Association of ITPKB, IL1R2 and COQ7 with Parkinson's disease in Taiwan

被引:3
|
作者
Fang, Hwa-Shin [1 ]
Wang, Chun-Chieh [2 ]
Chao, Chih-Ying [2 ]
Fan, Wen-Lang [3 ]
Su, Shih-Chi [4 ]
Wu, Yih-Ru [2 ,5 ]
机构
[1] Shin Kong Wu Ho Su Mem Hosp, Div Gen Med, Taipei, Taiwan
[2] Linkou Chang Gung Mem Hosp, Dept Neurol, Taoyuan, Taiwan
[3] Linkou Chang Gung Mem Hosp, Genom Med Core Lab, Taoyuan, Taiwan
[4] Chang Gung Mem Hosp, Whole Genome Res Core Lab Human Dis, Keelung, Taiwan
[5] Chang Gung Univ, Coll Med, Dept Neurol, Taoyuan, Taiwan
关键词
ITPKB; COQ7; Parkinson's disease; Disease association; DEFICIENCY; GENETICS;
D O I
10.1016/j.jfma.2021.06.016
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background/Purpose: Genetic and environmental factors play significant roles in the pathogenesis of Parkinson's disease (PD). Recently, 17 novel risk loci of PD were identified in a meta-analysis of genome-wide association study (GWAS) in the European populations. In order to clarify if these risk loci are associated with PD in Taiwanese population, we conducted a case-control study including 14 of the novel risk loci and analyzed the genetic distribution and allele frequency.Methods: A total of 2798 subjects were recruited in this study. Genotyping was performed in 672 PD patients and 609 healthy controls by using Mass ARRAY, and data of another 1517 healthy controls from Taiwan Biobank were also examined.Results: Our results show that the dominant models of ITPKB rs4653767 (OR (95% CI) = 0.832 (0.699, 0.990), p = 0.038), IL1R2 rs34043159 (OR (95% CI) = 0.812 (0.665, 0.992), p = 0.041) and COQ7 rs11343 (OR (95% CI) = 0.304 (0.180, 0.512), p < 0.001) were associated with PD. In allelic analysis, the T allele of IL1R2 rs34043159 (OR (95% CI) = 0.873 (0.772, 0.987), p = 0.03) and T allele of COQ7 rs11343 (OR (95% CI) = 0.098 (0.040, 0.238), p < 0.001) showed lower risk of PD. After Bonferroni correction, only dominant model and T allele of COQ7 rs11343 showed significantly reduced the risk of PD.Conclusion: This study suggests that ITPKB, IL1R2 and COQ7 have influence on the risk of PD in Taiwan.Copyright (c) 2021, Formosan Medical Association. Published by Elsevier Taiwan LLC. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/bync-nd/4.0/).
引用
收藏
页码:679 / 686
页数:8
相关论文
共 50 条
  • [21] COQ2 variants in Parkinson's disease and multiple system atrophy
    Mikasa, Michitaka
    Kanai, Kazuaki
    Li, Yuanzhe
    Yoshino, Hiroyo
    Mogushi, Kaoru
    Hayashida, Arisa
    Ikeda, Aya
    Kawajiri, Sumihiro
    Okuma, Yasuyuki
    Kashihara, Kenichi
    Sato, Tatsuya
    Kondo, Hiroshi
    Funayama, Manabu
    Nishioka, Kenya
    Hattori, Nobutaka
    JOURNAL OF NEURAL TRANSMISSION, 2018, 125 (06) : 937 - 944
  • [22] COQ2 variants in Parkinson’s disease and multiple system atrophy
    Michitaka Mikasa
    Kazuaki Kanai
    Yuanzhe Li
    Hiroyo Yoshino
    Kaoru Mogushi
    Arisa Hayashida
    Aya Ikeda
    Sumihiro Kawajiri
    Yasuyuki Okuma
    Kenichi Kashihara
    Tatsuya Sato
    Hiroshi Kondo
    Manabu Funayama
    Kenya Nishioka
    Nobutaka Hattori
    Journal of Neural Transmission, 2018, 125 : 937 - 944
  • [23] Sustained crosstalk between TLR2 and IL-1R1 exacerbates neurodegeneration in Parkinson's Disease
    Johnson, Marguerite Elizabeth
    Kortagere, Sandhya
    FASEB JOURNAL, 2018, 32 (01):
  • [24] IL1R2 polymorphisms and their interaction are associated with osteoporosis susceptibility in the Chinese Han population
    Rong, Kai
    Liang, Zhiquan
    Xiang, Wenyuan
    Wang, Zhan
    Wen, Fengli
    Lu, Laijin
    INTERNATIONAL JOURNAL OF IMMUNOGENETICS, 2021, 48 (06) : 510 - 525
  • [25] A whole genome methylation analysis of systemic lupus erythematosus: hypomethylation of the IL10 and IL1R2 promoters is associated with disease activity
    Lin, S-Y
    Hsieh, S-C
    Lin, Y-C
    Lee, C-N
    Tsai, M-H
    Lai, L-C
    Chuang, E. Y.
    Chen, P-C
    Hung, C-C
    Chen, L-Y
    Hsieh, W. S.
    Niu, D-M
    Su, Y-N
    Ho, H-N
    GENES AND IMMUNITY, 2012, 13 (03) : 214 - 220
  • [26] Impact of IL1R1 and IL1R2 gene polymorphisms on risk of osteonecrosis of the femoral head from a case-control study
    An, Feimeng
    Wang, Jiaqi
    Gao, Hongyan
    Liu, Chang
    Tian, Ye
    Jin, Tianbo
    Liu, Wanlin
    Wang, Jianzhong
    MOLECULAR GENETICS & GENOMIC MEDICINE, 2019, 7 (03):
  • [27] IL1R2在肿瘤发生发展中的作用
    刘颖婷
    卢斌峰
    蒋敬庭
    中国肿瘤生物治疗杂志, 2018, 25 (08) : 822 - 829
  • [28] LncRNA A2M-AS1 lessens the injury of cardiomyocytes caused by hypoxia and reoxygenation via regulating IL1R2
    Song, Xue-Lian
    Zhang, Fei-Fei
    Wang, Wen-Jing
    Li, Xin-Ning
    Dang, Yi
    Li, Ying-Xiao
    Yang, Qian
    Shi, Mei-Jing
    Qi, Xiao-Yong
    GENES & GENOMICS, 2020, 42 (12) : 1431 - 1441
  • [29] The Impacts of IL1R1 and IL1R2 Genetic Variants on Rheumatoid Arthritis Risk in the Chinese Han Population: A Case-Control Study
    Liu, Xiaoli
    Peng, Linna
    Li, Dandan
    He, Chunjuan
    Xing, Shishi
    Wang, Yuhe
    He, Yongjun
    INTERNATIONAL JOURNAL OF GENERAL MEDICINE, 2021, 14 : 2147 - 2159
  • [30] LncRNA A2M-AS1 lessens the injury of cardiomyocytes caused by hypoxia and reoxygenation via regulating IL1R2
    Xue-Lian Song
    Fei-Fei Zhang
    Wen-Jing Wang
    Xin-Ning Li
    Yi Dang
    Ying-Xiao Li
    Qian Yang
    Mei-Jing Shi
    Xiao-Yong Qi
    Genes & Genomics, 2020, 42 : 1431 - 1441