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Effects of novel glucose-lowering drugs on the lipid parameters: A systematic review and meta-analysis

AIM: We aim to evaluate the impacts of sodium-glucose co-transporter 2 inhibitors (SGLT-2), glucagon-like peptide 1 agonist (GLP-1RAs), and dipeptidyl peptidase-four (DPP4) inhibitors on the levels of high-density lipoprotein, low-density lipoprotein, triglyceride and total cholesterol. METHODS: The...

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Autores principales: Dar, Sophia, Siddiqi, Ahmed Kamal, Alabduladhem, Tamim Omar, Rashid, Ahmed Mustafa, Sarfraz, Saba, Maniya, Talha, Menezes, Ritesh G., Almas, Talal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9142616/
https://www.ncbi.nlm.nih.gov/pubmed/35637990
http://dx.doi.org/10.1016/j.amsu.2022.103633
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author Dar, Sophia
Siddiqi, Ahmed Kamal
Alabduladhem, Tamim Omar
Rashid, Ahmed Mustafa
Sarfraz, Saba
Maniya, Talha
Menezes, Ritesh G.
Almas, Talal
author_facet Dar, Sophia
Siddiqi, Ahmed Kamal
Alabduladhem, Tamim Omar
Rashid, Ahmed Mustafa
Sarfraz, Saba
Maniya, Talha
Menezes, Ritesh G.
Almas, Talal
author_sort Dar, Sophia
collection PubMed
description AIM: We aim to evaluate the impacts of sodium-glucose co-transporter 2 inhibitors (SGLT-2), glucagon-like peptide 1 agonist (GLP-1RAs), and dipeptidyl peptidase-four (DPP4) inhibitors on the levels of high-density lipoprotein, low-density lipoprotein, triglyceride and total cholesterol. METHODS: The MEDLINE database was searched from inception till October 2021, for randomized controlled trials assessing the effects of sodium-glucose co-transporter two inhibitors (SGLT-2), glucagon-like peptide 1 agonist (GLP-1RAs), and dipeptidyl peptidase-four (DPP4) inhibitors on lipid levels. RESULTS: A total of 57 trials were included in the analysis. Our pooled analysis demonstrates that SGLT-2 inhibitors significantly increase the levels of HDL (WMD = 0.07 mg/dL [0.06 to 0.08], P < 0.00001). SGLT-2 inhibitors were also found to be significantly associated with an increase in the levels of LDL (WMD = 0.11 mg/dL, [0.09–0.13 mg/dL, P < 0.00001). Pooled analysis also demonstrates that SGLT-2 inhibitors significantly reduce the levels of triglyceride (WMD = −0.10 mg/dL, [-0.13 to −0.06], P < 0.00001). Our pooled analysis demonstrates that SGLT-2 inhibitors significantly increased the levels of total cholesterol (WMD = 0.10 mg/dL, [0.06 to 0.15], P < 0.0001), whereas, GLP-1RAs significantly reduced the levels of total cholestrol (WMD = −0.18 mg/dL, [-0.34 to −0.02], P = 0.03). CONCLUSION: This is the first head-to-head study comparing the effects of 3-novel glucose-lowering agents to lipid parameters. However, more trials are crucial to better understand the impact of glucose-lowering drugs on lipid parameters.
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spelling pubmed-91426162022-05-29 Effects of novel glucose-lowering drugs on the lipid parameters: A systematic review and meta-analysis Dar, Sophia Siddiqi, Ahmed Kamal Alabduladhem, Tamim Omar Rashid, Ahmed Mustafa Sarfraz, Saba Maniya, Talha Menezes, Ritesh G. Almas, Talal Ann Med Surg (Lond) Systematic Review / Meta-analysis AIM: We aim to evaluate the impacts of sodium-glucose co-transporter 2 inhibitors (SGLT-2), glucagon-like peptide 1 agonist (GLP-1RAs), and dipeptidyl peptidase-four (DPP4) inhibitors on the levels of high-density lipoprotein, low-density lipoprotein, triglyceride and total cholesterol. METHODS: The MEDLINE database was searched from inception till October 2021, for randomized controlled trials assessing the effects of sodium-glucose co-transporter two inhibitors (SGLT-2), glucagon-like peptide 1 agonist (GLP-1RAs), and dipeptidyl peptidase-four (DPP4) inhibitors on lipid levels. RESULTS: A total of 57 trials were included in the analysis. Our pooled analysis demonstrates that SGLT-2 inhibitors significantly increase the levels of HDL (WMD = 0.07 mg/dL [0.06 to 0.08], P < 0.00001). SGLT-2 inhibitors were also found to be significantly associated with an increase in the levels of LDL (WMD = 0.11 mg/dL, [0.09–0.13 mg/dL, P < 0.00001). Pooled analysis also demonstrates that SGLT-2 inhibitors significantly reduce the levels of triglyceride (WMD = −0.10 mg/dL, [-0.13 to −0.06], P < 0.00001). Our pooled analysis demonstrates that SGLT-2 inhibitors significantly increased the levels of total cholesterol (WMD = 0.10 mg/dL, [0.06 to 0.15], P < 0.0001), whereas, GLP-1RAs significantly reduced the levels of total cholestrol (WMD = −0.18 mg/dL, [-0.34 to −0.02], P = 0.03). CONCLUSION: This is the first head-to-head study comparing the effects of 3-novel glucose-lowering agents to lipid parameters. However, more trials are crucial to better understand the impact of glucose-lowering drugs on lipid parameters. Elsevier 2022-04-16 /pmc/articles/PMC9142616/ /pubmed/35637990 http://dx.doi.org/10.1016/j.amsu.2022.103633 Text en © 2022 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Systematic Review / Meta-analysis
Dar, Sophia
Siddiqi, Ahmed Kamal
Alabduladhem, Tamim Omar
Rashid, Ahmed Mustafa
Sarfraz, Saba
Maniya, Talha
Menezes, Ritesh G.
Almas, Talal
Effects of novel glucose-lowering drugs on the lipid parameters: A systematic review and meta-analysis
title Effects of novel glucose-lowering drugs on the lipid parameters: A systematic review and meta-analysis
title_full Effects of novel glucose-lowering drugs on the lipid parameters: A systematic review and meta-analysis
title_fullStr Effects of novel glucose-lowering drugs on the lipid parameters: A systematic review and meta-analysis
title_full_unstemmed Effects of novel glucose-lowering drugs on the lipid parameters: A systematic review and meta-analysis
title_short Effects of novel glucose-lowering drugs on the lipid parameters: A systematic review and meta-analysis
title_sort effects of novel glucose-lowering drugs on the lipid parameters: a systematic review and meta-analysis
topic Systematic Review / Meta-analysis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9142616/
https://www.ncbi.nlm.nih.gov/pubmed/35637990
http://dx.doi.org/10.1016/j.amsu.2022.103633
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