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. 2018 Jan 3;20:2. doi: 10.1186/s12968-017-0419-6

Table 5.

Univariate and multivariate Cox proportional hazard analysis in patients without therapy at baseline

Univariate Multivariate Multivariate
HR (95% CI) P HR (95% CI) P HR (95% CI) P
Age,
per 1 year increase
1.053
(1.001–1.108)
0.046 1.067
(1.012–1.125)
0.011 1.060
(1.007–1.116)
0.025
NYHA 2.405
(1.450–3.988)
0.001 1.752
(1.010–3.039)
0.056 1.776
(0.924–3.414)
0.085
Mayo Stage 1.985
(1.212–3.252)
0.006 1.406
(0.736–2.683)
0.30 1.443
(0.779–2.672)
0.24
E/E’,
per 1 unit increase
1.073
(1.003–1.114)
0.042 1.235
(0.477–3.134)
0.28 1.296
(0.463–3.188)
0.40
LVEF,
per 1% increase
0.966
(0.939–0.994)
0.016 0.995
(0.960–1.033)
0.81 0.987
(0.954–1.021)
0.44
Septal thickness,
per 1 mm increase
1.115
(1.020–1.219)
0.017 1.112
(0.988–1.251)
0.078 1.086
(0.973–1.213)
0.041
ECV ≥44.0% 4.751
(1.572–14.360)
0.006 4.599
(1.493–14.165)
0.008
Global LGE 4.041
(1.452–11.246)
0.007 4.442
(1.578–12.389)
0.015

All significantly prognostic factors in univariate analysis were listed. Univariate analysis was not performed for native T1 because the Kaplan-Meier curves crossed each other (Tarone-Ware, P = 0.069). Univariate analysis was not performed for log (cTnI) and log (NT-proBNP), as they were included in Mayo Stage. All clinically and statistically significant variates in univariate analysis were put into the multivariate Cox model. ECV and LGE were put in separate models because of a correlation ρ of 0.889. Backward regression was chosen. HR Hazard ratio, CI Confidence interval, NYHA New York Heart Association, LVEF Left ventricle ejection fraction, LGE Late gadolinium enhancement, ECV Extracellular volume