Skip to main content
Top
Published in: Neurological Sciences 3/2016

01-03-2016 | Original Article

Association of the COQ2 V393A variant with risk of multiple system atrophy in East Asians: a case–control study and meta-analysis of the literature

Authors: QuanZhen Zhao, Xinglong Yang, SiJia Tian, Ran An, JinHua Zheng, Yanming Xu

Published in: Neurological Sciences | Issue 3/2016

Login to get access

Abstract

Recent studies in Japan have associated multiple system atrophy (MSA), a neurodegenerative disease of uncertain etiology, with polymorphism in the COQ2 gene. This led us to explore whether the same polymorphism is associated with MSA in Han Chinese and more broadly in East Asians. We conducted a case–control study with 82 Han Chinese with probable MSA and 484 gender- and age-matched healthy subjects, genotyping them using the ligase detection reaction. The results were meta-analyzed together with data from four previous studies to gain a broader picture of possible disease associations in East Asian populations. The COQ2 variants M78V and R337X were not detected in our Han Chinese patients or controls; only the heterozygous V393A variant (CT genotype) was detected. The frequency of this genotype was significantly higher in patients (7.3 %) than in controls (1.86 %; OR 4.17, 95 % CI 1.44–12.04, p = 0.004). Subgroup analysis among patients showed a significant association of V393A with MSA involving cerebellar signs (MSA-C; OR 4.59, 95 % CI 1.36–15.48, p = 0.007), but not with MSA involving parkinsonism (MSA-P). Meta-analysis of our results in Han Chinese with data from case–control studies in Japan, Korea, mainland China and Taiwan showed a significant association of V393A with MSA (OR 2.05, 95 % CI 1.29–3.25, p = 0.002), which subgroup analysis showed to be significant for MSA-C (OR 2.75, 95 % CI 1.98–3.84, p < 0.001) but not for MSA-P (OR 1.25, 95 % CI 0.64–2.46, p = 0.51). These findings provide evidence that the previously reported association of COQ2 V393A polymorphism with increased risk of MSA in Japanese also applies to Han Chinese, as well as more broadly to other East Asian populations. This association may be particularly strong for MSA-C.
Literature
1.
go back to reference Halliday GM, Holton JL, Revesz T et al (2011) Neuropathology underlying clinical variability in patients with synucleinopathies. Acta Neuropathol 122(2):187–204CrossRefPubMed Halliday GM, Holton JL, Revesz T et al (2011) Neuropathology underlying clinical variability in patients with synucleinopathies. Acta Neuropathol 122(2):187–204CrossRefPubMed
2.
go back to reference Wenning GK, Colosimo C (2010) Diagnostic criteria for multiple system atrophy and progressive supranuclear palsy. Rev Neurol (Paris) 166(10):829–833CrossRef Wenning GK, Colosimo C (2010) Diagnostic criteria for multiple system atrophy and progressive supranuclear palsy. Rev Neurol (Paris) 166(10):829–833CrossRef
3.
go back to reference Fujioka S, Ogaki K, Tacik PM et al (2014) Update on novel familial forms of Parkinson’s disease and multiple system atrophy. Parkinsonism Relat Disord 20(Suppl 1):S29–S34CrossRefPubMedPubMedCentral Fujioka S, Ogaki K, Tacik PM et al (2014) Update on novel familial forms of Parkinson’s disease and multiple system atrophy. Parkinsonism Relat Disord 20(Suppl 1):S29–S34CrossRefPubMedPubMedCentral
4.
go back to reference Nishimura M, Kuno S, Kaji R et al (2005) Influence of a tumor necrosis factor gene polymorphism in Japanese patients with multiple system atrophy. Neurosci Lett 374(3):218–221CrossRefPubMed Nishimura M, Kuno S, Kaji R et al (2005) Influence of a tumor necrosis factor gene polymorphism in Japanese patients with multiple system atrophy. Neurosci Lett 374(3):218–221CrossRefPubMed
5.
go back to reference Soma H, Yabe I, Takei A et al (2008) Associations between multiple system atrophy and polymorphisms of SLC1A4, SQSTM1, and EIF4EBP1 genes. Mov Disord 23(8):1161–1167CrossRefPubMed Soma H, Yabe I, Takei A et al (2008) Associations between multiple system atrophy and polymorphisms of SLC1A4, SQSTM1, and EIF4EBP1 genes. Mov Disord 23(8):1161–1167CrossRefPubMed
