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Plasma Amyloid Is Associated with White Matter and Subcortical Alterations and Is Modulated by Age and Seasonal Rhythms in Mouse Lemur Primates
Accumulation of amyloid-β (Aβ) peptides in the brain is a critical early event in the pathogenesis of Alzheimer's disease (AD), the most common age-related neurodegenerative disorder. There is increasing interest in measuring levels of plasma Aβ since this could help in diagnosis of brain patho...
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Published in: | Frontiers in aging neuroscience 2018-02, Vol.10, p.35-35 |
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description | Accumulation of amyloid-β (Aβ) peptides in the brain is a critical early event in the pathogenesis of Alzheimer's disease (AD), the most common age-related neurodegenerative disorder. There is increasing interest in measuring levels of plasma Aβ since this could help in diagnosis of brain pathology. However, the value of plasma Aβ in such a diagnosis is still controversial and factors modulating its levels are still poorly understood. The mouse lemur (
) is a primate model of cerebral aging which can also present with amyloid plaques and whose Aβ is highly homologous to humans'. In an attempt to characterize this primate model and to evaluate the potential of plasma Aβ as a biomarker for brain alterations, we measured plasma Aβ
concentration in 21 animals aged from 5 to 9.5 years. We observed an age-related increase in plasma Aβ
levels. We then evaluated the relationships between plasma Aβ
levels and cerebral atrophy in these mouse lemurs. Voxel-based analysis of cerebral MR images (adjusted for the age/sex/brain size of the animals), showed that low Aβ
levels are associated with atrophy of several white matter and subcortical brain regions. These results suggest that low Aβ
levels in middle-aged/old animals are associated with brain deterioration. One special feature of mouse lemurs is that their metabolic and physiological parameters follow seasonal changes strictly controlled by illumination. We evaluated seasonal-related variations of plasma Aβ
levels and found a strong effect, with higher plasma Aβ
concentrations in winter conditions compared to summer. This question of seasonal modulation of Aβ plasma levels should be addressed in clinical studies. We also focused on the amplitude of the difference between plasma Aβ
levels during the two seasons and found that this amplitude increases with age. Possible mechanisms leading to these seasonal changes are discussed. |
doi_str_mv | 10.3389/fnagi.2018.00035 |
format | article |
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) is a primate model of cerebral aging which can also present with amyloid plaques and whose Aβ is highly homologous to humans'. In an attempt to characterize this primate model and to evaluate the potential of plasma Aβ as a biomarker for brain alterations, we measured plasma Aβ
concentration in 21 animals aged from 5 to 9.5 years. We observed an age-related increase in plasma Aβ
levels. We then evaluated the relationships between plasma Aβ
levels and cerebral atrophy in these mouse lemurs. Voxel-based analysis of cerebral MR images (adjusted for the age/sex/brain size of the animals), showed that low Aβ
levels are associated with atrophy of several white matter and subcortical brain regions. These results suggest that low Aβ
levels in middle-aged/old animals are associated with brain deterioration. One special feature of mouse lemurs is that their metabolic and physiological parameters follow seasonal changes strictly controlled by illumination. We evaluated seasonal-related variations of plasma Aβ
levels and found a strong effect, with higher plasma Aβ
concentrations in winter conditions compared to summer. This question of seasonal modulation of Aβ plasma levels should be addressed in clinical studies. We also focused on the amplitude of the difference between plasma Aβ
levels during the two seasons and found that this amplitude increases with age. Possible mechanisms leading to these seasonal changes are discussed.</description><identifier>ISSN: 1663-4365</identifier><identifier>EISSN: 1663-4365</identifier><identifier>DOI: 10.3389/fnagi.2018.00035</identifier><identifier>PMID: 29491833</identifier><language>eng</language><publisher>Switzerland: Frontiers Research Foundation</publisher><subject>Age ; Aging ; Alzheimer ; Alzheimer's disease ; Amyloid ; Animals ; Atrophy ; Biomarkers ; brain morphometry ; Dementia ; Diabetes ; Diagnosis ; lemur ; Life Sciences ; Metabolism ; Metabolites ; Monkeys & apes ; Neurobiology ; Neurodegenerative diseases ; Neurons and Cognition ; Neuroscience ; Pathology ; Peptides ; Physiology ; plasma amyloid ; Plasma levels ; Primates ; Proteins ; Seasonal variations ; seasons ; Senile plaques ; Substantia alba</subject><ispartof>Frontiers in aging neuroscience, 2018-02, Vol.10, p.35-35</ispartof><rights>2018. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><rights>Copyright © 2018 Gary, Hérard, Hanss and Dhenain. 