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
	Mutations	B	S.E.	Wald	df	Sig.	Exp (B)
Model 1	m.1555A>G	−0,163	0,042	14,952	1	0,000	0,850
	m.3256C>T	0,033	0,051	0,417	1	0,519	1033
	m.14846G>A	−0,026	0,029	0,845	1	0,358	0,974
	m.5178C>A	0,034	0,045	0,560	1	0,454	1034
	m.652delG	0,052	0,022	5761	1	0,016	1054
	m.12315G>A	0,122	0,027	20,958	1	0,000	1130
	m.13513G>A	−0,046	0,017	6951	1	0,008	1047
	m.14459G>A	0,030	0,015	3971	1	0,046	0,970
	m.15059G>A	0,052	0,020	6836	1	0,009	1054
	m.652insG	0,077	0,081	0,901	1	0,343	1080
	m.3336T>C	0,052	0,028	3420	1	0,064	1054
	Constant	−2384	1308	3321	1	0,068	0,092

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.