0
We're unable to sign you in at this time. Please try again in a few minutes.
Retry
We were able to sign you in, but your subscription(s) could not be found. Please try again in a few minutes.
Retry
There may be a problem with your account. Please contact the AMA Service Center to resolve this issue.
Contact the AMA Service Center:
Telephone: 1 (800) 262-2350 or 1 (312) 670-7827  *   Email: subscriptions@jamanetwork.com
Error Message ......
Original Contribution |

Association of Glucocerebrosidase Mutations With Dementia With Lewy Bodies FREE

Lorraine N. Clark, PhD; Lykourgos A. Kartsaklis, MD; Rebecca Wolf Gilbert, MD; Beatriz Dorado, PhD; Barbara M. Ross, BSc; Sergey Kisselev, BSc; Miguel Verbitsky, PhD; Helen Mejia-Santana, MSc; Lucien J. Cote, MD; Howard Andrews, PhD; Jean-Paul Vonsattel, MD; Stanley Fahn, MD; Richard Mayeux, MD, MSc; Lawrence S. Honig, MD, PhD; Karen Marder, MD, MPH
[+] Author Affiliations

Author Affiliations: Taub Institute for Research on Alzheimer's Disease and the Aging Brain (Drs Clark, Dorado, Verbitsky, Vonsattel, Mayeux, Honig, and Marder and Ms Ross), Department of Pathology (Drs Clark, Dorado, and Vonsattel, Ms Ross, and Mr Kisselev), Center for Human Genetics (Dr Clark), Gertrude H. Sergievsky Center (Drs Kartsaklis, Cote, Andrews, Mayeux, Honig, and Marder and Ms Mejia-Santana), Department of Neurology (Drs Wolf Gilbert, Cote, Fahn, Mayeux, Honig, and Marder), Mailman School of Public Health (Dr Mayeux), and Department of Psychiatry (Drs Mayeux and Marder), Columbia University, New York, New York.


Arch Neurol. 2009;66(5):578-583. doi:10.1001/archneurol.2009.54.
Text Size: A A A
Published online

Background  Mutations in the glucocerebrosidase (GBA) gene are associated with Lewy body (LB) disorders.

Objective  To determine the relationship of GBA mutations and APOE4 genotype to LB and Alzheimer disease (AD) pathological findings.

Design  Case-control study.

Setting  Academic research.

Participants  The 187 subjects included patients with primary neuropathological diagnoses of LB disorders with or without AD changes (95 cases), randomly selected patients with AD (without significant LB pathological findings; 60 cases), and controls with neither LB nor AD pathological findings (32 cases).

Main Outcome Measures  GBA mutation status, APOE4 genotype, LB pathological findings (assessed according to the third report of the Dementia With Lewy Body Consortium), and Alzheimer plaque and tangle pathological findings (rated by criteria of Braak and Braak, the Consortium to Establish a Registry for Alzheimer Disease, and the National Institute on Aging–Reagan Institute).

Results  GBA mutations were found in 18% (34 of 187) of all subjects, including 28% (27 of 95) of those with primary LB pathological findings compared with 10% (6 of 60) of those with AD pathological findings and 3% (1 of 32) of those without AD or LB pathological findings (P=.001). GBA mutation status was significantly associated with the presence of cortical LBs (odds ratio, 6.48; 95% confidence interval, 2.45-17.16; P<.001), after adjusting for sex, age at death, and presence of APOE4. GBA mutation carriers were significantly less likely to meet AD pathological diagnostic (National Institute on Aging–Reagan Institute intermediate or high likelihood) criteria (odds ratio, 0.35; 95% confidence interval, 0.15-0.79; P=.01) after adjustment for sex, age at death, and APOE4.

Conclusion  GBA mutations may be associated with pathologically “purer” LB disorders, characterized by more extensive (cortical) LB, and less severe AD pathological findings and may be a useful marker for LB disorders.

