In a prospective MRI study the presence, appearance, volume, and regional cerebral blood flow (rCBF) correlates of periventricular hyperintensities (PVHs) and deep white matter hyperintensities (DWMHs) were examined in 18 patients with probable Alzheimer's disease and in 10 age matched healthy control subjects, all without major cerebrovascular risk factors. The 133Xe inhalation method and the [9"-Tc]-d,l-hexamethyl-propyleneamine-oxime (HMPAO) technique with single photon emission computed tomography (SPECT) were used to measure rCBF. Rating scores for PVHs were significantly higher in the Alzheimer's disease group (p < 0.01) and correlated significantly with the volume ofventricles (p < 0.05) and with systolic arterial blood pressure (p < 0.01), but not with rCBF.By contrast, there was no significant difference in the rating scores or volumes of DWMHs between the two groups, although three patients had extensive DWMH lesions in the central white matter. In the group of patients with Alzheimer's disease as a whole, the volume of DWMHs correlated well with rCBF in the hippocampal region (r = -0-72; p < 0'001), but not (0-79 (1-55)) (5-39 (11 3)) Total volume of ventricles (cm3) 24-5 (8 9-56 2) 46-9 (18-6-127-2) NS (mean (SD)) (31-1 (17-8)) (54-2 (33-1)) Values are median (range) unless stated otherwise. Control = healthy control subjects; Alzheimer's disease = patients with a clinical diagnosis of probable Alzheimer's disease; MMSE = mini mental state examination'4; GDS = global deterioration scale'5; PVH = periventricular hyperintensities; DWMH = deep white matter hyperintensities. **p < 0-01, NS = nonsignificant (patients with Alzheimer's disease v control subjects, Wilcoxon two sample rank sum test). study reported elsewhere,8 and the present report includes only patients in whom a cranial MRI study was available. In one patient (case 04-19), the diagnosis was later confirmed by postmortem neuropathological examination. All patients underwent an extensive study programme to rule out any other disorders that might be associated with dementia, cognitive dysfunction, or altered rCBF.8 Briefly, cranial x ray CT was without focal pathology and without periventricular hypodensity in all patients. No patient had a history of psychiatric or neurological disease, except for Alzheimer's disease. All patients had Hamilton" depression scores below or at 10. Cerebrovascular risk factors were minimised: patients with diabetes mellitus, moderate to severe impairment of cardiac or pulmonary function, significant stenosis of the carotid arteries on Doppler examination, chronic arterial hypertension, or increased cholesterol concentrations in the blood were excluded. Resting systolic/diastolic blood pressure was below 180/100 on the study day. The severity of dementia was documented (