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. 2017 Oct 28;6(11):e006524. doi: 10.1161/JAHA.117.006524

Table 3.

Subgroup Analysis for the Associations Between Choline Metabolite Score and Risk of CVD

Characteristics HR (95% CI) Per SD Increment P Value for Interaction
Sex
Men (n=452) 2.31 (1.13–4.71) 0.83
Women (n=528) 2.23 (1.03–4.83)
Age, y
≤65 (n=338) 2.67 (1.06–6.69) 0.49
>65 (n=598) 2.42 (1.27–4.64)
Obesity, kg/m2
≤30 (n=535) 2.65 (1.31–5.35) 0.79
>30 (n=445) 2.04 (0.92–4.52)
Smoking status
Current/former smoking (n=402) 2.45 (1.19–5.06) 0.63
Ever smoking (n=578) 2.40 (1.09–5.28)
Family history of CHD
Yes (n=237) 2.19 (1.22–3.95) 0.15
No (n=743) 3.78 (0.84–5.42)
Baseline type 2 diabetes mellitus
Yes (n=486) 2.22 (1.00–4.92) 0.87
No (n=494) 2.37 (1.20–4.69)
Baseline hypertension
Yes (n=817) 1.94 (1.08–3.46) 0.36
No (n=163) 3.12 (0.75–5.65)
Baseline dyslipidemia
Yes (n=692) 2.55 (1.31–4.94) 0.73
No (n=288) 2.03 (0.86–4.78)

Multivariate adjusted HRs (95% CIs) of incident CVD for 1‐SD increment in the baseline choline metabolite score. Data were adjusted for age, sex, body mass index, physical activity (metabolic equivalent task units in min/d), family history of premature heart disease, smoking, hypertension, dyslipidemia, and diabetes mellitus and stratified by intervention group, except for the stratification variable in each model. P values for interaction were derived from Cox models adjusted as above, including an interaction term between the stratification variable and the choline metabolite score. CHD indicates coronary heart disease; CI, confidence interval; CVD, cardiovascular disease; and HR, hazard ratio.