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本文引用的文献

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Comparing 3 T and 1.5 T MRI for tracking Alzheimer's disease progression with tensor-based morphometry.比较 3T 和 1.5T MRI 基于张量的形态测量学追踪阿尔茨海默病的进展。
Hum Brain Mapp. 2010 Apr;31(4):499-514. doi: 10.1002/hbm.20882.
2
Fat and carbohydrate intake modify the association between genetic variation in the FTO genotype and obesity.脂肪和碳水化合物的摄入量会改变 FTO 基因型的遗传变异与肥胖之间的关联。
Am J Clin Nutr. 2009 Nov;90(5):1418-25. doi: 10.3945/ajcn.2009.27958. Epub 2009 Sep 2.
3
Brain structure and obesity.脑结构与肥胖。
Hum Brain Mapp. 2010 Mar;31(3):353-64. doi: 10.1002/hbm.20870.
4
Caloric restriction delays disease onset and mortality in rhesus monkeys.热量限制可延缓恒河猴疾病的发作和死亡。
Science. 2009 Jul 10;325(5937):201-4. doi: 10.1126/science.1173635.
5
Loss-of-function mutation in the dioxygenase-encoding FTO gene causes severe growth retardation and multiple malformations.编码双加氧酶的FTO基因功能丧失性突变会导致严重的生长发育迟缓及多种畸形。
Am J Hum Genet. 2009 Jul;85(1):106-11. doi: 10.1016/j.ajhg.2009.06.002. Epub 2009 Jun 25.
6
Physical activity attenuates the body mass index-increasing influence of genetic variation in the FTO gene.体育活动减弱了FTO基因中遗传变异对体重指数增加的影响。
Am J Clin Nutr. 2009 Aug;90(2):425-8. doi: 10.3945/ajcn.2009.27652. Epub 2009 Jun 24.
7
FTO gene variation and measures of body mass in an African population.非洲人群中FTO基因变异与体重测量
BMC Med Genet. 2009 Mar 5;10:21. doi: 10.1186/1471-2350-10-21.
8
Altered executive function in obesity. Exploration of the role of affective states on cognitive abilities.肥胖中的执行功能改变。探索情感状态对认知能力的作用。
Appetite. 2009 Apr;52(2):535-9. doi: 10.1016/j.appet.2009.01.003.
9
Inactivation of the Fto gene protects from obesity.Fto基因失活可预防肥胖。
Nature. 2009 Apr 16;458(7240):894-8. doi: 10.1038/nature07848. Epub 2009 Feb 22.
10
Automated 3D mapping of hippocampal atrophy and its clinical correlates in 400 subjects with Alzheimer's disease, mild cognitive impairment, and elderly controls.对400名患有阿尔茨海默病、轻度认知障碍的受试者以及老年对照者进行海马萎缩的自动三维测绘及其临床相关性研究。
Hum Brain Mapp. 2009 Sep;30(9):2766-88. doi: 10.1002/hbm.20708.

常见的肥胖相关 FTO 基因等位基因与健康老年人的脑容量减少有关。

A commonly carried allele of the obesity-related FTO gene is associated with reduced brain volume in the healthy elderly.

机构信息

Laboratory of Neuroimaging, Department of Neurology, University of California School of Medicine, Los Angeles, CA 90095, USA.

出版信息

Proc Natl Acad Sci U S A. 2010 May 4;107(18):8404-9. doi: 10.1073/pnas.0910878107. Epub 2010 Apr 19.

DOI:10.1073/pnas.0910878107
PMID:20404173
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2889537/
Abstract

A recently identified variant within the fat mass and obesity-associated (FTO) gene is carried by 46% of Western Europeans and is associated with an approximately 1.2 kg higher weight, on average, in adults and an approximately 1 cm greater waist circumference. With >1 billion overweight and 300 million obese persons worldwide, it is crucial to understand the implications of carrying this very common allele for the health of our aging population. FTO is highly expressed in the brain and elevated body mass index (BMI) is associated with brain atrophy, but it is unknown how the obesity-associated risk allele affects human brain structure. We therefore generated 3D maps of regional brain volume differences in 206 healthy elderly subjects scanned with MRI and genotyped as part of the Alzheimer's Disease Neuroimaging Initiative. We found a pattern of systematic brain volume deficits in carriers of the obesity-associated risk allele versus noncarriers. Relative to structure volumes in the mean template, FTO risk allele carriers versus noncarriers had an average brain volume difference of approximately 8% in the frontal lobes and 12% in the occipital lobes-these regions also showed significant volume deficits in subjects with higher BMI. These brain differences were not attributable to differences in cholesterol levels, hypertension, or the volume of white matter hyperintensities; which were not detectably higher in FTO risk allele carriers versus noncarriers. These brain maps reveal that a commonly carried susceptibility allele for obesity is associated with structural brain atrophy, with implications for the health of the elderly.

摘要

最近在脂肪量和肥胖相关(FTO)基因中发现的一个变体,在 46%的西欧人中携带,并且与成年人的平均体重增加约 1.2 公斤,腰围增加约 1 厘米有关。在全球范围内,超重的人数超过 10 亿,肥胖的人数超过 3 亿,因此了解携带这种非常常见的等位基因对我们老龄化人口健康的影响至关重要。FTO 在大脑中高度表达,而升高的体重指数(BMI)与大脑萎缩有关,但尚不清楚与肥胖相关的风险等位基因如何影响人类大脑结构。因此,我们在 206 名健康的老年受试者中生成了 MRI 扫描的局部脑容量差异的 3D 图谱,并对他们进行了基因分型,这些受试者是阿尔茨海默病神经影像学倡议的一部分。我们发现,与非携带者相比,携带肥胖相关风险等位基因的受试者存在系统性的脑容量不足。与平均模板的结构体积相比,FTO 风险等位基因携带者与非携带者的额叶脑容量差异约为 8%,枕叶脑容量差异约为 12%-这些区域在 BMI 较高的受试者中也表现出明显的体积不足。这些大脑差异不是由于胆固醇水平、高血压或白质高信号体积的差异造成的;在 FTO 风险等位基因携带者与非携带者之间,这些差异并不明显。这些大脑图谱表明,肥胖的常见易感等位基因与结构脑萎缩有关,这对老年人的健康有影响。