Mitochondrial DNA sequence associations with dementia and amyloid-β in elderly African Americans
Identifieur interne : 000C88 ( Main/Exploration ); précédent : 000C87; suivant : 000C89Mitochondrial DNA sequence associations with dementia and amyloid-β in elderly African Americans
Auteurs : Gregory J. Tranah [États-Unis] ; Jennifer S. Yokoyama [États-Unis] ; Shana M. Katzman [États-Unis] ; Michael A. Nalls [États-Unis] ; Anne B. Newman [États-Unis] ; Tamara B. Harris [États-Unis] ; Matteo Cesari [France] ; Todd M. Manini [États-Unis] ; Nicholas J. Schork [États-Unis] ; Steven R. Cummings [États-Unis] ; Yongmei Liu [États-Unis] ; Kristine Yaffe [États-Unis]Source :
- Neurobiology of aging [ 0197-4580 ] ; 2013.
Abstract
Mitochondrial dysfunction occurs early in the course of several neurodegenerative diseases, and is potentially related to increased oxidative damage and amyloid-β (Aβ) formation in Alzheimer’s disease. The goals of this study were to assess mtDNA sequence associations with dementia risk, 10-year cognitive change, and markers of oxidative stress and Aβ among 1089 African-Americans in the population-based Health, Aging, and Body Composition Study. Participants were free of dementia at baseline, and incidence was determined in 187 (18%) cases over 10 to 12 follow-up years. Haplogroup L1 participants were at increased risk for developing dementia (odds ratio = 1.88, 95% confidence interval = 1.23–2.88,
Url:
DOI: 10.1016/j.neurobiolaging.2013.05.023
PubMed: 24140124
PubMed Central: 4019378
Affiliations:
- France, États-Unis
- Californie, Caroline du Nord, Floride, Maryland, Midi-Pyrénées, Occitanie (région administrative), Pennsylvanie
- Pittsburgh, Toulouse
- Université de Pittsburgh
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Le document en format XML
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<front><div type="abstract" xml:lang="en"><p id="P1">Mitochondrial dysfunction occurs early in the course of several neurodegenerative diseases, and is potentially related to increased oxidative damage and amyloid-β (Aβ) formation in Alzheimer’s disease. The goals of this study were to assess mtDNA sequence associations with dementia risk, 10-year cognitive change, and markers of oxidative stress and Aβ among 1089 African-Americans in the population-based Health, Aging, and Body Composition Study. Participants were free of dementia at baseline, and incidence was determined in 187 (18%) cases over 10 to 12 follow-up years. Haplogroup L1 participants were at increased risk for developing dementia (odds ratio = 1.88, 95% confidence interval = 1.23–2.88, <italic>p</italic>
= 0.004), lower plasma Aβ42 levels (<italic>p</italic>
= 0.03), and greater 10-year decline on the Digit Symbol Substitution Test (<italic>p</italic>
= 0.04) when compared with common haplogroup L3. The p.V193I, <italic>ND2</italic>
substitution was associated with significantly higher Aβ42 levels (<italic>p</italic>
= 0.0012), and this association was present in haplogroup L3 (<italic>p</italic>
= 0.018) but not L1 (<italic>p</italic>
= 0.90) participants. All associations were independent of potential confounders, including APOEε4 status and nuclear genetic ancestry. Identification of mtDNA sequence variation associated with dementia risk and cognitive decline may contribute to the development of new treatment targets and diagnostic tests that identify responders to interventions targeting mitochondria.</p>
</div>
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<name sortKey="Manini, Todd M" sort="Manini, Todd M" uniqKey="Manini T" first="Todd M." last="Manini">Todd M. Manini</name>
<name sortKey="Nalls, Michael A" sort="Nalls, Michael A" uniqKey="Nalls M" first="Michael A." last="Nalls">Michael A. Nalls</name>
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<name sortKey="Schork, Nicholas J" sort="Schork, Nicholas J" uniqKey="Schork N" first="Nicholas J." last="Schork">Nicholas J. Schork</name>
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<name sortKey="Yokoyama, Jennifer S" sort="Yokoyama, Jennifer S" uniqKey="Yokoyama J" first="Jennifer S." last="Yokoyama">Jennifer S. Yokoyama</name>
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<country name="France"><region name="Occitanie (région administrative)"><name sortKey="Cesari, Matteo" sort="Cesari, Matteo" uniqKey="Cesari M" first="Matteo" last="Cesari">Matteo Cesari</name>
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