Lewy body (LB) disorders include Parkinson disease (PD), dementia with LBs (DLB), and LB variant of Alzheimer disease (LBV-AD). They have in common pathologically the presence of aberrant intracellular α-synuclein aggregates (LBs and Lewy neurites). Clinically, these disorders tend to have symptoms of parkinsonism and dementia.1,2 It is common for Alzheimer disease (AD) and LB disorders to overlap; both may occur in the same brain (eg, LBV-AD).

We and others have shown that mutations in the glucocerebrosidase gene (GBA; OMIM 606463) are a risk factor for PD316 and neuropathologically confirmed DLB.17,18 In the present study, we have sequenced the GBA gene and performed APOE (OMIM 107741) genotype in 187 brains without and with LB and AD pathological findings. We report the clinical and pathological characteristics of GBA mutation carriers and the relation of mutation status to pathological changes.

BRAIN MATERIAL

Brain tissue samples were obtained from the Columbia University New York Brain Bank, including samples from patients seen at the Alzheimer Disease Research Center and the Center for Parkinson Disease and Other Movement Disorders. The 187 patients included all cases with frozen brain tissue between 2001 and 2007 with primary neuropathological diagnoses of LB disorders with or without AD changes (95 cases), randomly selected cases of AD (without significant LB pathological findings; 60 cases), and controls with neither LB nor AD pathological findings (32 cases). Lewy body pathological findings were assessed according to the third report of the DLB consortium and used α-synuclein immunohistochemistry, with LBs characterized as being brainstem-predominant or “cortical” (limbic or neocortical).19 Alzheimer plaque and tangle pathological features were detected by means of hematoxylin-eosin and Bielschowsky stains and β-amyloid and AT-8 immunohistochemistry, and were rated by means of Braak and Braak, Consortium to Establish a Registry for Alzheimer Disease, and National Institute on Aging–Reagan Institute (NIA-RI) criteria.20 All cases with either Braak and Braak stage III or greater neurofibrillary pathological findings and/or plaque-based possible, probable, or definite AD by the Consortium to Establish a Registry for Alzheimer Disease criteria were rated as having “any Alzheimer pathological findings.” Neuropathological findings were described as per the National Alzheimer Coordinating Center Neuropathology Manual Version 9.1.21 Only cases that met NIA-RI criteria for intermediate or high likelihood of AD were deemed to have an “AD pathological diagnosis.” Cases with cortical LB by consortium criteria were considered DLB if they did not have a concomitant AD pathological diagnosis and LBV-AD if they did. Clinical information on dementia was available in 85 of 95 brains with primary pathological diagnoses of LB disorders, in 60 of 60 cases with AD, and in only 9 of 32 cases with neither AD nor LB pathological findings.

MOLECULAR GENETIC ANALYSIS

Frozen cerebellar tissue was used to extract DNA by means of a kit (Gentra Puregene; Qiagen, Valencia, California) following the manufacturer's instructions. All GBA exons were sequenced by means of polymerase chain reaction and sequencing primers described previously.22 Cycle sequencing in forward and reverse directions was performed on purified polymerase chain reaction products and run on a genetic analyzer (ABI 3700; Applied Biosystems, Foster City, California). Sequence chromatograms were viewed and genotypes determined by means of Sequencher (Gene Codes Corp, Ann Arbor, Michigan). APOE4 genotyping was performed by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry on the Sequenom, Inc (San Diego, California) platform as described previously.23

STATISTICAL ANALYSIS

Continuous and categorical variables were compared by t tests and χ2 tests, respectively. Logistic regression models were constructed to examine the association of GBA mutation carrier status with the presence of each pathological diagnosis adjusting for sex, age at death, and the presence of APOE4.

