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Overexpression of Cell Cycle Proteins of Peripheral Lymphocytes in Patients with Alzheimer's Disease
Psychiatry Investigation ; : 127-134, 2016.
Article in English | WPRIM | ID: wpr-108175
ABSTRACT

OBJECTIVE:

Biological markers for Alzheimer's disease (AD) will help clinicians make objective diagnoses early during the course of dementia. Previous studies have suggested that cell cycle dysregulation begins earlier than the onset of clinical manifestations in AD.

METHODS:

We examined the lymphocyte expression of cell cycle proteins in AD patients, dementia controls (DC), and normal controls (NC). One-hundred seventeen subjects (36 AD, 31 DC, and 50 NC) were recruited. The cell cycle proteins CDK2, CDK4, CDK6, cyclin B, and cyclin D were measured in peripheral lymphocytes. Cell cycle protein expression in the three groups was compared after adjusting for age and sex.

RESULTS:

The levels of cell cycle proteins CDK2, CDK4, CDK6, cyclin B, and cyclin D were significantly higher in AD patients than in the NC subjects. The DC group manifested intermediate levels of cell cycle proteins compared with the AD patients and the NC subjects. The present study indicates that cell cycle proteins are upregulated in the peripheral lymphocytes of AD patients.

CONCLUSION:

Cell cycle dysregulation in peripheral lymphocytes may present a promising starting point for identifying peripheral biomarkers of AD.
Subject(s)

Full text: Available Index: WPRIM (Western Pacific) Main subject: Lymphocytes / Biomarkers / Cell Cycle / Cyclins / Cell Cycle Proteins / Cyclin B / Dementia / Diagnosis / Cyclin D / Alzheimer Disease Type of study: Diagnostic study Limits: Humans Language: English Journal: Psychiatry Investigation Year: 2016 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Lymphocytes / Biomarkers / Cell Cycle / Cyclins / Cell Cycle Proteins / Cyclin B / Dementia / Diagnosis / Cyclin D / Alzheimer Disease Type of study: Diagnostic study Limits: Humans Language: English Journal: Psychiatry Investigation Year: 2016 Type: Article