An investigation of the correlation between the S-glutathionylated GAPDH levels in blood and Alzheimer’s disease progression

Autor: Chia Fan Tsai, Cho Chen Hsieh, Wei Jung Chen, Muh-Shi Lin, Kuan Hung Lin, Chen Wei Tsai, Chai Ching Lin
Rok vydání: 2020
Předmět:
Male
0301 basic medicine
Physiology
Apoptosis
Disease
Alzheimer's Disease
Diagnostic Radiology
0302 clinical medicine
Outpatients
Blood plasma
Medicine and Health Sciences
Enzyme-Linked Immunoassays
Glyceraldehyde 3-phosphate dehydrogenase
Depression (differential diagnoses)
Aged
80 and over

Multidisciplinary
Cell Death
biology
Radiology and Imaging
Neurodegenerative Diseases
Blood Proteins
Middle Aged
Prognosis
Glutathione
Magnetic Resonance Imaging
Body Fluids
Blood
Neurology
Cell Processes
Disease Progression
Medicine
Female
Anatomy
Research Article
Adult
medicine.medical_specialty
Patients
Imaging Techniques
Science
Tau protein
Research and Analysis Methods
Blood Plasma
03 medical and health sciences
stomatognathic system
Alzheimer Disease
Diagnostic Medicine
Internal medicine
Mental Health and Psychiatry
medicine
Humans
Dementia
Immunoassays
Aged
business.industry
Case-control study
Biology and Life Sciences
Cell Biology
medicine.disease
Health Care
030104 developmental biology
Endocrinology
Case-Control Studies
Immunologic Techniques
biology.protein
Glyceraldehyde-3-Phosphate Dehydrogenase (Phosphorylating)
business
Protein Processing
Post-Translational

030217 neurology & neurosurgery
Follow-Up Studies
Zdroj: PLoS ONE
PLoS ONE, Vol 15, Iss 5, p e0233289 (2020)
ISSN: 1932-6203
DOI: 10.1371/journal.pone.0233289
Popis: Alzheimer's disease (AD) is a progressive neurodegenerative disease characterized by two aggregates, namely, amyloid-β (Aβ) plaques and neurofibrillary tangles (NFTs) of hyperphosphorylated tau protein (tau-p), which are released into the blood in a very small amount and cannot be easily detected. An increasing number of recent studies have suggested that S-glutathionylated glyceraldehyde 3-phosphate dehydrogenase (GAPDH) is highly correlated with Aβ in patients with AD and that S-glutathionylated GAPDH plays a role as a proapoptotic factor in AD. We found that S-glutathionylated GAPDH is abundant in the blood of AD patients, which is unusual because S-glutathionylated GAPDH cannot exist in the blood under normal conditions. The aim of this study was to further explore the correlation between the S-glutathionylated GAPDH levels in blood plasma and AD progression. As controls, we recruited 191 people without AD, which included 111 healthy individuals and 37 patients with depression and insomnia, in the psychosomatic clinic. Moreover, 47 patients with AD (aged 40-89 years) were recruited at the neurology clinic. The blood S-glutathionylated GAPDH levels in the AD patients were significantly (p < 0.001) higher (752.7 ± 301.7 ng/dL) than those in the controls (59.92 ± 122.4 ng/dL), irrespective of gender and age. For AD diagnosis, the criterion blood S-glutathionylated GAPDH level > 251.62 ng/dL exhibited 95.74% sensitivity and 92.67% specificity. In fact, the individuals aged 70-89 years, namely, 37 patients from the psychosomatic clinic and 42 healthy individuals, showed significant blood S-glutathionylated GAPDH levels (230.5 ± 79.3 and 8.05 ± 20.51 ng/dL, respectively). This finding might indicate neurodegenerative AD progression in psychosomatic patients and suggests that the degree of neuronal apoptosis during AD progression might be sensitively evaluated based on the level of S-glutathionylated GAPDH in blood.
Databáze: OpenAIRE