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PMID: 11145497 Published · ppublish English Letter Research Support, Non-U.S. Gov't

Increased risk of stroke in patients with the A12308G polymorphism in mitochondria.

Lancet (London, England) ·Vol. 356 ·No. 9247 ·2000-12-16 ·Pages 2068-9

Pulkes T, Sweeney MG, Hanna MG

Abstract

Factors which increase the risk of stroke in patients with the A3243G (mitochondrial encephalomyopathy, lactic acidosis, and stroke [MELAS]) mutation in human mitochondrial DNA are unclear. Previous work on lung-cancer cells with an A3243G mutation showed that a mutation in the mitochondrial transfer gene for leucine tRNA(Leu(CUN)) was able to ameliorate the A3243G-induced biochemical phenotype. We analysed the tRNA(Leu(CUN)) gene in 48 unrelated A3243G cases. We showed that a polymorphism, A12308G, in tRNA(Leu(CUN)) increases the risk of developing stroke in patients with the A3243G mutation (relative risk=2.17). This may have implications for genetic counselling.

MeSH Terms
DNA Mutational Analysis DNA, Mitochondrial/genetics Haplotypes Humans MELAS Syndrome/complications,genetics Phenotype Point Mutation Polymorphism, Genetic RNA, Transfer, Leu/analysis,genetics Stroke/complications,genetics
Chemicals
DNA, Mitochondrial RNA, Transfer, Leu
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Pulkes T
Sweeney M G
Hanna M G
Article Info
Journal
Lancet (London, England)
Abbr.
Lancet
ISSN
0140-6736
Published
2000-12-16
Pages
2068-9
Language
English
Region
England
NLM ID
2985213R
Subset
IM
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