腰肌弥散张量指数随年龄的变化

BJR|Open Pub Date : 2024-01-13 DOI:10.1093/bjro/tzae002
Andrew D Weedall, A. Dallaway, John Hattersley, Michael Diokno, Charles E Hutchinson, Adrian J Wilson, S. Wayte
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引用次数: 0

摘要

为了研究年轻和年长成年男性脊柱肌肉中弥散张量成像(DTI)参数和质子密度脂肪分数(PDFF)的差异,12 名年轻(19-30 岁)和 12 名年长(61-81 岁)身体健康、喜欢运动的男性参与者接受了腰椎 T1W、T2W、Dixon 和弥散张量成像检查。在多裂肌(MF)、竖脊肌内侧和外侧(ESmed、ESlat)和腰四头肌(QL)中测定了 DTI 的特征值(λ1、λ2、λ3)分数各向异性(FA)和平均扩散率(MD)以及 PDFF。采用双向方差分析研究年龄和肌肉的差异,并对单块肌肉的年龄差异进行 t 检验。 方差分析结果表明,除 λ1 和 PDFF 外,所有 DTI 参数和 PDFF 随年龄均有显著差异(p < 0.01),随肌肉也有显著差异(p < 0.01)。在 ESlat 和 QL 的所有 DTI 测量中,老年组的特征值和 MD 平均值较低,FA 较高,差异具有统计学意义(p < 0.01),但在 ESmed 中,只有 λ3 和 MD 的差异具有统计学意义(p < 0.05)。 随着年龄的增长,肌肉 DTI 参数的差异来自于细胞内和细胞外空间的变化,不能完全用纤维长度和直径来解释。 以往对年龄的研究使用的是年龄间隔不均匀的小群体。而我们的研究使用了两个定义明确且相互独立的年龄组。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Changes in lumbar muscle diffusion tensor indices with age
To investigate differences in diffusion tensor imaging (DTI) parameters and proton density fat fraction (PDFF) in the spinal muscles of younger and older adult males, Twelve younger (19-30years) and 12 older (61-81years) healthy, physically active male participants underwent T1W, T2W, Dixon and Diffusion Tensor imaging of the lumbar spine. The eigenvalues (λ1, λ2, λ3) fractional anisotropy (FA) and mean diffusivity (MD) from the DTI together with the PDFF were determined in the multifidus (MF), medial and lateral erector spinae (ESmed, ESlat) and quadratus lumborum (QL) muscles. A two-way ANOVA was used to investigate differences with age and muscle and t-tests for differences in individual muscles with age. The ANOVA gave significant differences with age for all DTI parameters and the PDFF (p < 0.01) and with muscle (p < 0.01) for all DTI parameters except for λ1 and for the PDFF. The mean of the eigenvalues and MD were lower and the FA higher in the older age group with differences reaching statistical significance for all DTI measures for ESlat and QL (p < 0.01) but only in ESmed for λ3 and MD (p < 0.05). Differences in DTI parameters of muscle with age result from changes in both in the intra- and extra-cellular space and cannot be uniquely explained in terms of fibre length and diameter. Previous studies looking at age have used small groups with uneven age spacing. Our study uses two well defined and separated age groups.
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