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Article type: Article Commentary
Authors: Atwood, Craig S.a; * | Perry, Georgeb
Affiliations: [a] Geriatric Research, Education and Clinical Center, Veterans Administration Hospital and Department of Medicine, University of Wisconsin, Madison, WI, USA | [b] Department of Neuroscience, Development and Regenerative Biology, University of Texas at San Antonio, San Antonio, TX, USA
Correspondence: [*] Correspondence to: Craig S. Atwood, PhD, University of Wisconsin-Madison School of Medicine and Public Health, Wm S. Middleton Memorial VA (GRECC 11G), 2500 Overlook Terrace, Madison, WI 53705, USA. Tel.: +1 608 256 1901/Ext. 11664; E-mail: csa@medicine.wisc.edu.
Abstract: The questionable approval of aducanumab and the recent approval of lecanemab (Leqembi; Eisai and Biogen) by the FDA has raised the issue of safety (stroke, meningitis, and encephalitis) over efficacy (slowing of cognitive decline). This communication recounts the important physiological functions of amyloid-β as a barrier protein with unique sealant and anti-pathogenic activities important for maintaining vascular integrity coupled with innate immune functions that prevent encephalitis and meningitis. The approval of a drug that obviates both of these purposive functions increases the risk of hemorrhage, edema and downstream pathogenic outcomes and should be clearly outlined to patients.
Keywords: Adverse events, amyloid-β, ARIA, cognition, edema, hemorrhage, innate immunity, lecanemab, pathogen, stroke
DOI: 10.3233/JAD-230040
Journal: Journal of Alzheimer's Disease, vol. 92, no. 3, pp. 799-801, 2023
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