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. 2022 Oct 18;23(20):12481. doi: 10.3390/ijms232012481

Table 4.

Association between the severity of NAFLD at baseline and increasing levels of worsening of glycaemic control at follow-up in postmenopausal women with type 2 diabetes.

Ordered Logistic Regression Models Odds Ratios (95% CI) p-Value
Unadjusted model
NAFLD and clinically significant fibrosis § 6.16 (1.48–25.7) 0.013
Adjusted model 1
NAFLD and clinically significant fibrosis 6.15 (1.47–25.9) 0.013
Age (years) 1.01 (0.95–1.08) 0.733
BMI (kg/m2) 0.97 (0.87–1.06) 0.462
Adjusted model 2
NAFLD and clinically significant fibrosis 6.11 (1.46–26.6) 0.014
Age (years) 1.01 (0.95–1.09) 0.696
BMI (kg/m2) 0.96 (0.86–1.06) 0.431
GLP-1 receptor agonist use 1.53 (0.28–8.21) 0.621
Adjusted model 3
NAFLD and clinically significant fibrosis 6.97 (1.62–30.0) 0.009
Age (years) 0.99 (0.92–1.06) 0.801
BMI (kg/m2) 0.96 (0.86–1.06) 0.385
SGLT-2 inhibitor use 0.14 (0.01–1.69) 0.123
Adjusted model 4
NAFLD and clinically significant fibrosis 5.96 (1.42–25.1) 0.015
Age (years) 1.01 (0.95–1.08) 0.665
BMI (kg/m2) 0.96 (0.87–1.07) 0.481
Pioglitazone use 1.25 (0.40–31.0) 0.982

Sample size, n = 61. Data are expressed as odds ratio and 95% confidence intervals (CI) as tested by ordered logistic regression analyses. The presence of four increasing categories of worsening of glycaemic control at follow-up (i.e., arbitrarily defined as HbA1c increases ≤ 0.19%, from 0.20% to 0.49%, from 0.50% to 0.99% and ≥1%, respectively) was the ordinal dependent variable in all these models. All covariates included in these regression models were recorded at baseline. § Clinically significant fibrosis was defined by LSM ≥ 7 kPa on Fibroscan®.