A β 1-15/16 as a marker for γ -secretase inhibition in Alzheimer’s disease

Amyloid- β (A β ) producing enzymes are key targets for disease-modifying Alzheimer’s disease (AD) therapies since A β trafficking is at the core of AD pathogenesis. Development of such drugs might benefit from the identification of markers indicating in vivo drug effects in the central nervous system. We have previously shown that A β 1-15 is produced by concerted β - and α secretase cleavage of amyloid- β protein precursor (A β PP). Here, we test the hypothesis that this pathway is more engaged upon γ -secretase inhibition in humans and cerebrospinal fluid (CSF) levels of A β 1-15/16 represent a biomarker for this effect. Twenty healthy men were treated with placebo (n=5) or the γ -secretase inhibitor semagacestat (100 mg [n=5], 140 mg [n=5], or 280 mg [n=5]). CSF samples were collected hourly over 36 hours and 10 time points were analyzed by immunoassay for A β 1-15/16 , A β x-38 , A β x-40 , A β x-42 , sA β PP α and sA β PP β . The CSF concentration of A β 1-15/16 showed a dose-dependent response over 36 hours. In the 280 mg treatment group, a transient increase was seen with a maximum of 180% relative to baseline at 9 hours post administration of semagacestat. The concentrations of A β x-38 , A β x-40 and A β x-42 decreased the first 9 hours followed by increased concentrations after 36 hours relative to baseline. No significant changes were detected for CSF sA β PP α and sA β PP β .Our data shows that CSF levels of A β 1-15/16 increase during treatment with semagacestat supporting its feasibility as a pharmacodynamic biomarker for drug candidates aimed at inhibiting γ -secretase-mediated A β PP-processing.

[1]  K. Blennow,et al.  A novel pathway for amyloid precursor protein processing , 2011, Neurobiology of Aging.

[2]  M. Citron,et al.  Alzheimer's disease: strategies for disease modification , 2010, Nature Reviews Drug Discovery.

[3]  K. Blennow,et al.  Mass spectrometric characterization of brain amyloid beta isoform signatures in familial and sporadic Alzheimer’s disease , 2010, Acta Neuropathologica.

[4]  M. Bielefeld-Sévigny AlphaLISA immunoassay platform- the "no-wash" high-throughput alternative to ELISA. , 2009, Assay and drug development technologies.

[5]  A. Fleisher,et al.  Phase 2 safety trial targeting amyloid beta production with a gamma-secretase inhibitor in Alzheimer disease. , 2008, Archives of neurology.

[6]  B. de Strooper,et al.  1-(3′,4′-Dichloro-2-fluoro[1,1′-biphenyl]-4-yl)-cyclopropanecarboxylic Acid (CHF5074), a Novel γ-Secretase Modulator, Reduces Brain β-Amyloid Pathology in a Transgenic Mouse Model of Alzheimer's Disease without Causing Peripheral Toxicity , 2007, Journal of Pharmacology and Experimental Therapeutics.

[7]  Henrik Zetterberg,et al.  Characterization of amyloid beta peptides in cerebrospinal fluid by an automated immunoprecipitation procedure followed by mass spectrometry. , 2007, Journal of proteome research.

[8]  Timothy Harrison,et al.  The Novel γ Secretase Inhibitor N-[cis-4-[(4-Chlorophenyl)sulfonyl]-4-(2,5-difluorophenyl)cyclohexyl]-1,1,1-trifluoromethanesulfonamide (MRK-560) Reduces Amyloid Plaque Deposition without Evidence of Notch-Related Pathology in the Tg2576 Mouse , 2007, Journal of Pharmacology and Experimental Therapeutics.

[9]  E. Reiman,et al.  Alzheimer's disease a century later. , 2006, The Journal of clinical psychiatry.

[10]  David M Holtzman,et al.  Human amyloid-β synthesis and clearance rates as measured in cerebrospinal fluid in vivo , 2006, Nature Medicine.

[11]  D. Selkoe Alzheimer's disease. , 2011, Cold Spring Harbor perspectives in biology.

[12]  B. de Strooper,et al.  Aph-1, Pen-2, and Nicastrin with Presenilin generate an active gamma-Secretase complex. , 2003, Neuron.

[13]  C. Vigo‐Pelfrey,et al.  Characterization of beta-amyloid peptide from human cerebrospinal fluid. , 1993, Journal of neurochemistry.