{"title":"缺血性脑卒中-1.6 ppm时核Overhauser增强效应的不对称分析。","authors":"Yu Zhao, Aqeela Afzal, Zhongliang Zu","doi":"10.1002/mp.17677","DOIUrl":null,"url":null,"abstract":"<div>\n \n \n <section>\n \n <h3> Background</h3>\n \n <p>The nuclear Overhauser enhancement (NOE)-mediated saturation transfer effect at -1.6 ppm, termed NOE(-1.6 ppm), has demonstrated potential for detecting ischemic stroke. However, the quantification of the NOE(-1.6 ppm) effect usually relies on a multiple-pool Lorentzian fit method, which necessitates a time-consuming acquisition of the entire chemical exchange saturation transfer (CEST) Z-spectrum with high-frequency resolution, thus hindering its clinical applications.</p>\n </section>\n \n <section>\n \n <h3> Purpose</h3>\n \n <p>This study aims to assess the feasibility of employing asymmetry analysis, a rapid CEST data acquisition and analysis method, for quantifying the NOE(-1.6 ppm) effect in an animal model of ischemic stroke.</p>\n </section>\n \n <section>\n \n <h3> Methods</h3>\n \n <p>We examined potential contaminations from guanidinium/amine CEST, NOE(-3.5 ppm), and asymmetric magnetization transfer (MT) effects, which could reduce the specificity of the asymmetry analysis of NOE(-1.6 ppm). First, a Lorentzian difference (LD) analysis was used to mitigate direct water saturation and MT effects, providing separate estimations of the contributions from the guanidinium/amine CEST and NOE effects. Then, the asymmetry analysis of the LD fitted spectrum was compared with the asymmetry analysis of the raw CEST Z-spectrum to evaluate the contribution of the asymmetric MT effect at -1.6 ppm.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>Results show that the variations of the LD quantified NOE(-1.6 ppm) in stroke lesions are much greater than that of the CEST signals at +1.6 ppm and NOE(-3.5 ppm), suggesting that NOE(-1.6 ppm) has a dominating contribution to the asymmetry analysis at -1.6 ppm compared with the guanidinium/amine CEST and NOE(-3.5 ppm) in ischemic stroke. The NOE(-1.6 ppm) variations in the asymmetry analysis of the raw CEST Z-spectrum are close to those in the asymmetry analysis of the LD fitted spectrum, revealing that the NOE(-1.6 ppm) dominates over the asymmetric MT effects.</p>\n </section>\n \n <section>\n \n <h3> Conclusion</h3>\n \n <p>Our study demonstrates that the asymmetry analysis can quantify the NOE(-1.6 ppm) contrast in ischemic stroke with high specificity, thus presenting a viable alternative for rapid mapping of ischemic stroke.</p>\n </section>\n </div>","PeriodicalId":18384,"journal":{"name":"Medical physics","volume":"52 5","pages":"2922-2937"},"PeriodicalIF":3.2000,"publicationDate":"2025-02-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/mp.17677","citationCount":"0","resultStr":"{\"title\":\"Asymmetry analysis of nuclear Overhauser enhancement effect at -1.6 ppm in ischemic stroke\",\"authors\":\"Yu Zhao, Aqeela Afzal, Zhongliang Zu\",\"doi\":\"10.1002/mp.17677\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n \\n <section>\\n \\n <h3> Background</h3>\\n \\n <p>The nuclear Overhauser enhancement (NOE)-mediated saturation transfer effect at -1.6 ppm, termed NOE(-1.6 ppm), has demonstrated potential for detecting ischemic stroke. However, the quantification of the NOE(-1.6 ppm) effect usually relies on a multiple-pool Lorentzian fit method, which necessitates a time-consuming acquisition of the entire chemical exchange saturation transfer (CEST) Z-spectrum with high-frequency resolution, thus hindering its clinical applications.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Purpose</h3>\\n \\n <p>This study aims to assess the feasibility of employing asymmetry analysis, a rapid CEST data acquisition and analysis method, for quantifying the NOE(-1.6 ppm) effect in an animal model of ischemic stroke.