Mosconi Lisa, De Santi Susan, Li Juan, Tsui Wai Hon, Li Yi, Boppana Madhu, Laska Eugene, Rusinek Henry, de Leon Mony J
New York University School of Medicine, New York, NY 10016, USA.
Neurobiol Aging. 2008 May;29(5):676-92. doi: 10.1016/j.neurobiolaging.2006.12.008. Epub 2007 Jan 11.
This longitudinal study used FDG-PET imaging to predict and monitor cognitive decline from normal aging.
Seventy-seven 50-80-year-old normal (NL) elderly received longitudinal clinical examinations over 6-14 years (561 person-years, mean per person 7.2 years). All subjects had a baseline FDG-PET scan and 55 subjects received follow-up PET exams. Glucose metabolic rates (MRglc) in the hippocampus and cortical regions were examined as predictors and correlates of clinical decline.
Eleven NL subjects developed dementia, including six with Alzheimer's disease (AD), and 19 declined to mild cognitive impairment (MCI), on average 8 years after the baseline exam. The baseline hippocampal MRglc predicted decline from NL to AD (81% accuracy), including two post-mortem confirmed cases, from NL to other dementias (77% accuracy), and from NL to MCI (71% accuracy). Greater rates of hippocampal and cortical MRglc reductions were found in the declining as compared to the non-declining NL.
Hippocampal MRglc reductions using FDG-PET during normal aging predict cognitive decline years in advance of the clinical diagnosis. Future studies are needed to increase preclinical specificity in differentiating dementing disorders.
本纵向研究采用氟代脱氧葡萄糖正电子发射断层扫描(FDG-PET)成像来预测和监测正常衰老过程中的认知衰退。
77名年龄在50至80岁的正常(NL)老年人在6至14年期间(共561人年,平均每人7.2年)接受了纵向临床检查。所有受试者均进行了基线FDG-PET扫描,55名受试者接受了随访PET检查。检测海马体和皮质区域的葡萄糖代谢率(MRglc),将其作为临床衰退的预测指标和相关因素。
11名NL受试者发展为痴呆,其中6例为阿尔茨海默病(AD),19例衰退为轻度认知障碍(MCI),平均在基线检查后8年出现。基线海马体MRglc可预测从NL发展为AD(准确率81%),包括2例尸检确诊病例,从NL发展为其他痴呆(准确率77%),以及从NL发展为MCI(准确率71%)。与未衰退的NL相比,衰退的NL海马体和皮质MRglc降低率更高。
在正常衰老过程中,使用FDG-PET检测到的海马体MRglc降低可在临床诊断前数年预测认知衰退。未来需要开展研究以提高在区分痴呆症方面的临床前特异性。