Association of chronic fatigue syndrome with premature telomere attrition.
Identifieur interne : 000A21 ( Main/Exploration ); précédent : 000A20; suivant : 000A22Association of chronic fatigue syndrome with premature telomere attrition.
Auteurs : Mangalathu S. Rajeevan [États-Unis] ; Janna Murray [États-Unis] ; Lisa Oakley [États-Unis] ; Jin-Mann S. Lin [États-Unis] ; Elizabeth R. Unger [États-Unis]Source :
- Journal of translational medicine [ 1479-5876 ] ; 2018.
Descripteurs français
- KwdFr :
- MESH :
- métabolisme : Syndrome de fatigue chronique, Télomère.
- Adulte d'âge moyen, Femelle, Homéostasie des télomères, Humains, Mâle.
English descriptors
- KwdEn :
- MESH :
- metabolism : Fatigue Syndrome, Chronic, Telomere.
- Female, Humans, Male, Middle Aged, Telomere Homeostasis.
Abstract
Chronic fatigue syndrome (CFS), also known as myalgic encephalomyelitis (ME), is a severely debilitating condition of unknown etiology. The symptoms and risk factors of ME/CFS share features of accelerated aging implicated in several diseases. Using telomere length as a marker, this study was performed to test the hypothesis that ME/CFS is associated with accelerated aging.
DOI: 10.1186/s12967-018-1414-x
PubMed: 29486769
Affiliations:
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Le document en format XML
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Rajeevan</name><affiliation wicri:level="1"><nlm:affiliation>Division of High-Consequence Pathogens & Pathology, Centers for Disease Control and Prevention, 1600 Clifton Road, Atlanta, GA, 30329, USA. mor4@cdc.gov.</nlm:affiliation><country xml:lang="fr">États-Unis</country><wicri:regionArea>Division of High-Consequence Pathogens & Pathology, Centers for Disease Control and Prevention, 1600 Clifton Road, Atlanta, GA, 30329</wicri:regionArea><wicri:noRegion>30329</wicri:noRegion></affiliation></author><author><name sortKey="Murray, Janna" sort="Murray, Janna" uniqKey="Murray J" first="Janna" last="Murray">Janna Murray</name><affiliation wicri:level="1"><nlm:affiliation>Division of High-Consequence Pathogens & Pathology, Centers for Disease Control and Prevention, 1600 Clifton Road, Atlanta, GA, 30329, USA.</nlm:affiliation><country xml:lang="fr">États-Unis</country><wicri:regionArea>Division of High-Consequence Pathogens & Pathology, Centers for Disease Control and Prevention, 1600 Clifton Road, Atlanta, GA, 30329</wicri:regionArea><wicri:noRegion>30329</wicri:noRegion></affiliation></author><author><name sortKey="Oakley, Lisa" sort="Oakley, Lisa" uniqKey="Oakley L" first="Lisa" last="Oakley">Lisa Oakley</name><affiliation wicri:level="1"><nlm:affiliation>Division of High-Consequence Pathogens & Pathology, Centers for Disease Control and Prevention, 1600 Clifton Road, Atlanta, GA, 30329, USA.</nlm:affiliation><country xml:lang="fr">États-Unis</country><wicri:regionArea>Division of High-Consequence Pathogens & Pathology, Centers for Disease Control and Prevention, 1600 Clifton Road, Atlanta, GA, 30329</wicri:regionArea><wicri:noRegion>30329</wicri:noRegion></affiliation></author><author><name sortKey="Lin, Jin Mann S" sort="Lin, Jin Mann S" uniqKey="Lin J" first="Jin-Mann S" last="Lin">Jin-Mann S. 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Unger</name><affiliation wicri:level="1"><nlm:affiliation>Division of High-Consequence Pathogens & Pathology, Centers for Disease Control and Prevention, 1600 Clifton Road, Atlanta, GA, 30329, USA.</nlm:affiliation><country xml:lang="fr">États-Unis</country><wicri:regionArea>Division of High-Consequence Pathogens & Pathology, Centers for Disease Control and Prevention, 1600 Clifton Road, Atlanta, GA, 30329</wicri:regionArea><wicri:noRegion>30329</wicri:noRegion></affiliation></author></analytic><series><title level="j">Journal of translational medicine</title><idno type="eISSN">1479-5876</idno><imprint><date when="2018" type="published">2018</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Fatigue Syndrome, Chronic (metabolism)</term><term>Female</term><term>Humans</term><term>Male</term><term>Middle Aged</term><term>Telomere (metabolism)</term><term>Telomere Homeostasis</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Adulte d'âge moyen</term><term>Femelle</term><term>Homéostasie des télomères</term><term>Humains</term><term>Mâle</term><term>Syndrome de fatigue chronique (métabolisme)</term><term>Télomère (métabolisme)</term></keywords><keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Fatigue Syndrome, Chronic</term><term>Telomere</term></keywords><keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr"><term>Syndrome de fatigue chronique</term><term>Télomère</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Female</term><term>Humans</term><term>Male</term><term>Middle Aged</term><term>Telomere Homeostasis</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Adulte d'âge moyen</term><term>Femelle</term><term>Homéostasie des télomères</term><term>Humains</term><term>Mâle</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Chronic fatigue syndrome (CFS), also known as myalgic encephalomyelitis (ME), is a severely debilitating condition of unknown etiology. The symptoms and risk factors of ME/CFS share features of accelerated aging implicated in several diseases. Using telomere length as a marker, this study was performed to test the hypothesis that ME/CFS is associated with accelerated aging.</div></front></TEI><affiliations><list><country><li>États-Unis</li></country></list><tree><country name="États-Unis"><noRegion><name sortKey="Rajeevan, Mangalathu S" sort="Rajeevan, Mangalathu S" uniqKey="Rajeevan M" first="Mangalathu S" last="Rajeevan">Mangalathu S. Rajeevan</name></noRegion><name sortKey="Lin, Jin Mann S" sort="Lin, Jin Mann S" uniqKey="Lin J" first="Jin-Mann S" last="Lin">Jin-Mann S. Lin</name><name sortKey="Murray, Janna" sort="Murray, Janna" uniqKey="Murray J" first="Janna" last="Murray">Janna Murray</name><name sortKey="Oakley, Lisa" sort="Oakley, Lisa" uniqKey="Oakley L" first="Lisa" last="Oakley">Lisa Oakley</name><name sortKey="Unger, Elizabeth R" sort="Unger, Elizabeth R" uniqKey="Unger E" first="Elizabeth R" last="Unger">Elizabeth R. Unger</name></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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