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  Greater monoamine oxidase a binding in perimenopausal age as measured with carbon 11–labeled harmine positron emission tomography

Rekkas, P. V., Wilson, A. A., Lee, V. W. H., Yogalingam, P., Sacher, J., Rusjan, P., et al. (2014). Greater monoamine oxidase a binding in perimenopausal age as measured with carbon 11–labeled harmine positron emission tomography. JAMA Psychiatry, 71(8), 873-879. doi:10.1001/jamapsychiatry.2014.250.

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Item Permalink: http://hdl.handle.net/11858/00-001M-0000-0019-C17B-8 Version Permalink: http://hdl.handle.net/21.11116/0000-0003-819A-D
Genre: Journal Article

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 Creators:
Rekkas, Paraskevi Vivien1, Author
Wilson, Alan A.1, Author
Lee, Vivian Wai Han1, Author
Yogalingam, Priyanga1, Author
Sacher, Julia2, Author              
Rusjan, Pablo1, Author
Houle, Sylvain1, Author
Stewart, Donna E.3, Author
Kolla, Nathan J.1, Author
Kish, Stephen1, Author
Chiuccariella, Lina1, Author
Meyer, Jeffrey H.1, Author
Affiliations:
1Centre for Addiction and Mental Health, University of Toronto, ON, Canada, ou_persistent22              
2Department Neurology, MPI for Human Cognitive and Brain Sciences, Max Planck Society, ou_634549              
3Department of Psychiatry, University Health Network, University of Toronto, ON, Canada, ou_persistent22              

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 Abstract: Importance Perimenopause is a period of high risk for mood disorders, and it has been proposed that perimenopause is also a window of risk for processes linked to later dementia. However, in human perimenopause, the neurobiological changes implicated in the genesis of mood disorders or dementia have not been identified. Monoamine oxidase A (MAO-A) is an important brain enzyme that creates oxidative stress, influences apoptosis, and metabolizes monoamines. After declines in estrogen level, MAO-A density may be elevated for a month or longer, and repeated declines in estrogen level occur with greater magnitude during perimenopause. Objective To investigate whether MAO-A total distribution volume (VT), an index of MAO-A density, is elevated in women of perimenopausal age (41-51 years). Design, Setting, and Participants In a cross-sectional study at a tertiary care psychiatric hospital, 58 women underwent carbon 11–labeled harmine positron emission tomography. These included 19 young women of reproductive age (mean [SD], 28.26 [5.05] years), 27 women of perimenopausal age (mean [SD] age, 45.21 [3.41] years; including 14 women with change in menstrual cycle length with a mean [SD] age of 45.50 [4.00] years and 13 women with no change in menstrual cycle length with a mean [SD] age of 44.92 [2.81] years), and 12 women in menopause (mean [SD] age, 56.25 [3.19] years). Main Outcomes and Measures Values of MAO-A VT in the prefrontal cortex, anterior cingulate cortex, dorsal striatum, ventral striatum, thalamus, hippocampus, and midbrain. Results On average, MAO-A VT in perimenopausal age was elevated by 34% compared with reproductive age and by 16% compared with menopause (multivariate analysis of variance, group effect, F16,94 = 3.03; P < .001). Within the perimenopausal age group, meeting Stages of Reproductive Aging Workshop criteria for perimenopause, which is mainly based on menstrual cycle length, was not associated with MAO-A VT (F8,18 = 0.548; P = .81) but tendency to cry was positively correlated with MAO-A VT in the prefrontal cortex (r = 0.54; P = .008). Conclusions and Relevance To our knowledge, this is the first report of a change in a central biomarker during perimenopausal age that is also present during major depressive episodes and high-risk states for major depressive episodes. The functions of MAO-A influence oxidative stress and apoptosis, 2 processes implicated as excessive in both mood disorders and dementia. Hence, greater MAO-A VT during perimenopause may represent a new target for assessing novel interventions to prevent mood disorders and reduce longer-term risk of neurodegenerative disease.

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Language(s): eng - English
 Dates: 2014-01-202013-12-042014-02-072014-06-042014-08
 Publication Status: Published in print
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Method: Peer
 Identifiers: DOI: 10.1001/jamapsychiatry.2014.250
PMID: 24898155
PMC: PMC4942269
 Degree: -

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Title: JAMA Psychiatry
Source Genre: Journal
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Publ. Info: Chicago, Ill. : American Medical Association
Pages: - Volume / Issue: 71 (8) Sequence Number: - Start / End Page: 873 - 879 Identifier: Other: 2168-6238
CoNE: https://pure.mpg.de/cone/journals/resource/2168-6238