JAOA Vol 105 No 3 March 2005 145-158
Cholinesterase Inhibitors in the Treatment of Dementia
Jay M. Ellis, DO
From Neuroscience Research of the Berkshires in Pittsfield, Mass.
Address correspondence to Jay M. Ellis, DO, Director, Neuroscience Research of
the Berkshires, 100 Wendell Ave, Pittsfield, MA 01201-6941.E-mail:
IMdocjay{at}aol.com
Dementia associated with probable Alzheimer's disease (AD) is one of the
most common types of dementia. Patients with AD often have cholinergic
deficits in association with the disease. The cholinesterase inhibitors
donepezil hydrochloride, galantamine hydrobromide, and rivastigmine tartrate
are the current mainstays of symptomatic treatment for patients with AD. In
clinical trials for all three agents, beneficial effects on standard measures
of cognitive and global function have been observed in patients with mild to
moderate AD. Although none of the cholinesterase inhibitors has been approved
for treatment of patients in advanced stages of AD, all three agents have had
beneficial cognitive effects among patients with less severe forms of the
disease. The author provides information on recommended dosing for all three
medications, noting that cholinesterase inhibitors must be titrated carefully.
When administered with caution, galantamine, rivastigmine, and donepezil are
generally well-tolerated pharmacologic treatment options. The author notes
that, after patients and their caregivers understand that no change in status
is considered an "improvement" and a desirable clinical outcome
for patients with AD, if no benefits are achieved with the use of one
cholinesterase inhibitor, switching to another medication in this class might
be beneficial. The author further suggests that the benefits found in
cholinesterase inhibitors for patients with AD might also be applicable to
patients with other types of dementia such as vascular dementia and dementia
with Lewy bodies as cholinergic deficits have been reported in association
with these types of dementia as well.
This article has been cited by other articles:

|
 |

|
 |
 
A. Bekker, M. Haile, K. Gingrich, L. Wenning, A. Gorny, D. Quartermain, and T. Blanck
Physostigmine Reverses Cognitive Dysfunction Caused by Moderate Hypoxia in Adult Mice
Anesth. Analg.,
September 1, 2007;
105(3):
739 - 743.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
E. Groner, Y. Ashani, D. Schorer-Apelbaum, J. Sterling, Y. Herzig, and M. Weinstock
The Kinetics of Inhibition of Human Acetylcholinesterase and Butyrylcholinesterase by Two Series of Novel Carbamates
Mol. Pharmacol.,
June 1, 2007;
71(6):
1610 - 1617.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
J. L. Whitwell, S. D. Weigand, M. M. Shiung, B. F. Boeve, T. J. Ferman, G. E. Smith, D. S. Knopman, R. C. Petersen, E. E. Benarroch, K. A. Josephs, et al.
Focal atrophy in dementia with Lewy bodies on MRI: a distinct pattern from Alzheimer's disease
Brain,
March 1, 2007;
130(3):
708 - 719.
[Abstract]
[Full Text]
[PDF]
|
 |
|
Copyright © 2005 by the American Osteopathic Association.
| |
|