Suppr超能文献

海马体代谢减退预示着正常衰老过程中的认知衰退。

Hippocampal hypometabolism predicts cognitive decline from normal aging.

作者信息

Mosconi Lisa, De Santi Susan, Li Juan, Tsui Wai Hon, Li Yi, Boppana Madhu, Laska Eugene, Rusinek Henry, de Leon Mony J

机构信息

New York University School of Medicine, New York, NY 10016, USA.

出版信息

Neurobiol Aging. 2008 May;29(5):676-92. doi: 10.1016/j.neurobiolaging.2006.12.008. Epub 2007 Jan 11.

Abstract

OBJECTIVE

This longitudinal study used FDG-PET imaging to predict and monitor cognitive decline from normal aging.

METHODS

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.

RESULTS

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.

CONCLUSIONS

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.

摘要

目的

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。

方法

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。

结果

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。

结论

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。

相似文献

1
Hippocampal hypometabolism predicts cognitive decline from normal aging.
Neurobiol Aging. 2008 May;29(5):676-92. doi: 10.1016/j.neurobiolaging.2006.12.008. Epub 2007 Jan 11.
2
Reduced hippocampal metabolism in MCI and AD: automated FDG-PET image analysis.
Neurology. 2005 Jun 14;64(11):1860-7. doi: 10.1212/01.WNL.0000163856.13524.08.
3
Regional analysis of FDG and PIB-PET images in normal aging, mild cognitive impairment, and Alzheimer's disease.
Eur J Nucl Med Mol Imaging. 2008 Dec;35(12):2169-81. doi: 10.1007/s00259-008-0833-y. Epub 2008 Jun 20.
4
FDG-PET changes in brain glucose metabolism from normal cognition to pathologically verified Alzheimer's disease.
Eur J Nucl Med Mol Imaging. 2009 May;36(5):811-22. doi: 10.1007/s00259-008-1039-z. Epub 2009 Jan 14.
5
Multicenter standardized 18F-FDG PET diagnosis of mild cognitive impairment, Alzheimer's disease, and other dementias.
J Nucl Med. 2008 Mar;49(3):390-8. doi: 10.2967/jnumed.107.045385. Epub 2008 Feb 20.
6
Prediction of cognitive decline in normal elderly subjects with 2-[(18)F]fluoro-2-deoxy-D-glucose/poitron-emission tomography (FDG/PET).
Proc Natl Acad Sci U S A. 2001 Sep 11;98(19):10966-71. doi: 10.1073/pnas.191044198. Epub 2001 Aug 28.
9
Brain glucose metabolism in the early and specific diagnosis of Alzheimer's disease. FDG-PET studies in MCI and AD.
Eur J Nucl Med Mol Imaging. 2005 Apr;32(4):486-510. doi: 10.1007/s00259-005-1762-7.
10
Cerebral metabolic changes accompanying conversion of mild cognitive impairment into Alzheimer's disease: a PET follow-up study.
Eur J Nucl Med Mol Imaging. 2003 Aug;30(8):1104-13. doi: 10.1007/s00259-003-1194-1. Epub 2003 May 23.

引用本文的文献

2
Computational Risk Stratification of Preclinical Alzheimer's in Younger Adults.
Diagnostics (Basel). 2025 May 26;15(11):1327. doi: 10.3390/diagnostics15111327.
3
Irisin: A Multifaceted Hormone Bridging Exercise and Disease Pathophysiology.
Int J Mol Sci. 2024 Dec 16;25(24):13480. doi: 10.3390/ijms252413480.
5
High caloric intake improves neuronal metabolism and functional hyperemia in a rat model of early AD pathology.
Theranostics. 2024 Oct 28;14(19):7405-7423. doi: 10.7150/thno.98793. eCollection 2024.
7
Phosphoglycerate kinase is a central leverage point in Parkinson's disease-driven neuronal metabolic deficits.
Sci Adv. 2024 Aug 23;10(34):eadn6016. doi: 10.1126/sciadv.adn6016. Epub 2024 Aug 21.
9
WNKs regulate mouse behavior and alter central nervous system glucose uptake and insulin signaling.
bioRxiv. 2024 Jun 22:2024.06.09.598125. doi: 10.1101/2024.06.09.598125.

本文引用的文献

1
Mild cognitive impairment.
Lancet. 2006 Apr 15;367(9518):1262-70. doi: 10.1016/S0140-6736(06)68542-5.
4
Visual rating of medial temporal lobe metabolism in mild cognitive impairment and Alzheimer's disease using FDG-PET.
Eur J Nucl Med Mol Imaging. 2006 Feb;33(2):210-21. doi: 10.1007/s00259-005-1956-z. Epub 2005 Nov 26.
7
Reduced hippocampal metabolism in MCI and AD: automated FDG-PET image analysis.
Neurology. 2005 Jun 14;64(11):1860-7. doi: 10.1212/01.WNL.0000163856.13524.08.
8
Brain glucose metabolism in the early and specific diagnosis of Alzheimer's disease. FDG-PET studies in MCI and AD.
Eur J Nucl Med Mol Imaging. 2005 Apr;32(4):486-510. doi: 10.1007/s00259-005-1762-7.
9
MCI conversion to dementia and the APOE genotype: a prediction study with FDG-PET.
Neurology. 2004 Dec 28;63(12):2332-40. doi: 10.1212/01.wnl.0000147469.18313.3b.
10
Mixed-effects and fMRI studies.
Neuroimage. 2005 Jan 1;24(1):244-52. doi: 10.1016/j.neuroimage.2004.08.055.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验