Clinical Study

Possible Involvement of a Mitochondrial Translation Initiation Factor 3 Variant Causing Decreased mRNA Levels in Parkinson's Disease

Table 1

Association analysis of MTIF3 rs7669 genotype and allele frequencies in Parkinson’s disease (PD).

MTIF3Familial PD (n= 90)Sporadic PD (n= 291)Combined samples (n= 381)Controls (n= 322)

Genotypes
CC (%)59 (65.6)168 (57.7)227 (59.6)211 (65.5)
CT (%)28 (31.1)108 (37.1)136 (35.7)96 (29.8)
TT (%)3 (3.3)15 (5.2)18 (4.7)15 (4.7)
Alleles
C (%)146 (81.1)444 (76.3)590 (77.4)518 (80.4)
T (%)34 (18.9)138 (23.7)172 (22.6)126 (19.6)
Odds ratio1.045 (0.686–1.59)0.783 (0.596–1.03)0.834 (0.644–1.08)
Combined genotypes
CC/CT (%)87 (96.7)276 (94.8)363 (95.3)307 (95.3)
TT (%)3 (3.3)15 (5.2)18 (4.7)15 (4.7)
Odds ratio1.42 (0.401–5.01)0.899 (0.432–1.87)0.985 (0.488–1.99)
TT/CT (%)31 (34.4)123 (42.3)154 (40.4)111 (34.5)
CC (%)59 (65.6)168 (57.7)227 (59.6)211 (65.5)
P  =  .0473
Odds ratio0.999 (0.612–1.63)1.39 (1.01–1.93)1.29 (0.948–1.75)

aChi-square test (χ 2) (2DF) for contingency table, (1DF) for contingency table.