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Association between Plasma Ceramides and Phosphatidylcholines and Hippocampal Brain Volume in Late Onset Alzheimer's Disease.

Identifieur interne : 001160 ( PubMed/Checkpoint ); précédent : 001159; suivant : 001161

Association between Plasma Ceramides and Phosphatidylcholines and Hippocampal Brain Volume in Late Onset Alzheimer's Disease.

Auteurs : Min Kim [Royaume-Uni] ; Alejo Nevado-Holgado [Royaume-Uni] ; Luke Whiley [Royaume-Uni] ; Stuart G. Snowden [Royaume-Uni] ; Hilkka Soininen [Finlande] ; Iwona Kloszewska [Pologne] ; Patrizia Mecocci [Italie] ; Magda Tsolaki [Grèce] ; Bruno Vellas [France] ; Madhav Thambisetty [États-Unis] ; Richard J B. Dobson [Royaume-Uni] ; John F. Powell [Royaume-Uni] ; Michelle K. Lupton [Australie] ; Andy Simmons [Royaume-Uni] ; Latha Velayudhan [Royaume-Uni] ; Simon Lovestone [Royaume-Uni] ; Petroula Proitsi [Royaume-Uni] ; Cristina Legido-Quigley [Royaume-Uni]

Source :

RBID : pubmed:27911300

Abstract

Lipids such as ceramides and phosphatidylcholines (PC) have been found altered in the plasma of Alzheimer's disease (AD) patients in a number of discovery studies. For this reason, the levels of 6 ceramides and 3 PCs, with different fatty acid length and saturation levels, were measured in the plasma from 412 participants (AD n = 205, Control n = 207) using mass spectrometry coupled with ultra-performance liquid chromatography. After this, associations with AD status, brain atrophy, and age-related effects were studied. In the plasma of AD participants, cross-sectional analysis revealed elevated levels of three ceramides (Cer16:0 p < 0.01, Cer18:0 p < 0.01, Cer24:1 p < 0.05). In addition, two PCs in AD plasma (PC36:5 p < 0.05, PC38:6 p < 0.05) were found to be depleted compared to the control group, with PC36:5 also associating with hippocampal atrophy (p < 0.01). Age-specific analysis further revealed that levels of Cer16:0, Cer18:0, and Cer20:0 were associated with hippocampal atrophy only in younger participants (age < 75, p < 0.05), while all 3 PCs did so in the older participants (age > 75, p < 0.05). PC36:5 was associated with AD status in the younger group (p < 0.01), while PC38:6 and 40:6 did so in the older group (p < 0.05). In this study, elevated ceramides and depleted PCs were found in the plasma from 205 AD volunteers. Our findings also suggest that dysregulation in PC and ceramide metabolism could be occurring in different stages of AD progression.

