Abstract Th0048: How do novel type 2 diabetes mellitus (T2DM) medications affect lipid parameters in patients with metabolic dysfunction–associated steatotic liver disease (MASLD) and type 2 diabetes

Introduction: Metabolic dysfunction–associated steatotic liver disease (MASLD) is highly associated with T2DM and is a common cause of chronic liver disease and cardiovascular disease (CVD). Our goal was to examine the effects of various antidiabetic agents such as Metformin, sodium-glucose transport protein-2 inhibitors (SGLT2i), glucagon-like peptide 1 receptor analogs (GLP-1RAs), compared to insulin(ins) alone, as the control, in T2DM patients with liver fibrosis (based on FIB-4 score) as major comorbidities. We also wanted to investigate how do these agents affect the lipid parameters. Methods: We conducted a cross-sectional chart review of patients with using FIB-4 score at or above 1.3 and 1.8, to detect subjects at risk for liver hepato-steatosis at the DC VAMC Diabetes Clinic for over 24 months. We screened a total of 255 patients based on the inclusion criteria. Results: Patients had a mean age of 72.64±0.67 and were mostly on ins alone (32.23%). The mean BMI was 30.43±0.58 and A1C was 7.8±0.13. Using Mann-Whitney test, Metformin (+/- insulin) group had significantly lower FIB-4 score of 1.76±0.08 (n = 24) compared to SGLT2-i (+/- insulin or metformin) with 2.29±0.2 (p=0.0370) (n=32), while GLP-1RA(+/-ins or met) had a FIB-4 score of 1.9±0.1 (n= 30). Insulin only group had the highest FIB-4 of 2.36±0.22 (n = 41). The lipid panels were also analyzed with the mean LDL of GLP-1RA(+/-ins or met) had 70.40 ±6.065, SGLT2i(+/-ins or met) had 66.00 ±4.312, Metformin(+/-ins) had 79.79 ±8.026, and ins only had 71.95 ±6.463. The mean HDL for GLP-1RA(+/-ins or met) had 45.77±2.378, SGLT2i(+/-ins or met) had 43.31 ±2.897, Metformin(+/-ins) had 46.46±2.341, ins only had 56.20±2.695. The mean total cholesterol of GLP-1RA(+/-ins or met) was 140.2±7.653, SGLT2i(+/-ins or met) had 132.3±4.671, Metformin(+/-ins) had 146.3±8.659, ins only had 149.3±7.134. The mean triglyceride of GLP-1RA(+/-ins or met) had 134.4±10.68, SGLT2i(+/-ins or met) had 162.5±17.52, Metformin(+/-ins) 114.2±7.849, ins only had 120.8±11.99. Conclusion: In our predominantly African-American cohort, Metformin group appears to have the lowest FIB-4 score compared to other regimens with GLP1A coming at a close second. Additionally, the lipid parameters LDL, HDL, and total cholesterol seem to be similar across the medication groups except for triglyceride, where SGLT2i seems to be associated with statistically significant higher values compared to non-SGLT2i groups, particularly Metformin group.

Authors

Institutions

Publication Details

Journal
Arteriosclerosis Thrombosis and Vascular Biology
Published
2025-04-01
DOI
https://doi.org/10.1161/atv.45.suppl_1.th0048
Primary Topic
Liver Disease Diagnosis and Treatment
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Abstract Th0048: How do novel type 2 diabetes mellitus (T2DM) medications affect lipid parameters in patients with metabolic dysfunction–associated steatotic liver disease (MASLD) and type 2 diabetes

Sabyasachi Sen, Jessica Khoury, Shannen Nicole Dean Ubalde
Arteriosclerosis Thrombosis and Vascular Biology
Liver Disease Diagnosis and Treatment
article

Abstract Th0048: How do novel type 2 diabetes mellitus (T2DM) medications affect lipid parameters in patients with metabolic dysfunction–associated steatotic liver disease (MASLD) and type 2 diabetes

Sabyasachi Sen, Jessica Khoury, Shannen Nicole Dean Ubalde
article en

Abstract

Introduction: Metabolic dysfunction–associated steatotic liver disease (MASLD) is highly associated with T2DM and is a common cause of chronic liver disease and cardiovascular disease (CVD). Our goal was to examine the effects of various antidiabetic agents such as Metformin, sodium-glucose transport protein-2 inhibitors (SGLT2i), glucagon-like peptide 1 receptor analogs (GLP-1RAs), compared to insulin(ins) alone, as the control, in T2DM patients with liver fibrosis (based on FIB-4 score) as major comorbidities. We also wanted to investigate how do these agents affect the lipid parameters. Methods: We conducted a cross-sectional chart review of patients with using FIB-4 score at or above 1.3 and 1.8, to detect subjects at risk for liver hepato-steatosis at the DC VAMC Diabetes Clinic for over 24 months. We screened a total of 255 patients based on the inclusion criteria. Results: Patients had a mean age of 72.64±0.67 and were mostly on ins alone (32.23%). The mean BMI was 30.43±0.58 and A1C was 7.8±0.13. Using Mann-Whitney test, Metformin (+/- insulin) group had significantly lower FIB-4 score of 1.76±0.08 (n = 24) compared to SGLT2-i (+/- insulin or metformin) with 2.29±0.2 (p=0.0370) (n=32), while GLP-1RA(+/-ins or met) had a FIB-4 score of 1.9±0.1 (n= 30). Insulin only group had the highest FIB-4 of 2.36±0.22 (n = 41). The lipid panels were also analyzed with the mean LDL of GLP-1RA(+/-ins or met) had 70.40 ±6.065, SGLT2i(+/-ins or met) had 66.00 ±4.312, Metformin(+/-ins) had 79.79 ±8.026, and ins only had 71.95 ±6.463. The mean HDL for GLP-1RA(+/-ins or met) had 45.77±2.378, SGLT2i(+/-ins or met) had 43.31 ±2.897, Metformin(+/-ins) had 46.46±2.341, ins only had 56.20±2.695. The mean total cholesterol of GLP-1RA(+/-ins or met) was 140.2±7.653, SGLT2i(+/-ins or met) had 132.3±4.671, Metformin(+/-ins) had 146.3±8.659, ins only had 149.3±7.134. The mean triglyceride of GLP-1RA(+/-ins or met) had 134.4±10.68, SGLT2i(+/-ins or met) had 162.5±17.52, Metformin(+/-ins) 114.2±7.849, ins only had 120.8±11.99. Conclusion: In our predominantly African-American cohort, Metformin group appears to have the lowest FIB-4 score compared to other regimens with GLP1A coming at a close second. Additionally, the lipid parameters LDL, HDL, and total cholesterol seem to be similar across the medication groups except for triglyceride, where SGLT2i seems to be associated with statistically significant higher values compared to non-SGLT2i groups, particularly Metformin group.

Arteriosclerosis Thrombosis and Vascular BiologyVol. 45(Suppl_1)
George Washington University (US)
Good health and well-being
Openalex Percentile: Top 79%
Liver Disease Diagnosis and Treatment
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.