6.
go back to reference Multiple-System Atrophy Research Collaboration (2013) Mutations in COQ2 in familial and sporadic multiple-system atrophy. N Engl J Med 369(3):233–244CrossRef Multiple-System Atrophy Research Collaboration (2013) Mutations in COQ2 in familial and sporadic multiple-system atrophy. N Engl J Med 369(3):233–244CrossRef
7.
go back to reference Jellinger KA (2014) Neuropathology of multiple system atrophy: new thoughts about pathogenesis. Mov Disord 29(14):1720–1741CrossRefPubMed Jellinger KA (2014) Neuropathology of multiple system atrophy: new thoughts about pathogenesis. Mov Disord 29(14):1720–1741CrossRefPubMed
8.
go back to reference Lin CH, Tan EK, Yang CC et al (2015) COQ2 gene variants associate with cerebellar subtype of multiple system atrophy in Chinese. Mov Disord 30(3):436–437CrossRefPubMed Lin CH, Tan EK, Yang CC et al (2015) COQ2 gene variants associate with cerebellar subtype of multiple system atrophy in Chinese. Mov Disord 30(3):436–437CrossRefPubMed
9.
go back to reference Jeon BS, Farrer MJ, Bortnick SF et al (2014) Mutant COQ2 in multiple-system atrophy. N Engl J Med 371(1):80CrossRefPubMed Jeon BS, Farrer MJ, Bortnick SF et al (2014) Mutant COQ2 in multiple-system atrophy. N Engl J Med 371(1):80CrossRefPubMed
10.
go back to reference Chen YP, Zhao B, Cao B et al (2015) Mutation scanning of the COQ2 gene in ethnic Chinese patients with multiple-system atrophy. Neurobiol Aging 36(2):1222.e7–11 Chen YP, Zhao B, Cao B et al (2015) Mutation scanning of the COQ2 gene in ethnic Chinese patients with multiple-system atrophy. Neurobiol Aging 36(2):1222.e7–11
11.
12.
go back to reference Thomas G, Sinville R, Sutton S et al (2004) Capillary and microelectrophoretic separations of ligase detection reaction products produced from low-abundant point mutations in genomic DNA. Electrophoresis 25(10–11):1668–1677CrossRefPubMed Thomas G, Sinville R, Sutton S et al (2004) Capillary and microelectrophoretic separations of ligase detection reaction products produced from low-abundant point mutations in genomic DNA. Electrophoresis 25(10–11):1668–1677CrossRefPubMed
13.
go back to reference Begg CB, Mazumdar M (1994) Operating characteristics of a rank correlation test for publication bias. Biometrics 50:1088–1101CrossRefPubMed Begg CB, Mazumdar M (1994) Operating characteristics of a rank correlation test for publication bias. Biometrics 50:1088–1101CrossRefPubMed
15.
go back to reference Hayashino Y, Noguchi Y, Fukui T (2005) Systematic evaluation and comparison of statistical tests for publication bias. J Epidemiol 15:235–243CrossRefPubMed Hayashino Y, Noguchi Y, Fukui T (2005) Systematic evaluation and comparison of statistical tests for publication bias. J Epidemiol 15:235–243CrossRefPubMed
16.
go back to reference Lin CH, Lin HI, Chen ML, Wu RM (2014) COQ2p, V393A variant, rs148156462, is not associated with Parkinson’s disease in a Taiwanese population. Neurobiol Aging 36(1):546.e17–8 Lin CH, Lin HI, Chen ML, Wu RM (2014) COQ2p, V393A variant, rs148156462, is not associated with Parkinson’s disease in a Taiwanese population. Neurobiol Aging 36(1):546.e17–8
17.
go back to reference Schottlaender LV, Houlden H, Atrophy Multiple-System, (MSA) Brain Bank Collaboration (2014) Mutant COQ2 in multiple-system atrophy. N Engl J Med 371(1):81PubMed Schottlaender LV, Houlden H, Atrophy Multiple-System, (MSA) Brain Bank Collaboration (2014) Mutant COQ2 in multiple-system atrophy. N Engl J Med 371(1):81PubMed
18.
go back to reference Ogaki K, Fujioka S, Heckman MG et al (2014) Analysis of COQ2 gene in multiple system atrophy. Mol Neurodegener 5(9):44CrossRef Ogaki K, Fujioka S, Heckman MG et al (2014) Analysis of COQ2 gene in multiple system atrophy. Mol Neurodegener 5(9):44CrossRef
19.
go back to reference Sharma M, Wenning G, Krüger R et al (2014) Mutant COQ2 in multiple-system atrophy. N Engl J Med 371(1):80–81CrossRefPubMed Sharma M, Wenning G, Krüger R et al (2014) Mutant COQ2 in multiple-system atrophy. N Engl J Med 371(1):80–81CrossRefPubMed
