Literature DB >> 27521182

LRRK2 variation and dementia with Lewy bodies.

Michael G Heckman1, Alexandra I Soto-Ortolaza2,3, Monica Y Sanchez Contreras2, Melissa E Murray2, Otto Pedraza4, Nancy N Diehl1, Ronald Walton2, Catherine Labbé2, Oswaldo Lorenzo-Betancor2, Ryan J Uitti5, Jay van Gerpen5, Nilüfer Ertekin-Taner5, Glenn E Smith6, Kejal Kantarci7, Rodolfo Savica8, David T Jones8, Jonathan Graff-Radford8, David S Knopman8, Val J Lowe7, Clifford R Jack7, Ronald C Petersen8, Joseph E Parisi8,9, Rosa Rademakers2, Zbigniew K Wszolek5, Neill R Graff-Radford5, Tanis J Ferman4, Dennis W Dickson2, Bradley F Boeve8, Owen A Ross2,3,10,11.   

Abstract

INTRODUCTION: The leucine-rich repeat kinase 2 (LRRK2) gene contains several variants that cause Parkinson's disease (PD) and others that modify PD risk. However, little is known about the role of LRRK2 in dementia with Lewy bodies (DLB). Aims of this study were to screen DLB patients for pathogenic LRRK2 variants and to evaluate associations between common LRRK2 variants and risk of DLB.
METHODS: 417 clinical DLB patients and 1790 controls were included in the primary analysis. Additionally, 355 Lewy body disease patients assessed as having a high likelihood of clinical DLB based on neuropathological findings were included in secondary analysis. Seven pathogenic LRRK2 variants were assessed in patients, while 17 common LRRK2 exonic variants and 1 GWAS-nominated common LRRK2 PD-risk variant were evaluated for association with DLB.
RESULTS: We identified carriers of 2 different pathogenic LRRK2 variants. One clinical DLB patient was a p.G2019S carrier, while in the pathological high likelihood DLB series there was one carrier of the p.R1441C mutation. However, examination of clinical records revealed the p.R1441C carrier to have PD with dementia. Evaluation of common variants did not reveal any associations with DLB risk after multiple testing adjustment. However, a non-significant trend similar to that previously reported for PD was observed for the protective p.N551K-R1398H-K1423K haplotype in the clinical DLB series (OR: 0.76, P = 0.061).
CONCLUSION: LRRK2 does not appear to play a major role in DLB, however further study of p.G2019S and the p.N551K-R1398H-K1423K haplotype is warranted to better understand their involvement in determining DLB risk.
Copyright © 2016 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Dementia with Lewy bodies; Genetics; LRRK2; Parkinson's disease

Mesh:

Substances:

Year:  2016        PMID: 27521182      PMCID: PMC5048558          DOI: 10.1016/j.parkreldis.2016.07.015

Source DB:  PubMed          Journal:  Parkinsonism Relat Disord        ISSN: 1353-8020            Impact factor:   4.891


  30 in total

1.  LRRK2 mutations on Crete: R1441H associated with PD evolving to PSP.

Authors:  Cleanthe Spanaki; Helen Latsoudis; Andreas Plaitakis
Journal:  Neurology       Date:  2006-10-24       Impact factor: 9.910

2.  Lrrk2 and Lewy body disease.

Authors:  Owen A Ross; Mathias Toft; Andrew J Whittle; Joseph L Johnson; Spiridon Papapetropoulos; Deborah C Mash; Irene Litvan; Mark F Gordon; Zbigniew K Wszolek; Matthew J Farrer; Dennis W Dickson
Journal:  Ann Neurol       Date:  2006-02       Impact factor: 10.422

3.  Validation of the neuropathologic criteria of the third consortium for dementia with Lewy bodies for prospectively diagnosed cases.

Authors:  Hiroshige Fujishiro; Tanis J Ferman; Bradley F Boeve; Glenn E Smith; Neill R Graff-Radford; Ryan J Uitti; Zbigniew K Wszolek; David S Knopman; Ronald C Petersen; Joseph E Parisi; Dennis W Dickson
Journal:  J Neuropathol Exp Neurol       Date:  2008-07       Impact factor: 3.685

4.  Lrrk2 G2019S substitution in frontotemporal lobar degeneration with ubiquitin-immunoreactive neuronal inclusions.

Authors:  Justus C Dächsel; Owen A Ross; Ignacio F Mata; Jennifer Kachergus; Mathias Toft; Ashley Cannon; Matt Baker; Jennifer Adamson; Mike Hutton; Dennis W Dickson; Matthew J Farrer
Journal:  Acta Neuropathol       Date:  2006-12-07       Impact factor: 17.088

5.  Screening for the LRRK2 G2019S and codon-1441 mutations in a pathological series of parkinsonian syndromes and frontotemporal lobar degeneration.

