Last David, Alsop David C, Abduljalil Amir M, Marquis Robert P, de Bazelaire Cedric, Hu Kun, Cavallerano Jerry, Novak Vera
Division of Gerontology, Beth Israel Deaconess Medical Center, Harvard Medical School, 110 Francis St., Boston, MA 02215, USA.
Diabetes Care. 2007 May;30(5):1193-9. doi: 10.2337/dc06-2052. Epub 2007 Feb 8.
The aim of this study was to evaluate the regional effects of type 2 diabetes and associated conditions on cerebral tissue volumes and cerebral blood flow (CBF) regulation.
CBF was examined in 26 diabetic (aged 61.6 +/- 6.6 years) and 25 control (aged 60.4 +/- 8.6 years) subjects using continuous arterial spin labeling (CASL) imaging during baseline, hyperventilation, and CO2 rebreathing. Regional gray and white matter, cerebrospinal fluid (CSF), and white matter hyperintensity (WMH) volumes were measured on a T1-weighted inversion recovery fast-gradient echo and a fluid attenuation inversion recovery magnetic resonance imaging at 3 Tesla.
The diabetic group had smaller global white (P = 0.006) and gray (P = 0.001) matter and larger CSF (36.3%, P < 0.0001) volumes than the control group. Regional differences were observed for white matter (-13.1%, P = 0.0008) and CSF (36.3%, P < 0.0001) in the frontal region, for CSF (20.9%, P = 0.0002) in the temporal region, and for gray matter (-3.0%, P = 0.04) and CSF (17.6%, P = 0.01) in the parieto-occipital region. Baseline regional CBF (P = 0.006) and CO2 reactivity (P = 0.005) were reduced in the diabetic group. Hypoperfusion in the frontal region was associated with gray matter atrophy (P < 0.0001). Higher A1C was associated with lower CBF (P < 0.0001) and greater CSF (P = 0.002) within the temporal region.
Type 2 diabetes is associated with cortical and subcortical atrophy involving several brain regions and with diminished regional cerebral perfusion and vasoreactivity. Uncontrolled diabetes may further contribute to hypoperfusion and atrophy. Diabetic metabolic disturbance and blood flow dysregulation that affects preferentially frontal and temporal regions may have implications for cognition and balance in elderly subjects with diabetes.
本研究旨在评估2型糖尿病及其相关病症对脑组织容量和脑血流量(CBF)调节的区域影响。
在基线、过度通气和二氧化碳再呼吸期间,使用连续动脉自旋标记(CASL)成像技术对26名糖尿病患者(年龄61.6±6.6岁)和25名对照者(年龄60.4±8.6岁)进行脑血流量检查。在3特斯拉的T1加权反转恢复快速梯度回波和液体衰减反转恢复磁共振成像上测量区域灰质、白质、脑脊液(CSF)和白质高信号(WMH)体积。
糖尿病组的全脑白质(P = 0.006)和灰质(P = 0.001)体积较对照组小,脑脊液体积更大(36.3%,P < 0.0001)。额叶区域的白质(-13.1%,P = 0.0008)和脑脊液(36.3%,P < 0.0001)、颞叶区域的脑脊液(20.9%,P = 0.0002)以及顶枕叶区域的灰质(-3.0%,P = 0.04)和脑脊液(17.6%,P = 0.01)存在区域差异。糖尿病组的基线区域脑血流量(P = 0.00)和二氧化碳反应性(P = 0.005)降低。额叶区域的灌注不足与灰质萎缩相关(P < 0.0001)。较高的糖化血红蛋白与颞叶区域较低的脑血流量(P < 0.0001)和更大的脑脊液体积(P = 0.002)相关。
2型糖尿病与涉及多个脑区的皮质和皮质下萎缩、区域脑灌注和血管反应性降低有关。未控制的糖尿病可能进一步导致灌注不足和萎缩。优先影响额叶和颞叶区域的糖尿病代谢紊乱和血流调节异常可能对老年糖尿病患者的认知和平衡产生影响。