{"title":"双相C-11 PiB PET图像检测脑淀粉样血管病Tau病理。","authors":"Meng-Ting Chiang, Chia-Ju Liu, Bo-Ching Lee, Ruoh-Fang Yen, Hsin-Hsi Tsai","doi":"10.1002/acn3.70021","DOIUrl":null,"url":null,"abstract":"<div>\n \n \n <section>\n \n <h3> Background</h3>\n \n <p>Cerebral amyloid angiopathy (CAA) is a major cause of lobar intracerebral hemorrhage and cognitive dysfunction in the elderly, and frequently coexists with Alzheimer's disease and tau pathology. Dual-phase <sup>11</sup>C-PiB PET detects amyloid deposition and cerebral perfusion changes and may have diagnostic value for identifying tau in CAA.</p>\n </section>\n \n <section>\n \n <h3> Methods</h3>\n \n <p>We prospectively enrolled patients with probable CAA for dynamic PiB and AV1451 scans. We compared early-phase (0–6 min after tracer injection) and late-phase (40–70 min) PiB PET between the tau(+) and tau(−) groups (based on AV1451 PET) and investigated their diagnostic values for detecting tau.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>CAA/tau(+) had lower early-phase temporal PiB uptake than CAA/tau(−) (<i>p</i> = 0.014) and higher late-phase uptake in the whole cortex and temporal and parietal lobes (all <i>p</i> < 0.05). Early-phase temporal PiB SUVR correlated with tau burden (<i>r</i> = −0.34, <i>p</i> = 0.038). Using Youden's cut-off, early-phase and late-phase PET had sensitivities of 55% and 80% and specificities of 85% and 65% for detecting tau, respectively. Combining early- and late-phase scans provided a rule-out sensitivity of 90% and rule-in specificity of 100% for tau pathology in CAA.</p>\n </section>\n \n <section>\n \n <h3> Conclusions</h3>\n \n <p>Dual-phase <sup>11</sup>C-PiB PET represents a reliable approach for assessing tau and could potentially identify CAA patients for tau biomarker testing.</p>\n </section>\n </div>","PeriodicalId":126,"journal":{"name":"Annals of Clinical and Translational Neurology","volume":"12 5","pages":"905-914"},"PeriodicalIF":3.9000,"publicationDate":"2025-03-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/acn3.70021","citationCount":"0","resultStr":"{\"title\":\"Dual-Phase C-11 PiB PET Images for Detecting Tau Pathology in Cerebral Amyloid Angiopathy\",\"authors\":\"Meng-Ting Chiang, Chia-Ju Liu, Bo-Ching Lee, Ruoh-Fang Yen, Hsin-Hsi Tsai\",\"doi\":\"10.1002/acn3.70021\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n \\n <section>\\n \\n <h3> Background</h3>\\n \\n <p>Cerebral amyloid angiopathy (CAA) is a major cause of lobar intracerebral hemorrhage and cognitive dysfunction in the elderly, and frequently coexists with Alzheimer's disease and tau pathology. Dual-phase <sup>11</sup>C-PiB PET detects amyloid deposition and cerebral perfusion changes and may have diagnostic value for identifying tau in CAA.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Methods</h3>\\n \\n <p>We prospectively enrolled patients with probable CAA for dynamic PiB and AV1451 scans. We compared early-phase (0–6 min after tracer injection) and late-phase (40–70 min) PiB PET between the tau(+) and tau(−) groups (based on AV1451 PET) and investigated their diagnostic values for detecting tau.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Results</h3>\\n \\n <p>CAA/tau(+) had lower early-phase temporal PiB uptake than CAA/tau(−) (<i>p</i> = 0.014) and higher late-phase uptake in the whole cortex and temporal and parietal lobes (all <i>p</i> < 0.05). Early-phase temporal PiB SUVR correlated with tau burden (<i>r</i> = −0.34, <i>p</i> = 0.038). Using Youden's cut-off, early-phase and late-phase PET had sensitivities of 55% and 80% and specificities of 85% and 65% for detecting tau, respectively. Combining early- and late-phase scans provided a rule-out sensitivity of 90% and rule-in specificity of 100% for tau pathology in CAA.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Conclusions</h3>\\n \\n <p>Dual-phase <sup>11</sup>C-PiB PET represents a reliable approach for assessing tau and could potentially identify CAA patients for tau biomarker testing.</p>\\n </section>\\n </div>\",\"PeriodicalId\":126,\"journal\":{\"name\":\"Annals of Clinical and Translational Neurology\",\"volume\":\"12 5\",\"pages\":\"905-914\"},\"PeriodicalIF\":3.9000,\"publicationDate\":\"2025-03-03\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1002/acn3.70021\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Annals of Clinical and Translational Neurology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/acn3.70021\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CLINICAL NEUROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Annals of Clinical and Translational Neurology","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/acn3.70021","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
Dual-Phase C-11 PiB PET Images for Detecting Tau Pathology in Cerebral Amyloid Angiopathy
Background
Cerebral amyloid angiopathy (CAA) is a major cause of lobar intracerebral hemorrhage and cognitive dysfunction in the elderly, and frequently coexists with Alzheimer's disease and tau pathology. Dual-phase 11C-PiB PET detects amyloid deposition and cerebral perfusion changes and may have diagnostic value for identifying tau in CAA.
Methods
We prospectively enrolled patients with probable CAA for dynamic PiB and AV1451 scans. We compared early-phase (0–6 min after tracer injection) and late-phase (40–70 min) PiB PET between the tau(+) and tau(−) groups (based on AV1451 PET) and investigated their diagnostic values for detecting tau.
Results
CAA/tau(+) had lower early-phase temporal PiB uptake than CAA/tau(−) (p = 0.014) and higher late-phase uptake in the whole cortex and temporal and parietal lobes (all p < 0.05). Early-phase temporal PiB SUVR correlated with tau burden (r = −0.34, p = 0.038). Using Youden's cut-off, early-phase and late-phase PET had sensitivities of 55% and 80% and specificities of 85% and 65% for detecting tau, respectively. Combining early- and late-phase scans provided a rule-out sensitivity of 90% and rule-in specificity of 100% for tau pathology in CAA.
Conclusions
Dual-phase 11C-PiB PET represents a reliable approach for assessing tau and could potentially identify CAA patients for tau biomarker testing.
期刊介绍:
Annals of Clinical and Translational Neurology is a peer-reviewed journal for rapid dissemination of high-quality research related to all areas of neurology. The journal publishes original research and scholarly reviews focused on the mechanisms and treatments of diseases of the nervous system; high-impact topics in neurologic education; and other topics of interest to the clinical neuroscience community.