Abstract

BackgroundLittle is known of vitamin D concentration in cerebrospinal fluid (CSF) in Alzheimer´s disease (AD) and its relation with CSF acetylcholinesterase (AChE) activity, a marker of cholinergic function.MethodsA cross-sectional study of 52 consecutive patients under primary evaluation of cognitive impairment and 17 healthy controls. The patients had AD dementia or mild cognitive impairment (MCI) diagnosed with AD dementia upon follow-up (n = 28), other dementias (n = 12), and stable MCI (SMCI, n = 12). We determined serum and CSF concentrations of calcium, parathyroid hormone (PTH), 25-hydroxyvitamin D (25OHD), and CSF activities of AChE and butyrylcholinesterase (BuChE). FindingsCSF 25OHD level was reduced in AD patients (P < 0.05), and CSF AChE activity was decreased both in patients with AD (P < 0.05) and other dementias (P < 0.01) compared to healthy controls. None of the measured variables differed between BuChE K-variant genotypes whereas the participants that were homozygous in terms of the apolipoprotein E (APOE) ε4 allele had decreased CSF AChE activity compared to subjects lacking the APOE ε4 allele (P = 0.01). In AD patients (n=28), CSF AChE activity correlated positively with CSF levels of total tau (T-tau) (r = 0.44, P < 0.05) and phosphorylated tau protein (P-tau) (r = 0.50, P < 0.01), but CSF activities of AChE or BuChE did not correlate with serum or CSF levels of 25OHD.ConclusionsIn this pilot study, both CSF 25OHD level and CSF AChE activity were reduced in AD patients. However, the lack of correlations between 25OHD levels and CSF activities of AChE or BuChE might suggest different mechanisms of action, which could have implications for treatment trials.

Highlights

  • Calcium influx into cells is a mediator of cellular metabolism, but unbuffered intracellular calcium could be neurotoxic for brain cells [1]

  • In this pilot study, both cerebrospinal fluid (CSF) 25OHD level and CSF AChE activity were reduced in Alzheimer’s disease (AD) patients

  • CSF 25OHD level was lower in AD patients compared to patients with other dementias and healthy controls (P = 0.01 and P = 0.03, respectively; Table 3)

Read more

Summary

Introduction

Calcium influx into cells is a mediator of cellular metabolism, but unbuffered intracellular calcium could be neurotoxic for brain cells [1]. Circulating calcium is dependent on parathyroid hormone (PTH) and vitamin D [2]. In human Alzheimer’s disease (AD), relatively little is known of possible interactions between the calcium/vitamin D system and the cholinergic system. The vitamin D receptor (VDR) is abundantly expressed in the human brain [3]. 1,25-dihydroxyvitamin D can decrease the activity of reactive oxygen species (ROS) [6], and the defective phagocytosis of soluble amyloid-β (Aβ) by macrophages in AD might be stimulated by vitamin D [7]. Little is known of vitamin D concentration in cerebrospinal fluid (CSF) in Alzheimers disease (AD) and its relation with CSF acetylcholinesterase (AChE) activity, a marker of cholinergic function

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call