2018 Gary, Hérard, Hanss and Dhenain</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c524t-c5bcd23de60c025e28e631e8ac3e550b9af9c3560c68860d1f6372bc7d0c44dd3</citedby><cites>FETCH-LOGICAL-c524t-c5bcd23de60c025e28e631e8ac3e550b9af9c3560c68860d1f6372bc7d0c44dd3</cites><orcidid>0000-0001-8260-9618 ; 0000-0001-8804-4101</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2300662981/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2300662981?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25731,27901,27902,36989,36990,44566,53766,53768,74869</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29491833$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-02155747$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Gary, Charlotte</creatorcontrib><creatorcontrib>Hérard, Anne-Sophie</creatorcontrib><creatorcontrib>Hanss, Zoé</creatorcontrib><creatorcontrib>Dhenain, Marc</creatorcontrib><title>Plasma Amyloid Is Associated with White Matter and Subcortical Alterations and Is Modulated by Age and Seasonal Rhythms in Mouse Lemur Primates</title><title>Frontiers in aging neuroscience</title><addtitle>Front Aging Neurosci</addtitle><description>Accumulation of amyloid-β (Aβ) peptides in the brain is a critical early event in the pathogenesis of Alzheimer's disease (AD), the most common age-related neurodegenerative disorder. There is increasing interest in measuring levels of plasma Aβ since this could help in diagnosis of brain pathology. However, the value of plasma Aβ in such a diagnosis is still controversial and factors modulating its levels are still poorly understood. The mouse lemur (
) is a primate model of cerebral aging which can also present with amyloid plaques and whose Aβ is highly homologous to humans'. In an attempt to characterize this primate model and to evaluate the potential of plasma Aβ as a biomarker for brain alterations, we measured plasma Aβ
concentration in 21 animals aged from 5 to 9.5 years. We observed an age-related increase in plasma Aβ
levels. We then evaluated the relationships between plasma Aβ
levels and cerebral atrophy in these mouse lemurs. Voxel-based analysis of cerebral MR images (adjusted for the age/sex/brain size of the animals), showed that low Aβ
levels are associated with atrophy of several white matter and subcortical brain regions. These results suggest that low Aβ
levels in middle-aged/old animals are associated with brain deterioration. One special feature of mouse lemurs is that their metabolic and physiological parameters follow seasonal changes strictly controlled by illumination. We evaluated seasonal-related variations of plasma Aβ
levels and found a strong effect, with higher plasma Aβ
concentrations in winter conditions compared to summer. This question of seasonal modulation of Aβ plasma levels should be addressed in clinical studies. We also focused on the amplitude of the difference between plasma Aβ
levels during the two seasons and found that this amplitude increases with age. Possible mechanisms leading to these seasonal changes are discussed.</description><subject>Age</subject><subject>Aging</subject><subject>Alzheimer</subject><subject>Alzheimer's disease</subject><subject>Amyloid</subject><subject>Animals</subject><subject>Atrophy</subject><subject>Biomarkers</subject><subject>brain morphometry</subject><subject>Dementia</subject><subject>Diabetes</subject><subject>Diagnosis</subject><subject>lemur</subject><subject>Life Sciences</subject><subject>Metabolism</subject><subject>Metabolites</subject><subject>Monkeys & apes</subject><subject>Neurobiology</subject><subject>Neurodegenerative diseases</subject><subject>Neurons and Cognition</subject><subject>Neuroscience</subject><subject>Pathology</subject><subject>Peptides</subject><subject>Physiology</subject><subject>plasma amyloid</subject><subject>Plasma levels</subject><subject>Primates</subject><subject>Proteins</subject><subject>Seasonal variations</subject><subject>seasons</subject><subject>Senile plaques</subject><subject>Substantia alba</subject><issn>1663-4365</issn><issn>1663-4365</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpdkktv1DAUhSMEolXpnhWyxAYWM_g9zgYpqoCONBUVD7G0HPtm4lESl9gpml_BX8aZKVXbjW3de77j1ymK1wQvGVPlh2YwW7-kmKglxpiJZ8UpkZItOJPi-YP1SXEe4w7PGoaxUC-LE1rykijGTou_152JvUFVv--Cd2gdURVjsN4kcOiPTy361foE6MqkBCMyg0Pfp9qGMXlrOlR1uWqSD0M89DJ_FdzUHfB6j6otHBkwMQwZ-NbuU9tH5IcsnCKgDfTTiK5H32cmvipeNKaLcH43nxU_P3_6cXG52Hz9sr6oNgsrKE95rK2jzIHEFlMBVIFkBJSxDITAdWma0jKRu1IpiR1pJFvR2q4ctpw7x86K9dHXBbPTN_Pu414H4_WhEMatNvMVO9BgDLek5iVQwm0NSjJrZdnwsgTOVZO9Ph69bqa6B2dhSKPpHpk-7gy-1dtwq4UiKyxxNnh_NGifYJfVRs81TIkQK766JVn77m6zMfyeICbd-2ih68wA-T01xbgUUlLBsvTtE-kuTGP-hKzKSciiUs2G-KiyY4hxhOb-BATrOWj6EDQ9B00fgpaRNw8vfA_8jxX7Bwh60A4</recordid><startdate>20180214</startdate><enddate>20180214</enddate><creator>Gary, Charlotte</creator><creator>Hérard, Anne-Sophie</creator><creator>Hanss, Zoé</creator><creator>Dhenain, Marc</creator><general>Frontiers Research Foundation</general><general>Frontiers</general><general>Frontiers Media S.A</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88I</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M2P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>1XC</scope><scope>VOOES</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0001-8260-9618</orcidid><orcidid>https://orcid.org/0000-0001-8804-4101</orcidid></search><sort><creationdate>20180214</creationdate><title>Plasma