Gérontopôle de Toulouse, Institut du Vieillissement, Centre Hospitalo-Universitaire de Toulouse, 37 allées Jules Guesdes, 31000 Toulouse, France.
Gérontopôle de Toulouse, Institut du Vieillissement, Centre Hospitalo-Universitaire de Toulouse, 37 allées Jules Guesdes, 31000 Toulouse, France; UMR INSERM, 1027 University of Toulouse III, Toulouse, France, Faculté de Médecine, 37 allées Jules Guesde 31000 Toulouse, France.
Maturitas. 2021 Oct;152:10-19. doi: 10.1016/j.maturitas.2021.06.010. Epub 2021 Jun 30.
Physical activity (PA) has been shown to modulate the detrimental effect of carrying the apolipoprotein-E epsilon 4 (APOE-ɛ4) allele on brain structure. However, the current literature mainly provides cross-sectional data, and longitudinal studies investigating the interaction between genotype and PA on white matter (WM) integrity are lacking.
We investigated both the cross-sectional and the longitudinal interactive effects of APOE-ɛ4 and PA on WM integrity in older adults.
Fractional anisotropy, as well as axial, radial, and mean diffusivity, extracted from brain diffusion tensor imaging (DTI) were used to assess WM integrity in non-demented older adults. They were categorized according to their APOE-ɛ4 status (carriers vs. non-carriers), and their level of total (TPA), moderate to vigorous (MVPA) and light (LPA) PA were assessed using a questionnaire. Mixed model regressions were performed to test the interactive effects of APOE-ɛ4 status and PA on WM integrity at baseline and over a 3-year follow-up.
190 subjects with a mean age 74.5 years (SD = 3.9) were examined. Despite a lack of cross-sectional associations, sensitivity analyses revealed that, in the carrier group only, higher levels of LPA, but not MVPA, were mainly associated with higher axial and mean diffusivity values over time.
This study partially confirms the previously reported interactive associations between PA, APOE-ɛ4 genotype and WM integrity, supporting the hypothesis that PA may protect against fiber loss in WM tracts containing crossing fibers. Future studies assessing sedentary behaviors in addition to PA could bring relevant contributions to the field. CLINICAL TRIAL REGISTRATION NUMBER FROM CLINICALTRIALS.GOV: NCT00672685.
已有研究表明,身体活动(PA)可调节载脂蛋白 E ɛ4(APOE-ɛ4)等位基因对大脑结构的不利影响。然而,目前的文献主要提供横断面数据,缺乏关于基因型和 PA 对大脑白质(WM)完整性之间相互作用的纵向研究。
我们研究了 APOE-ɛ4 和 PA 对老年人大脑 WM 完整性的横断面和纵向交互作用。
使用基于扩散张量成像(DTI)的各向异性分数,以及轴向、径向和平均弥散度来评估非痴呆老年人大脑 WM 完整性。根据他们的 APOE-ɛ4 状态(携带者与非携带者)进行分类,并使用问卷评估他们的总(TPA)、中高强度(MVPA)和低强度身体活动(LPA)水平。采用混合模型回归检验 APOE-ɛ4 状态和 PA 对 WM 完整性的交互作用,包括在基线和 3 年随访时的 WM 完整性。
共纳入 190 名平均年龄 74.5 岁(SD=3.9)的受试者。尽管横断面研究未发现两者之间的关联,但敏感性分析显示,仅在携带者组中,较高水平的 LPA,而非 MVPA,与随时间轴向和平均弥散度的升高相关。
本研究部分证实了之前报道的 PA、APOE-ɛ4 基因型与 WM 完整性之间的交互关联,支持了 PA 可能保护含有交叉纤维的 WM 束中纤维丢失的假说。未来研究在评估 PA 的同时评估久坐行为,可能会为该领域带来更多的贡献。临床试验注册编号:NCT00672685。