Evidence mapPaperPMID 34497814Full record

ReviewFrontiers in medicine2021

Sodium-Glucose Cotransporter-2 Inhibitor (SGLT2i) as a Primary Preventative Agent in the Healthy Individual: A Need of a Future Randomised Clinical Trial?

Dan Xu, Owain Chandler, Cleo Wee, Chau Ho, Jacquita S Affandi, Daya Yang, Xinxue Liao, Wei Chen, Yanbing Li, Christopher Reid and 1 more

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
3.1field-weighted citation impact, top 7% 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

8 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Exploring the Efficacy of Sotagliflozin on Heart and Kidney Health in Diabetic Patients: A Comprehensive Meta-Analysis.Indian journal of community medicine : official publication of Indian Association of Preventive & Social Medicine
    Review
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

11 authors at 3 institutions in 2 countries.

Dan XuFaculty of Health Sciences, CCRE, Curtin School of Population Health, Curtin University, Perth, WA, Australia.
Owain ChandlerFaculty of Health Sciences, Curtin Medical School, Curtin University, Perth, WA, Australia.
Cleo WeeFaculty of Health Sciences, Curtin Medical School, Curtin University, Perth, WA, Australia.
Chau HoFaculty of Health Sciences, CCRE, Curtin School of Population Health, Curtin University, Perth, WA, Australia.
Jacquita S AffandiFaculty of Health Sciences, CCRE, Curtin School of Population Health, Curtin University, Perth, WA, Australia.
Daya YangDepartment of Medical Education, First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Xinxue LiaoDepartment of Medical Education, First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Wei ChenDepartment of Medical Education, First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Yanbing LiDepartment of Medical Education, First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Christopher ReidFaculty of Health Sciences, CCRE, Curtin School of Population Health, Curtin University, Perth, WA, Australia.
Haipeng XiaoDepartment of Medical Education, First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Curtin University · AUSun Yat-sen University · CNThe First Affiliated Hospital, Sun Yat-sen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sodium-glucose cotransporter-2 inhibitors (SGLT2i) are a relatively novel class of drug for treating type 2 diabetes mellitus (T2DM) that inhibits glucose reabsorption in the renal proximal tubule to promote glycosuria and reduce blood glucose levels. SGLT2i has been clinically indicated for treating T2DM, with numerous recent publications focussing on both primary and secondary prevention of cardiovascular and renal events in Type 2 diabetic patients. The most recent clinical trials showed that SGLT2i have moderately significant beneficial effects on atherosclerotic major adverse cardiovascular events (MACE) in patients with histories of atherosclerotic cardiovascular disease. In this review and analysis, SGLT2i have however demonstrated clinically significant benefits in reducing hospitalisation for heart failure and worsening of chronic kidney disease (CKD) irrespective of pre-existing atherosclerotic cardiovascular disease or previous heart failure history. A meta-analysis suggests that all SGLT2 inhibitors demonstrated the therapeutic benefit on all-cause and cardiovascular mortality, as shown in EMPAREG OUTCOME study with a significant decrease in myocardial infarction, without increased stroke risk. All the above clinical trial recruited type 2 diabetic patients. This article aims to postulate and review the possible primary prevention role of SGLT2i in healthy individuals by reviewing the current literature and provide a prospective overview. The emphasis will include primary prevention of Type 2 Diabetes, Heart Failure, CKD, Hypertension, Obesity and Dyslipidaemia in healthy individuals, whom are defined as healthy, low or intermediate risks patients.

Indexed as

cardioprotectionchronic diseases preventionprimary preventionrenoprotectionSGLT2i inhibitor

Identifiers

PMID34497814
PMCPMC8419219
OpenAlexW3195454129

What Socratic holds

Textmetadata
LicenceCC BY
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.