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Total testosterone and neuropsychiatric symptoms in elderly men with Alzheimer’s disease
INTRODUCTION: There has been a significant increase in the use of testosterone in aging men, but little investigation into its impact on men with Alzheimer’s disease (AD). The findings of the few studies that have been done are inconsistent. In the present study, we investigated the relationship bet...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4416299/ https://www.ncbi.nlm.nih.gov/pubmed/25937840 http://dx.doi.org/10.1186/s13195-015-0107-4 |
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author | Hall, James R Wiechmann, April R Cunningham, Rebecca L Johnson, Leigh A Edwards, Melissa Barber, Robert C Singh, Meharvan Winter, Scott O’Bryant, Sid E |
author_facet | Hall, James R Wiechmann, April R Cunningham, Rebecca L Johnson, Leigh A Edwards, Melissa Barber, Robert C Singh, Meharvan Winter, Scott O’Bryant, Sid E |
author_sort | Hall, James R |
collection | PubMed |
description | INTRODUCTION: There has been a significant increase in the use of testosterone in aging men, but little investigation into its impact on men with Alzheimer’s disease (AD). The findings of the few studies that have been done are inconsistent. In the present study, we investigated the relationship between total testosterone (TT) and neuropsychiatric symptoms (NPS) in a well-characterized sample of elderly men with mild to moderate AD. METHODS: The sample, which was drawn from the Texas Alzheimer’s Research Care Consortium Longitudinal Research Cohort, included 87 men who met the criteria for mild to moderate AD. The occurrence of NPS was gathered from caregivers and/or family members with the Neuropsychiatric Inventory. TT was analyzed, and the sample was divided into a low-testosterone group (TT ≤2.5 ng/ml; n = 44) and a borderline/normal group (TT ≥2.6 ng/ml; n = 43). RESULTS: TT was correlated with symptoms of hallucinations, delusions, agitation, irritability and motor activity. The borderline/normal group was significantly more likely to have hallucinations (odds ratio (OR) = 5.56), delusions (OR = 3.87), motor activity (OR = 3.13) and irritability (OR = 2.77) than the low-testosterone group. Health status and apolipoprotein E ε4 status were not significant factors. CONCLUSIONS: The findings of the present study have implications for the use of testosterone replacement therapy in men with AD or the prodromal stage of the disease. |
format | Online Article Text |
id | pubmed-4416299 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-44162992015-05-02 Total testosterone and neuropsychiatric symptoms in elderly men with Alzheimer’s disease Hall, James R Wiechmann, April R Cunningham, Rebecca L Johnson, Leigh A Edwards, Melissa Barber, Robert C Singh, Meharvan Winter, Scott O’Bryant, Sid E Alzheimers Res Ther Research INTRODUCTION: There has been a significant increase in the use of testosterone in aging men, but little investigation into its impact on men with Alzheimer’s disease (AD). The findings of the few studies that have been done are inconsistent. In the present study, we investigated the relationship between total testosterone (TT) and neuropsychiatric symptoms (NPS) in a well-characterized sample of elderly men with mild to moderate AD. METHODS: The sample, which was drawn from the Texas Alzheimer’s Research Care Consortium Longitudinal Research Cohort, included 87 men who met the criteria for mild to moderate AD. The occurrence of NPS was gathered from caregivers and/or family members with the Neuropsychiatric Inventory. TT was analyzed, and the sample was divided into a low-testosterone group (TT ≤2.5 ng/ml; n = 44) and a borderline/normal group (TT ≥2.6 ng/ml; n = 43). RESULTS: TT was correlated with symptoms of hallucinations, delusions, agitation, irritability and motor activity. The borderline/normal group was significantly more likely to have hallucinations (odds ratio (OR) = 5.56), delusions (OR = 3.87), motor activity (OR = 3.13) and irritability (OR = 2.77) than the low-testosterone group. Health status and apolipoprotein E ε4 status were not significant factors. CONCLUSIONS: The findings of the present study have implications for the use of testosterone replacement therapy in men with AD or the prodromal stage of the disease. BioMed Central 2015-05-01 /pmc/articles/PMC4416299/ /pubmed/25937840 http://dx.doi.org/10.1186/s13195-015-0107-4 Text en © Hall et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Hall, James R Wiechmann, April R Cunningham, Rebecca L Johnson, Leigh A Edwards, Melissa Barber, Robert C Singh, Meharvan Winter, Scott O’Bryant, Sid E Total testosterone and neuropsychiatric symptoms in elderly men with Alzheimer’s disease |
title | Total testosterone and neuropsychiatric symptoms in elderly men with Alzheimer’s disease |
title_full | Total testosterone and neuropsychiatric symptoms in elderly men with Alzheimer’s disease |
title_fullStr | Total testosterone and neuropsychiatric symptoms in elderly men with Alzheimer’s disease |
title_full_unstemmed | Total testosterone and neuropsychiatric symptoms in elderly men with Alzheimer’s disease |
title_short | Total testosterone and neuropsychiatric symptoms in elderly men with Alzheimer’s disease |
title_sort | total testosterone and neuropsychiatric symptoms in elderly men with alzheimer’s disease |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4416299/ https://www.ncbi.nlm.nih.gov/pubmed/25937840 http://dx.doi.org/10.1186/s13195-015-0107-4 |
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