Skip to main content
. Author manuscript; available in PMC: 2020 Dec 1.
Published in final edited form as: Clin Gastroenterol Hepatol. 2019 May 9;17(13):2776–2784.e4. doi: 10.1016/j.cgh.2019.04.061

Table 4.

Duration of aspirin use1 and risk for developing incident advanced fibrosis2, among patients with NAFLD fibrosis stage 0-2 at enrollment (n=317)

Duration of daily aspirin use (years)1
Non-regular use (ref.) 0 to <2 years 2 to <4 years ≥4 years P for trend3
No. of patients with composite endpoint2 54 11 12 9
Age- and sex-adjusted* HR (95% CI) 1 0.85 (0.65-1.10) 0.60 (0.42-0.81) 0.47 (0.34-0.69) <0.0001
Multivariable Model¥; HR (95% CI) 1 0.90 (0.68-1.20) 0.64 (0.45-0.86) 0.50 (0.35-0.73) 0.026

Abbreviations: NAFLD, nonalcoholic fatty liver disease; No., number; HR, hazard ratio; CI, confidence interval

*

Model 1: see footnote for Table 3.

¥

Multivariable Model: see footnote for Table 3.

1

Aspirin use was defined as daily use of aspirin. Less frequent use or never-use was defined as non-regular use. Aspirin use data was ascertained and updated at each clinical follow-up visit and modeled as a time-varying exposure.

2

Incident advanced fibrosis was defined as the first recorded follow-up FIB-4 Index >2.67 or NFS >0.67 or APRI > 1.0.

3

P-trend across increasing categories of duration, among daily aspirin users.