Consensus Guidance for Genetic Counseling in GBA1 Variants: A Focus on Parkinson's Disease

被引:1
|
作者
Vieira, Sophia R. L. [1 ]
Mezabrovschi, Roxana [1 ]
Toffoli, Marco [1 ]
Del Pozo, Sara Lucas [1 ]
Menozzi, Elisa [1 ]
Mullin, Stephen [1 ,2 ]
Yalkic, Selen [1 ]
Limbachiya, Naomi [1 ]
Koletsi, Sofia [1 ,3 ]
Loefflad, Nadine [1 ]
Lopez, Grisel J. [4 ]
Gan-Or, Ziv [5 ,6 ]
Alcalay, Roy N. [7 ,8 ]
Sidransky, Ellen [3 ,4 ]
Schapira, Anthony H. V. [1 ,3 ]
机构
[1] Univ Coll London Queen Sq, Dept Clin & Movement Neurosci, Inst Neurol, London, England
[2] Univ Plymouth, Fac Hlth, Plymouth, England
[3] Aligning Sci Parkinsons Collaborat Res Network, Chevy Chase, MD USA
[4] Natl Human Genome Res Inst, Med Genet Branch, NIH, Bethesda, MD USA
[5] McGill Univ, Neuro Montreal Neurol Inst Hosp, Dept Neurol & Neurosurg, Montreal, PQ, Canada
[6] McGill Univ, Dept Human Genet, Montreal, PQ, Canada
[7] Columbia Univ, Irving Med Ctr, New York, NY USA
[8] Tel Aviv Univ, Tel Aviv Sourasky Med Ctr, Tel Aviv Sch Med, Tel Aviv, Israel
关键词
GBA1; Parkinson's; counseling; neurodegeneration; risk; GLUCOCEREBROSIDASE MUTATIONS; GAUCHER-DISEASE; ASSOCIATION; RISK; MULTICENTER; PROGRESSION; DEMENTIA; POLYMORPHISM; SURVIVAL; MOTOR;
D O I
10.1002/mds.30006
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Glucocerebrosidase (GBA1) variants constitute numerically the most common known genetic risk factor for Parkinson's disease (PD) and are distributed worldwide. Access to GBA1 genotyping varies across the world and even regionally within countries. Guidelines for GBA1 variant counseling are evolving. We review the current knowledge of the link between GBA1 and PD, and discuss the practicalities of GBA1 testing. Lastly, we provide a consensus for an approach to counseling people with GBA1 variants, notably the communication of PD risk. (c) 2024 The Author(s). Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.
引用
收藏
页码:2144 / 2154
页数:11
相关论文
共 50 条
  • [41] Generation of GBA1 isogenic iPSC lines to investigate the pathogenesis of GBA1-associated Parkinson disease
    Ma, Charis
    Chen, Yu
    Chen, Chase
    Sidransky, Ellen
    MOLECULAR GENETICS AND METABOLISM, 2024, 141 (02)
  • [42] Genetic variants of GBA and GLA in a Turkish cohort of Parkinson's disease: A preliminary report
    Yekeduz, Merve Koc
    Yilmaz, Rezzak
    Kayis, Gorkem
    Dogulu, Neslihan
    Oncul, Ummuhan
    Abali, Talha
    Temizyurek, Akar Diyar
    Celik, Gokalp
    Coklu, Hilal
    Gemci, Emine
    Yalcin, Ahmet
    Ceylaner, Serdar
    Akbostanci, M. Cenk
    Eminoglu, Fatma Tuba
    PARKINSONISM & RELATED DISORDERS, 2023, 110
  • [43] The Functional Consequences of the 'African GBA1 Allele' of rs3115534 in Parkinson's disease (PD)
    Radefeldt, M.
    Demuth, L.
    Al-Ali, R.
    Fischer, S.
    Beetz, C.
    Bauer, P.
    MOVEMENT DISORDERS, 2024, 39 : S750 - S750
  • [44] CSF d18:1 sphingolipid species in Parkinson disease and dementia with Lewy bodies with and without GBA1 variants
    Lerche, Stefanie
    Wurster, Isabel
    Valente, Enza Maria
    Avenali, Micol
    Samaniego, Daniela
    Martinez-Vicente, Marta
    Hernandez-Vara, Jorge
    Laguna, Ariadna
    Sturchio, Andrea
    Svenningsson, Per
    France, Nicholas P.