DOI: 10.3233/JAD-160645
PubMed: 27911300


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Le document en format XML

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<name sortKey="Lupton, Michelle K" sort="Lupton, Michelle K" uniqKey="Lupton M" first="Michelle K" last="Lupton">Michelle K. Lupton</name>
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<name sortKey="Velayudhan, Latha" sort="Velayudhan, Latha" uniqKey="Velayudhan L" first="Latha" last="Velayudhan">Latha Velayudhan</name>
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<title xml:lang="en">Association between Plasma Ceramides and Phosphatidylcholines and Hippocampal Brain Volume in Late Onset Alzheimer's Disease.</title>
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<name sortKey="Kim, Min" sort="Kim, Min" uniqKey="Kim M" first="Min" last="Kim">Min Kim</name>
<affiliation wicri:level="3">
<nlm:affiliation>Institute of Pharmaceutical Science, King's College London, London, UK.</nlm:affiliation>
<country xml:lang="fr">Royaume-Uni</country>
<wicri:regionArea>Institute of Pharmaceutical Science, King's College London, London</wicri:regionArea>
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<settlement type="city">Londres</settlement>
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<region type="région" nuts="1">Grand Londres</region>
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<author>
<name sortKey="Nevado Holgado, Alejo" sort="Nevado Holgado, Alejo" uniqKey="Nevado Holgado A" first="Alejo" last="Nevado-Holgado">Alejo Nevado-Holgado</name>
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<nlm:affiliation>Department of Psychiatry, University of Oxford, Oxford, UK.</nlm:affiliation>
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<wicri:regionArea>Department of Psychiatry, University of Oxford, Oxford</wicri:regionArea>
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<settlement type="city">Oxford</settlement>
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<name sortKey="Whiley, Luke" sort="Whiley, Luke" uniqKey="Whiley L" first="Luke" last="Whiley">Luke Whiley</name>
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<nlm:affiliation>Institute of Pharmaceutical Science, King's College London, London, UK.</nlm:affiliation>
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<name sortKey="Soininen, Hilkka" sort="Soininen, Hilkka" uniqKey="Soininen H" first="Hilkka" last="Soininen">Hilkka Soininen</name>
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<name sortKey="Kloszewska, Iwona" sort="Kloszewska, Iwona" uniqKey="Kloszewska I" first="Iwona" last="Kloszewska">Iwona Kloszewska</name>
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<nlm:affiliation>Department of Old Age Psychiatry & Psychotic Disorders, Medical University of Lodz, Lodz, Poland.</nlm:affiliation>
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<name sortKey="Mecocci, Patrizia" sort="Mecocci, Patrizia" uniqKey="Mecocci P" first="Patrizia" last="Mecocci">Patrizia Mecocci</name>
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<name sortKey="Tsolaki, Magda" sort="Tsolaki, Magda" uniqKey="Tsolaki M" first="Magda" last="Tsolaki">Magda Tsolaki</name>
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<nlm:affiliation>Third Department of Neurology, Memory and Dementia Centre, Medical School, Aristotle University of Thessaloniki, Thessaloniki, Greece.</nlm:affiliation>
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<name sortKey="Vellas, Bruno" sort="Vellas, Bruno" uniqKey="Vellas B" first="Bruno" last="Vellas">Bruno Vellas</name>
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<nlm:affiliation>Department of Internal and Geriatrics Medicine, INSERM U 1027, Gerontopole, Hôpitaux de Toulouse, Toulouse, France.</nlm:affiliation>
<country xml:lang="fr">France</country>
<wicri:regionArea>Department of Internal and Geriatrics Medicine, INSERM U 1027, Gerontopole, Hôpitaux de Toulouse, Toulouse</wicri:regionArea>
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<region type="region">Occitanie (région administrative)</region>
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<settlement type="city">Toulouse</settlement>
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<name sortKey="Thambisetty, Madhav" sort="Thambisetty, Madhav" uniqKey="Thambisetty M" first="Madhav" last="Thambisetty">Madhav Thambisetty</name>
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<nlm:affiliation>Clinical and Translational Neuroscience Unit, Laboratory of Behavioral Neuroscience, National Institute on Aging, Baltimore, MD, USA.</nlm:affiliation>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Clinical and Translational Neuroscience Unit, Laboratory of Behavioral Neuroscience, National Institute on Aging, Baltimore, MD</wicri:regionArea>
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<name sortKey="Dobson, Richard J B" sort="Dobson, Richard J B" uniqKey="Dobson R" first="Richard J B" last="Dobson">Richard J B. Dobson</name>
<affiliation wicri:level="3">
<nlm:affiliation>Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, UK.</nlm:affiliation>
<country xml:lang="fr">Royaume-Uni</country>
<wicri:regionArea>Institute of Psychiatry, Psychology & Neuroscience, King's College London, London</wicri:regionArea>
<placeName>
<settlement type="city">Londres</settlement>
<region type="country">Angleterre</region>
<region type="région" nuts="1">Grand Londres</region>
</placeName>
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</author>
<author>
<name sortKey="Powell, John F" sort="Powell, John F" uniqKey="Powell J" first="John F" last="Powell">John F. Powell</name>
<affiliation wicri:level="3">
