RESUMEN
The established biomarkers of Alzheimer's disease (AD) require invasive endeavours or presuppose sophisticated technical equipment. Consequently, new biomarkers are needed. Here, we report that plasma levels of soluble amyloid precursor protein ß (sAPPß), a protein of the initial phase of the amyloid cascade, were significantly lower in patients with symptomatic AD (21 with mild cognitive impairment due to AD and 44 with AD dementia) with AD-typical cerebral hypometabolic pattern compared with 27 cognitively healthy elderly individuals without preclinical AD. These findings yield further evidence for the potential of sAPPß in plasma as an AD biomarker candidate.
Asunto(s)
Enfermedad de Alzheimer/sangre , Precursor de Proteína beta-Amiloide/sangre , Disfunción Cognitiva/sangre , Anciano , Enfermedad de Alzheimer/diagnóstico , Biomarcadores/sangre , Disfunción Cognitiva/diagnóstico , Femenino , Humanos , Masculino , Persona de Mediana EdadRESUMEN
Cost- and time-effective markers of Alzheimer's disease (AD), reliable and feasible at the population level are urgently needed. Soluble amyloid-ß protein precursor ß (sAßPPß) in plasma has attracted scientific attention as a potential AD biomarker candidate. Here we report that plasma sAßPPß levels in patients with AD dementia and typical for AD cerebrospinal fluid (CSF) biomarker profiles (Nâ=â33) are significantly lower (pâ<â0.01) than those of cognitively healthy elderly individuals without AD (Nâ=â39), while CSF sAßPPß levels did not differ between the studied groups. This provides further evidence for the potential of sAßPPß in plasma as an AD biomarker candidate.