GBA MUTATIONS

Table 1 lists all cases with mutations, together with age at onset of cognitive or extrapyramidal motor disorder, initial clinical presentation, and pathological diagnosis. GBA mutations were found in 34 of the 187 subjects (18%). We classified mutation types in Table 1 as having null, severe, mild, or unknown phenotypic effect according to previously published studies.16,24 Overall, 5 of 34 subjects with a GBA mutation (15%) had a null or severe mutation, although none of these was homozygous. Among the 17 different GBA mutations found in 34 individuals, 14 were missense mutations, 1 was an insertion mutation, 1 was a silent mutation (synonymous substitution), and 1 was a nucleotide substitution located in the noncoding region of exon 1 (g.1444A>G; −15 of the ATG start codon). With the exception of 5 variants (g.1444 A>G, E388K, G389V, P171P, and N188R), all mutations have been reported previously.25 These 5 variants were not found in the 32 control brains reported on herein nor in an additional 179 controls described previously.10Table 2 shows basic demographic and neuropathological information on carriers and noncarriers of GBA mutations. There was no difference in age at death or duration of symptoms in the carriers compared with noncarriers. Carriers were younger at diagnosis of dementia (63.2 vs 69.1 years; P = .01). There was no difference in ethnicity between carriers and noncarriers.

Table Graphic Jump LocationTable 1. Characteristics of Autopsy Cases With Identified GBA Mutations
Table Graphic Jump LocationTable 2. Demographic and Neuropathological Characteristics of Subjects Examined at Autopsy
RELATIONSHIP OF GBA TO PATHOLOGICAL DIAGNOSES

GBA mutations were found in 28% (27 of 95) of those with primary pathological diagnoses of LB disorders, compared with 10% (6 of 60) of cases with primary AD and 3% (1 of 32) of control cases containing neither AD nor LB pathological findings (P < .001). GBA mutations were not significantly more frequent among primary AD cases than among controls. GBA mutation carriers were significantly more likely to have cortical LBs (28 of 34 [82%]) than were nonmutation carriers (66 of 153 [43%]; P < .001). Presence of a GBA mutation appeared to relate more to the presence of cortical LBs than to LBs confined to the subcortical regions, but there were only 14 cases of the latter (Table 2).

In contrast to the greater likelihood of GBA mutation carriers to have LBs, these carriers were significantly less likely to meet NIA-RI pathological criteria for AD (13 of 34 [38%]) than were GBA mutation noncarriers (96 of 153 [63%]; P = .01) (Table 2). No significant difference was seen among carriers and noncarriers of APOE4 among cases with any LB pathological findings, cortical LB pathological findings, or presence of any AD pathological changes. There were significantly more APOE4 carriers who had AD pathological findings; more APOE4 carriers met NIA-RI criteria for AD (59 of 79 [75%]) than did non–APOE4 carriers (50 of 107 [47%]; P < .001). Examining both APOE4 and GBA mutation status conjointly among the 109 cases with pathological diagnosis of AD, the least frequent category was that of persons who were GBA carriers and APOE4 noncarriers (6 of 109 [6%]; Table 3).

Table Graphic Jump LocationTable 3. Distribution of GBA and APOE4 by Pathological Diagnosis
RELATIONSHIP OF GBA MUTATION STATUS TO CORTICAL LB AND AD PATHOLOGICAL FINDINGS

In separate logistic models, GBA mutation carrier status was significantly associated with the presence of cortical LBs, not only adjusting for sex and age at death but also in models additionally including the presence of AD pathological findings, presence of APOE4, and a clinical diagnosis of dementia (Table 4). APOE4 was not independently associated with the presence of cortical LBs in any of the models. Analyses in which the dependent variable was the presence of any LB pathological finding, rather than just the presence of cortical LBs, gave similar results (because there were only 14 cases in which LB pathological findings were confined to the brainstem). As shown in Table 4, the presence of the GBA mutation was inversely associated with the presence of a pathological diagnosis of AD, even after adjustment for age at death, sex, and the presence of APOE4 (odds ratio, 0.35; 95% confidence interval, 0.15-0.79; P = .01), although APOE4 was significantly associated with AD pathological diagnosis in this model (3.97, 1.97-8.04; P < .001).

