van der Veen Pieternella H, Muller Majon, Vincken Koen L, Hendrikse Jeroen, Mali Willem P T M, van der Graaf Yolanda, Geerlings Mirjam I
From the Department of Radiology (P.H.v.d.V., J.H., W.P.T.M.M.), Julius Center for Health Sciences and Primary Care (P.H.v.d.V., M.M., Y.v.d.G., M.I.G.), and Image Sciences Institute (K.L.V.), University Medical Center Utrecht, Utrecht, The Netherlands; and Department of Gerontology and Geriatrics, Leiden University Medical Center, Leiden, The Netherlands (M.M.).
Stroke. 2015 May;46(5):1233-8. doi: 10.1161/STROKEAHA.114.008030. Epub 2015 Mar 24.
Cerebral small-vessel disease and cerebral blood flow (CBF) are interrelated. However, the direction of the relationship is unknown, and longitudinal studies are scarce. We investigated the longitudinal relationship between CBF and white matter hyperintensities (WMHs) and lacunes, as representatives of cerebral small-vessel disease, in patients with manifest arterial disease.
Within the Second Manifestations of Arterial Disease-Magnetic Resonance (SMART-MR) study, 1.5T brain magnetic resonance imaging, including an MR angiography, was obtained at baseline and after on ≈3.9 years of follow-up in 575 patients with manifest arterial disease (mean age, 57±10 years). Longitudinal associations of WMHs and lacunes with parenchymal CBF (pCBF; per 100-mL brain volume) were estimated using regression analyses, adjusted for age, sex, follow-up time, and baseline brain measures.
Baseline pCBF was not associated with progression of WMHs and lacunes over time. However, periventricular and deep WMHs at baseline were associated with decline in pCBF; mean (95% confidence interval) decline in pCBF per % intracranial volume increase in periventricular and deep WMH volume was -0.70 (-1.40 to -0.00) and -1.01 (-1.64 to -0.38) mL/min per 100-mL brain volume, respectively. These associations were partly explained by cardiovascular risk factors but remained significant for deep WMHs (mean decline [95% confidence interval] in pCBF per % intracranial volume increase in deep WMH volume was -0.92 [-1.56 to -0.28] mL/min per 100-mL brain volume). Lacunes were not associated with change in pCBF.
In patients with manifest arterial disease, baseline periventricular and deep WMH volumes were associated with decline in pCBF over time, but baseline pCBF was not associated with progression of WMHs and lacunes over time.
脑小血管疾病与脑血流量(CBF)相互关联。然而,这种关系的方向尚不清楚,且纵向研究较少。我们调查了明显动脉疾病患者中CBF与作为脑小血管疾病代表的白质高信号(WMH)和腔隙之间的纵向关系。
在动脉疾病的第二次磁共振成像(SMART-MR)研究中,对575例明显动脉疾病患者(平均年龄57±10岁)在基线时和随访约3.9年后进行了1.5T脑磁共振成像检查,包括磁共振血管造影。使用回归分析估计WMH和腔隙与实质CBF(pCBF;每100毫升脑体积)的纵向关联,并对年龄、性别、随访时间和基线脑测量进行了调整。
基线pCBF与WMH和腔隙随时间的进展无关。然而,基线时脑室周围和深部WMH与pCBF下降有关;脑室周围和深部WMH体积每增加1%颅内体积,pCBF每100毫升脑体积的平均(95%置信区间)下降分别为-0.70(-1.40至-0.00)和-1.01(-1.64至-0.38)毫升/分钟。这些关联部分由心血管危险因素解释,但深部WMH仍然显著(深部WMH体积每增加1%颅内体积,pCBF每100毫升脑体积的平均下降[95%置信区间]为-0.92[-1.56至-0.28]毫升/分钟)。腔隙与pCBF的变化无关。
在明显动脉疾病患者中,基线时脑室周围和深部WMH体积与pCBF随时间下降有关,但基线pCBF与WMH和腔隙随时间的进展无关。