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Mitochondrial DNA Haplogroup Distribution in Chaoshanese with and Without Myopia

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Journal Mol Vis
Date 2010 Mar 9
PMID 20208987
Citations 30
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Abstract

Purpose: Mitochondrial DNA (mtDNA) haplogroups affect the clinical expression of Leber hereditary optic neuropathy, age-related macular degeneration, and other diseases. The objective of this study is to investigate whether an mtDNA background is associated with myopia.

Methods: Blood DNA was obtained from 192 college students, including 96 individuals with moderate-to-high myopia and 96 controls without myopia. All the subjects were from a well-known isolated population living in the Chaoshan area of east Guangdong Province and speaking one of the four major dialects in southern China. The mtDNA haplogroups in the 192 subjects were determined by sequencing the mtDNA control region and partial coding regions as well as by analysis of restriction fragment length polymorphisms. Each mtDNA was classified according to the updated version of the Eastern Asian haplogroup system.

Results: Sixteen mtDNA haplogroups were recognized in the 192 subjects. The overall matrilineal structures of the samples with and without myopia were similar and had genetic imprints showing their ethno-origin. There was no statistical difference in frequencies of haplogroup distribution between subjects with and without myopia (chi(2) test, p=0.556).

Conclusions: We failed to identify clues that suggest an involvement of mtDNA background in the predisposition to myopia.

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References
1.
Jones M, Manwaring N, Wang J, Rochtchina E, Mitchell P, Sue C . Mitochondrial DNA haplogroups and age-related maculopathy. Arch Ophthalmol. 2007; 125(9):1235-40. DOI: 10.1001/archopht.125.9.1235. View

2.
Hudson G, Carelli V, Spruijt L, Gerards M, Mowbray C, Achilli A . Clinical expression of Leber hereditary optic neuropathy is affected by the mitochondrial DNA-haplogroup background. Am J Hum Genet. 2007; 81(2):228-33. PMC: 1950812. DOI: 10.1086/519394. View

3.
Fukui H, Moraes C . The mitochondrial impairment, oxidative stress and neurodegeneration connection: reality or just an attractive hypothesis?. Trends Neurosci. 2008; 31(5):251-6. PMC: 2731695. DOI: 10.1016/j.tins.2008.02.008. View

4.
Ban M, Elson J, Walton A, Turnbull D, Compston A, Chinnery P . Investigation of the role of mitochondrial DNA in multiple sclerosis susceptibility. PLoS One. 2008; 3(8):e2891. PMC: 2494944. DOI: 10.1371/journal.pone.0002891. View

5.
Andrew T, Maniatis N, Carbonaro F, Liew S, Lau W, Spector T . Identification and replication of three novel myopia common susceptibility gene loci on chromosome 3q26 using linkage and linkage disequilibrium mapping. PLoS Genet. 2008; 4(10):e1000220. PMC: 2556391. DOI: 10.1371/journal.pgen.1000220. View