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Letter to the Editor | Open Access

Implication of the LINGO2 gene in the predisposition to movement disorders

Department of Biochemistry, Faculty of Medicine, Hasanuddin University, Makassar 90245, South Sulawesi, Indonesia
Department of Neurology, Faculty of Medicine, Hasanuddin University, Makassar 90245, South Sulawesi, Indonesia
National Research and Innovation Agency (BRIN), Jakarta 10340, Indonesia
Department of Biochemistry, Faculty of Medicine and Health Sciences, Maulana Malik Ibrahim State Islamic University of Malang, Batu 65151, East Java, Indonesia
Department of General Surgery, Weston General Hospital, Grange Rd, Weston super Mare BS23 4QT, UK

§ These authors contributed equally to this work.

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Abstract

Previous reports on the pathogenesis of age-related movement disorders, such as Parkinson’s disease (PD) and essential tremor (ET), have demonstrated the potential implications of LINGO1 (leucine-rich repeat and immunoglobulin domain-containing protein) gene. Although LINGO2 has a high degree of homology with LINGO1, but it is less characterized and the role of LINGO2 in the development of PD/ET remains unreported. Hence, this meta-analysis was conducted to evaluate the role of LINGO2 in PD/ET pathogenesis. A total of 4 studies, which complied with the Hardy-Weinberg equilibrium, were included in the meta-analysis. Analysis of the pooled odds ratio and confidence interval of the studies were performed for five genetic models, namely: allelic, dominant, recessive, homozygous, and heterozygous. No significant association was observed between the LINGO2 polymorphism and PD/ET, although subgroup analysis through conventional meta-analysis indicated that the recessive models of rs7033345 and rs10812774 are significantly associated with predisposition to ET in the Asian population. However, trial sequential analyses for both polymorphisms were unlikely to reveal any robust effect. Hence, studies with larger samples on this association are needed in the future to corroborate our results.

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Brain Science Advances
Pages 257-262
Cite this article:
Soraya GV, Ulhaq ZS, Garcia CP. Implication of the LINGO2 gene in the predisposition to movement disorders. Brain Science Advances, 2021, 7(4): 257-262. https://doi.org/10.26599/BSA.2021.9050018

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Published: 10 January 2022
© The authors 2021.

This article is published with open access at journals.sagepub.com/home/BSA

Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/ en-us/nam/open-access-at-sage).

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