Association of Rare Variants in ARSA with Parkinson's Disease

被引:2
|
作者
Senkevich, Konstantin [1 ,2 ]
Beletskaia, Mariia [3 ]
Dworkind, Aliza [4 ]
Yu, Eric [5 ]
Ahmad, Jamil [2 ]
Ruskey, Jennifer A. [1 ,2 ]
Asayesh, Farnaz [1 ,5 ]
Spiegelman, Dan [1 ]
Fahn, Stanley [6 ]
Waters, Cheryl [6 ]
Monchi, Oury [7 ,8 ,9 ]
Dauvilliers, Yves [10 ]
Dupre, Nicolas [11 ,12 ]
Greenbaum, Lior [13 ,14 ,15 ]
Hassin-Baer, Sharon [15 ,16 ]
Nagornov, Ilya [17 ]
Tyurin, Alexandr [3 ]
Miliukhina, Irina [18 ]
Timofeeva, Alla [3 ]
Emelyanov, Anton [3 ]
Trempe, Jean-Francois [19 ,20 ]
Zakharova, Ekaterina [17 ]
Alcalay, Roy N. [6 ,21 ]
Pchelina, Sofya [3 ]
Gan-Or, Ziv [1 ,2 ]
机构
[1] McGill Univ, Neuro Montreal Neurol Inst, Montreal, PQ, Canada
[2] McGill Univ, Dept Neurol & Neurosurg, Montreal, PQ, Canada
[3] First Pavlov State Med Univ St Petersburg, St Petersburg, Russia
[4] McGill Univ, Dept Physiol, Montreal, PQ, Canada
[5] McGill Univ, Dept Human Genet, Montreal, PQ, Canada
[6] Columbia Univ, Dept Neurol, Coll Phys & Surg, Med Ctr, New York, NY USA
[7] Univ Calgary, Dept Clin Neurosci, Calgary, AB, Canada
[8] Univ Calgary, Dept Radiol, Calgary, AB, Canada
[9] Cumming Sch Med, Hotchkiss Brain Inst, Calgary, AB, Canada
[10] Univ Montpellier, Natl Reference Ctr Narcolepsy, Sleep Unit,CHU Montpellier, Dept Neurol,Gui de Chauliac Hosp, Montpellier, France
[11] Univ Laval, Div Neurosci, CHU Quebec, Quebec City, PQ, Canada
[12] Univ Laval, Dept Med, Fac Med, Quebec City, PQ, Canada
[13] Sheba Med Ctr, Danek Gertner Inst Human Genet, Ramat Gan, Israel
[14] Joseph Sagol Neurosci Ctr, Sheba Med Ctr, Ramat Gan, Israel
[15] Tel Aviv Univ, Sackler Fac Med, Tel Aviv, Israel
[16] Sheba Med Ctr, Movement Disorders Inst, Dept Neurol, Tel Aviv, Israel
[17] Res Ctr Med Genet, Moscow, Russia
[18] Inst Human Brain RAS, St Petersburg, Russia
[19] McGill Univ, Dept Pharmacol & Therapeut, Montreal, PQ, Canada
[20] McGill Univ, Ctr Rech Biol Struct, Montreal, PQ, Canada
[21] Tel Aviv Sourasky Med Ctr, Div Movement Disorders, Tel Aviv, Israel
基金
美国国家卫生研究院;
关键词
lysosomal genes; Parkinson's disease; ARSA; rare variants; GENERAL FRAMEWORK; METAANALYSIS; RISK; INSIGHTS;
D O I
10.1002/mds.29521
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
BackgroundSeveral lysosomal genes are associated with Parkinson's disease (PD), yet the association between PD and ARSA remains unclear. ObjectivesTo study rare ARSA variants in PD. MethodsTo study rare ARSA variants (minor allele frequency < 0.01) in PD, we performed burden analyses in six independent cohorts with 5801 PD patients and 20,475 controls, followed by a meta-analysis. ResultsWe found evidence for associations between functional ARSA variants and PD in four cohorts (P & LE; 0.05 in each) and in the meta-analysis (P = 0.042). We also found an association between loss-of-function variants and PD in the United Kingdom Biobank cohort (P = 0.005) and in the meta-analysis (P = 0.049). These results should be interpreted with caution as no association survived multiple comparisons correction. Additionally, we describe two families with potential co-segregation of ARSA p.E382K and PD. ConclusionsRare functional and loss-of-function ARSA variants may be associated with PD. Further replications in large case-control/familial cohorts are required. & COPY; 2023 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.
