Evidence map›Paper›PMID 36232780›Full record

ArticleInternational journal of molecular sciences2022

Lipids Alterations Associated with Metformin in Healthy Subjects: An Investigation Using Mass Spectrometry Shotgun Approach.

Lina A Dahabiyeh, Muhammad Mujammami, Reem H AlMalki, Tawfiq Arafat, Hicham Benabdelkamel, Assim A Alfadda, Anas M Abdel Rahman

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In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.5field-weighted citation impact, top 18% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 17 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 5 institutions in 3 countries.

Lina A DahabiyehDepartment of Pharmaceutical Sciences, School of Pharmacy, The University of Jordan, Amman 11942, Jordan.ORCID 0000-0002-4688-7052
Muhammad MujammamiEndocrinology and Diabetes Unit, Department of Medicine, College of Medicine, King Saud University, Riyadh 12372, Saudi Arabia.
Reem H AlMalkiDepartment of Botany and Microbiology, College of Science, King Saud University, Riyadh 11451, Saudi Arabia.ORCID 0000-0001-5221-5634
Tawfiq ArafatJordan Center for Pharmaceutical Research, Amman 11195, Jordan.
Hicham BenabdelkamelProteomics Resource Unit, Obesity Research Center, College of Medicine, King Saud University, Riyadh 12372, Saudi Arabia.ORCID 0000-0001-9745-2959
Assim A AlfaddaEndocrinology and Diabetes Unit, Department of Medicine, College of Medicine, King Saud University, Riyadh 12372, Saudi Arabia.ORCID 0000-0002-4792-5188
Anas M Abdel RahmanMetabolomics Section, Department of Clinical Genomics, Center for Genome Medicine, King Faisal Specialist Hospital and Research Centre (KFSHRC), Riyadh 11564, Saudi Arabia.ORCID 0000-0002-9527-9424
King Saud University · SAKing Abdulaziz University · SAKing Faisal Specialist Hospital & Research Centre · SAMemorial University of Newfoundland · CAUniversity of Jordan · JO

Funding

This research was funded by the University Diabetes Center, King Saud University 00001111
6 · The paper itself

Abstract

Metformin is an orally effective insulin-sensitizing drug widely prescribed for treating type 2 diabetes mellitus (T2DM). Metformin has been reported to alter lipid metabolism. However, the molecular mechanisms behind its impact on lipid metabolism remain partially explored and understood. In the current study, mass spectrometry-based lipid profiling was used to investigate the lipidomic changes in the serum of 26 healthy individuals after a single-dose intake of metformin. Samples were analyzed at five-time points: preadministration, before the maximum concentration of metformin (Cmax), Cmax, after Cmax, and 36 h post-administration. A total of 762 molecules were significantly altered between the five-time points. Based on a comparison between baseline level and Cmax, metformin significantly increased and decreased the level of 33 and 192 lipids, respectively (FDR ≤ 0.05 and fold change cutoff of 1.5). The altered lipids are mainly involved in arachidonic acid metabolism, steroid hormone biosynthesis, and glycerophospholipid metabolism. Furthermore, several lipids acted in an opposed or similar manner to metformin levels and included fatty acyls, sterol lipids, glycerolipids, and glycerophospholipids. The significantly altered lipid species pointed to fundamental lipid signaling pathways that could be linked to the pleiotropic effects of metformin in T2DM, insulin resistance, polycystic ovary syndrome, cancer, and cardiovascular diseases.

Indexed as

Diabetes Mellitus, Type 2Insulin ResistanceMetforminPolycystic Ovary SyndromeArachidonic AcidFemaleGlycerophospholipidsHealthy VolunteersHumansHypoglycemic AgentsInsulinMass SpectrometrySteroidsSterolsArachidonic AcidGlycerophospholipidsHypoglycemic AgentsInsulinMetforminSteroidsSterolsarachidonic acidcancerglycerophospholipidhydroxyeicosatetraenoic acids (HETE)metforminsphingosine-1-phosphateT2DM

Identifiers

PMID36232780
PMCPMC9569788
OpenAlexW4297977811

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.