Chen_2019_J.Clin.Med_8_

Reference

Title : Serum Level and Activity of Butylcholinesterase: A Biomarker for Post-Stroke Dementia - Chen_2019_J.Clin.Med_8_
Author(s) : Chen YC , Chou WH , Fang CP , Liu TH , Tsou HH , Wang Y , Liu YL
Ref : J Clin Med , 8 : , 2019
Abstract :

Cholinergic neurotransmission regulates the immune response and inhibits cytokine release after stroke. The changes in the level/activity of blood cholinesterase (ChE) in patients with post-stroke dementia (PSD) are less known. This study aimed to examine post-stroke plasma acetylcholinesterase (AChE) and butylcholinesterase (BChE) and determine whether they are biomarkers for PSD. Thirty patients with PSD, 87 post-stroke patients without dementia (PSNoD), and 117 age- and gender-matched healthy controls were recruited. Missense genetic variants AChE rs1799806 and BChE rs1803274 were genotyped. The plasma AChE level did not differ between the PSD and PSNoD groups. However, BChE levels were significantly lower in the PSD than in the PSNoD group (3300.66 +/- 515.35 vs 3855.74 +/- 677.60 ng/mL, respectively; p = 0.0033). The activities of total ChE, BChE, and AChE were all lower in the PSD group (19,563.33 +/- 4366.03, 7650.17 +/- 1912.29, 11,913.17 +/- 2992.42 mU/mL, respectively) than in the PSNoD group (23,579.08 +/- 5251.55, 9077.72 +/- 1727.28, and 14,501.36 +/- 4197.17 mU/mL, respectively). When further adjusting for age and sex, significance remained in BChE level and activity and in total ChE activity. BChE rs1803274 was associated with reduced BChE activity, while AChE rs1799806 did not influence AChE activity. The level and activity of BChE, but not of AChE, were decreased in PSD patients and may therefore aid in PSD diagnosis.

PubMedSearch : Chen_2019_J.Clin.Med_8_
PubMedID: 31653081

Related information

Citations formats

Chen YC, Chou WH, Fang CP, Liu TH, Tsou HH, Wang Y, Liu YL (2019)
Serum Level and Activity of Butylcholinesterase: A Biomarker for Post-Stroke Dementia
J Clin Med 8 :

Chen YC, Chou WH, Fang CP, Liu TH, Tsou HH, Wang Y, Liu YL (2019)
J Clin Med 8 :