Magnetic Resonance Imaging Improves Cerebrospinal Fluid Biomarkers in the Early Detection of Alzheimer's Disease

Article type: Research Article

Authors: Brys, Miroslaw^a | Glodzik, Lidia^a | Mosconi, Lisa^a | Switalski, Remigiusz^a | De Santi, Susan^a | Pirraglia, Elizabeth^a | Rich, Kenneth^a | Kim, Byeong C.^c | Mehta, Pankaj^d | Zinkowski, Ray^e | Pratico, Domenico^f | Wallin, Anders^g | Zetterberg, Henrik^g | Tsui, Wai H.^a | Rusinek, Henry^a | Blennow, Kaj^g | de Leon, Mony J.^{a; b; *}

Affiliations: [a] New York University School of Medicine, Center for Brain Health, NY, USA | [b] Nathan Kline Institute, Orangeburg, NY, USA | [c] Chonnam National University Medical School, Gwangju, Korea | [d] Institute for Basic Research, Staten Island, NY, USA | [e] Applied Neurosolutions, Vernon Hills, IL, USA | [f] Temple University, School of Medicine, Philadelphia, PA, USA | [g] University of Göteborg, Göteborg, Sweden

Correspondence: [*] Corresponding author: Mony J. de Leon, Center for Brain Health, 550 First Avenue MHL-400, New York, NY 10016, USA. Tel.: +1 212 263 7563; E-mail: [email protected].

Abstract: Little is known of combined utility of magnetic resonance imaging (MRI) and cerebrospinal fluid (CSF) biomarkers for prediction of Alzheimer's disease (AD) and longitudinal data is scarce. We examined these biomarkers at baseline and longitudinally in incipient AD. Forty-five subjects [21 controls (NL-NL), 16 stable MCI (MCI-MCI), 8 MCI who declined to AD (MCI-AD)] received MRI and lumbar puncture at baseline and after 2 years. CSF measures included total and phosphorylated tau (T-tau, P-tau231), amyloid-β (Aβ42/Aβ40) and isoprostane. Voxel-based morphometry identified gray matter concentration (GMC) differences best distinguishing study groups and individual GMC values were calculated. Rate of medial temporal lobe (MTL) atrophy was examined using regional boundary shift (rBS) method. At baseline, for MRI, MCI-AD showed reduced GMC-MTL, and for CSF higher CSF T-tau, P-tau231, IP and lower Aβ42/Aβ40 as compared with MCI-MCI or NL-NL. Longitudinally, rBS-MTL atrophy was higher in MCI-AD than in either MCI-MCI or NL-NL, particularly in the left hemisphere. CSF data showed longitudinally greater increases of isoprostane in MCI-AD as compared with NL-NL. Combining baseline CSF-P-tau231 and GMC-MTL significantly increased overall prediction of AD from 74% to 84% (pstep < 0.05). These results provide support for including multiple modalities of biomarkers in the identification of memory clinic patients at increased risk for dementia.

Keywords: Alzheimer's disease, brain atrophy, cerebrospinal fluid biomarkers, early diagnosis

DOI: 10.3233/JAD-2009-0968

Journal: Journal of Alzheimer's Disease, vol. 16, no. 2, pp. 351-362, 2009