通过[11C]亮氨酸 PET 对临床阿尔茨海默病的区域脑蛋白合成进行定量成像。

IF 3 4区 医学 Q2 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
Karl Herholz, Adam McMahon, Jennifer C Thompson, Matthew Jones, Herve Boutin, Jamil Gregory, Christine A Parker, Rainer Hinz
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引用次数: 0

摘要

目的:蛋白质合成对维持人脑的完整性和功能至关重要,蛋白质合成与长期记忆的形成特别相关。实验和临床观察表明,这一过程在阿尔茨海默氏症痴呆症和其他神经退行性疾病中受到干扰。使用[11C]亮氨酸进行正电子发射断层扫描(PET)的体内研究为测量人脑区域脑蛋白合成率(rCPS)提供了一种独特的可能性,并可确定阿尔茨海默氏症(AD)是否会改变这种合成率,从而为未来的治疗干预提供目标:在这项首次人体研究中,我们通过[11C]亮氨酸 PET 测量了四名阿尔茨海默病患者(年龄为 57-73 岁)的 rCPS,并将结果与六名健康对照者(其中三名年龄匹配,另外三名为年轻对照者)进行了比较。量化 rCPS 还需要在至少禁食六小时后进行 90 分钟 PET 扫描期间测量血浆中的氨基酸(AA)水平以及游离和蛋白结合的[11C]亮氨酸:以 nmol/g/min 的绝对单位测量,AD 患者的 rCPS 率介于 1.81 和 2.53 之间,匹配对照组介于 2.10 和 2.54 之间,年轻对照组介于 2.21 和 2.35 之间。各组之间的平均值和中位值没有明显差异。rCPS 的比率还取决于计算中是否包含血浆 AA 水平的校正。当考虑以胼胝体为参照区域的区域值时,患者的 rCPS 有受损的趋势,这在顶叶皮层最为突出,但没有达到显著性。将rCPS与全球皮质平均值标准化后,也观察到了类似的结果:总之,这项首次使用[11C]亮氨酸评估AD患者区域蛋白质合成的人体研究表明,大脑蛋白质合成测量中的差异来源可能来自哪里,以及这种差异的潜在程度。这项研究还表明,阿尔茨海默病患者的 rCPS 有受损的趋势,这需要进一步研究,包括因萎缩而可能产生的部分体积效应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Quantitative Imaging of Regional Cerebral Protein Synthesis in Clinical Alzheimer's Disease by [11C]Leucine PET.

Purpose: Protein synthesis is essential to maintain integrity and function of the human brain, and protein synthesis is associated specifically with the formation of long-term memory. Experimental and clinical observations indicate that this process is disturbed in Alzheimer's dementia and other neurodegenerative diseases. In-vivo investigation with positron emission tomography (PET) using [11C]leucine provides a unique possibility to measure regional cerebral protein synthesis (rCPS) rates in human brain and to determine whether it is altered in Alzheimer's disease (AD), and thus may provide a target for future therapeutic interventions.

Procedures: In this first human study, we measured rCPS by [11C]leucine PET in four patients with AD (age 57-73 years) and compared the results with six healthy controls (three of whom were age matched and the other three were young controls). Quantification of rCPS also required measurement of amino acid (AA) levels and of free and protein-bound [11C]leucine in plasma during the 90 min PET scans conducted following at least six hours of fasting.

Results: Rates of rCPS measured in absolute units of nmol/g/min ranged between 1.81 and 2.53 in AD patients, 2.10 and 2.54 in matched controls, and 2.21 to 2.35 in the young controls. Mean and median values did not show significant differences between the groups. Rates of rCPS also depended upon whether corrections for plasma AA levels were included in the calculations. When considering regional values relative to the corpus callosum as a reference region, there was a tendency towards impairment of rCPS in patients, which was most prominent in the parietal cortex, but did not reach significance. Similar findings were observed with normalisation of rCPS to global cortical mean.

Conclusions: In summary, this first human study assessing regional protein synthesis with [11C]leucine in AD has demonstrated where the sources of variance in measurements of cerebral protein synthesis may arise, along with the potential magnitude of this variance. This study also indicates that there is a tendency towards impairment of rCPS in patients with Alzheimer's disease, which requires further investigation including possible partial volume effects due to atrophy.

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来源期刊
CiteScore
6.90
自引率
3.20%
发文量
95
审稿时长
3 months
期刊介绍: Molecular Imaging and Biology (MIB) invites original contributions (research articles, review articles, commentaries, etc.) on the utilization of molecular imaging (i.e., nuclear imaging, optical imaging, autoradiography and pathology, MRI, MPI, ultrasound imaging, radiomics/genomics etc.) to investigate questions related to biology and health. The objective of MIB is to provide a forum to the discovery of molecular mechanisms of disease through the use of imaging techniques. We aim to investigate the biological nature of disease in patients and establish new molecular imaging diagnostic and therapy procedures. Some areas that are covered are: Preclinical and clinical imaging of macromolecular targets (e.g., genes, receptors, enzymes) involved in significant biological processes. The design, characterization, and study of new molecular imaging probes and contrast agents for the functional interrogation of macromolecular targets. Development and evaluation of imaging systems including instrumentation, image reconstruction algorithms, image analysis, and display. Development of molecular assay approaches leading to quantification of the biological information obtained in molecular imaging. Study of in vivo animal models of disease for the development of new molecular diagnostics and therapeutics. Extension of in vitro and in vivo discoveries using disease models, into well designed clinical research investigations. Clinical molecular imaging involving clinical investigations, clinical trials and medical management or cost-effectiveness studies.
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