Mallinckrodt Institute of Radiology, Washington University in St. Louis, St. Louis, Missouri, USA.
Washington University School of Medicine, Division of Public Health Sciences, Department of Surgery, St. Louis, Missouri, USA.
Aging Dis. 2024 Aug 1;15(4):1843-1854. doi: 10.14336/AD.2023.0707.
Obesity and excess adiposity at midlife are risk factors for Alzheimer disease (AD). Visceral fat is known to be associated with insulin resistance and a pro-inflammatory state, the two mechanisms involved in AD pathology. We assessed the association of obesity, MRI-determined abdominal adipose tissue volumes, and insulin resistance with PET-determined amyloid and tau uptake in default mode network areas, and MRI-determined brain volume and cortical thickness in AD cortical signature in the cognitively normal midlife population. Thirty-two middle-aged (age: 51.27±6.12 years, 15 males, body mass index (BMI): 32.28±6.39 kg/m2) cognitively normal participants, underwent bloodwork, brain and abdominal MRI, and amyloid and tau PET scan. Visceral and subcutaneous adipose tissue (VAT, SAT) were semi-automatically segmented using VOXel Analysis Suite (Voxa). FreeSurfer was used to automatically segment brain regions using a probabilistic atlas. PET scans were acquired using [11C]PiB and AV-1451 tracers and were analyzed using PET unified pipeline. The association of brain volumes, cortical thicknesses, and PiB and AV-1451 standardized uptake value ratios (SUVRs) with BMI, VAT/SAT ratio, and insulin resistance were assessed using Spearman's partial correlation. VAT/SAT ratio was associated significantly with PiB SUVRs in the right precuneus cortex (p=0.034) overall, controlling for sex. This association was significant only in males (p=0.044), not females (p=0.166). Higher VAT/SAT ratio and PiB SUVRs in the right precuneus cortex were associated with lower cortical thickness in AD-signature areas predominantly including bilateral temporal cortices, parahippocampal, medial orbitofrontal, and cingulate cortices, with age and sex as covariates. Also, higher BMI and insulin resistance were associated with lower cortical thickness in bilateral temporal poles. In midlife cognitively normal adults, we demonstrated higher amyloid pathology in the right precuneus cortex in individuals with a higher VAT/SAT ratio, a marker of visceral obesity, along with a lower cortical thickness in AD-signature areas associated with higher visceral obesity, insulin resistance, and amyloid pathology.
肥胖和中年时期的多余脂肪是阿尔茨海默病(AD)的风险因素。众所周知,内脏脂肪与胰岛素抵抗和促炎状态有关,这两种机制都与 AD 病理有关。我们评估了肥胖、MRI 确定的腹部脂肪组织体积以及胰岛素抵抗与默认模式网络区域的 PET 确定的淀粉样蛋白和 tau 摄取、AD 皮质特征中的 MRI 确定的脑体积和皮质厚度之间的关系在认知正常的中年人群中。32 名中年(年龄:51.27±6.12 岁,15 名男性,体重指数(BMI):32.28±6.39 kg/m2)认知正常参与者接受了血液检查、脑部和腹部 MRI 以及淀粉样蛋白和 tau PET 扫描。使用 VOXel 分析套件(Voxa)半自动分割内脏和皮下脂肪(VAT、SAT)。使用 FreeSurfer 使用概率图谱自动分割大脑区域。使用 [11C]PiB 和 AV-1451 示踪剂采集 PET 扫描,并使用 PET 统一管道进行分析。使用 Spearman 部分相关评估脑体积、皮质厚度以及 PiB 和 AV-1451 标准化摄取比值(SUVRS)与 BMI、VAT/SAT 比值和胰岛素抵抗的相关性。VAT/SAT 比值与右楔前叶皮质的 PiB SUVR 总体上显著相关(p=0.034),控制性别。这种相关性仅在男性中显著(p=0.044),而在女性中不显著(p=0.166)。右楔前叶皮质中较高的 VAT/SAT 比值和 PiB SUVR 与 AD 特征区域的皮质厚度较低相关,这些区域主要包括双侧颞叶、海马旁回、内侧眶额和扣带回皮质,以年龄和性别为协变量。此外,较高的 BMI 和胰岛素抵抗与双侧颞极皮质厚度降低有关。在认知正常的中年成年人中,我们发现在具有较高 VAT/SAT 比值的个体中,右楔前叶皮质的淀粉样蛋白病理学更高,同时 AD 特征区域的皮质厚度更低,与更高的内脏肥胖、胰岛素抵抗和淀粉样蛋白病理学有关。