Table Graphic Jump LocationTable 4. Association of GBA Mutation With the Presence of Cortical Lewy Bodies or AD Pathological Diagnosis

We have shown that carriers of GBA mutations are significantly more likely than noncarriers to have cortical LB pathological findings. This is true when adjusting for sex, age at death, the presence of AD pathological findings, APOE4, and clinical diagnosis of dementia. The presence of a GBA mutation is not associated with AD pathological findings, whereas APOE4 is independently associated with AD diagnostic pathological findings in the same model, suggesting that GBA mutation status may be a useful clinical marker in the accurate diagnosis of LB disorders.

GBA mutations are not exclusively present in cases with LBs, even in this autopsy series of elderly persons. One case with no significant AD or LB pathological findings and 10 cases with autopsy-proved primary AD (4 of which lacked any LB pathological findings) nonetheless had GBA mutations. A previous report analyzing GBA status in a clinic-based series of 74 Ashkenazi patients with AD genotyped for only 6 mutations (N370S, L444P, 84GG, IVS+1, V394L, and R496H) found that 4% (3 of 74) carried a GBA mutation. This is not dissimilar from our observed mutation frequency of 10% (6 of 60) in cases with primary pathological diagnoses of AD; 2 of these cases had rare LBs, but 4 had complete absence of any discernible LBs. The mutations in these 6 cases were all of the mild or unknown function type.

Two previously published studies have examined GBA genotype in neuropathologically confirmed DLB cases from autopsy series.17,18 Mata et al18 examined 57 cases with DLB (54 had autopsies) and found a mutation frequency of only 3.5%, but they sequenced for only 2 GBA mutations (N370S and L444P). Goker-Alpan et al17 did perform full genotyping of GBA in 63 cases with LB pathological findings including 35 with cortical LBs (DLB or LBV-AD) and 28 with pure PD. They found an overall GBA mutation frequency of 14% (9 of 63) among the LB cases but 29% (8 of 28) among the cases with cortical LB.17 Thus, the frequency of GBA mutations of 28% that we found in a set of LB cases (of which few had pure PD pathological findings) is similar to that observed in the previous studies. Our study, which examined not only individuals with LB pathological findings but also those with AD and some with neither AD nor LB pathological findings and included genotyping for APOE, shows that GBA is a marker for cortical LB pathological findings, independent of AD pathological features, and is unrelated to APOE genotype.

We, like Goker-Alpan et al,17 observed a higher frequency of GBA mutation carriers among those with cortical LBs than among those with only brainstem LBs (pure PD), although we had proportionately few cases with pure PD. If this finding should be further confirmed, there are several possible explanations, including that GBA relates specifically to cortical LB degeneration, as differentiated from pure PD, or that GBA relates to some combination of age at onset, rapidity of disease progression, and mortality. We are currently expanding our studies to distinguish between these possibilities.

It is unclear whether specific mutations in the GBA gene are more likely to be associated with specific phenotypic responses. In the study of Goker-Alpan et al, 9 of 63 subjects with LBs (14%) carried a GBA mutation including N370S (n = 5), R120W (n = 1), A359X (n = 1), T267I (n = 1), and I161N (n = 1).17 We also found that N370S was the most frequent mutation in subjects with LBs; this mutation was found in 29% (10 of 34) of our GBA mutation carriers. We also observed additional mutations that have been previously reported in PD cases and that are reported to be pathogenic in cases of Gaucher disease.25 Five mutations identified in our study are novel. Three of these are missense mutations, 1 is a silent mutation (synonymous substitution), and 1 nucleotide substitution is located in the noncoding promoter region of exon 1. Currently, the pathogenicity of these mutations is unknown, and functional studies will be needed to determine their effects on the GBA protein. The mechanism by which GBA mutations might increase the likelihood of LB disease, such as DLB, is unclear. The mutations are nearly exclusively heterozygous and many are deemed “mild” for Gaucher disease even if homozygous, so it is unlikely but possible that gene product insufficiency might be the predisposing factor. More likely, alterations in GBA might affect lysosomal protein degradational processes, increasing the likelihood of aberrant α-synuclein processing, and LB neurodegeneration.

