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An Update on the Effect Of Sodium Glucose Cotransporter 2 Inhibitors on Non-Alcoholic Fatty Liver Disease: A Systematic Review of Clinical Trials
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Abstract:
Non-alcoholic fatty liver disease (NAFLD) is one of the main causes of liver disease,
specifically chronic liver disease. Type 2 diabetes (T2DM) is associated with the risk of NAFLD
given that patients usually have insulin resistance as one of the observed complications with
NAFLD. Hypoglycemic agents, including sodium glucose cotransporter 2 (SGLT-2), have shown
to improve NAFLD. The objective of this study is to evaluate the effect of SGLT-2 inhibitors on
NAFLD patients’ outcomes, whether they have T2DM or not. We conducted a comprehensive
search using the PubMed and Ovid databases to identify published studies that addressed the use of
SGLT-2 inhibitors in NAFLD patients. The outcomes assessed include changes in liver enzymes,
lipid profiles, weight changes, the fibrosis-4-index (FIB4), and magnetic resonance imaging proton
density-based fat fraction (MRI-PDFF). Only clinical trials that met the quality measures were included
in this review. Out of 382 potential studies, we included 16 clinical trials that discussed the
use of SGLT-2 inhibitors in NAFLD patients. A total of 753 patients were enrolled in these trials.
The majority of the trials reported positive effects of SGLT-2 inhibitors on liver enzymes; alanine
transaminase (ALT), aspartate aminotransferase (AST), and gamma-glutamyl transferase. All 10
trials that reported changes in body mass index (BMI) from baseline showed a statistically significant
reduction with SGLT-2 inhibitor use, while 11 studies reported a significant increase in high
density lipoprotein (HDL) levels, 3 studies reported a reduction in triglycerides (TG) levels, and 2
studies showed a decrease in low density lipoprotein (LDL) levels. The available evidence shows
that the use of SGLT-2 inhibitors in NAFLD is associated with positive outcomes on liver enzymes,
lipid profiles, and BMI. Further studies with larger sample size and longer follow-up time
are warranted.
Bentham Science Publishers Ltd.
Title: An Update on the Effect Of Sodium Glucose Cotransporter 2 Inhibitors on
Non-Alcoholic Fatty Liver Disease: A Systematic Review of Clinical Trials
Description:
Abstract:
Non-alcoholic fatty liver disease (NAFLD) is one of the main causes of liver disease,
specifically chronic liver disease.
Type 2 diabetes (T2DM) is associated with the risk of NAFLD
given that patients usually have insulin resistance as one of the observed complications with
NAFLD.
Hypoglycemic agents, including sodium glucose cotransporter 2 (SGLT-2), have shown
to improve NAFLD.
The objective of this study is to evaluate the effect of SGLT-2 inhibitors on
NAFLD patients’ outcomes, whether they have T2DM or not.
We conducted a comprehensive
search using the PubMed and Ovid databases to identify published studies that addressed the use of
SGLT-2 inhibitors in NAFLD patients.
The outcomes assessed include changes in liver enzymes,
lipid profiles, weight changes, the fibrosis-4-index (FIB4), and magnetic resonance imaging proton
density-based fat fraction (MRI-PDFF).
Only clinical trials that met the quality measures were included
in this review.
Out of 382 potential studies, we included 16 clinical trials that discussed the
use of SGLT-2 inhibitors in NAFLD patients.
A total of 753 patients were enrolled in these trials.
The majority of the trials reported positive effects of SGLT-2 inhibitors on liver enzymes; alanine
transaminase (ALT), aspartate aminotransferase (AST), and gamma-glutamyl transferase.
All 10
trials that reported changes in body mass index (BMI) from baseline showed a statistically significant
reduction with SGLT-2 inhibitor use, while 11 studies reported a significant increase in high
density lipoprotein (HDL) levels, 3 studies reported a reduction in triglycerides (TG) levels, and 2
studies showed a decrease in low density lipoprotein (LDL) levels.
The available evidence shows
that the use of SGLT-2 inhibitors in NAFLD is associated with positive outcomes on liver enzymes,
lipid profiles, and BMI.
Further studies with larger sample size and longer follow-up time
are warranted.
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