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Article
September 1993

Temporal Lobe Regions on Magnetic Resonance Imaging Identify Patients With Early Alzheimer's Disease

Author Affiliations

From the Departments of Anatomy and Neurobiology (Drs Killiany and Moss) and Neurology (Dr Moss), Boston University School of Medicine; Departments of Psychiatry and Neurology, Massachusetts General Hospital, Harvard Medical School (Dr Albert); and Department of Radiology, Brigham and Women's Hospital, Harvard Medical School (Drs Sandor and Jolesz and Mr Tieman), Boston, Mass.

Arch Neurol. 1993;50(9):949-954. doi:10.1001/archneur.1993.00540090052010
Abstract

• Objective.  —The goal of the study was to examine the volume of selected brain regions in a group of mildly impaired patients with Alzheimer's disease (AD). Five regions were selected for analysis, all of which have been reported to show substantial change in the majority of patients with AD at some time in the course of disease.

Design.  —Case-control study with the experimenter "blinded."

Setting.  —Hospital-based magnetic resonance imaging center.

Participants.  —Fifteen subjects, eight patients with the diagnosis of probable dementia of the Alzheimer type made in concordance with National Institute of Neurological and Communicative Diseases and Stroke/Alzheimer's Disease and Related Disorders Association criteria and seven age-matched healthy control subjects.

Results.  —Three of the volumetric measures were significantly different between patients with AD and controls: the hippocampus, the temporal horn of the lateral ventricles, and the temporal lobe. Two of the measures did not significantly differentiate patients with AD and controls: the amygdala and the basal forebrain. A discriminant function analysis demonstrated that a linear combination of the volumes of the hippocampus and the temporal horn of the lateral ventricles differentiated 100% of the patients and controls from one another.

Conclusions.  —The results suggest that the hippocampus and the temporal horn of the lateral ventricles may be useful as antemortem markers of AD in mildly impaired patients.

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