Authors:  Carles Gaig; Mario Ezquerra; Maria José Martí; Francesc Valldeoriola; Esteban Muñoz; Albert Lladó; Maria Jesús Rey; Adriana Cardozo; José Luis Molinuevo; Eduardo Tolosa
Journal:  J Neurol Sci       Date:  2008-03-19       Impact factor: 3.181

6.  Corticobasal syndrome and primary progressive aphasia as manifestations of LRRK2 gene mutations.

Authors:  A S Chen-Plotkin; W Yuan; C Anderson; E McCarty Wood; H I Hurtig; C M Clark; B L Miller; V M-Y Lee; J Q Trojanowski; M Grossman; V M Van Deerlin
Journal:  Neurology       Date:  2007-10-03       Impact factor: 9.910

7.  Early-onset familial lewy body dementia with extensive tauopathy: a clinical, genetic, and neuropathological study.

Authors:  Jordi Clarimón; Laura Molina-Porcel; Teresa Gómez-Isla; Rafael Blesa; Cristina Guardia-Laguarta; Anna González-Neira; Montserrat Estorch; Josep Ma Grau; Lluís Barraquer; Carles Roig; Isidre Ferrer; Alberto Lleó
Journal:  J Neuropathol Exp Neurol       Date:  2009-01       Impact factor: 3.685

8.  APOE ε4 increases risk for dementia in pure synucleinopathies.

Authors:  Debby Tsuang; James B Leverenz; Oscar L Lopez; Ronald L Hamilton; David A Bennett; Julie A Schneider; Aron S Buchman; Eric B Larson; Paul K Crane; Jeffrey A Kaye; Patricia Kramer; Randy Woltjer; John Q Trojanowski; Daniel Weintraub; Alice S Chen-Plotkin; David J Irwin; Jacqueline Rick; Gerard D Schellenberg; G Stennis Watson; Walter Kukull; Peter T Nelson; Gregory A Jicha; Janna H Neltner; Doug Galasko; Eliezer Masliah; Joseph F Quinn; Kathryn A Chung; Dora Yearout; Ignacio F Mata; Jia Y Wan; Karen L Edwards; Thomas J Montine; Cyrus P Zabetian
Journal:  JAMA Neurol       Date:  2013-02       Impact factor: 18.302

9.  Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease.

Authors:  Mike A Nalls; Nathan Pankratz; Christina M Lill; Chuong B Do; Dena G Hernandez; Mohamad Saad; Anita L DeStefano; Eleanna Kara; Jose Bras; Manu Sharma; Claudia Schulte; Margaux F Keller; Sampath Arepalli; Christopher Letson; Connor Edsall; Hreinn Stefansson; Xinmin Liu; Hannah Pliner; Joseph H Lee; Rong Cheng; M Arfan Ikram; John P A Ioannidis; Georgios M Hadjigeorgiou; Joshua C Bis; Maria Martinez; Joel S Perlmutter; Alison Goate; Karen Marder; Brian Fiske; Margaret Sutherland; Georgia Xiromerisiou; Richard H Myers; Lorraine N Clark; Kari Stefansson; John A Hardy; Peter Heutink; Honglei Chen; Nicholas W Wood; Henry Houlden; Haydeh Payami; Alexis Brice; William K Scott; Thomas Gasser; Lars Bertram; Nicholas Eriksson; Tatiana Foroud; Andrew B Singleton
Journal:  Nat Genet       Date:  2014-07-27       Impact factor: 38.330

10.  Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodies.

Authors:  Jose Bras; Rita Guerreiro; Lee Darwent; Laura Parkkinen; Olaf Ansorge; Valentina Escott-Price; Dena G Hernandez; Michael A Nalls; Lorraine N Clark; Lawrence S Honig; Karen Marder; Wiesje M Van Der Flier; Afina Lemstra; Philip Scheltens; Ekaterina Rogaeva; Peter St George-Hyslop; Elisabet Londos; Henrik Zetterberg; Sara Ortega-Cubero; Pau Pastor; Tanis J Ferman; Neill R Graff-Radford; Owen A Ross; Imelda Barber; Anne Braae; Kristelle Brown; Kevin Morgan; Walter Maetzler; Daniela Berg; Claire Troakes; Safa Al-Sarraj; Tammaryn Lashley; Yaroslau Compta; Tamas Revesz; Andrew Lees; Nigel Cairns; Glenda M Halliday; David Mann; Stuart Pickering-Brown; Dennis W Dickson; Andrew Singleton; John Hardy
Journal:  Hum Mol Genet       Date:  2014-06-27       Impact factor: 6.150

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  11 in total

1.  Multiple variants in families with amyotrophic lateral sclerosis and frontotemporal dementia related to C9orf72 repeat expansion: further observations on their oligogenic nature.

