Oxidative Medicine and Cellular Longevity / 2017 / Article / Tab 5

Research Article

Role of Mitochondrial Genome Mutations in Pathogenesis of Carotid Atherosclerosis

Table 5

The analysis of included variables and the coefficient of link force and direction.

Analyzed variables
MutationsBS.E.WalddfSig.Exp (B)

Model 1m.1555A>G−0,1630,04214,95210,0000,850
m.3256C>T0,0330,0510,41710,5191033
m.14846G>A−0,0260,0290,84510,3580,974
m.5178C>A0,0340,0450,56010,4541034
m.652delG0,0520,022576110,0161054
m.12315G>A0,1220,02720,95810,0001130
m.13513G>A−0,0460,017695110,0081047
m.14459G>A0,0300,015397110,0460,970
m.15059G>A0,0520,020683610,0091054
m.652insG0,0770,0810,90110,3431080
m.3336T>C0,0520,028342010,0641054
Constant−23841308332110,0680,092

Coefficient B indicates the link direction; Significant correlation of mutations with atherosclerotic plaques in carotid arteries (); Correlation of mutations with atherosclerotic plaques at level of significance.

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