Structural and vascular alterations of deep cervical lymph nodes in amyloid PET-positive Alzheimer's disease patients

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Authors: Tae Hyung Kim, Jin Geun Kwon, Jimmy Sung- Chuan Chao, Jae Woo Kim, Changsik John Pak, Hak-Soo Suh, Jae-Sung Lim, Joon Pio Hong
Cited by: 2
References: 35

Abstract

• This study is the first to assess deep cervical lymph nodes in Alzheimer’s disease. • High-frequency color Doppler ultrasound revealed distinct lymph node alterations. • Zone 5 nodes in AD were fewer, irregularly shaped, and showed reduced vascularity. • A lymph node–based ultrasound scores distinguished AD from controls with 0.81 AUC. • Findings support lymphatic dysfunction as a novel biomarker in AD pathophysiology. Impaired clearance of brain-derived waste via the glymphatic–lymphatic system has been implicated in Alzheimer’s disease (AD) pathogenesis. Although animal studies highlight the role of deep cervical lymph nodes (dCLNs) in draining brain interstitial solutes, their characteristics in AD patients remain unknown. This study assessed structural and vascular alterations of dCLNs in AD using high-frequency color Doppler ultrasound (HFCDU). Twenty-five patients with amyloid PET–positive AD and 25 age-matched cognitively normal controls underwent HFCDU of dCLNs at neck zone 2–5. Lymph node number, shape, morphology, vascularity (via Superb Microvascular Imaging, SMI), and Solbiati index were quantified. Between-group differences were analyzed using logistic regression and receiver operating characteristic (ROC) analyses, and a simplified diagnostic score was developed from discriminative features. A total of 482 lymph nodes were analyzed (210 from AD, 272 from controls). AD patients had fewer oval-shaped nodes (50% vs. 83%, p

Fields of Study & Subjects

Cerebrospinal fluid and hydrocephalus Dementia and Cognitive Impairment Research Alzheimer's disease research and treatments

Publication details

Journal / source
Cerebral Circulation - Cognition and Behavior
Publisher
Elsevier BV
Volume
10
Pages
100533–100533
Publication date
1 January 2026
Language
EN