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A DLST genotype associated with reduced risk for Alzheimer's disease

Sheu, KFR (author)
Brown, AM (author)
Kristal, BS (author)
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Kalaria, RN (author)
Lilius, L (author)
Karolinska Institutet
Lannfelt, L (author)
Blass, JP (author)
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 (creator_code:org_t)
1999-04-01
1999
English.
In: Neurology. - : Ovid Technologies (Wolters Kluwer Health). - 0028-3878 .- 1526-632X. ; 52:7, s. 1505-1507
  • Journal article (peer-reviewed)
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  • Article abstract Recent studies suggest that variants of the DLST gene alter the risk of AD. DLST encodes the core subunit of the mitochondrial α-ketoglutarate dehydrogenase complex, which is deficient in AD. The authors report that in 247 US white subjects, homozygosity for DLST A19,117, T19,183 was associated with a reduced risk of AD (odds ratio [OR] = 0.35, p = 0.018). The reduced risk was marked in subjects who did not carry the apolipoprotein (APOE)-4 allele (OR = 0.16, p = 0.014). Further study of DLST in AD appears warranted.

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