Phreedom Pharma, Saskatoon, Sask., Canada.
J Psychiatry Neurosci. 2010 Jan;35(1):59-62. doi: 10.1503/jpn.090059.
Plasmalogens, which are key structural phospholipids in brain membranes, are decreased in the brain and serum of patients with Alzheimer disease (AD). We performed this pilot study to evaluate the relation between the levels of circulating plasmalogens and Alzheimer Disease Assessment Scale-Cognitive (ADAS-Cog) scores in patients with AD.
We evaluated participants' ADAS-Cog scores and serum plasmalogen levels. For the 40 included AD patients with an ADAS-Cog score between 20 and 46, were tested their ADAS-Cog score 1 year later. The levels of docosahexaenoic acid plasmalogen were measured by use of liquid chromatography-tandem mass spectrometry.
We found that the ADAS-Cog score increased significantly in AD patients with circulating plasmalogen levels that were <or= 75% of that of age-matched controls at entry into the study. There was no change in score among participants with normal serum plasmalogen levels at baseline (> 75%).
This was a pilot study with 40 patients, and the results require validation in a larger population.
Our study demonstrates that decreased levels of plasmalogen precursors in the central nervous system correlate with functional decline (as measured by ADAS-Cog scores) in AD patients. The use of both ADAS-Cog and serum plasmalogen data may be a more accurate way of predicting cognitive decline in AD patients, and may be used to decrease the risk of including patients with no cognitive decline in the placebo arm of a drug trial.
神经髓磷脂,是大脑膜的关键结构磷脂,在阿尔茨海默病(AD)患者的大脑和血清中减少。我们进行了这项初步研究,以评估循环神经髓磷脂水平与 AD 患者阿尔茨海默病评估量表-认知(ADAS-Cog)评分之间的关系。
我们评估了参与者的 ADAS-Cog 评分和血清神经髓磷脂水平。对于 40 名 AD 患者,他们的 ADAS-Cog 评分在 20 到 46 之间,一年后测试他们的 ADAS-Cog 评分。通过使用液相色谱-串联质谱法测量二十二碳六烯酸神经髓磷脂的水平。
我们发现,在进入研究时,循环神经髓磷脂水平<或=年龄匹配对照的 75%的 AD 患者的 ADAS-Cog 评分显著增加。基线时血清神经髓磷脂水平正常(> 75%)的参与者的评分没有变化。
这是一项有 40 名患者的初步研究,结果需要在更大的人群中验证。
我们的研究表明,中枢神经系统神经髓磷脂前体水平降低与 AD 患者的功能下降(如 ADAS-Cog 评分所示)相关。使用 ADAS-Cog 和血清神经髓磷脂数据可能是更准确地预测 AD 患者认知下降的方法,并且可以用于降低在药物试验安慰剂组中不包括认知下降患者的风险。