicting infection at the time of cutoff analysis was 5.16 log10 cp/mL, with 60% sensitivity and 81% specificity. Machine learning models improved performance, with sensitivity and specificity 0.805 and 0.735, respectively.

Conclusions: TTV viremia may serve as a biomarker for infection risk, particularly when used with other clinical variables. The identified TTV threshold of 5.16 log10 cp/mL offers a practical tool for clinical decision-making, particularly when integrated with a machine learning model. Further studies with larger cohorts are needed to validate these findings and refine clinical applications.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Infectious Disease Reports
Infectious Disease Reports INFECTIOUS DISEASES-
CiteScore
5.10
自引率
0.00%
发文量
82
审稿时长
11 weeks
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信