Correspondence: Karen Marder, MD, MPH, Columbia University, 630 W 168th St, Unit 16, New York, NY 10032 (ksm1@columbia.edu).

Accepted for Publication: August 20, 2008.

Author Contributions:Study concept and design: Clark, Kartsaklis, Mayeux, Honig, and Marder. Acquisition of data: Clark, Kartsaklis, Wolf Gilbert, Dorado, Ross, Kisselev, Verbitsky, Mejia-Santana, Cote, Andrews, Vonsattel, Fahn, and Honig. Analysis and interpretation of data: Clark, Kartsaklis, Wolf Gilbert, Dorado, Mejia-Santana, Mayeux, and Honig. Drafting of the manuscript: Clark, Kartsaklis, Wolf Gilbert, Dorado, Ross, Verbitsky, Mejia-Santana, Vonsattel, Honig, and Marder. Critical revision of the manuscript for important intellectual content: Clark, Kisselev, Cote, Andrews, Fahn, Mayeux, and Honig. Statistical analysis: Kartsaklis, Andrews, and Honig. Obtained funding: Clark, Wolf Gilbert, Cote, and Honig. Administrative, technical, and material support: Clark, Ross, Verbitsky, Andrews, Vonsattel, Honig, and Marder. Study supervision: Clark, Verbitsky, Mejia-Santana, and Mayeux. Neuropathological evaluation: Vonsattel.

Financial Disclosure: None reported.

Funding/Support: This study was supported by National Institutes of Health grants R21NS050487 (Dr Clark), R01NS36630 (Dr Marder), UL1RR024156 (Dr Marder), T32NS007155 (Dr Wolf Gilbert), R37AG15473 (Dr Mayeux), and P50AG08702 (Michael L. Shelanski, MD, PhD); the Hellenic Republic State Scholarships Foundation (Dr Kartsaklis); the Parkinson's Disease Foundation (Drs Clark and Marder); and the Henry Panasci Fund (Dr Honig).

Role of the Sponsor: None of the sponsors or funders had any role in the design and conduct of the study; in the collection, analysis, and interpretation of the data; or in the preparation, review, or approval of the manuscript.

Additional Contributions: Asa Abeliovich, MD, PhD (Columbia University) shared specimens and Arlene Lawton, RN, and Carol Moskowitz, NP, assisted with clinical information.

