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. 2011 Sep;12(6):443–450. doi: 10.2174/138920211797248600

Table 3.

History of Candidate Gene Association Studies in Ménière’s disease. None of them were Replicated in an Independent Population

Gene Paper Phenotype Cases Controls Odds ratio P value
HLA-DRB1*1201 Koyama S et al. 1993 Sporadic MD 20 0,04
COCH Fransen E et al. 1999 Familial MD 23 119
HLA-DRB1*09 Meng X et al. 2001 Sporadic MD 60 85 0,2 0,01
Antiquitin Lynch M et al. 2002 Familial MD 9
HLA-Cw*07 Melchiorri L et al. 2002 Sporadic MD 41 101 3,6 6,9.E-3
HLA-DRB1*0405 Koo JW et al. 2003 Sporadic MD 41 226 8,51 0,006
KCNE1 Doi K et al. 2005 Sporadic MD 63 205 NC NC
KCNE3 Doi K et al. 2005 Sporadic MD 63 237 NC NC
HLA-DRB1*1101 Lopez-Escamez JA et al. 2007 Sporadic MD 80 250 3,65 0,029
Alpha-adducin Teggi R et al. 2008 Sporadic MD 28 48 0,0034
HSP 70 Kawaguchi S et al. 2008 Sporadic MD 49 100 <0,001
PARP-1 Lopez-Escamez JA et al. 2009 Bilateral MD 80 371 7,33 0,012
PTPN22 Lopez-Escamez JA et al. 2010 Bilateral MD 52 348 2,25 0,04
FcγRIIIa Lopez-Escamez JA et al. 2011 Sporadic MD 156 626 1,49 0,054
NOS1/NOS2A* Gazquez I et al., 2011 Sporadic MD 381 667 0.89 0.56
*

A CCTTT microsatellite was initially associated in Galicia population, OR=0.37, corrected p=0.04.