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Aging of the cingulum in the human brain: Preliminary study of a diffusion tensor imaging study

机译:人脑扣带的老化:扩散张量成像研究的初步研究

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The cingulum, a major structure of the limbic system, is closely associated with memory function. In the current study, we investigated aging of the cingulum according to the location of the cingulum in each part of the cingulum after dividing the cingulum into five parts in normal subjects, using DTT parameters (fractional anisotropy (FA) and fiber number (FN)). Ninety healthy subjects (males: 44, females: 46, mean age: 49.0 years; range: 20-78 years) were enrolled in this study. Subjects were categorized according to six groups by age intervals of 10 years; each age group consisted of 15 subjects. The cingulum was divided into five parts (anterior, anterior superior, posterior superior cingulum, posterior, and inferior cingulum). The FA and FN of each part were measured. The FA value indicates the degree of directionality and integrity of white matter microstructures such as axons, myelin, and microtubules, and the FN reflects the total number of fibers in a neural tract. Age-related decline in the FA value may indicate demyelination, and a decline in the number of myelinated fibers of a neural tract can also lead to a decline of the FN. Significant differences in the FA value of the anterior cingulum and anterior superior cingulum, and the FN of the inferior cingulum were observed between age groups (AVOVA, p<0.05). A significant decrease was observed in the FA values of the anterior and anterior superior cingulum of the 60s and 70s age groups compared with those of the 20s and 30s age groups, and in the FN of the inferior cingulum of the 60s and 70s age groups compared with that of the 20s age group (LSD post hoc test, p<0.05). Aging of the cingulum began at both ends of the cingulum in the 20s or 30s, and progressed steadily at a near continuous rate over the lifespan and a significant degenerative aging effect at both ends of the cingulum occurred into the 60s, compared with the 20s or 30s. (C) 2015 Elsevier Ireland Ltd. All rights reserved.
机译:扣带是边缘系统的主要结构,与记忆功能密切相关。在当前的研究中,我们使用DTT参数(分数各向异性(FA)和纤维数(FN)),将正常人将其分为五个部分,然后根据在每个部分的扣带位置调查扣带的老化情况。 )。这项研究纳入了90名健康受试者(男性:44岁,女性:46岁,平均年龄:49.0岁;范围:20-78岁)。按照10岁年龄组将受试者分为六组。每个年龄段由15名受试者组成。扣带分为五个部分(前扣带,前扣带,后扣带,后扣带和下扣带)。测量每个部分的FA和FN。 FA值表示白质微结构(如轴突,髓磷脂和微管)的方向性和完整性,而FN则反映神经道中纤维的总数。 FA值与年龄相关的下降可能表明脱髓鞘,而神经束的髓鞘纤维数量下降也可能导致FN下降。在不同年龄组之间,前扣带和前扣带的FA值以及下扣带的FN值存在显着差异(AVOVA,p <0.05)。与20s和30s年龄组的前扣带和前上扣带的FA值相比,20s和30s年龄组的FA值显着降低,并且60s和70s年龄组的下扣带的FN相比与20岁年龄组的水平相同(LSD事后检验,p <0.05)。扣带的老化始于20s或30s的扣带两端,并在整个寿命中以接近连续的速率稳定地发展,并且扣带两端的显着退化性衰老效应发生在60年代,而20s或30s则如此。 30多岁(C)2015 Elsevier Ireland Ltd.保留所有权利。

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