<nlm:affiliation>Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, UK.</nlm:affiliation>
<country xml:lang="fr">Royaume-Uni</country>
<wicri:regionArea>Institute of Psychiatry, Psychology & Neuroscience, King's College London, London</wicri:regionArea>
<placeName>
<settlement type="city">Londres</settlement>
<region type="country">Angleterre</region>
<region type="région" nuts="1">Grand Londres</region>
</placeName>
</affiliation>
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<author>
<name sortKey="Lupton, Michelle K" sort="Lupton, Michelle K" uniqKey="Lupton M" first="Michelle K" last="Lupton">Michelle K. Lupton</name>
<affiliation wicri:level="1">
<nlm:affiliation>Genetic Epidemiology, QIMR Berghofer Medical Research Institute, Brisbane, Qld, Australia.</nlm:affiliation>
<country xml:lang="fr">Australie</country>
<wicri:regionArea>Genetic Epidemiology, QIMR Berghofer Medical Research Institute, Brisbane, Qld</wicri:regionArea>
<wicri:noRegion>Qld</wicri:noRegion>
</affiliation>
</author>
<author>
<name sortKey="Simmons, Andy" sort="Simmons, Andy" uniqKey="Simmons A" first="Andy" last="Simmons">Andy Simmons</name>
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<nlm:affiliation>Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, UK.</nlm:affiliation>
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<author>
<name sortKey="Velayudhan, Latha" sort="Velayudhan, Latha" uniqKey="Velayudhan L" first="Latha" last="Velayudhan">Latha Velayudhan</name>
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<author>
<name sortKey="Lovestone, Simon" sort="Lovestone, Simon" uniqKey="Lovestone S" first="Simon" last="Lovestone">Simon Lovestone</name>
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<nlm:affiliation>Department of Psychiatry, University of Oxford, Oxford, UK.</nlm:affiliation>
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<name sortKey="Proitsi, Petroula" sort="Proitsi, Petroula" uniqKey="Proitsi P" first="Petroula" last="Proitsi">Petroula Proitsi</name>
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<author>
<name sortKey="Legido Quigley, Cristina" sort="Legido Quigley, Cristina" uniqKey="Legido Quigley C" first="Cristina" last="Legido-Quigley">Cristina Legido-Quigley</name>
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<nlm:affiliation>Institute of Pharmaceutical Science, King's College London, London, UK.</nlm:affiliation>
<country xml:lang="fr">Royaume-Uni</country>
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<series>
<title level="j">Journal of Alzheimer's disease : JAD</title>
<idno type="eISSN">1875-8908</idno>
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<date when="2017" type="published">2017</date>
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<div type="abstract" xml:lang="en">Lipids such as ceramides and phosphatidylcholines (PC) have been found altered in the plasma of Alzheimer's disease (AD) patients in a number of discovery studies. For this reason, the levels of 6 ceramides and 3 PCs, with different fatty acid length and saturation levels, were measured in the plasma from 412 participants (AD n = 205, Control n = 207) using mass spectrometry coupled with ultra-performance liquid chromatography. After this, associations with AD status, brain atrophy, and age-related effects were studied. In the plasma of AD participants, cross-sectional analysis revealed elevated levels of three ceramides (Cer16:0 p < 0.01, Cer18:0 p < 0.01, Cer24:1 p < 0.05). In addition, two PCs in AD plasma (PC36:5 p < 0.05, PC38:6 p < 0.05) were found to be depleted compared to the control group, with PC36:5 also associating with hippocampal atrophy (p < 0.01). Age-specific analysis further revealed that levels of Cer16:0, Cer18:0, and Cer20:0 were associated with hippocampal atrophy only in younger participants (age < 75, p < 0.05), while all 3 PCs did so in the older participants (age > 75, p < 0.05). PC36:5 was associated with AD status in the younger group (p < 0.01), while PC38:6 and 40:6 did so in the older group (p < 0.05). In this study, elevated ceramides and depleted PCs were found in the plasma from 205 AD volunteers. Our findings also suggest that dysregulation in PC and ceramide metabolism could be occurring in different stages of AD progression.</div>
</front>
</TEI>
<pubmed>
<MedlineCitation Status="In-Process" Owner="NLM">
<PMID Version="1">27911300</PMID>
<DateCreated>
<Year>2016</Year>
<Month>12</Month>
<Day>02</Day>
</DateCreated>
<DateRevised>
<Year>2017</Year>
<Month>11</Month>
<Day>18</Day>
</DateRevised>
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<Journal>
<ISSN IssnType="Electronic">1875-8908</ISSN>
<JournalIssue CitedMedium="Internet">
<Volume>60</Volume>
<Issue>3</Issue>
<PubDate>
<Year>2017</Year>
</PubDate>
</JournalIssue>
<Title>Journal of Alzheimer's disease : JAD</Title>
<ISOAbbreviation>J. Alzheimers Dis.</ISOAbbreviation>
</Journal>
<ArticleTitle>Association between Plasma Ceramides and Phosphatidylcholines and Hippocampal Brain Volume in Late Onset Alzheimer's Disease.</ArticleTitle>
<Pagination>
<MedlinePgn>809-817</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.3233/JAD-160645</ELocationID>
<Abstract>
