The Challenge and Opportunity to Diagnose Parkinson's Disease in Midlife

Parkinson's disease (PD) is the most common neurodegenerative movement disorder that affects extensive regions of the nervous system. Its current clinical diagnosis is based on motor symptoms that appear late during disease progression when substantial proportions of the nigrostriatal dopaminer...

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Main Authors: Alexander Kilzheimer, Thomas Hentrich, Simone Burkhardt, Julia M. Schulze-Hentrich
Format: Article
Language:English
Published: Frontiers Media S.A. 2019-12-01
Series:Frontiers in Neurology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fneur.2019.01328/full
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spelling doaj-64726dde3be649ebae9484406686eabc2020-11-25T01:17:08ZengFrontiers Media S.A.Frontiers in Neurology1664-22952019-12-011010.3389/fneur.2019.01328484578The Challenge and Opportunity to Diagnose Parkinson's Disease in MidlifeAlexander KilzheimerThomas HentrichSimone BurkhardtJulia M. Schulze-HentrichParkinson's disease (PD) is the most common neurodegenerative movement disorder that affects extensive regions of the nervous system. Its current clinical diagnosis is based on motor symptoms that appear late during disease progression when substantial proportions of the nigrostriatal dopaminergic neuron population are lost already. Although disturbances in sleep and other biofunctions often surface years prior to motor impairments and point to a long prodromal phase, these phenotypic signs in a person's midlife lack predictive power. They do, however, signal the unfolding of the disease and suggest molecular correlates that begin deviating early on. Revealing such trajectories, hence, promises not only a better understanding of prodromal PD but may also enable a much-needed earlier diagnosis. A nexus that may harbor such molecular trajectories is the epigenome as key etiological factors of PD—genetics, age, and environment—influence this substrate. An earlier diagnosis would also allow earlier interventions and lifestyle adjustments to improve brain function and reduce symptoms. In this review, we describe the challenges of diagnosing PD early on and highlight the opportunities that may arise from steering research efforts towards comprehensive interrogations of molecular layers during the long-time neglected midlife phase. In particular, we emphasize how existing cohorts of at-risk individuals, available animal models, and suitable markers may come together and aid in revealing molecular trajectories that offer diagnostic utility for PD in its prodromal stage.https://www.frontiersin.org/article/10.3389/fneur.2019.01328/fullParkinson's diseaseprodromalmidlifemolecular prodromebiomarkerdiagnosis
collection DOAJ
language English
format Article
sources DOAJ
author Alexander Kilzheimer
Thomas Hentrich
Simone Burkhardt
Julia M. Schulze-Hentrich
spellingShingle Alexander Kilzheimer
Thomas Hentrich
Simone Burkhardt
Julia M. Schulze-Hentrich
The Challenge and Opportunity to Diagnose Parkinson's Disease in Midlife
Frontiers in Neurology
Parkinson's disease
prodromal
midlife
molecular prodrome
biomarker
diagnosis
author_facet Alexander Kilzheimer
Thomas Hentrich
Simone Burkhardt
Julia M. Schulze-Hentrich
author_sort Alexander Kilzheimer
title The Challenge and Opportunity to Diagnose Parkinson's Disease in Midlife
title_short The Challenge and Opportunity to Diagnose Parkinson's Disease in Midlife
title_full The Challenge and Opportunity to Diagnose Parkinson's Disease in Midlife
title_fullStr The Challenge and Opportunity to Diagnose Parkinson's Disease in Midlife
title_full_unstemmed The Challenge and Opportunity to Diagnose Parkinson's Disease in Midlife
title_sort challenge and opportunity to diagnose parkinson's disease in midlife
publisher Frontiers Media S.A.
series Frontiers in Neurology
issn 1664-2295
publishDate 2019-12-01
description Parkinson's disease (PD) is the most common neurodegenerative movement disorder that affects extensive regions of the nervous system. Its current clinical diagnosis is based on motor symptoms that appear late during disease progression when substantial proportions of the nigrostriatal dopaminergic neuron population are lost already. Although disturbances in sleep and other biofunctions often surface years prior to motor impairments and point to a long prodromal phase, these phenotypic signs in a person's midlife lack predictive power. They do, however, signal the unfolding of the disease and suggest molecular correlates that begin deviating early on. Revealing such trajectories, hence, promises not only a better understanding of prodromal PD but may also enable a much-needed earlier diagnosis. A nexus that may harbor such molecular trajectories is the epigenome as key etiological factors of PD—genetics, age, and environment—influence this substrate. An earlier diagnosis would also allow earlier interventions and lifestyle adjustments to improve brain function and reduce symptoms. In this review, we describe the challenges of diagnosing PD early on and highlight the opportunities that may arise from steering research efforts towards comprehensive interrogations of molecular layers during the long-time neglected midlife phase. In particular, we emphasize how existing cohorts of at-risk individuals, available animal models, and suitable markers may come together and aid in revealing molecular trajectories that offer diagnostic utility for PD in its prodromal stage.
topic Parkinson's disease
prodromal
midlife
molecular prodrome
biomarker
diagnosis
url https://www.frontiersin.org/article/10.3389/fneur.2019.01328/full
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