引用
收藏
页码:1806 / 1812
页数:7
相关论文
共 50 条
  • [41] PTPA variants are rare in early-onset and familial Parkinson's disease
    Dulski, Jaroslaw
    Soto-Beasley, Alexandra, I
    Uitti, Ryan J.
    Wszolek, Zbigniew K.
    Ross, Owen A.
    BRAIN, 2023, 146 (12) : E125 - E127
  • [42] Common and rare GCH1 variants are associated with Parkinson's disease
    Rudakou, Uladzislau
    Bencheikh, Bouchra Ouled Amar
    Ruskey, Jennifer A.
    Krohn, Lynne
    Laurent, Sandra B.
    Spiegelman, Dan
    Liong, Christopher
    Fahn, Stanley
    Waters, Cheryl
    Monchi, Oury
    Fon, Edward A.
    Dauvilliers, Yves
    Alcalay, Roy N.
    Dupre, Nicolas
    Gan-Or, Ziv
    NEUROBIOLOGY OF AGING, 2019, 73 : 231.e1 - 231.e6
  • [43] Are rare heterozygous SYNJ1 variants associated with Parkinson's disease?
    Senkevich, Konstantin
    Parlar, Sitki Cem
    Chantereault, Cloe
    Yu, Eric
    Ahmad, Jamil
    Ruskey, Jennifer A.
    Asayesh, Farnaz
    Spiegelman, Dan
    Waters, Cheryl
    Monchi, Oury
    Dauvilliers, Yves
    Dupre, Nicolas
    Miliukhina, Irina
    Timofeeva, Alla
    Emelyanov, Anton
    Pchelina, Sofya
    Greenbaum, Lior
    Hassin-Baer, Sharon
    Alcalay, Roy N.
    Gan-Or, Ziv
    NPJ PARKINSONS DISEASE, 2024, 10 (01)
  • [44] Rare variants analysis of cutaneous malignant melanoma genes in Parkinson's disease
    Lubbe, S. J.
    Escott-Price, V.
    Brice, A.
    Gasser, T.
    Pittman, A. M.
    Bras, J.
    Hardy, J.
    Heutink, P.
    Wood, N. M.
    Singleton, A. B.
    Grosset, D. G.
    Carroll, C. B.
    Law, M. H.
    Demenais, F.
    Iles, M. M.
    Bishop, D. T.
    Newton-Bishop, J.
    Williams, N. M.
    Morris, H. R.
    NEUROBIOLOGY OF AGING, 2016, 48 : 222.e1 - 222.e7
  • [45] Association of rare variants in neurodegenerative genes with familial Alzheimer's disease
    Zhang, Weiwei
    Jiao, Bin
    Xiao, Tingting
    Liu, Xixi
    Liao, Xinxin
    Xiao, Xuewen
    Guo, Lina
    Yuan, Zhenhua
    Yan, Xinxiang
    Tang, Beisha
    Shen, Lu
    ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY, 2020, 7 (10): : 1985 - 1995
  • [46] Cohen's h for detection of disease association with rare genetic variants
    Wen, Shu-Hui
    Yeh, Jih-I
    BMC GENOMICS, 2014, 15
  • [47] Cohen’s h for detection of disease association with rare genetic variants
    Shu-Hui Wen
    Jih-I Yeh
    BMC Genomics, 15
  • [48] Association of SNCA variants with α-synuclein of gastric and colonic mucosa in Parkinson's disease
    Chung, Sun Ju
    Koenig, Inke R.
    Lohmann, Katja
    Hinrichs, Frauke
    Kim, Juyeon
    Ryu, Ho-Sung
    Lee, Hyo Jeong
    Kim, Kiju
    Lee, Jeong Hoon
    Jung, Kee Wook
    Kim, Mi Jung
    Kim, Mi-Jung
    Kim, Young Jin
    Yun, Sung-Cheol
    Hong, Seung-Mo
    Myung, Seung-Jae
    Klein, Christine
    PARKINSONISM & RELATED DISORDERS, 2019, 61 : 151 - 155
  • [49] Familial variants of Parkinson's disease
    Gwinn-Hardy, K
    Hanson, M
    Wszolek, Z
    Adam, A
    Singleton, A
    Adler, CH
    Caviness, JN
    Bower, J
    Hickey, S
    Chen, JY
    Waseem, S
    Farrer, M
    MAPPING THE PROGRESS OF ALZHEIMER'S AND PARKINSON'S DISEASE, 2002, 51 : 281 - 284
  • [50] Common variants in Parkinson's disease
    Ross, Owen A.
    Farrer, Matthew J.
    Wu, Ruey-Meei
    MOVEMENT DISORDERS, 2007, 22 (06) : 899 - 900