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. Author manuscript; available in PMC: 2020 Dec 1.
Published in final edited form as: J Intern Med. 2019 Aug 23;286(6):711–722. doi: 10.1111/joim.12964

Table 2.

Incidence rate and hazard ratio for chronic kidney disease (CKD) in NAFLD compared to non- NAFLD patients, primary analysis and subanalyses by age and gender

NAFLD Status No of patients Person years No of events Crude incidence per 1000 person-years Adjusted HR of CKD (95% CI) P-value***
Baseline covariates adjusted* Baseline and time-varying covariates adjusted**
Primary analysis NAFLD 262,619 707,310 5,766 8.2 1.41 (1.36, 1.46) 1.58 (1.52, 1.66)
Non-NAFLD 769,878 1,572,889 8,655 5.5 Reference Reference
Age
 18–49 NAFLD 113,293 303,861 798 2.6 1.49 (1.35, 1.65) 1.66 (1.47, 1.88) <0.001
Non-NAFLD 317,052 651,841 915 1.4 Reference Reference
 50–59 NAFLD 87,991 249,790 1,930 7.7 1.48 (1.39, 1.57) 1.60 (1.47, 1.73)
Non-NAFLD 260,349 576,143 2,489 4.3 Reference Reference
 >= 60 NAFLD 61,228 153,443 3,031 19.8 1.31 (1.25, 1.37) 1.56 (1.47, 1.67)
Non-NAFLD 183,558 369,791 5,241 14.2 Reference Reference
Gender
 Male NAFLD 123,527 328,401 3,074 9.4 1.58 (1.50, 1.66) 1.70 (1.59, 1.81) 0.001
Non-NAFLD 366,955 746,076 3,989 5.3 Reference Reference
 Female NAFLD 139,064 378,858 2,690 7.1 1.33 (1.26, 1.40) 1.47 (1.38, 1.58)
Non-NAFLD 401,258 817,245 4,313 5.3 Reference Reference

Abbreviations: NAFLD Non-alcoholic fatty liver disease, CKD chronic kidney disease, CI confidence interval, HR hazard ratio

*

Adjusted for age, gender, diabetes, hypertension, obesity, hyperlipidemia, coronary artery disease, peripheral vascular disease, cerebrovascular disease, heart failure, and chronic obstructive pulmonary disease, angiotensin-converting-enzyme inhibitors, and angiotensin II receptor blockers, mean number of outpatient visits, and mean number of inpatient visits, cirrhosis, decompensated cirrhosis, and hepatocellular carcinoma.

**

Time varying covariates include age, gender, diabetes, hypertension, obesity, hyperlipidemia, coronary artery disease, peripheral vascular disease, cerebrovascular disease, heart failure, and chronic obstructive pulmonary disease, angiotensin-converting-enzyme inhibitors, and angiotensin II receptor blockers, cirrhosis, decompensated cirrhosis, and hepatocellular carcinoma.

***

P-value for interaction