20.
go back to reference Ozawa T, Revesz T, Paviour D et al (2012) Difference in MSA phenotype distribution between populations: genetics or environment? J Parkinsons Dis 2(1):7–18PubMed Ozawa T, Revesz T, Paviour D et al (2012) Difference in MSA phenotype distribution between populations: genetics or environment? J Parkinsons Dis 2(1):7–18PubMed
21.
go back to reference Fontaine E, Ichas F, Bernardi P (1998) A ubiquinone-binding site regulates the mitochondrial permeability transition pore. J Biol Chem 273(40):25734–25740CrossRefPubMed Fontaine E, Ichas F, Bernardi P (1998) A ubiquinone-binding site regulates the mitochondrial permeability transition pore. J Biol Chem 273(40):25734–25740CrossRefPubMed
22.
go back to reference Turunen M, Wehlin M, Sjöberg J et al (2002) β2-Integrin and lipid modifications indicate a non-antioxidant mechanism for the anti-atherogenic effect of dietary coenzyme Q10. Biochem Biophys Res Commun 296(2):255–260CrossRefPubMed Turunen M, Wehlin M, Sjöberg J et al (2002) β2-Integrin and lipid modifications indicate a non-antioxidant mechanism for the anti-atherogenic effect of dietary coenzyme Q10. Biochem Biophys Res Commun 296(2):255–260CrossRefPubMed
23.
go back to reference Quinzii CM, Lopez LC, Von-Moltke J et al (2008) Respiratory chain dysfunction and oxidative stress correlate with severity of primary CoQ10 deficiency. FASEB J Off Publ Fed Am Soc Exp Biol 2(6):1874–1885 Quinzii CM, Lopez LC, Von-Moltke J et al (2008) Respiratory chain dysfunction and oxidative stress correlate with severity of primary CoQ10 deficiency. FASEB J Off Publ Fed Am Soc Exp Biol 2(6):1874–1885
24.
go back to reference Turunen M, Olsson J, Dallner G (2004) Metabolism and function of coenzyme Q. Biochim Biophys Acta 1660(1–2):171–199CrossRefPubMed Turunen M, Olsson J, Dallner G (2004) Metabolism and function of coenzyme Q. Biochim Biophys Acta 1660(1–2):171–199CrossRefPubMed
25.
go back to reference Quinzii CM, López LC, Von-Moltke J et al (2008) Respiratory chain dysfunction and oxidative stress correlate with severity of primary CoQ10 deficiency. FASEB J 22(6):1874–1885CrossRefPubMedPubMedCentral Quinzii CM, López LC, Von-Moltke J et al (2008) Respiratory chain dysfunction and oxidative stress correlate with severity of primary CoQ10 deficiency. FASEB J 22(6):1874–1885CrossRefPubMedPubMedCentral
26.
go back to reference Quinzii CM, Lopez LC, Gilkerson RW et al (2010) Reactive oxygen species, oxidative stress, and cell death correlate with level of CoQ10 deficiency. FASEB J Off Publ Fed Am Soc Exp Biol 2(10):3733–3743 Quinzii CM, Lopez LC, Gilkerson RW et al (2010) Reactive oxygen species, oxidative stress, and cell death correlate with level of CoQ10 deficiency. FASEB J Off Publ Fed Am Soc Exp Biol 2(10):3733–3743
27.
go back to reference Yamashita T, Ando Y, Obayashi K et al (2000) Oxidative injury is present in Purkinje cells in patients with olivopontocerebellar atrophy. J Neurol Sci 175(2):107–110CrossRefPubMed Yamashita T, Ando Y, Obayashi K et al (2000) Oxidative injury is present in Purkinje cells in patients with olivopontocerebellar atrophy. J Neurol Sci 175(2):107–110CrossRefPubMed
28.
go back to reference Vanacore N, Bonifati V, Fabbrini G et al (2005) Case-control study of multiple system atrophy. Mov Disord 20(2):158–163CrossRefPubMed Vanacore N, Bonifati V, Fabbrini G et al (2005) Case-control study of multiple system atrophy. Mov Disord 20(2):158–163CrossRefPubMed
Metadata
Title
Association of the COQ2 V393A variant with risk of multiple system atrophy in East Asians: a case–control study and meta-analysis of the literature
Authors
QuanZhen Zhao
Xinglong Yang
SiJia Tian
Ran An
JinHua Zheng
Yanming Xu
Publication date
01-03-2016
Publisher
Springer Milan
Published in
Neurological Sciences / Issue 3/2016
Print ISSN: 1590-1874
Electronic ISSN: 1590-3478
DOI
https://doi.org/10.1007/s10072-015-2414-8

Other articles of this Issue 3/2016

Neurological Sciences 3/2016 Go to the issue