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Lack of evidence for an association between the V393A variant of COQ2 and amyotrophic lateral sclerosis in a Han Chinese population

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Abstract

Amyotrophic lateral sclerosis (ALS) is a progressive disorder involving the degeneration of motor neurons. ALS shares pathogenic characteristics and genetic risk factors with multiple system atrophy (MSA). Here we examine whether a variant of the COQ2 gene associated with MSA in Japanese is also associated with ALS in Han Chinese. The ligase detection reaction was used to measure the frequency of the V393A variant of COQ2 in 282 patients with ALS and 491 healthy controls. The ALS and control groups showed no significant differences in genotype frequencies (OR 1.298, 95 %CI 0.396–4.253, p = 0.666) or allele frequencies (OR 1.314, 95 %CI 0.403–4.286, p = 0.650) at the V393A locus of COQ2. We also conducted a meta-analysis and combined our data with the previous Japanese research, but still failed to detect an association between V393A and ALS. In conclusion, This case–control study shows no evidence for an association between ALS and the V393A variant of COQ2 in Han Chinese and together with the Japanese research suggests that this polymorphism may not be linked to the risk of ALS in East Asians in general.

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Acknowledgments

This research was supported by the National Natural Science Foundation of China (No. 81471300), the Sichuan Province Applied Basic Research Program (No. 2014JY0247), the Sichuan Key Project of Science and Technology (No. 2010SZ0086) and the Ministry of Science and Technology of China (2012AA02A514). We thank all the patients and controls involved in this research.

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The authors declare no conflicts of interest.

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Correspondence to Yanming Xu.

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X. Yang, J. Xi and R. An contributed equally to this work.

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Yang, X., Xi, J., An, R. et al. Lack of evidence for an association between the V393A variant of COQ2 and amyotrophic lateral sclerosis in a Han Chinese population. Neurol Sci 36, 1211–1215 (2015). https://doi.org/10.1007/s10072-015-2083-7

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  • DOI: https://doi.org/10.1007/s10072-015-2083-7

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