    Barlow, Carrolee
    Sankaranarayanan, Sethu
    Brockmann, Kathrin
    NPJ PARKINSONS DISEASE, 2024, 10 (01)
  • [45] Mild cognitive impairment among LRRK2 and GBA1 patients with Parkinson's disease
    Thaler, Avner
    Livne, Vered
    Rubinstein, Einat
    Omer, Nurit
    Faust-Socher, Achinoam
    Cohen, Batsheva
    Giladi, Nir
    Shirvan, Julia C.
    Cedarbaum, Jesse M.
    Gana-Weisz, Mali
    Goldstein, Orly
    Orr-Urtreger, Avi
    Alcalay, Roy N.
    Mirelman, Anat
    PARKINSONISM & RELATED DISORDERS, 2024, 123
  • [46] First clinicogenetic description of Parkinson's disease related to S107L GBA1 mutation
    Hertz, E.
    Thornqvist, M.
    Holmberg, B.
    Machaczka, M.
    Sidransky, E.
    Svenningsson, P.
    EUROPEAN JOURNAL OF NEUROLOGY, 2018, 25 : 192 - 192
  • [47] VALIDATION OF STRATEGIES FOR MEASURING BLOOD GLUCOCEREBROSIDASE ENZYME ACTIVITY IN PARKINSON'S DISEASE WITH GBA1 VARIANT
    Park, K. -S.
    Hwangbo, J.
    Lee, J. -H.
    PARKINSONISM & RELATED DISORDERS, 2024, 122
  • [48] A Large-Scale Full GBA1 Gene Screening in Parkinson's Disease in the Netherlands.
    den Heijer, Jonas M.
    Cullen, Valerie C.
    Quadri, Marialuisa
    Schmitz, Arnoud
    Hilt, Dana C.
    Lansbury, Peter
    Berendse, Henk W.
    van de Berg, Wilma D. J.
    de Bie, Rob M. A.
    Boertien, Jeffrey M.
    Boon, Agnita J. W.
    Contarino, M. Fiorella
    van Hilten, Jacobus J.
    Hoff, Jorrit, I
    van Mierlo, Tom
    Munts, Alex G.
    van der Plas, Anne A.
    Ponsen, Mirthe M.
    Baas, Frank
    Majoor-Krakauer, Danielle
    Bonifati, Vincenzo
    van Laar, Teus
    Groeneveld, Geert J.
    MOVEMENT DISORDERS, 2020, 35 (09) : 1667 - 1674
  • [49] Lewy pathology formation in patient-derived GBA1 Parkinson's disease midbrain organoids
    Frattini, Emanuele
    Faustini, Gaia
    Lopez, Gianluca
    Carsana, Emma Veronica
    Tosi, Mattia
    Trezzi, Ilaria
    Magni, Manuela
    Solda, Giulia
    Straniero, Letizia
    Facchi, Daniele
    Samarani, Maura
    Marta-Ariza, Mitchell
    De Luca, Chiara Maria Giulia
    Vezzoli, Elena
    Pittaro, Alessandra
    Stepanyan, Astghik
    Silipigni, Rosamaria
    Rosety, Isabel
    Schwamborn, Jens C.
    Sardi, Sergio Pablo
    Moda, Fabio
    Corti, Stefania
    Comi, Giacomo P.
    Blandini, Fabio
    Tritsch, Nicolas X.
    Bortolozzi, Mario
    Ferrero, Stefano
    Cribiu, Fulvia Milena
    Wisniewski, Thomas
    Asselta, Rosanna
    Aureli, Massimo
    Bellucci, Arianna
    Di Fonzo, Alessio
    BRAIN, 2025,
  • [50] Comorbidities in Genetic Parkinson's disease (PD): Comparison Between LRRK2, GBA1, and Non-Mutated PD
    Di Rauso, G.
    Pirone, F.
    Franco, G.
    Arienti, F.
    Trezzi, I.
    Frattini, E.
    Cavallieri, F.
    Rispoli, V.
    Valzania, F.
    Monfrini, E.
    Di Fonzo, A.
    MOVEMENT DISORDERS, 2024, 39 : S773 - S773