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Brain type carnosinase in dementia: a pilot study

BACKGROUND: The pathological processes underlying dementia are poorly understood and so are the markers which identify them. Carnosinase is a dipeptidase found almost exclusively in brain and serum. Carnosinase and its substrate carnosine have been linked to neuropathophysiological processes. METHOD...

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Autores principales: Balion, Cynthia M, Benson, Carolyn, Raina, Parminder S, Papaioannou, Alexandra, Patterson, Christopher, Ismaila, Afisi S
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2200655/
https://www.ncbi.nlm.nih.gov/pubmed/17983474
http://dx.doi.org/10.1186/1471-2377-7-38
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author Balion, Cynthia M
Benson, Carolyn
Raina, Parminder S
Papaioannou, Alexandra
Patterson, Christopher
Ismaila, Afisi S
author_facet Balion, Cynthia M
Benson, Carolyn
Raina, Parminder S
Papaioannou, Alexandra
Patterson, Christopher
Ismaila, Afisi S
author_sort Balion, Cynthia M
collection PubMed
description BACKGROUND: The pathological processes underlying dementia are poorly understood and so are the markers which identify them. Carnosinase is a dipeptidase found almost exclusively in brain and serum. Carnosinase and its substrate carnosine have been linked to neuropathophysiological processes. METHODS: Carnosinase activity was measured by a flourometric method in 37 patients attending a Geriatric Outpatient Clinic. There were 17 patients without dementia, 13 had Alzheimer's disease (AD) and 7 had mixed dementia (MD). RESULTS: The range of serum carnosinase activity for patients without dementia was 14.5 – 78.5 μmol/ml/h. There was no difference in carnosinase activity between patients without dementia (40.3 ± 15.2 μmol/ml/h) and patients with AD (44.4 ± 12.4 μmol/ml/h) or MD (26.6 ± 15 μmol/ml/h). However, levels in the MD group were significantly lower than the AD group (p = 0.01). This difference remained significant after adjusting for gender, MMSE score, exercise, but not age, one at a time and all combined. The effect of other medical conditions did not remove the significance between the AD and MD groups. The MD group, but not the AD group, demonstrated a significant trend with carnosinase activity decreasing with duration of disease (from first recorded date of diagnosis to date of blood collection) (r = -0.76, p = 0.049). There was no association with carnosinase activity and MMSE score in the AD or MD group. Both AD and MD patients on any dementia medication (donepezil, galantamine, memantine) had higher carnosinase activity compared to those not taking a dementia medication. Carnosinase activity was higher in patients who regularly exercised (n = 20) compared to those who did not exercise regularly (n = 17)(p = 0.006). CONCLUSION: This exploratory study has shown altered activities of the enzyme carnosinase in patients with dementia.
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spelling pubmed-22006552008-01-16 Brain type carnosinase in dementia: a pilot study Balion, Cynthia M Benson, Carolyn Raina, Parminder S Papaioannou, Alexandra Patterson, Christopher Ismaila, Afisi S BMC Neurol Research Article BACKGROUND: The pathological processes underlying dementia are poorly understood and so are the markers which identify them. Carnosinase is a dipeptidase found almost exclusively in brain and serum. Carnosinase and its substrate carnosine have been linked to neuropathophysiological processes. METHODS: Carnosinase activity was measured by a flourometric method in 37 patients attending a Geriatric Outpatient Clinic. There were 17 patients without dementia, 13 had Alzheimer's disease (AD) and 7 had mixed dementia (MD). RESULTS: The range of serum carnosinase activity for patients without dementia was 14.5 – 78.5 μmol/ml/h. There was no difference in carnosinase activity between patients without dementia (40.3 ± 15.2 μmol/ml/h) and patients with AD (44.4 ± 12.4 μmol/ml/h) or MD (26.6 ± 15 μmol/ml/h). However, levels in the MD group were significantly lower than the AD group (p = 0.01). This difference remained significant after adjusting for gender, MMSE score, exercise, but not age, one at a time and all combined. The effect of other medical conditions did not remove the significance between the AD and MD groups. The MD group, but not the AD group, demonstrated a significant trend with carnosinase activity decreasing with duration of disease (from first recorded date of diagnosis to date of blood collection) (r = -0.76, p = 0.049). There was no association with carnosinase activity and MMSE score in the AD or MD group. Both AD and MD patients on any dementia medication (donepezil, galantamine, memantine) had higher carnosinase activity compared to those not taking a dementia medication. Carnosinase activity was higher in patients who regularly exercised (n = 20) compared to those who did not exercise regularly (n = 17)(p = 0.006). CONCLUSION: This exploratory study has shown altered activities of the enzyme carnosinase in patients with dementia. BioMed Central 2007-11-05 /pmc/articles/PMC2200655/ /pubmed/17983474 http://dx.doi.org/10.1186/1471-2377-7-38 Text en Copyright © 2007 Balion et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Balion, Cynthia M
Benson, Carolyn
Raina, Parminder S
Papaioannou, Alexandra
Patterson, Christopher
Ismaila, Afisi S
Brain type carnosinase in dementia: a pilot study
title Brain type carnosinase in dementia: a pilot study
title_full Brain type carnosinase in dementia: a pilot study
title_fullStr Brain type carnosinase in dementia: a pilot study
title_full_unstemmed Brain type carnosinase in dementia: a pilot study
title_short Brain type carnosinase in dementia: a pilot study
title_sort brain type carnosinase in dementia: a pilot study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2200655/
https://www.ncbi.nlm.nih.gov/pubmed/17983474
http://dx.doi.org/10.1186/1471-2377-7-38
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