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. Author manuscript; available in PMC: 2020 Aug 21.
Published in final edited form as: Stroke. 2019 Feb;50(2):298–304. doi: 10.1161/STROKEAHA.118.021856

Table 2:

Predictors of favorable outcome after stroke in the SiGN/GISCOME cohort

Predictor Outcome OR 95%CI p-value
unfavorable (n=889) favorable (n=1609) univariate multivariate
Female sex (n)§ 459 (51.6) 580 (36.0) 8.107 0.75–96.33 <0.001 0.081
Age (mean±SD) 73.7±12.9 64.3±13.7 0.943 0.93–0.95 <0.001 <0.001
TOAST/CCS etiology n.d. n.d. 1.01 0.94–1.09 <0.001 0.709
NIHSS (median)$ 7 [0–41] 3 [0–30] 0.822 0.80–0.84 <0.001 <0.001
Imbalance (median/mean) $ 0/1.18 [0–48] 0/0.90 [0–27] 0.94 0.91–0.98 0.91 0.0036
Imbalance with ohnologs (median/mean) $ 0/0.69 [0–48] 0/0.37 [0–27] 0.93 0.89–0.98 0.093 0.002
Imbalance without ohnologs (median/mean) $ 0/0.49 [0–14] 0/0.53 [0–13] 0.99 0.92–1.07 0.19 0.89

The association between functional outcome and different types of genetic imbalance was assessed by multivariate logistic regression analysis (model 1: continuous genetic imbalance), adjusted for age, sex and ancestry-derived principal components 1–10 as potential confounders, and including stroke etiology (TOAST/CCS) and stroke severity (NIHSS) as additional covariates. NIHSS indicates NIH stroke scale; TOAST, Trial of Org 10172 in Acute Stroke Treatment stroke sub classification; CCS, Causative Classification System; OR, model-adjusted odds ratio of favorable outcome; 95%CI: 95% confidence interval of OR

§

percentage in brackets

$

range in square brackets.

Univariate p-values obtained by non-model-based methods: χ2-squared test, Student’s t test or Mann-Whitney U-test, as appropriate