<AbstractText>Lipids such as ceramides and phosphatidylcholines (PC) have been found altered in the plasma of Alzheimer's disease (AD) patients in a number of discovery studies. For this reason, the levels of 6 ceramides and 3 PCs, with different fatty acid length and saturation levels, were measured in the plasma from 412 participants (AD n = 205, Control n = 207) using mass spectrometry coupled with ultra-performance liquid chromatography. After this, associations with AD status, brain atrophy, and age-related effects were studied. In the plasma of AD participants, cross-sectional analysis revealed elevated levels of three ceramides (Cer16:0 p < 0.01, Cer18:0 p < 0.01, Cer24:1 p < 0.05). In addition, two PCs in AD plasma (PC36:5 p < 0.05, PC38:6 p < 0.05) were found to be depleted compared to the control group, with PC36:5 also associating with hippocampal atrophy (p < 0.01). Age-specific analysis further revealed that levels of Cer16:0, Cer18:0, and Cer20:0 were associated with hippocampal atrophy only in younger participants (age < 75, p < 0.05), while all 3 PCs did so in the older participants (age > 75, p < 0.05). PC36:5 was associated with AD status in the younger group (p < 0.01), while PC38:6 and 40:6 did so in the older group (p < 0.05). In this study, elevated ceramides and depleted PCs were found in the plasma from 205 AD volunteers. Our findings also suggest that dysregulation in PC and ceramide metabolism could be occurring in different stages of AD progression.</AbstractText>
</Abstract>
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<Author ValidYN="Y">
<LastName>Kim</LastName>
<ForeName>Min</ForeName>
<Initials>M</Initials>
<AffiliationInfo>
<Affiliation>Institute of Pharmaceutical Science, King's College London, London, UK.</Affiliation>
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<LastName>Nevado-Holgado</LastName>
<ForeName>Alejo</ForeName>
<Initials>A</Initials>
<AffiliationInfo>
<Affiliation>Department of Psychiatry, University of Oxford, Oxford, UK.</Affiliation>
</AffiliationInfo>
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</AffiliationInfo>
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</AffiliationInfo>
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<ForeName>Iwona</ForeName>
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<ForeName>Patrizia</ForeName>
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</AffiliationInfo>
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<Initials>M</Initials>
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</AffiliationInfo>
</Author>
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<LastName>Vellas</LastName>
<ForeName>Bruno</ForeName>
<Initials>B</Initials>
<AffiliationInfo>
<Affiliation>Department of Internal and Geriatrics Medicine, INSERM U 1027, Gerontopole, Hôpitaux de Toulouse, Toulouse, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Thambisetty</LastName>
<ForeName>Madhav</ForeName>
<Initials>M</Initials>
<AffiliationInfo>
<Affiliation>Clinical and Translational Neuroscience Unit, Laboratory of Behavioral Neuroscience, National Institute on Aging, Baltimore, MD, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Dobson</LastName>
<ForeName>Richard J B</ForeName>
<Initials>RJB</Initials>
<AffiliationInfo>
<Affiliation>Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, UK.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Powell</LastName>
<ForeName>John F</ForeName>
<Initials>JF</Initials>
<AffiliationInfo>
<Affiliation>Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, UK.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Lupton</LastName>
<ForeName>Michelle K</ForeName>
<Initials>MK</Initials>
<AffiliationInfo>
<Affiliation>Genetic Epidemiology, QIMR Berghofer Medical Research Institute, Brisbane, Qld, Australia.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Simmons</LastName>
<ForeName>Andy</ForeName>
<Initials>A</Initials>
<AffiliationInfo>
<Affiliation>Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, UK.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>National Institute for Health Research (NIHR) Biomedical Research Centre (BRC) for Mental Health at South London and Maudsley NHS Foundation Trust, UK.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Velayudhan</LastName>
<ForeName>Latha</ForeName>
<Initials>L</Initials>
<AffiliationInfo>
<Affiliation>Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, UK.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Lovestone</LastName>
<ForeName>Simon</ForeName>
<Initials>S</Initials>
<AffiliationInfo>
<Affiliation>Department of Psychiatry, University of Oxford, Oxford, UK.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Proitsi</LastName>
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<LastName>Legido-Quigley</LastName>
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<AffiliationInfo>
<Affiliation>Institute of Pharmaceutical Science, King's College London, London, UK.</Affiliation>
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</Author>
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<Language>eng</Language>
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<Grant>
<Agency>Wellcome Trust</Agency>
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<Keyword MajorTopicYN="N">brain atrophy</Keyword>
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</country>
<country name="Grèce">
<noRegion>
<name sortKey="Tsolaki, Magda" sort="Tsolaki, Magda" uniqKey="Tsolaki M" first="Magda" last="Tsolaki">Magda Tsolaki</name>
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<country name="France">
<region name="Occitanie (région administrative)">
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<country name="États-Unis">
<region name="Maryland">
<name sortKey="Thambisetty, Madhav" sort="Thambisetty, Madhav" uniqKey="Thambisetty M" first="Madhav" last="Thambisetty">Madhav Thambisetty</name>
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<country name="Australie">
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<name sortKey="Lupton, Michelle K" sort="Lupton, Michelle K" uniqKey="Lupton M" first="Michelle K" last="Lupton">Michelle K. Lupton</name>
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