Authors:  Maria Pia Giannoccaro; Anna Bartoletti-Stella; Silvia Piras; Annalisa Pession; Patrizia De Massis; Federico Oppi; Michelangelo Stanzani-Maserati; Elena Pasini; Simone Baiardi; Patrizia Avoni; Piero Parchi; Rocco Liguori; Sabina Capellari
Journal:  J Neurol       Date:  2017-06-15       Impact factor: 4.849

Review 2.  Neuropathology of genetic synucleinopathies with parkinsonism: Review of the literature.

Authors:  Susanne A Schneider; Roy N Alcalay
Journal:  Mov Disord       Date:  2017-11       Impact factor: 10.338

Review 3.  Dementia with Lewy bodies and Parkinson's disease-dementia: current concepts and controversies.

Authors:  Kurt A Jellinger
Journal:  J Neural Transm (Vienna)       Date:  2017-12-08       Impact factor: 3.575

4.  GTP-binding inhibitors increase LRRK2-linked ubiquitination and Lewy body-like inclusions.

Authors:  Joseph M Thomas; Xiaobo Wang; Gongbo Guo; Tianxia Li; Bingling Dai; Leslie G Nucifora; Frederick C Nucifora; Zhaohui Liu; Fengtian Xue; Chunfeng Liu; Christopher A Ross; Wanli W Smith
Journal:  J Cell Physiol       Date:  2020-03-17       Impact factor: 6.384

5.  Case-control analysis of LRRK2 protective variants in Essential Tremor.

Authors:  Adeline S L Ng; Ebonne Y L Ng; Yi Jayne Tan; Kumar M Prakash; Wing Lok Au; Louis C S Tan; Eng-King Tan
Journal:  Sci Rep       Date:  2018-03-28       Impact factor: 4.379

Review 6.  The Genetics of Dementia with Lewy Bodies: Current Understanding and Future Directions.

Authors:  Tatiana Orme; Rita Guerreiro; Jose Bras
Journal:  Curr Neurol Neurosci Rep       Date:  2018-08-10       Impact factor: 5.081

7.  Role of LRRK2 variant p.Gly2019Ser in patients with Parkinsonism.

Authors:  Dipanwita Sadhukhan; Arindam Biswas; Arunima Bhaduri; Neelanjana Sarkar; Atanu Biswas; Shyamal K Das; Tapas K Banerjee; Kunal Ray; Jharna Ray
Journal:  Indian J Med Res       Date:  2020-06       Impact factor: 2.375

8.  Association between CSF alpha-synuclein seeding activity and genetic status in Parkinson's disease and dementia with Lewy bodies.

Authors:  Kathrin Brockmann; Corinne Quadalti; Stefanie Lerche; Marcello Rossi; Isabel Wurster; Simone Baiardi; Benjamin Roeben; Angela Mammana; Milan Zimmermann; Ann-Kathrin Hauser; Christian Deuschle; Claudia Schulte; Katharina Waniek; Ingolf Lachmann; Simon Sjödin; Ann Brinkmalm; Kaj Blennow; Henrik Zetterberg; Thomas Gasser; Piero Parchi
Journal:  Acta Neuropathol Commun       Date:  2021-10-30       Impact factor: 7.801

Review 9.  Dementia with Lewy bodies: an update and outlook.

Authors:  Tiago Fleming Outeiro; David J Koss; Daniel Erskine; Lauren Walker; Marzena Kurzawa-Akanbi; David Burn; Paul Donaghy; Christopher Morris; John-Paul Taylor; Alan Thomas; Johannes Attems; Ian McKeith
Journal:  Mol Neurodegener       Date:  2019-01-21       Impact factor: 14.195

10.  Novel Associations of BST1 and LAMP3 With REM Sleep Behavior Disorder.

Authors:  Kheireddin Mufti; Eric Yu; Uladzislau Rudakou; Lynne Krohn; Jennifer A Ruskey; Farnaz Asayesh; Sandra B Laurent; Dan Spiegelman; Isabelle Arnulf; Michele T M Hu; Jacques Y Montplaisir; Jean-François Gagnon; Alex Desautels; Yves Dauvilliers; Gian Luigi Gigli; Mariarosaria Valente; Francesco Janes; Andrea Bernardini; Birgit Högl; Ambra Stefani; Evi Holzknecht; Karel Sonka; David Kemlink; Wolfgang Oertel; Annette Janzen; Giuseppe Plazzi; Elena Antelmi; Michela Figorilli; Monica Puligheddu; Brit Mollenhauer; Claudia Trenkwalder; Friederike Sixel-Döring; Valérie Cochen De Cock; Christelle Charley Monaca; Anna Heidbreder; Luigi Ferini-Strambi; Femke Dijkstra; Mineke Viaene; Beatriz Abril; Bradley F Boeve; Jean-François Trempe; Guy A Rouleau; Ronald B Postuma; Ziv Gan-Or
Journal:  Neurology       Date:  2021-01-04       Impact factor: 9.910

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