Evidence mapPaperPMID 40486606Full record

ReviewAnnals of medicine and surgery (2012)2025

"Is sotagliflozin a 'wonder drug'? A review of its impact on cardiovascular, diabetic, renal, neuroprotective, and hepatic outcomes".

Eeshal Fatima, Hamza Irfan, Faiza Fatima, Jyoti Jain, Obaid Ur Rehman, Ayesha Sehar, Bilal Ahmad, Sanjana Kumari, Aymar Akilimali

Abstract readReview
In one paragraph

Review in Annals of medicine and surgery (2012), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
field-weighted citation impact
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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
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

9 authors.

Eeshal FatimaDepartment of Internal Medicine, Services Institute of Medical Sciences, Lahore, Pakistan.
Hamza IrfanDepartment of Internal Medicine, Shaikh Khalifa Bin Zayed Al Nahyan Medical and Dental College, Lahore, Pakistan.ORCID https://orcid.org/0000-0002-0967-7523
Faiza FatimaDepartment of Internal Medicine, Services Institute of Medical Sciences, Lahore, Pakistan.ORCID https://orcid.org/0009-0006-4871-6595
Jyoti JainDepartment of Internal Medicine, All India Institute of Medical Sciences, Jodhpur, India.
Obaid Ur RehmanDepartment of Internal Medicine, Services Institute of Medical Sciences, Lahore, Pakistan.ORCID https://orcid.org/0009-0000-8302-2173
Ayesha SeharDepartment of Internal Medicine, King Edward Medical University, Lahore, Pakistan.
Bilal AhmadDepartment of Internal Medicine, Shaikh Khalifa Bin Zayed Al Nahyan Medical and Dental College, Lahore, Pakistan.ORCID https://orcid.org/0009-0005-8911-0955
Sanjana KumariDepartment of Internal Medicine, Dow University of Health Sciences, Karachi, Pakistan.ORCID https://orcid.org/0000-0001-5998-0427
Aymar AkilimaliDepartment of Internal Medicine, Department of Research, Medical Research Circle (MedReC), Goma, DR Congo.ORCID https://orcid.org/0000-0001-9393-1215

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Heart failure (HF) and diabetes mellitus frequently co-occur, with an incidence of HF among diabetics ranging from 9% to 22%. Clinical research underscores that shared pathophysiological pathways link these conditions, driving advancements in therapeutic strategies that target neuro-hormonal modulation and sodium-glucose co-transporter 2 (SGLT2) inhibition. The SOLOIST-WHF and SCORED trials highlighted the efficacy of sotagliflozin, a dual sodium-glucose co-transporters 1/2 (SGLT1/2) inhibitor, in patients with HF and chronic kidney disease (CKD), demonstrating reductions in cardiovascular mortality and HF-related hospitalizations. Trials with other SGLT2 inhibitors, like dapagliflozin and empagliflozin, in HF, diabetes, and renal disease also showed significant reductions in major adverse cardiovascular events, hospitalizations, and improved kidney function. Furthermore, SGLT2 inhibitors have shown neuroprotective effects, potentially benefiting patients with Alzheimer's and Parkinson's diseases. Dual SGLT1/2 inhibitors, by targeting glucose transport in the renal and intestinal systems, not only reduce blood glucose but also improve insulin sensitivity, weight loss, and cardiovascular health. Sotagliflozin specifically impacts postprandial glucose absorption, mitigating the risks of hypoglycemia and hyperglycemia-related complications. In diabetic CKD, SGLT inhibitors promote renal protection by reducing glucose reabsorption, diuresis, and systemic inflammation. Neuroprotective effects of these agents, including reduced oxidative stress and inflammatory markers, show promise in treating neurodegenerative diseases. While adverse effects like hypoglycemia and ketoacidosis remain concerns, tailored dosing, and monitoring strategies may mitigate these risks. Thus, SGLT inhibitors, especially dual inhibitors like sotagliflozin, offer broad therapeutic benefits in diabetes, HF, CKD, and potentially neurological conditions.

Indexed as

chronic kidney diseasediabetes mellitusdual SGLT1/2 inhibitorsheart failuresotagliflozin

Identifiers

PMID40486606
PMCPMC12140779

What Socratic holds

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LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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 Socratic graph.