Effect of SGLT2 Inhibitors on Type 2 Diabetes Mellitus With Non-Alcoholic Fatty Liver Disease: A Meta-Analysis of Randomized Controlled Trials - PubMed (original) (raw)

Meta-Analysis

Effect of SGLT2 Inhibitors on Type 2 Diabetes Mellitus With Non-Alcoholic Fatty Liver Disease: A Meta-Analysis of Randomized Controlled Trials

Qiong Wei et al. Front Endocrinol (Lausanne). 2021.

Abstract

Objective: Clinical trials showed that sodium-glucose cotransporter 2 (SGLT2) inhibitors can improve non-alcoholic fatty liver disease (NAFLD). In this work, a meta-analysis of randomized controlled trials was conducted to evaluate the effect of SGLT2 inhibitors on type 2 diabetes mellitus (T2DM) with NAFLD.

Methods: PubMed, Embase, Web of Science, and Cochrane Libraries were used for the systematic literature review to determine eligible studies. A randomized effect model was adapted to perform a meta-analysis on these eligible studies to estimate the combined effect sizes. Differences were expressed as the weighted average difference (WMD) of the continuous results and the 95% confidence interval (CI).

Results: Ten randomized controlled trials with 573 participants were included. SGLT2 inhibitors significantly reduced the levels of alanine transaminase (WMD -5.36 [95% CI: -8.86, -1.85], p = 0.003) and Aspartate Transaminase (WMD -2.56 [95% CI: -3.83, -1.29], p <0.0001). In terms of body composition, liver proton density fat fraction (WMD -2.20 [95% CI: -3.67, -0.74], p = 0.003), visceral fat mass area (WMD -20.71 [95% CI: -28.19, -13.23], p <0.00001), subcutaneous fat areas (WMD -14.68 [95% CI: -26.96, -2.40], p = 0.02) were also significantly reduced.

Conclusion: SGLT2 inhibitors can remarkably reduce hepatic enzymes, hepatic fat and improve body composition. Thus, they may become a new treatment option for NAFLD.

Systematic review registration: PROSPERO, identifier CRD42020215570.

Keywords: liver proton density fat fraction; non-alcoholic fatty liver disease; sodium-glucose cotransporter 2 inhibitors; type 2 diabetes mellitus; visceral fat mass area.

Copyright © 2021 Wei, Xu, Guo, Li and Li.

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Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

Figure 1

Figure 1

Summary of study identification, inclusion, and exclusion.

Figure 2

Figure 2

Quality evaluation chart of included studies.

Figure 3

Figure 3

Meta-analysis of the effect of SGLT2 inhibitors on glycemic indices compared with the control group.

Figure 4

Figure 4

Meta-analysis of the effect of SGLT2 inhibitors on liver function compared with the control group.

Figure 5

Figure 5

Meta-analysis of the effect of SGLT2 inhibitors on body composition compared with the control group.

Figure 6

Figure 6

Meta-analysis of AST level comparisons between SGLT2 inhibitors and the control group based on the control.

Figure 7

Figure 7

Meta-analysis of body weight level comparisons between SGLT2 inhibitors and the control group based on the control.

References

    1. Targher G, Lonardo A, Byrne CD. Nonalcoholic Fatty Liver Disease and Chronic Vascular Complications of Diabetes Mellitus. Nat Rev Endocrinol (2018) 14(2):99–114. 10.1038/nrendo.2017.173 - DOI - PubMed
    1. Schuppan D, Schattenberg JM. Non-Alcoholic Steatohepatitis: Pathogenesis and Novel Therapeutic Approaches. J Gastroenterol Hepatol (2013) 28 Suppl 1:68–76. 10.1111/jgh.12212 - DOI - PubMed
    1. Marchesini G, Brizi M, Morselli-Labate AM, Bianchi G, Bugianesi E, Mccullough AJ, et al. Association of Nonalcoholic Fatty Liver Disease With Insulin Resistance. Am J Med (1999) 107(5):450–5. 10.1016/S0002-9343(99)00271-5 - DOI - PubMed
    1. Gusdon AM, Song KX, Qu S. Nonalcoholic Fatty Liver Disease: Pathogenesis and Therapeutics From a Mitochondria-Centric Perspective. Oxid Med Cell Longev (2014) 2014:637027. 10.1155/2014/637027 - DOI - PMC - PubMed
    1. Targher G, Byrne CD, Lonardo A, Zoppini G, Barbui C. Non-Alcoholic Fatty Liver Disease and Risk of Incident Cardiovascular Disease: A Meta-Analysis. J Hepatol (2016) 65(3):589–600. 10.1016/j.jhep.2016.05.013 - DOI - PubMed

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