Journal Article DZNE-2026-00695

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Brain-first versus body-first Parkinson's disease: Differential findings on pupillary, brainstem and vagus sonography.

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2026
Steinkopff [Darmstadt]

Journal of neurology 273(8), 444 () [10.1007/s00415-026-13973-0]

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Abstract: In Parkinson's disease (PD), two pathogenetic subtypes have been proposed: a 'brain-first', with α-synuclein pathology arising in one hemisphere and spreading secondarily to the peripheral autonomic nervous system, and a 'body-first' subtype, with the pathology originating in the enteric or peripheral autonomic nervous system and subsequently spreading symmetrically to the brain. To dissect these subtypes, we assessed the association between pupillary dysfunction, mesencephalic raphe and substantia nigra changes, vagus nerve atrophy and vagal electrocardiographic parameters in PD patients and controls.In this single-center cross-sectional study, we included 54 people with PD and 60 matched healthy controls. Participants underwent clinical assessments, electrocardiography, and sonographic measurements of substantia nigra echoic area, midbrain raphe echo-score and vagus nerve caliber. Dynamic ultrasound pupillometry was performed in drug-naïve de novo PD patients and matched controls. The brain-first and body-first subtypes were classified based on the REM-sleep Behavior Disorder Screening Questionnaire and gastrointestinal symptoms.Vagal atrophy increased with disease duration and severity. During the first decade of motor disease, vagal atrophy and dysfunction occurred in body-first but not brain-first PD. Sympathetic pupillary innervation was reduced in de novo body-first but not brain-first PD patients. However, parasympathetic pupillary innervation was reduced in both subtypes at the de novo stage. Substantia nigra hyperechoic area was asymmetrical in brain-first but more symmetrical in body-first PD.Our findings support the concept of two subtypes of PD in which the mesencephalic and vagal parasympathetic systems are affected in opposite sequences. Ultrasonic and electrocardiographic examination could facilitate early subtyping.

Keyword(s): Humans (MeSH) ; Parkinson Disease: diagnostic imaging (MeSH) ; Parkinson Disease: physiopathology (MeSH) ; Parkinson Disease: complications (MeSH) ; Parkinson Disease: pathology (MeSH) ; Parkinson Disease: classification (MeSH) ; Male (MeSH) ; Female (MeSH) ; Cross-Sectional Studies (MeSH) ; Aged (MeSH) ; Middle Aged (MeSH) ; Vagus Nerve: diagnostic imaging (MeSH) ; Vagus Nerve: physiopathology (MeSH) ; Vagus Nerve: pathology (MeSH) ; Brain Stem: diagnostic imaging (MeSH) ; Brain Stem: physiopathology (MeSH) ; Ultrasonography (MeSH) ; Parkinson’s disease ; Pupillary reflex ; Substantia nigra ; Transcranial ultrasound ; Ultrasonography ; Vagus nerve

Classification:

Contributing Institute(s):
  1. Clinical Dementia Research (Rostock /Greifswald) (AG Teipel)
  2. Non-Motor Symptoms in Parkinson's disease (AG Storch)
Research Program(s):
  1. 353 - Clinical and Health Care Research (POF4-353) (POF4-353)

Appears in the scientific report 2026
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Medline ; Creative Commons Attribution CC BY 4.0 ; OpenAccess ; BIOSIS Previews ; Biological Abstracts ; Clarivate Analytics Master Journal List ; Current Contents - Life Sciences ; DEAL Springer ; Ebsco Academic Search ; Essential Science Indicators ; IF >= 5 ; JCR ; NationallizenzNationallizenz ; SCOPUS ; Science Citation Index Expanded ; Web of Science Core Collection
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Document types > Articles > Journal Article
Institute Collections > ROS DZNE > ROS DZNE-AG Storch
Institute Collections > ROS DZNE > ROS DZNE-AG Teipel
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 Record created 2026-07-07, last modified 2026-07-10