Dickson  DW Alpha-synuclein and the Lewy body disorders. Curr Opin Neurol 2001;14 (4) 423- 432
PubMed
Lippa  CFDuda  JEGrossman  M  et al. DLB/PDD Working Group, DLB and PDD boundary issues: diagnosis, treatment, molecular pathology, and biomarkers. Neurology 2007;68 (11) 812- 819
PubMed
Lwin  AOrvisky  EGoker-Alpan  OLaMarca  MESidransky  E Glucocerebrosidase mutations in subjects with parkinsonism. Mol Genet Metab 2004;81 (1) 70- 73
PubMed
Aharon-Peretz  JRosenbaum  HGershoni-Baruch  R Mutations in the glucocerebrosidase gene and Parkinson's disease in Ashkenazi Jews. N Engl J Med 2004;351 (19) 1972- 1977
PubMed
Clark  LNNicolai  AAfridi  S  et al.  Pilot association study of the β-glucocerebrosidase N370S allele and Parkinson's disease in subjects of Jewish ethnicity. Mov Disord 2005;20 (1) 100- 103
PubMed
Sato  CMorgan  ALang  AE  et al.  Analysis of the glucocerebrosidase gene in Parkinson's disease. Mov Disord 2005;20 (3) 367- 370
PubMed
Eblan  MJNguyen  JZiegler  SG  et al.  Glucocerebrosidase mutations are also found in subjects with early-onset parkinsonism from Venezuela. Mov Disord 2006;21 (2) 282- 283
PubMed
Toft  MPielsticker  LRoss  OAAasly  JOFarrer  MJ Glucocerebrosidase gene mutations and Parkinson disease in the Norwegian population. Neurology 2006;66 (3) 415- 417
PubMed
Bras  JPaisan-Ruiz  CGuerreiro  R  et al.  Complete screening for glucocerebrosidase mutations in Parkinson disease patients from Portugal [published online December 19, 2007]. Neurobiol Aging
PubMed10.1016/j.neurobiolaging.2007.11.016
Clark  LNRoss  BMWang  Y  et al.  Mutations in the glucocerebrosidase gene are associated with early-onset Parkinson disease. Neurology 2007;69 (12) 1270- 1277
PubMed
De Marco  EVAnnesi  GTarantino  P  et al.  Glucocerebrosidase gene mutations are associated with Parkinson's disease in southern Italy. Mov Disord 2008;23 (3) 460- 463
PubMed
Spitz  MRozenberg  Rda Veiga Pereira  LReis Barbosa  E Association between Parkinson's disease and glucocerebrosidase mutations in Brazil. Parkinsonism Relat Disord 2008;14 (1) 58- 62
PubMed
Tan  EKTong  JFook-Chong  S  et al.  Glucocerebrosidase mutations and risk of Parkinson disease in Chinese patients. Arch Neurol 2007;64 (7) 1056- 1058
PubMed
Wu  YRChen  CMChao  CY  et al.  Glucocerebrosidase gene mutation is a risk factor for early onset of Parkinson disease among Taiwanese. J Neurol Neurosurg Psychiatry 2007;78 (9) 977- 979
PubMed
Ziegler  SGEblan  MJGutti  U  et al.  Glucocerebrosidase mutations in Chinese subjects from Taiwan with sporadic Parkinson disease. Mol Genet Metab 2007;91 (2) 195- 200
PubMed
Gan-Or  ZGiladi  NRozovski  U  et al.  Genotype-phenotype correlations between GBA mutations and Parkinson disease risk and onset. Neurology 2008;70 (24) 2277- 2283
PubMed
Goker-Alpan  OGiasson  BIEblan  MJ  et al.  Glucocerebrosidase mutations are an important risk factor for Lewy body disorders. Neurology 2006;67 (5) 908- 910
PubMed
Mata  IFSamii  ASchneer  SH  et al.  Glucocerebrosidase gene mutations a risk factor for Lewy body disorders. Arch Neurol 2008;65 (3) 379- 382
PubMed
McKeith  IGDickson  DWLowe  J  et al. Consortium on DLB, Diagnosis and management of dementia with Lewy bodies: third report of the DLB Consortium. Neurology 2005;65 (12) 1863- 1872
PubMed
Mirra  SSHeyman  A McKeel  D  et al.  The Consortium to Establish a Registry for Alzheimer's Disease (CERAD), part II: standardization of the neuropathologic assessment of Alzheimer's disease. Neurology 1991;41 (4) 479- 486
PubMed
National Alzheimer's Coordinating Center, NACC Neuropathology (NP) Diagnosis Coding Guidebook.  Seattle University of Washington2005-2008;http://www.alz.washington.edu/NONMEMBER/NP/npguide9.pdf. Accessed February 5, 2009
Stone  DLTayebi  NOrvisky  EStubblefield  BMadike  VSidransky  E Glucocerebrosidase gene mutations in patients with type 2 Gaucher disease. Hum Mutat 2000;15 (2) 181- 188
PubMed
Ghebranious  NIvacic  LMallum  JDokken  C Detection of APOE E2, E3 and E4 alleles using MALDI-TOF mass spectrometry and the homogeneous mass-extend technology. Nucleic Acids Res 2005;33 (17) e149
PubMed10.1093/nar/gni155
Beutler  EGelbart  TScott  R Hematologically important mutations: Gaucher disease. Blood Cells Mol Dis 2005;35 (3) 355- 364
PubMed
Hruska  KSLaMarca  MEScott  RCSidransky  E Gaucher disease: mutation and polymorphism spectrum in the glucocerebrosidase gene. Hum Mutat 2008;29 (5) 567- 583
PubMed