Amyloid Is Associated with White Matter and Subcortical Alterations and Is Modulated by Age and Seasonal Rhythms in Mouse Lemur Primates</title><author>Gary, Charlotte ; Hérard, Anne-Sophie ; Hanss, Zoé ; Dhenain, Marc</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c524t-c5bcd23de60c025e28e631e8ac3e550b9af9c3560c68860d1f6372bc7d0c44dd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Age</topic><topic>Aging</topic><topic>Alzheimer</topic><topic>Alzheimer's disease</topic><topic>Amyloid</topic><topic>Animals</topic><topic>Atrophy</topic><topic>Biomarkers</topic><topic>brain morphometry</topic><topic>Dementia</topic><topic>Diabetes</topic><topic>Diagnosis</topic><topic>lemur</topic><topic>Life Sciences</topic><topic>Metabolism</topic><topic>Metabolites</topic><topic>Monkeys & apes</topic><topic>Neurobiology</topic><topic>Neurodegenerative diseases</topic><topic>Neurons and Cognition</topic><topic>Neuroscience</topic><topic>Pathology</topic><topic>Peptides</topic><topic>Physiology</topic><topic>plasma amyloid</topic><topic>Plasma levels</topic><topic>Primates</topic><topic>Proteins</topic><topic>Seasonal variations</topic><topic>seasons</topic><topic>Senile plaques</topic><topic>Substantia alba</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gary, Charlotte</creatorcontrib><creatorcontrib>Hérard, Anne-Sophie</creatorcontrib><creatorcontrib>Hanss, Zoé</creatorcontrib><creatorcontrib>Dhenain, Marc</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health Medical collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biological Sciences</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>ProQuest Science Journals</collection><collection>Biological Science Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Frontiers in aging neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gary, Charlotte</au><au>Hérard, Anne-Sophie</au><au>Hanss, Zoé</au><au>Dhenain, Marc</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Plasma Amyloid Is Associated with White Matter and Subcortical Alterations and Is Modulated by Age and Seasonal Rhythms in Mouse Lemur Primates</atitle><jtitle>Frontiers in aging neuroscience</jtitle><addtitle>Front Aging Neurosci</addtitle><date>2018-02-14</date><risdate>2018</risdate><volume>10</volume><spage>35</spage><epage>35</epage><pages>35-35</pages><issn>1663-4365</issn><eissn>1663-4365</eissn><abstract>Accumulation of amyloid-β (Aβ) peptides in the brain is a critical early event in the pathogenesis of Alzheimer's disease (AD), the most common age-related neurodegenerative disorder. There is increasing interest in measuring levels of plasma Aβ since this could help in diagnosis of brain pathology. However, the value of plasma Aβ in such a diagnosis is still controversial and factors modulating its levels are still poorly understood. The mouse lemur (
) is a primate model of cerebral aging which can also present with amyloid plaques and whose Aβ is highly homologous to humans'. In an attempt to characterize this primate model and to evaluate the potential of plasma Aβ as a biomarker for brain alterations, we measured plasma Aβ
concentration in 21 animals aged from 5 to 9.5 years. We observed an age-related increase in plasma Aβ
levels. We then evaluated the relationships between plasma Aβ
levels and cerebral atrophy in these mouse lemurs. Voxel-based analysis of cerebral MR images (adjusted for the age/sex/brain size of the animals), showed that low Aβ
levels are associated with atrophy of several white matter and subcortical brain regions. These results suggest that low Aβ
levels in middle-aged/old animals are associated with brain deterioration. One special feature of mouse lemurs is that their metabolic and physiological parameters follow seasonal changes strictly controlled by illumination. We evaluated seasonal-related variations of plasma Aβ
levels and found a strong effect, with higher plasma Aβ
concentrations in winter conditions compared to summer. This question of seasonal modulation of Aβ plasma levels should be addressed in clinical studies. We also focused on the amplitude of the difference between plasma Aβ
levels during the two seasons and found that this amplitude increases with age. Possible mechanisms leading to these seasonal changes are discussed.</abstract><cop>Switzerland</cop><pub>Frontiers Research Foundation</pub><pmid>29491833</pmid><doi>10.3389/fnagi.2018.00035</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0001-8260-9618</orcidid><orcidid>https://orcid.org/0000-0001-8804-4101</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Age Aging Alzheimer Alzheimer's disease Amyloid Animals Atrophy Biomarkers brain morphometry Dementia Diabetes Diagnosis lemur Life Sciences Metabolism Metabolites Monkeys & apes Neurobiology Neurodegenerative diseases Neurons and Cognition Neuroscience Pathology Peptides Physiology plasma amyloid Plasma levels Primates Proteins Seasonal variations seasons Senile plaques Substantia alba |
title | Plasma Amyloid Is Associated with White Matter and Subcortical Alterations and Is Modulated by Age and Seasonal Rhythms in Mouse Lemur Primates |
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