Overlapping pathological features of Alzheimer’s and Parkinson’s diseases: Clinical implications and future directions for improving diagnostic precision
Jul 2026· Life Sciences, Medicine and Biomedicine· Vol 10· 0 citations
TL;DR
This article explores these overlapping features, including memory and executive function deficits, neuropsychiatric symptoms such as depression and apathy, and motor signs like bradykinesia and rigidity, and discusses the diagnostic challenges arising from these overlaps.
Abstract
Alzheimer's disease (AD) and Parkinson's disease (PD) are two of the most common neurodegenerative disorders, each with distinct clinical and pathological features, yet sharing significant overlaps that complicate diagnosis and management. AD is primarily characterized by cognitive decline stemming from amyloid-beta plaques and tau tangles, while PD is defined by motor dysfunction caused by alpha-synuclein-containing Lewy bodies. Despite these differences, both diseases exhibit overlapping cognitive, neuropsychiatric, and motor symptoms, along with shared underlying mechanisms like neuroinflammation and abnormal protein aggregation. This article explores these overlapping features, including memory and executive function deficits, neuropsychiatric symptoms such as depression and apathy, and motor signs like bradykinesia and rigidity. It also discusses the diagnostic challenges arising from these overlaps, highlighting the limitations of current tools and the promise of a multi-modal diagnostic strategy that integrates clinical evaluation, advanced neuroimaging, and emerging biomarkers. The review concludes by outlining future research directions, emphasizing the potential of advanced imaging, early detection of dual pathologies, and the development of integrated therapeutic approaches to enable precision medicine for these complex disorders.
Canine cognitive dysfunction syndrome (CCDS) shares notable clinical and molecular similarities with Alzheimer's disease (AD), supporting the value of cross-species translational research to enhance diagnostic and therapeutic approaches for both conditions. These disorders are progressive neurological diseases characte...
Evilly Lopes-Gomes, F. F. B. Resende, Alexandra Mazer Greuel et al.· Journal of Alzheimer's Disea...· 0 citations
This chapter highlights a overview of blood-based biomarkers emerging in the field of AD and PD, exploring the clinical utility of core pathology markers (Aβ42/40, p-tau species, and α-synuclein), alongside other neurodegenerative markers such as neurofilament light chain and glial activation markers like GFAP.
Priya, Radhika Mittal, Jyotirmoy Banerjee et al.· International review of neur...· 0 citations
The current understanding of the genetic and physiological mechanisms underlying Alzheimer’s disease is reviewed and modern approaches for diagnosis and treatment are discussed.
Zahraa Mohammed Fakheir, S. A. H. Jasim· Journal of Genetic and Envir...· 0 citations
A practical multi-axis framework comprising clinical phenotype, AD biological context (AD pathology plus co-pathologies and molecular modifiers), network topography (regional patterns) and tempo (rate of clinical and biomarker progression) is proposed to reduce diagnostic mismatches, make cohorts more comparable and su...
L. Grinberg, M. Murray· Nature Reviews Neurology· 0 citations
A combination of biomarker-guided diagnostics with mechanism-based therapies might enable precision medicine approaches and improve clinical outcomes in AD.
Alzheimer’s disease (AD) is the leading cause of dementia and a heterogeneous neurodegenerative disorder characterized by amyloid-β (Aβ) and tau pathology, impaired proteostasis, neurovascular dysfunction, maladaptive glial and immune responses, and synaptic dysfunction. Human genetic evidence supports an upstream role...
P. Chmielewski· Cells· 0 citations
We use cookies to run the site and, with your consent, for analytics and to show ads.
See our Cookie Policy.