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Gene overview of all published PD-association studies for BDNF
Gene:
BDNF
(MGC34632)
View on AlzGene
View on MSGene
View on SZGene
Protein:
brain-derived neurotrophic factor
(neurotrophin)
Chromosome:
11
(View:
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
21
22
X
Y
MT
)
Status:
Updated 27 November 2011
1. Case-Control Studies (by ethnic group)
PD Cases
Normal Controls
Study
Population
Source
# Polys
# Subjects
(% women)
DX
Onset Age
(range)
Age
(range)
# Subjects
(% women)
Age
(range)
Result
Caucasian
Cramer, 2009
USA
CL
1
(detail)
53
(36%)
C
-
65 + 10
(-)
54
(-)
55 + 15
(-)
Negative
Fung, 2006
Overlaps with
Simon-Sanchez, 2009 (USA)
CL
4
(detail)
267
(-)
C
-
-
270
(-)
68
(55-88)
n.a.
Gao, 2010
Spain
CL
1
(detail)
193
(42%)
-
56.9 + 12
(-)
66.1 + 10.4
(-)
300
(38%)
61.7 + 12.2
(-)
Negative
Guerini, 2009
Italy
CL
1
(detail)
294
(46%)
C
61.2
(-)
69.5
(33-86)
233
(66%)
61.5
(26-86)
Positive
Hakansson, 2003
Sweden
CL
1
(detail)
257
(-)
C
60
(-)
-
307
(-)
-
Negative
Karakasis, 2011
Greece
CL
1
(detail)
184
(-)
C
-
63.9 + 0.7
(-)
113
(-)
71.6 + 0.5
(-)
Negative
Karamohamed, 2005
Overlaps with
Parsian, 2004
CL
5
(detail)
597
(-)
C
-
-
130
(-)
-
Positive
Liu, 2005
USA
CL
3
(detail)
600
(-)
C
-
-
280
(-)
-
n.a.
Pankratz, 2008
USA (PROGENI, GenePD)
CL
9
(detail)
857
(41%)
C
61.9 + 10.8
(-)
-
867
(60%)
54.8 + 13.1
(-)
Negative
Parsian, 2004
USA
CL
2
(detail)
358
(35%)
C
60
(21-85)
67.6
(-)
195
(35%)
62 + 14
(-)
Positive
Saarela, 2006
Finland
CL
2
(detail)
52
(52%)
M
76.2 + 6
(-)
-
101
(55%)
79 + 9.3
(-)
Negative
Simon-Sanchez, 2009
USA, Germany (GWAS)
CL,PO
2
(detail)
1745
(45%)
C
55.8
(7-98)
-
4047
(50%)
-
Negative
Simon-Sanchez, 2009
USA (NINDS-GWAS)
CL
7
(detail)
931
(40%)
C
-
-
790
(58%)
-
Negative
Xiromerisiou, 2007
Greece
CL
8
(detail)
242
(41%)
C
63.3 + 9.6
(-)
69.8 + 8.7
(-)
203
(46%)
68.3 + 12.8
(-)
Negative
Xiromerisiou, 2007
Overlaps with
Simon-Sanchez, 2009 (USA)
CL
8
(detail)
271
(46%)
C
55 + 15.1
(-)
63 + 13.3
(-)
231
(44%)
68.7 + 15.2
(-)
n.a.
Xiromerisiou, 2007
Finland
CL
8
(detail)
145
(41%)
C
61.1 + 8.5
(-)
66.8 + 8.6
(-)
133
(36%)
66.6 + 9.1
(-)
Negative
Asian
Chen, 2007
Taiwan
CL
1
(detail)
356
(46%)
C
63.5 + 9.2
(41-84)
69.2 + 9.1
(-)
325
(48%)
62.6 + 10.4
(40-94)
Negative
Chen, 2011
China
CL
4
(detail)
266
(35%)
C
-
65 + 10.5
(-)
400
(59%)
64.5 + 5.7
(-)
Positive
Hong, 2003
Taiwan
CL
1
(detail)
107
(28%)
C
64 + 11.4
(-)
68.2 + 10.4
(-)
103
(33%)
66.3 + 14.2
(-)
Negative
Lin, 2010
Taiwan
CL
1
(detail)
453
(43%)
C
-
57.9 + 11.7
(-)
291
(56%)
59.2 + 14.6
(-)
Positive
Masaki, 2003
Japan
CL
1
(detail)
291
(-)
C
-
65.7 + 8.9
(-)
291
(-)
65.6 + 9.2
(-)
Positive
Mizuta, 2006
Overlaps with
Momose, 2002
CL
1
(detail)
190
(-)
C
-
-
190
(-)
-
n.a.
Momose, 2002
Japan
CL
1
(detail)
232
(51%)
C
54.1 + 10.5
(24-80)
-
249
(49%)
-
Positive
Nishimura, 2005
Japan
CL
2
(detail)
327
(61%)
C
-
66.4 + 9.9
(35-88)
275
(61%)
68.4 + 10.5
(35-92)
Negative
Toda, 2003
Overlaps with
Momose, 2002
CL
1
(detail)
232
(51%)
C
54.1 + 10.5
(24-80)
-
249
(49%)
-
n.a.
Other/Mixed
Benitez, 2010
Colombia
CL
1
(detail)
104
(49%)
C
53.7 + 13.4
(-)
60.1 + 12.6
(-)
136
(54%)
62.4 + 9.5
(-)
Negative
Contact us
if you are an author of an association study regarding this gene and do not find your study in this table or find errors in the representation of your study details.
2. Family-Based Studies (by ethnic group)
Affecteds
Unaffecteds
Study
Population
# Polys
# Families
# Subjects
(% women)
DX
Onset Age
(range)
Age
(range)
# Subjects
(% women)
Age
(range)
Result
Caucasian
Liu, 2005
Overlaps with
Liu, 2005 (CC)
3
(detail)
600
(-)
C
-
-
320
(-)
-
Negative
Maraganore, 2005
USA
1
(detail)
443
443
(39%)
C
61
(31-94)
68
(33-96)
443
(52%)
66
(29-90)
Negative
Contact us
if you are an author of an association study regarding this gene and do not find your study in this table or find errors in the representation of your study details.
Source:
Source of case population -> “CL” (clinic-based), “PO” (population-based), or “CO” (community-based).
# Polys:
Number of polymorphisms tested per gene and per sample.
Onset Age and Age:
Mean or median age at onset or examination, respectively.
DX:
Criteria used to determine PD diagnosis -> "C" (clinical PD diagnosis), "N" (neuropathological PD diagnosis), "M" (mixed, i.e. PD sample contains both clinical and neuropathological cases), "U" (unknown).
Result:
Overall conclusion reached by authors of the original publication (“positive” usually indicates significant (P<0.05) association in at least one of the performed analyses, and “negative” indicates no evidence for significant association, while “trend” indicates results in between).
(-)
: Either no data provided or in case of overlap, data included in original study.
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Studies: 881
Genes: 915
Polymorphisms: 3446
Meta-analyses: 889
GEO-PD Meeting 2012
PDmutDB
Curated by the VIB Department of Molecular Genetics of the University of Antwerp
Parkinson's disease Mutation Database
Curated by Parkinson's Institute from Leiden University Medical Center
Mutation Database for Parkinson's Disease
Curated by the Institute for Infocomm Research in Singapore
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is supported by a grant from
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An up-to-date collection of all published genetic association studies.
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