Role of Mitochondrial Genome Mutations in Pathogenesis of Carotid Atherosclerosis

Table 10

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

Analyzed variables
	Mutations	B	S.E.	Wald	df	Sig.	Exp(B)
Model 1	m.1555A>G	−0,177	0,079	5017	1	0,025	0,838
	m.3256C>T	0,098	0,071	1916	1	0,166	1103
	m.14846G>A	−0,108	0,051	4483	1	0,034	0,898
	m.5178C>A	0,079	0,078	1024	1	0,312	0,924
	m.652delG	0,006	0,036	0,032	1	0,857	0,994
	m.12315G>A	0,027	0,030	0,806	1	0,369	1028
	m.13513G>A	−0,023	0,023	1001	1	0,317	1023
	m.14459G>A	0,018	0,026	0,463	1	0,496	0,982
	m.15059G>A	0,026	0,023	1273	1	0,259	1027
	m.652insG	−0,187	0,156	1439	1	0,230	1205
	m.3336T>C	0,028	0,028	1036	1	0,309	1028
	Constant	1350	1913	0,498	1	0,480	3858

Coefficient B indicated the link direction; Significant correlation of mutations with atherosclerotic plaques in carotid arteries ().