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Methods</h3>\\n \\n <p>We examined potential contaminations from guanidinium/amine CEST, NOE(-3.5 ppm), and asymmetric magnetization transfer (MT) effects, which could reduce the specificity of the asymmetry analysis of NOE(-1.6 ppm). First, a Lorentzian difference (LD) analysis was used to mitigate direct water saturation and MT effects, providing separate estimations of the contributions from the guanidinium/amine CEST and NOE effects. Then, the asymmetry analysis of the LD fitted spectrum was compared with the asymmetry analysis of the raw CEST Z-spectrum to evaluate the contribution of the asymmetric MT effect at -1.6 ppm.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Results</h3>\\n \\n <p>Results show that the variations of the LD quantified NOE(-1.6 ppm) in stroke lesions are much greater than that of the CEST signals at +1.6 ppm and NOE(-3.5 ppm), suggesting that NOE(-1.6 ppm) has a dominating contribution to the asymmetry analysis at -1.6 ppm compared with the guanidinium/amine CEST and NOE(-3.5 ppm) in ischemic stroke. The NOE(-1.6 ppm) variations in the asymmetry analysis of the raw CEST Z-spectrum are close to those in the asymmetry analysis of the LD fitted spectrum, revealing that the NOE(-1.6 ppm) dominates over the asymmetric MT effects.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Conclusion</h3>\\n \\n <p>Our study demonstrates that the asymmetry analysis can quantify the NOE(-1.6 ppm) contrast in ischemic stroke with high specificity, thus presenting a viable alternative for rapid mapping of ischemic stroke.</p>\\n </section>\\n </div>\",\"PeriodicalId\":18384,\"journal\":{\"name\":\"Medical physics\",\"volume\":\"52 5\",\"pages\":\"2922-2937\"},\"PeriodicalIF\":3.2000,\"publicationDate\":\"2025-02-11\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1002/mp.17677\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Medical physics\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/mp.17677\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Medical physics","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/mp.17677","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING","Score":null,"Total":0}
Asymmetry analysis of nuclear Overhauser enhancement effect at -1.6 ppm in ischemic stroke
Background
The nuclear Overhauser enhancement (NOE)-mediated saturation transfer effect at -1.6 ppm, termed NOE(-1.6 ppm), has demonstrated potential for detecting ischemic stroke. However, the quantification of the NOE(-1.6 ppm) effect usually relies on a multiple-pool Lorentzian fit method, which necessitates a time-consuming acquisition of the entire chemical exchange saturation transfer (CEST) Z-spectrum with high-frequency resolution, thus hindering its clinical applications.
Purpose
This study aims to assess the feasibility of employing asymmetry analysis, a rapid CEST data acquisition and analysis method, for quantifying the NOE(-1.6 ppm) effect in an animal model of ischemic stroke.
Methods
We examined potential contaminations from guanidinium/amine CEST, NOE(-3.5 ppm), and asymmetric magnetization transfer (MT) effects, which could reduce the specificity of the asymmetry analysis of NOE(-1.6 ppm). First, a Lorentzian difference (LD) analysis was used to mitigate direct water saturation and MT effects, providing separate estimations of the contributions from the guanidinium/amine CEST and NOE effects. Then, the asymmetry analysis of the LD fitted spectrum was compared with the asymmetry analysis of the raw CEST Z-spectrum to evaluate the contribution of the asymmetric MT effect at -1.6 ppm.
Results
Results show that the variations of the LD quantified NOE(-1.6 ppm) in stroke lesions are much greater than that of the CEST signals at +1.6 ppm and NOE(-3.5 ppm), suggesting that NOE(-1.6 ppm) has a dominating contribution to the asymmetry analysis at -1.6 ppm compared with the guanidinium/amine CEST and NOE(-3.5 ppm) in ischemic stroke. The NOE(-1.6 ppm) variations in the asymmetry analysis of the raw CEST Z-spectrum are close to those in the asymmetry analysis of the LD fitted spectrum, revealing that the NOE(-1.6 ppm) dominates over the asymmetric MT effects.
Conclusion
Our study demonstrates that the asymmetry analysis can quantify the NOE(-1.6 ppm) contrast in ischemic stroke with high specificity, thus presenting a viable alternative for rapid mapping of ischemic stroke.
期刊介绍:
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