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. 2008 Sep 8;168(8):855–865. doi: 10.1093/aje/kwn206

Table 4.

Observed (O) and Expected (E) Numbers of Studies with Statistically Significant (P < 0.05) Results in AlzGene Meta-Analyses with Formally Statistically Significant Associationsa

Gene Polymorphism Odds Ratio 95% Confidence Interval No. of Studies O E
P Value
Main Analysis Sensitivity Analysis 1 Main Analysis Sensitivity Analysis 1
ACE rs1800764 (ACE7) 0.83 0.72, 0.95 5 0 1.09 0.44 0.59 1.00
ACE rs4291 (ACE6) 0.86 0.75, 0.99 5 0 0.72 0.34 1.00 1.00
ACE rs4362 (ACE2) 0.83 0.70, 0.99 3 0 0.63 0.27 1.00 1.00
APOC1 Ins/del (HpaI)b 2.07 1.67, 2.57 13 8 10.79 5.32 0.05 0.16
APOE promoter rs405509 (Th1/E47cs) 0.79 0.71, 0.87 15 5 5.88 2.03 0.79 0.04*
APOE promoter rs440446 (+113) 0.58 0.50, 0.68 4 3 3.68 1.92 0.28 0.36
APOE promoter rs449647 (−491) 0.72 0.63, 0.81 36 13 10.79 4.01 0.47 ≤0.001*
CH25H rs13500 1.44 1.08, 1.93 7 4 2.46 0.86 0.25 0.01*
CHRNB2 rs4845378 0.67 0.50, 0.90 4 1 0.95 0.35 1.00 0.30
CST3 5′-UTR-157 1.23 1.03, 1.47 4 0 0.79 0.33 1.00 1.00
CST3 5′-UTR-72 1.28 1.05, 1.56 3 0 0.81 0.30 0.57 1.00
CST3 rs1064039 1.15 1.02, 1.31 9 1 1.04 0.57 1.00 0.44
DAPK1 rs4877365 0.80 0.69, 0.92 3 1 1.27 0.44 1.00 0.38
DAPK1 rs4878104 0.87 0.79, 0.95 6 1 1.49 0.60 1.00 0.47
DNFB31 rs2274159 1.18 1.05, 1.34 3 1 0.99 0.37 1.00 0.33
GAPDHS rs12984928 0.82 0.71, 0.95 3 1 1.24 0.44 1.00 0.38
GAPDHS rs4806173 0.81 0.71, 0.94 3 2 1.34 0.46 0.59 0.06*
IL1b rs1143634 (+3953) 1.18 1.03, 1.34 7 1 0.98 0.47 1.00 0.39
LOC439999 rs498055 1.18 1.03, 1.34 7 3 1.83 0.70 0.39 0.03*
LPL rs320 (HindIII) 0.73 0.59, 0.90 3 1 1.15 0.40 1.00 0.35
MAPT rs1467967 (promoter) 0.86 0.75, 1.00 4 0 0.65 0.31 1.00 0.56
MAPT rs242557 (promoter) 1.34 1.01, 1.53 4 0 1.20 0.45 0.59 0.07*
MAPT rs2471738 (intron 9) 1.42 1.20, 1.70 4 2 1.89 0.64 1.00 0.12
NCSTN −119 intron 16 1.38 1.03, 1.83 3 1 0.72 0.31 0.56 0.28
POMT1 rs2018621 1.70 1.24, 2.34 3 2 1.34 0.42 0.59 0.05*
PON1 rs662 (R192Q) 0.86 0.77, 0.97 8 1 1.02 0.51 1.00 0.41
PRNP rs1799990 (M129V) 0.89 0.81, 0.98 10 1 1.26 0.69 1.00 0.51
SOAT1 rs1044925 1.31 1.11, 1.55 4 1 1.26 0.45 1.00 0.38
SORCS1 rs600879 1.24 1.04, 1.47 4 1 0.85 0.37 1.00 0.32
SORL1 rs2070045 1.20 1.02, 1.41 5 1 1.55 0.60 1.00 0.47
SORL1 rs2282649 1.14 1.03, 1.26 5 1 1.00 0.44 1.00 0.37
SORL1 rs3824968 1.21 1.01, 1.45 5 2 1.83 0.67 1.00 0.13
SORL1 rs661057 0.84 0.73, 0.96 5 1 1.81 0.63 0.66 0.49
SORL1 rs668387 0.82 0.69, 0.98 5 2 2.10 0.74 1.00 0.16
TF rs1049296 (P570S) 1.21 1.07, 1.39 13 2 1.92 0.90 1.00 0.23
TFAM rs2306604 0.78 0.62, 0.98 3 0 0.62 0.23 1.00 1.00
TGFB1 rs9282871 (Leu10Pro) 0.87 0.77, 0.99 3 0 0.67 0.29 1.00 1.00
TNF −863 0.71 0.53, 0.96 3 2 1.01 0.37 0.26 0.04*
TNF rs4647198 (−1031) 1.37 1.05, 1.78 3 1 0.73 0.26 0.57 0.24
hCG2039140c rs1903908 1.23 1.06, 1.44 4 0 1.03 0.42 0.58 1.00

Abbreviations: ACE, angiotensin-converting enzyme; ABCA1, ATP-binding cassette transporter A1; APOC1, apolipoprotein C1; APOE, apolipoprotein E; CH25H, cholesterol 25-hydroxylase; CHRNB2, cholinergic receptor, nicotinic, beta 2; CST3, cystatin 3; DAPK1, death-associated protein kinase 1; DFNB31, deafness, autosomal recessive 31; GAPDHS, glyceraldehyde-3-phosphate dehydrogenase, spermatogenic; IL1b, interleukin-1b; LOC439999, similar to ribosomal protein S3a; LPL, lipoprotein lipase; MAPT, microtubule-associated protein; NCSTN, nicastrin; POMT1, protein-O-mannosyltransferase 1; PON1, paraoxonase 1; PRNP, prion protein; SOAT1, sterol O-acyltransferase 1; SORCS1, sortilin-related VPS10 domain containing receptor 1; SORL1, sortilin-related receptor, L(DLR class) A repeats-containing; TF, transferring; TFAM, transcription factor A, mitochondrial; TGFB1, transforming growth factor, beta 1; TNF, tumor necrosis factor; UTR, untranslated region.

*

P < 0.10 for an excess of O over E.

a

The main results assume that the plausible effect in each meta-analysis is given by the summary effect (odds ratio) of the meta-analysis. Also shown are results from evaluations using half of the log odds ratio (“Sensitivity Analysis 1”) as the plausible effect.

b

Note that for this polymorphism, there is seemingly an excess of E over O—probably a chance finding resulting from the high number of analyses conducted. The signal of this single nucleotide polymorphism is probably due to high linkage disequilibrium with the APOE ϵ2/3/4 single nucleotide polymorphism.

c

This gene does not yet have an official name.