Figures

Tables

Table Graphic Jump LocationTable 1. Characteristics of Autopsy Cases With Identified GBA Mutations
Table Graphic Jump LocationTable 2. Demographic and Neuropathological Characteristics of Subjects Examined at Autopsy
Table Graphic Jump LocationTable 3. Distribution of GBA and APOE4 by Pathological Diagnosis
Table Graphic Jump LocationTable 4. Association of GBA Mutation With the Presence of Cortical Lewy Bodies or AD Pathological Diagnosis

References

Dickson  DW Alpha-synuclein and the Lewy body disorders. Curr Opin Neurol 2001;14 (4) 423- 432
PubMed
Lippa  CFDuda  JEGrossman  M  et al. DLB/PDD Working Group, DLB and PDD boundary issues: diagnosis, treatment, molecular pathology, and biomarkers. Neurology 2007;68 (11) 812- 819
PubMed
Lwin  AOrvisky  EGoker-Alpan  OLaMarca  MESidransky  E Glucocerebrosidase mutations in subjects with parkinsonism. Mol Genet Metab 2004;81 (1) 70- 73
PubMed
Aharon-Peretz  JRosenbaum  HGershoni-Baruch  R Mutations in the glucocerebrosidase gene and Parkinson's disease in Ashkenazi Jews. N Engl J Med 2004;351 (19) 1972- 1977
PubMed
Clark  LNNicolai  AAfridi  S  et al.  Pilot association study of the β-glucocerebrosidase N370S allele and Parkinson's disease in subjects of Jewish ethnicity. Mov Disord 2005;20 (1) 100- 103
PubMed
Sato  CMorgan  ALang  AE  et al.  Analysis of the glucocerebrosidase gene in Parkinson's disease. Mov Disord 2005;20 (3) 367- 370
PubMed
Eblan  MJNguyen  JZiegler  SG  et al.  Glucocerebrosidase mutations are also found in subjects with early-onset parkinsonism from Venezuela. Mov Disord 2006;21 (2) 282- 283
PubMed
Toft  MPielsticker  LRoss  OAAasly  JOFarrer  MJ Glucocerebrosidase gene mutations and Parkinson disease in the Norwegian population. Neurology 2006;66 (3) 415- 417
PubMed
Bras  JPaisan-Ruiz  CGuerreiro  R  et al.  Complete screening for glucocerebrosidase mutations in Parkinson disease patients from Portugal [published online December 19, 2007]. Neurobiol Aging
PubMed10.1016/j.neurobiolaging.2007.11.016
Clark  LNRoss  BMWang  Y  et al.  Mutations in the glucocerebrosidase gene are associated with early-onset Parkinson disease. Neurology 2007;69 (12) 1270- 1277
PubMed
De Marco  EVAnnesi  GTarantino  P  et al.  Glucocerebrosidase gene mutations are associated with Parkinson's disease in southern Italy. Mov Disord 2008;23 (3) 460- 463
PubMed
Spitz  MRozenberg  Rda Veiga Pereira  LReis Barbosa  E Association between Parkinson's disease and glucocerebrosidase mutations in Brazil. Parkinsonism Relat Disord 2008;14 (1) 58- 62
PubMed
Tan  EKTong  JFook-Chong  S  et al.  Glucocerebrosidase mutations and risk of Parkinson disease in Chinese patients. Arch Neurol 2007;64 (7) 1056- 1058
PubMed
Wu  YRChen  CMChao  CY  et al.  Glucocerebrosidase gene mutation is a risk factor for early onset of Parkinson disease among Taiwanese. J Neurol Neurosurg Psychiatry 2007;78 (9) 977- 979
PubMed
Ziegler  SGEblan  MJGutti  U  et al.  Glucocerebrosidase mutations in Chinese subjects from Taiwan with sporadic Parkinson disease. Mol Genet Metab 2007;91 (2) 195- 200
PubMed
Gan-Or  ZGiladi  NRozovski  U  et al.  Genotype-phenotype correlations between GBA mutations and Parkinson disease risk and onset. Neurology 2008;70 (24) 2277- 2283
PubMed
Goker-Alpan  OGiasson  BIEblan  MJ  et al.  Glucocerebrosidase mutations are an important risk factor for Lewy body disorders. Neurology 2006;67 (5) 908- 910
PubMed
Mata  IFSamii  ASchneer  SH  et al.  Glucocerebrosidase gene mutations a risk factor for Lewy body disorders. Arch Neurol 2008;65 (3) 379- 382
PubMed
McKeith  IGDickson  DWLowe  J  et al. Consortium on DLB, Diagnosis and management of dementia with Lewy bodies: third report of the DLB Consortium. Neurology 2005;65 (12) 1863- 1872
PubMed
Mirra  SSHeyman  A McKeel  D  et al.  The Consortium to Establish a Registry for Alzheimer's Disease (CERAD), part II: standardization of the neuropathologic assessment of Alzheimer's disease. Neurology 1991;41 (4) 479- 486
PubMed
National Alzheimer's Coordinating Center, NACC Neuropathology (NP) Diagnosis Coding Guidebook.  Seattle University of Washington2005-2008;http://www.alz.washington.edu/NONMEMBER/NP/npguide9.pdf. Accessed February 5, 2009
Stone  DLTayebi  NOrvisky  EStubblefield  BMadike  VSidransky  E Glucocerebrosidase gene mutations in patients with type 2 Gaucher disease. Hum Mutat 2000;15 (2) 181- 188
PubMed
Ghebranious  NIvacic  LMallum  JDokken  C Detection of APOE E2, E3 and E4 alleles using MALDI-TOF mass spectrometry and the homogeneous mass-extend technology. Nucleic Acids Res 2005;33 (17) e149
PubMed10.1093/nar/gni155
Beutler  EGelbart  TScott  R Hematologically important mutations: Gaucher disease. Blood Cells Mol Dis 2005;35 (3) 355- 364
PubMed
Hruska  KSLaMarca  MEScott  RCSidransky  E Gaucher disease: mutation and polymorphism spectrum in the glucocerebrosidase gene. Hum Mutat 2008;29 (5) 567- 583
PubMed

