Correlation analysis of peripheral platelet markers and disease phenotypes in Alzheimer's disease
INTRODUCTION Platelets serve as the primary peripheral reservoir of amyloid beta (Aβ). However, there is limited research on platelet markers in routine blood examinations, particularly with regard to the large platelet ratio (P‐LCR) in Alzheimer's disease (AD). METHODS This study included 512...
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Published in | Alzheimer's & dementia Vol. 20; no. 6; pp. 4366 - 4372 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
John Wiley and Sons Inc
01.06.2024
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Subjects | |
Online Access | Get full text |
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Summary: | INTRODUCTION
Platelets serve as the primary peripheral reservoir of amyloid beta (Aβ). However, there is limited research on platelet markers in routine blood examinations, particularly with regard to the large platelet ratio (P‐LCR) in Alzheimer's disease (AD).
METHODS
This study included 512 AD patients and 205 healthy controls (HCs). Platelet markers and apolipoprotein E (APOE) 4 status were assessed in all participants.
RESULTS
The study revealed that P‐LCR was significantly elevated in AD patients compared to HCs. In AD patients carrying APOE4, P‐LCR significantly negatively correlated with Montreal Cognitive Assessment scores. There was an observed increasing trend in the rate of change in P‐LCR with disease progression. Binary logistic regression analysis indicated that P‐LCR may constitute a risk factor for AD, after adjusting for age, sex, APOE4, and body mass index.
DISCUSSION
P‐LCR is associated with disease severity in AD patients carrying APOE4. P‐LCR may be a promising marker to reflect platelet activity in AD patients.
Highlights
P‐LCR significantly negatively correlated with MoCA scores in AD patients with APOE4.
The rate of change in P‐LCR showed an increasing trend with disease progression.
P‐LCR may be a risk factor for AD. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1552-5260 1552-5279 1552-5279 |
DOI: | 10.1002/alz.13841 |