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Pilot data on telmisartan short-term effects on glucose metabolism in the olfactory tract in Alzheimer's disease

The possible effect of antihypertensive therapy on Alzheimer's disease (AD) has been studied, and angiotensin II receptor blockers (ARBs) have been suggested to exert an effect on cognitive decline. The purpose of this study is to clarify the functional effects of telmisartan, a long-acting ARB...

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Autores principales: Imabayashi, Etsuko, Matsuda, Hiroshi, Yoshimaru, Kimiko, Kuji, Ichiei, Seto, Akira, Shimano, Yasumasa, Ito, Kimiteru, Kikuta, Daisuke, Shimazu, Tomokazu, Araki, Nobuo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Inc 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3236542/
https://www.ncbi.nlm.nih.gov/pubmed/22399085
http://dx.doi.org/10.1002/brb3.13
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author Imabayashi, Etsuko
Matsuda, Hiroshi
Yoshimaru, Kimiko
Kuji, Ichiei
Seto, Akira
Shimano, Yasumasa
Ito, Kimiteru
Kikuta, Daisuke
Shimazu, Tomokazu
Araki, Nobuo
author_facet Imabayashi, Etsuko
Matsuda, Hiroshi
Yoshimaru, Kimiko
Kuji, Ichiei
Seto, Akira
Shimano, Yasumasa
Ito, Kimiteru
Kikuta, Daisuke
Shimazu, Tomokazu
Araki, Nobuo
author_sort Imabayashi, Etsuko
collection PubMed
description The possible effect of antihypertensive therapy on Alzheimer's disease (AD) has been studied, and angiotensin II receptor blockers (ARBs) have been suggested to exert an effect on cognitive decline. The purpose of this study is to clarify the functional effects of telmisartan, a long-acting ARB, on AD brain using prospective longitudinal (18)F-fluorodeoxyglucose positron emission tomography (FDG-PET) studies. For this purpose, brain glucose metabolism of four hypertensive patients with AD was examined with FDG-PET before and after administration of telmisartan. Studied subjects underwent three FDG-PET studies at intervals of 12 weeks. Antihypertensive treatment except for telmisartan was started after the first FDG-PET and continued for 24 weeks. Then 40–80 mg of telmisartan was added after the second FDG-PET and continued for 12 weeks.Glucose metabolism was significantly decreased during the first 12 weeks without telmisartan use at an area (−10, 21, −22, x, y, z; Z = 3.56) caudal to the left rectal gyrus and the olfactory sulcus corresponding to the left olfactory tract. In contrast, the introduction of telmisartan during the following 12 weeks preserved glucose metabolism at areas (5, 19, −20, x, y, z; Z = 3.09; 6, 19, −22, x, y, z; Z = 2.88) caudal to the bilateral rectal gyri and olfactory sulci corresponding to the bilateral olfactory tracts. No areas showed decreased glucose metabolism after the introduction of telmisartan. In AD, amyloid-β deposition is observed in the anterior olfactory nucleus (AON) of the olfactory tract. Glucose metabolism in AON may be progressively decreased and preserved by telmisartan.
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spelling pubmed-32365422011-12-23 Pilot data on telmisartan short-term effects on glucose metabolism in the olfactory tract in Alzheimer's disease Imabayashi, Etsuko Matsuda, Hiroshi Yoshimaru, Kimiko Kuji, Ichiei Seto, Akira Shimano, Yasumasa Ito, Kimiteru Kikuta, Daisuke Shimazu, Tomokazu Araki, Nobuo Brain Behav Original Research The possible effect of antihypertensive therapy on Alzheimer's disease (AD) has been studied, and angiotensin II receptor blockers (ARBs) have been suggested to exert an effect on cognitive decline. The purpose of this study is to clarify the functional effects of telmisartan, a long-acting ARB, on AD brain using prospective longitudinal (18)F-fluorodeoxyglucose positron emission tomography (FDG-PET) studies. For this purpose, brain glucose metabolism of four hypertensive patients with AD was examined with FDG-PET before and after administration of telmisartan. Studied subjects underwent three FDG-PET studies at intervals of 12 weeks. Antihypertensive treatment except for telmisartan was started after the first FDG-PET and continued for 24 weeks. Then 40–80 mg of telmisartan was added after the second FDG-PET and continued for 12 weeks.Glucose metabolism was significantly decreased during the first 12 weeks without telmisartan use at an area (−10, 21, −22, x, y, z; Z = 3.56) caudal to the left rectal gyrus and the olfactory sulcus corresponding to the left olfactory tract. In contrast, the introduction of telmisartan during the following 12 weeks preserved glucose metabolism at areas (5, 19, −20, x, y, z; Z = 3.09; 6, 19, −22, x, y, z; Z = 2.88) caudal to the bilateral rectal gyri and olfactory sulci corresponding to the bilateral olfactory tracts. No areas showed decreased glucose metabolism after the introduction of telmisartan. In AD, amyloid-β deposition is observed in the anterior olfactory nucleus (AON) of the olfactory tract. Glucose metabolism in AON may be progressively decreased and preserved by telmisartan. Blackwell Publishing Inc 2011-11 /pmc/articles/PMC3236542/ /pubmed/22399085 http://dx.doi.org/10.1002/brb3.13 Text en © 2011 The Authors. Published by Wiley Periodicals, Inc.
spellingShingle Original Research
Imabayashi, Etsuko
Matsuda, Hiroshi
Yoshimaru, Kimiko
Kuji, Ichiei
Seto, Akira
Shimano, Yasumasa
Ito, Kimiteru
Kikuta, Daisuke
Shimazu, Tomokazu
Araki, Nobuo
Pilot data on telmisartan short-term effects on glucose metabolism in the olfactory tract in Alzheimer's disease
title Pilot data on telmisartan short-term effects on glucose metabolism in the olfactory tract in Alzheimer's disease
title_full Pilot data on telmisartan short-term effects on glucose metabolism in the olfactory tract in Alzheimer's disease
title_fullStr Pilot data on telmisartan short-term effects on glucose metabolism in the olfactory tract in Alzheimer's disease
title_full_unstemmed Pilot data on telmisartan short-term effects on glucose metabolism in the olfactory tract in Alzheimer's disease
title_short Pilot data on telmisartan short-term effects on glucose metabolism in the olfactory tract in Alzheimer's disease
title_sort pilot data on telmisartan short-term effects on glucose metabolism in the olfactory tract in alzheimer's disease
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3236542/
https://www.ncbi.nlm.nih.gov/pubmed/22399085
http://dx.doi.org/10.1002/brb3.13
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