Correspondence

CME
Also Meets CME requirements for:
Browse CME for all U.S. States
Accreditation Information
The American Medical Association is accredited by the Accreditation Council for Continuing Medical Education to provide continuing medical education for physicians. The AMA designates this journal-based CME activity for a maximum of 1 AMA PRA Category 1 CreditTM per course. Physicians should claim only the credit commensurate with the extent of their participation in the activity. Physicians who complete the CME course and score at least 80% correct on the quiz are eligible for AMA PRA Category 1 CreditTM.
Note: You must get at least of the answers correct to pass this quiz.
Please click the checkbox indicating that you have read the full article in order to submit your answers.
Your answers have been saved for later.
You have not filled in all the answers to complete this quiz
The following questions were not answered:
Sorry, you have unsuccessfully completed this CME quiz with a score of
The following questions were not answered correctly:
Commitment to Change (optional):
Indicate what change(s) you will implement in your practice, if any, based on this CME course.
Your quiz results:
The filled radio buttons indicate your responses. The preferred responses are highlighted
For CME Course: A Proposed Model for Initial Assessment and Management of Acute Heart Failure Syndromes
Indicate what changes(s) you will implement in your practice, if any, based on this CME course.
Submit a Comment

Multimedia

Some tools below are only available to our subscribers or users with an online account.

Web of Science® Times Cited: 61

Related Content

Customize your page view by dragging & repositioning the boxes below.

See Also...
Articles Related By Topic
Related Collections
PubMed Articles