Literature DB >> 22194196

Clinical and pathological characteristics of LRRK2 G2019S patients with PD.

Markos Poulopoulos1, Etty Cortes, Jean-Paul G Vonsattel, Stanley Fahn, Cheryl Waters, Lucien J Cote, Carol Moskowitz, Lawrence S Honig, Lorraine N Clark, Karen S Marder, Roy N Alcalay.   

Abstract

The objective of this study is to describe the neuropathologic findings in three LRRK2 G2019S carriers with Parkinson's disease (PD). We cross-referenced a list of 956 PD individuals that had been previously genotyped in clinical studies at Columbia University, with 282 subjects with a parkinsonian syndrome who came to autopsy in our brain bank since 1991. We found three autopsies of G2019S mutation carriers. Pathological analyses of the samples were blind to the genetic findings. We retrospectively reviewed the clinical records of the three patients. All three had a clinical and pathological diagnosis of PD. Cognitive impairment was a late feature in two out of three patients. Cortical involvement varied significantly: one had diffuse Lewy body (LB) pathology, tau inclusions, and amyloid pathology consistent with advanced Alzheimer's disease; one had diffuse cortical LB; and one had only brainstem predominant LB pathology. Cognitive impairment may be a long-term complication in G2019S mutation carriers. However, the extent of cortical involvement is variable. Larger longitudinal follow-up of LRRK2 G2019S mutation carriers is required to assess for risk factors for cortical involvement and dementia.

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Year:  2011        PMID: 22194196      PMCID: PMC3335886          DOI: 10.1007/s12031-011-9696-y

Source DB:  PubMed          Journal:  J Mol Neurosci        ISSN: 0895-8696            Impact factor:   3.444


  23 in total

1.  Involvement of the cerebral cortex in Parkinson disease linked with G2019S LRRK2 mutation without cognitive impairment.

Authors:  Anna Gomez; Isidre Ferrer
Journal:  Acta Neuropathol       Date:  2010-03-16       Impact factor: 17.088

2.  Hyposmia in G2019S LRRK2-related parkinsonism: clinical and pathologic data.

Authors:  L Silveira-Moriyama; L C Guedes; A Kingsbury; H Ayling; K Shaw; E R Barbosa; V Bonifati; N P Quinn; P Abou-Sleiman; N W Wood; A Petrie; C Sampaio; J J Ferreira; J Holton; T Revesz; A J Lees
Journal:  Neurology       Date:  2008-09-23       Impact factor: 9.910

3.  G2019S LRRK2 mutation causing Parkinson's disease without Lewy bodies.

Authors:  Carles Gaig; María José Martí; Mario Ezquerra; Maria Jesús Rey; Adriana Cardozo; Eduardo Tolosa
Journal:  J Neurol Neurosurg Psychiatry       Date:  2007-01-08       Impact factor: 10.154

4.  Parkinsonism, Lrrk2 G2019S, and tau neuropathology.

Authors:  A Rajput; D W Dickson; C A Robinson; O A Ross; J C Dächsel; S J Lincoln; S A Cobb; M L Rajput; M J Farrer
Journal:  Neurology       Date:  2006-10-24       Impact factor: 9.910

5.  Predictors of parkin mutations in early-onset Parkinson disease: the consortium on risk for early-onset Parkinson disease study.

Authors:  Karen S Marder; Ming X Tang; Helen Mejia-Santana; Llency Rosado; Elan D Louis; Cynthia L Comella; Amy Colcher; Andrew D Siderowf; Danna Jennings; Martha A Nance; Susan Bressman; William K Scott; Caroline M Tanner; Susan F Mickel; Howard F Andrews; Cheryl Waters; Stanley Fahn; Barbara M Ross; Lucien J Cote; Steven Frucht; Blair Ford; Roy N Alcalay; Michael Rezak; Kevin Novak; Joseph H Friedman; Ronald F Pfeiffer; Laura Marsh; Brad Hiner; Gregory D Neils; Miguel Verbitsky; Sergey Kisselev; Elise Caccappolo; Ruth Ottman; Lorraine N Clark
Journal:  Arch Neurol       Date:  2010-06

6.  Leucine-rich repeat kinase 2 gene-associated disease: redefining genotype-phenotype correlation.

Authors:  Christian Wider; Dennis W Dickson; Zbigniew K Wszolek
Journal:  Neurodegener Dis       Date:  2010-03-03       Impact factor: 2.977

7.  G2019S mutation in the leucine-rich repeat kinase 2 gene is not associated with multiple system atrophy.

Authors:  Laurie J Ozelius; Tatiana Foroud; Susanne May; Geetha Senthil; Paola Sandroni; Phillip A Low; Stephen Reich; Amy Colcher; Matthew B Stern; William G Ondo; Joseph Jankovic; Neng Huang; Caroline M Tanner; Peter Novak; Sid Gilman; Frederick J Marshall; G Frederick Wooten; Thomas C Chelimsky; Clifford W Shults
Journal:  Mov Disord       Date:  2007-03-15       Impact factor: 10.338

8.  Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study.

