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

被引:21
作者
Tsai, Chen Wei [1 ]
Tsai, Chia Fan [2 ]
Lin, Kuan Hung [3 ]
Chen, Wei Jung [1 ]
Lin, Muh Shi [1 ,4 ,5 ,6 ]
Hsieh, Cho Chen [7 ]
Lin, Chai Ching [1 ]
机构
[1] Natl Ilan Univ, Coll Bioresources, Dept Biotechnol & Anim Sci, Yilan, Taiwan
[2] Taipei Vet Gen Hosp, Dept Psychiat, Taipei, Taiwan
[3] Taiwan Adventist Hosp, Dept Neurol, Taipei, Taiwan
[4] Kuang Tien Gen Hosp, Dept Surg, Taichung, Taiwan
[5] Hung Kuang Univ, Coll Med & Hlth Care, Dept Biotechnol, Taichung, Taiwan
[6] Hung Kuang Univ, Coll Med & Hlth Care, Dept Hlth Business Adm, Taichung, Taiwan
[7] Dr Power Stem Int Grp Co Ltd, Taichung, Taiwan
关键词
GLYCERALDEHYDE-3-PHOSPHATE DEHYDROGENASE GAPDH; AMYLOID-BETA-PROTEIN; FUNCTIONAL DIVERSITY; INDUCED APOPTOSIS; TRANSFER-RNA; IDENTIFICATION; DEPRESSION; SEQUENCE; DEMENTIA; BINDING;
D O I
10.1371/journal.pone.0233289
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Alzheimer's disease (AD) is a progressive neurodegenerative disease characterized by two aggregates, namely, amyloid-beta (A beta) 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 A beta 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.
引用
收藏
页数:12
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