AlzGene - Gene overview of all published AD-association studies for LDLR
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 Gene: LDLR  (FH; FHC)  Entrez Gene    View on ALSGene
 Protein: low density lipoprotein receptor   ProteinLink
 Chromosome: 19   (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 18 April 2011
Meta-Analysis
1. Case-Control Studies (by ethnic group)
      AD Cases Normal Controls    
Study Population Source # Polys # Subjects
(% women)
DX Onset Age
(range)
Age
(range)
# Subjects
(% women)
Age
(range)
Result Comment
 Caucasian
Cheng, 2005
USA CL  2  (detail)  180
(71%)
C70.8 + 8.1
(50-92)
-141
(59%)
72.3 + 8.4
(51-89)
Positive
Corder, 2006
Overlaps with
Cheng, 2005
CL  2  (detail)  ------n.a.
Giedraitis, 2009
Sweden (ULSAM) CL  4  (detail)  86
(0%)
C80.2
(72-85)
-404
(0%)
81.8
(80-84)
Negative
Gopalraj, 2004
USA (UKY) CL,CO  3  (detail)  118
(73%)
C74.3 + 6.1
(-)
-133
(62%)
79 + 8
(-)
Positive
Gopalraj, 2004
USA (ROS) CO  3  (detail)  86
(57%)
C-88 + 6.1
(-)
69
(48%)
82 + 6.3
(-)
Positive
Lamsa, 2007
Finland CL  6  (detail)  405
(69%)
C71.6 + 7.3
(-)
-463
(60%)
69.9 + 5.1
(-)
Positive
Lendon, 1997
Unknown CL  1  (detail)  115
(50%)
C69.9 + 10.4
(-)
76.9 + 10.4
(-)
70
(57%)
79.8 + 10.7
(-)
Negative
Li, 2008
Canada CL  2  (detail)  753
(58%)
C71.9 + 8.5
(-)
77.8 + 8.6
(-)
736
(64%)
73.4 + 7.9
(-)
Negative
Papassotiropoulos, 2005
I (Greece) CL  1  (detail)  134
(-)
C--45
(-)
-Negative
Papassotiropoulos, 2005
II (Germany, Switzerland) CL  1  (detail)  150
(-)
C--216
(-)
-Negative
Randall, 2009
Overlaps with
Cheng, 2005
CL  2  (detail)  181
(71%)
C--119
(52%)
-n.a.
Reiman, 2007
USA, Netherlands CL  1  (detail)  861
(-)
M-74.9 + 6.6
(-)
550
(-)
77.4 + 7.3
(-)
Negative
Retz, 2001
Germany CL  2  (detail)  63
(68%)
C66.6 + 11.9
(-)
73.7 + 9.3
(-)
162
(62%)
70.6 + 8.2
(-)
Trend
Rodriguez, 2005
Overlaps with
Rodriguez, 2006
CL  1  (detail)  274
(68%)
C71.6 + 8.6
(48-94)
75.4 + 8.7
(50-97)
283
(71%)
80.5 + 7.9
(63-100)
n.a.
Rodriguez, 2006
Spain CL  3  (detail)  322
(68%)
C72 + 8.5
(48-94)
75.6 + 8.6
(50-97)
314
(71%)
80.4 + 7.7
(63-100)
Negative
Scacchi, 2001
Italy CL  1  (detail)  85
(76%)
C-86.1 + 3.8
(81-95)
156
(58%)
83.9 + 3.1
(80-99)
Negative
Zou, 2008
USA (MCJ) CL  1  (detail)  577
(63%)
C-78.4 + 6.7
(-)
566
(60%)
78 + 7.6
(-)
Negative
Zou, 2008
USA (RS-AUT) CL  1  (detail)  1090
(61%)
M-81.6 + 6.7
(-)
1126
(54%)
78.5 + 6
(-)
Positive
Zou, 2008
USA (ROS) CL  1  (detail)  84
(56%)
N-87.7 + 6.4
(-)
69
(48%)
81.4 + 6.5
(-)
Trend
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 Comment
 Other/Mixed
Bertram, 2005
USA (NIMH)  3  (detail)  202440
(-)
M71.2 + 7.4
(-)
-348
(-)
-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 AD diagnosis ->  "C" (clinical AD diagnosis), "N" (neuropathological AD diagnosis), "M" (mixed, i.e. AD 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); results obtained in duplicate or largely overlapping samples are listed as "n.a.".
(-) :  Either no data provided or in case of overlap, data included in original study.
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Studies: 1395
Genes: 695
Polymorphisms: 2973
Meta-analyses: 320
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