Authors:  Daniel G Healy; Mario Falchi; Sean S O'Sullivan; Vincenzo Bonifati; Alexandra Durr; Susan Bressman; Alexis Brice; Jan Aasly; Cyrus P Zabetian; Stefano Goldwurm; Joaquim J Ferreira; Eduardo Tolosa; Denise M Kay; Christine Klein; David R Williams; Connie Marras; Anthony E Lang; Zbigniew K Wszolek; Jose Berciano; Anthony H V Schapira; Timothy Lynch; Kailash P Bhatia; Thomas Gasser; Andrew J Lees; Nicholas W Wood
Journal:  Lancet Neurol       Date:  2008-06-06       Impact factor: 44.182

9.  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

10.  The Sydney multicenter study of Parkinson's disease: the inevitability of dementia at 20 years.

Authors:  Mariese A Hely; Wayne G J Reid; Michael A Adena; Glenda M Halliday; John G L Morris
Journal:  Mov Disord       Date:  2008-04-30       Impact factor: 10.338

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  25 in total

1.  Neuropsychological performance in LRRK2 G2019S carriers with Parkinson's disease.

Authors:  Roy N Alcalay; Helen Mejia-Santana; Anat Mirelman; Rachel Saunders-Pullman; Deborah Raymond; Christina Palmese; Elise Caccappolo; Laurie Ozelius; Avi Orr-Urtreger; Lorraine Clark; Nir Giladi; Susan Bressman; Karen Marder
Journal:  Parkinsonism Relat Disord       Date:  2014-11-20       Impact factor: 4.891

Review 2.  LRRK2, a puzzling protein: insights into Parkinson's disease pathogenesis.

Authors:  A Raquel Esteves; Russell H Swerdlow; Sandra M Cardoso
Journal:  Exp Neurol       Date:  2014-06-04       Impact factor: 5.330

Review 3.  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 4.  Role of protein kinase A in regulating mitochondrial function and neuronal development: implications to neurodegenerative diseases.

Authors:  Ruben K Dagda; Tania Das Banerjee
Journal:  Rev Neurosci       Date:  2015       Impact factor: 4.353

Review 5.  The neuropathology of genetic Parkinson's disease.

Authors:  Markos Poulopoulos; Oren A Levy; Roy N Alcalay
Journal:  Mov Disord       Date:  2012-03-26       Impact factor: 10.338

Review 6.  LRRK2 links genetic and sporadic Parkinson's disease.

Authors:  Jillian H Kluss; Adamantios Mamais; Mark R Cookson
Journal:  Biochem Soc Trans       Date:  2019-03-05       Impact factor: 5.407

Review 7.  α-Synuclein oligomers and clinical implications for Parkinson disease.

Authors:  Lorraine V Kalia; Suneil K Kalia; Pamela J McLean; Andres M Lozano; Anthony E Lang
Journal:  Ann Neurol       Date:  2012-12-07       Impact factor: 10.422

Review 8.  Parkinson's disease.

Authors:  Timothy R Mhyre; James T Boyd; Robert W Hamill; Kathleen A Maguire-Zeiss
Journal:  Subcell Biochem       Date:  2012

9.  Cognitive and motor function in long-duration PARKIN-associated Parkinson disease.

Authors:  Roy N Alcalay; Elise Caccappolo; Helen Mejia-Santana; Ming Xin Tang; Llency Rosado; Martha Orbe Reilly; Diana Ruiz; Elan D Louis; Cynthia L Comella; Martha A Nance; Susan B Bressman; William K Scott; Caroline M Tanner; Susan F Mickel; Cheryl H Waters; Stanley Fahn; Lucien J Cote; Steven J Frucht; Blair Ford; Michael Rezak; Kevin E Novak; Joseph H Friedman; Ronald F Pfeiffer; Laura Marsh; Bradley Hiner; Haydeh Payami; Eric Molho; Stewart A Factor; John G Nutt; Carmen Serrano; Maritza Arroyo; Ruth Ottman; Michael W Pauciulo; William C Nichols; Lorraine N Clark; Karen S Marder
Journal:  JAMA Neurol       Date:  2014-01       Impact factor: 18.302

10.  REM sleep behavior disorder, as assessed by questionnaire, in G2019S LRRK2 mutation PD and carriers.

Authors:  Rachel Saunders-Pullman; Roy N Alcalay; Anat Mirelman; Cuiling Wang; Marta San Luciano; Roberto A Ortega; Amanda Glickman; Deborah Raymond; Helen Mejia-Santana; Nancy Doan; Brooke Johannes; Kira Yasinovsky; Laurie Ozelius; Lorraine Clark; Avi Orr-Utreger; Karen Marder; Nir Giladi; Susan B Bressman
Journal:  Mov Disord       Date:  2015-09-14       Impact factor: 10.338

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