Strobel Joachim, Yousefzadeh-Nowshahr Elham, Deininger Katharina, Bohn Karl Peter, von Arnim Christine A F, Otto Markus, Solbach Christoph, Anderl-Straub Sarah, Polivka Dörte, Fissler Patrick, Glatting Gerhard, Riepe Matthias W, Higuchi Makoto, Beer Ambros J, Ludolph Albert, Winter Gordon
Department of Nuclear Medicine, Ulm University Medical Center, 89081 Ulm, Germany.
Department of Geriatrics, University Medical Center Göttingen, 37073 Göttingen, Germany.
Biomedicines. 2024 Jul 1;12(7):1460. doi: 10.3390/biomedicines12071460.
Accurately diagnosing Alzheimer's disease (AD) and frontotemporal lobar degeneration (FTLD) is challenging due to overlapping symptoms and limitations of current imaging methods. This study investigates the use of [11C]PBB3 PET/CT imaging to visualize tau pathology and improve diagnostic accuracy. Given diagnostic challenges with symptoms and conventional imaging, [11C]PBB3 PET/CT's potential to enhance accuracy was investigated by correlating tau pathology with cerebrospinal fluid (CSF) biomarkers, positron emission tomography (PET), computed tomography (CT), amyloid-beta, and Mini-Mental State Examination (MMSE). We conducted [11C]PBB3 PET/CT imaging on 24 patients with suspected AD or FTLD, alongside [11C]PiB PET/CT (13 patients) and [18F]FDG PET/CT (15 patients). Visual and quantitative assessments of [11C]PBB3 uptake using standardized uptake value ratios (SUV-Rs) and correlation analyses with clinical assessments were performed. The scans revealed distinct tau accumulation patterns; 13 patients had no or faint uptake (PBB3-negative) and 11 had moderate to pronounced uptake (PBB3-positive). Significant inverse correlations were found between [11C]PBB3 SUV-Rs and MMSE scores, but not with CSF-tau or CSF-amyloid-beta levels. Here, we show that [11C]PBB3 PET/CT imaging can reveal distinct tau accumulation patterns and correlate these with cognitive impairment in neurodegenerative diseases. Our study demonstrates the potential of [11C]PBB3-PET imaging for visualizing tau pathology and assessing disease severity, offering a promising tool for enhancing diagnostic accuracy in AD and FTLD. Further research is essential to validate these findings and refine the use of tau-specific PET imaging in clinical practice, ultimately improving patient care and treatment outcomes.
由于症状重叠以及当前成像方法的局限性,准确诊断阿尔茨海默病(AD)和额颞叶痴呆(FTLD)具有挑战性。本研究调查了[11C]PBB3 PET/CT成像用于可视化tau病理并提高诊断准确性的情况。鉴于症状和传统成像的诊断挑战,通过将tau病理与脑脊液(CSF)生物标志物、正电子发射断层扫描(PET)、计算机断层扫描(CT)、淀粉样蛋白β以及简易精神状态检查表(MMSE)相关联,研究了[11C]PBB3 PET/CT提高准确性的潜力。我们对24例疑似AD或FTLD的患者进行了[11C]PBB3 PET/CT成像,同时还对13例患者进行了[11C]PiB PET/CT成像以及对15例患者进行了[18F]FDG PET/CT成像。使用标准化摄取值比率(SUV-Rs)对[11C]PBB3摄取进行了视觉和定量评估,并与临床评估进行了相关性分析。扫描显示出不同的tau聚集模式;13例患者无摄取或摄取微弱(PBB3阴性),11例患者有中度至明显摄取(PBB3阳性)。在[11C]PBB3 SUV-Rs与MMSE评分之间发现了显著的负相关,但与CSF-tau或CSF-淀粉样蛋白β水平无关。在此,我们表明[11C]PBB3 PET/CT成像可以揭示不同的tau聚集模式,并将这些模式与神经退行性疾病中的认知障碍相关联。我们的研究证明了[11C]PBB3-PET成像在可视化tau病理和评估疾病严重程度方面的潜力,为提高AD和FTLD的诊断准确性提供了一种有前景的工具。进一步的研究对于验证这些发现并完善tau特异性PET成像在临床实践中的应用至关重要,最终改善患者护理和治疗结果。