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Chinese Journal of Clinicians(Electronic Edition) ›› 2018, Vol. 12 ›› Issue (03): 129-134. doi: 10.3877/cma.j.issn.1674-0785.2018.03.001

Special Issue:

• Clinical Researches •     Next Articles

Effect of atorvastatin intervention on carotid atherosclerosis in patients with type 2 diabetes mellitus

Yan Wu1, Huaiguo Zhang1,(), Cunfu Liang1, Xiangwen Xu1, Haiying Fan1, Rui Tao1, Lingling Wang1, Bin Li1, Shufa Li1   

  1. 1. Department of General Practice, Linyi People′s Hospital, Linyi 276003, China
  • Received:2017-09-07 Online:2018-02-01 Published:2018-02-01
  • Contact: Huaiguo Zhang
  • About author:
    Corresponding author: Zhang Huaiguo, Email:

Abstract:

Objective

To investigate the effect of atorvastatin intervention on glucose and lipid metabolism, inflammatory cytokine levels, and carotid atherosclerosis in patients with type 2 diabetes mellitus.

Methods

A total of 196 patients with type 2 diabetes mellitus treated at our hospital between January 2015 and December 2016 were collected and divided into either a control group (n=98) or an atorvastatin group (n=98) according to treatment method. The patients in both groups were treated with basic treatment, and the patients in the atorvastatin group were additionally treated with atorvastatin. The changes of glucose metabolism, lipid metabolism, inflammatory cytokine levels, and carotid artery atherosclerosis-related indexes were analyzed and compared between the two groups.

Results

After treatment, FPG, HbA1c, INS, and HOMA-IR levels were not statistically significant between the two groups of patients [(6.42±1.21) mmol/L vs (6.27±1.05) mmol/L, t=0.406, P=0.572; (6.21±0.65)% vs (6.08±0.73)%, t=0.662, P=0.339; (13.04±1.21)% vs (12.83±1.15)%, t=0.316, P=0.606; (3.75±0.27) vs (3.64±0.35), t=0.283, P=0.692), respectively]. TC, TG, and LDL-C were significantly lower and HDL-C was significantly higher in the atorvastatin group than in the control group [(3.18±0.33) vs (4.76±0.39), t=2.738, P=0.009; (1.69±0.14) vs (2.13±0.31), t=3.012, P=0.003; (1.74±0.27) vs (3.08±0.39), t=3.974, P=0.001; (1.26±0.21) vs (1.04±0.15), t=2.458, P=0.014), respectively]. CRP, IL-6, TNF-α, ICAM-1, VCAM-1, and Selectin levels were significantly lower in the atorvastatin group than in the control group [(0.83±0.09) vs (0.92±0.11), t=2.576, P=0.036; (1.83±0.25) vs (2.32±0.36), t=3.119, P=0.025; (33.83±4.15) vs (41.92±6.11), t=3.102, P=0.029; (198.83±14.15) vs (210.92±15.11), t=2.583, P=0.035; (457.83±41.15) vs (501.92±38.11), t=2.104, P=0.043; (20.04±1.91) vs (25.83±2.09), t=2.722, P=0.031), respectively]. IMT, plaque thickness, plaque size, and plaque number were significantly lower in the atorvastatin group than in the control group [(1.05±0.12) mm vs (1.30±0.16) mm, t=3.501, P=0.012; (2.64±0.37) mm vs (3.23±0.55) mm, t=3.164, P=0.019; (0.078±0.021) cm2 vs (0.093±0.025) cm2, t=4.068, P=0.001; (3.54±0.62) vs (4.23±0.92), t=2.083, P=0.042, respectively]. In multivariate logistic regression analysis, IMT was significantly associated with atorvastatin, HDL-C, TC, TG, LDL, CRP, IL-6, and TNF-α.

Conclusion

Atorvastatin can regulate lipid metabolism and reduce inflammatory cytokine levels and carotid atherosclerosis in patients with type 2 diabetes mellitus.

Key words: Type 2 diabetes mellitus, Atorvastatin, Glucose and lipid metabolism, Inflammatory cytokine levels, Carotid atherosclerosis

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