Okamura Nobuyuki, Fodero-Tavoletti Michelle T, Kudo Yukitsuka, Rowe Christopher C, Furumoto Shozo, Arai Hiroyuki, Masters Colin L, Yanai Kazuhiko, Villemagne Victor L
Tohoku University, Pharmacology, Sendai, Japan.
Expert Opin Med Diagn. 2009 Nov;3(6):705-16. doi: 10.1517/17530050903133790. Epub 2009 Jul 29.
There is an urgent need for early diagnosis and treatment of dementia to ease caregiver burden and medical costs associated with the increasing number of affected patients. Molecular imaging with target-specific ligands is contributing to the early diagnosis of dementia and the evaluation of anti-dementia therapy.
This article reviews recent advances in the molecular imaging field applied to dementia. To illustrate the utility of molecular imaging in the clinical management of dementia, results from recently published papers using new imaging probes are compared with those from conventional imaging strategies.
The recent development of β-sheet binding agents including FDDNP, PIB, SB-13, BF-227 and BAY94-9172 enables the non-invasive detection of amyloid deposition in the brain. These agents would be useful for the early and accurate diagnosis of Alzheimer's disease, patient selection for disease-modifying therapeutic trials and monitoring the effect of anti-amyloid therapy. Also, monitoring neurotransmitter function contributes to the differential diagnosis of dementia and refinement of treatment protocols. New targets for molecular imaging are focusing on protein misfolding diseases associated with the neurotoxic deposition of aggregated tau, α-synuclein and prion proteins.
迫切需要对痴呆症进行早期诊断和治疗,以减轻与受影响患者数量增加相关的护理负担和医疗成本。使用靶向特异性配体的分子成像有助于痴呆症的早期诊断和抗痴呆治疗的评估。
本文综述了应用于痴呆症的分子成像领域的最新进展。为了说明分子成像在痴呆症临床管理中的效用,将最近发表的使用新型成像探针的论文结果与传统成像策略的结果进行了比较。
包括FDDNP、PIB、SB-13、BF-227和BAY94-9172在内的β-折叠结合剂的最新进展使得能够无创检测大脑中的淀粉样蛋白沉积。这些试剂将有助于阿尔茨海默病的早期准确诊断、疾病修饰治疗试验的患者选择以及监测抗淀粉样蛋白治疗的效果。此外,监测神经递质功能有助于痴呆症的鉴别诊断和治疗方案的优化。分子成像的新靶点聚焦于与聚集的tau、α-突触核蛋白和朊病毒蛋白的神经毒性沉积相关的蛋白质错误折叠疾病。