Evidence mapPaperPMID 35235172Full record

ReviewCurrent hypertension reports2022

Targeting Features of the Metabolic Syndrome Through Sympatholytic Effects of SGLT2 Inhibition.

Lakshini Y Herat, Jennifer Matthews, Omar Azzam, Markus P Schlaich, Vance B Matthews

Open access · hybridAbstract readReview
In one paragraph

Review in Current hypertension reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

17 citing papers in PubMed, 28 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Observational
  8. Emerging Perspectives on the Impact of Diabetes Mellitus and Anti-Diabetic Drugs on Premenstrual Syndrome. A Narrative Review.Diabetes therapy : research, treatment and education of diabetes and related disorders · 2024
    Review
  9. Review
  10. SGLT2 and SGLT1 inhibitors suppress the activities of the RVLM neurons in newborn Wistar rats.Hypertension research : official journal of the Japanese Society of Hypertension · 2024
    Article
  11. Review
  12. Article
  13. Review
  14. Review
  15. Review
  16. International journal of molecular sciences · 2022
    Article
  17. 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

5 authors at 1 institution in 1 country.

Lakshini Y HeratDobney Hypertension Centre, School of Biomedical Science - Royal Perth Hospital Unit, University of Western Australia, MRF Building, Level 3, Rear 50 Murray St, Perth, WA, 6000, Australia.ORCID 0000-0001-9818-006X
Jennifer MatthewsDobney Hypertension Centre, School of Biomedical Science - Royal Perth Hospital Unit, University of Western Australia, MRF Building, Level 3, Rear 50 Murray St, Perth, WA, 6000, Australia.
Omar AzzamDobney Hypertension Centre, School of Biomedical Science - Royal Perth Hospital Unit, University of Western Australia, MRF Building, Level 3, Rear 50 Murray St, Perth, WA, 6000, Australia.
Markus P SchlaichDobney Hypertension Centre, School of Biomedical Science - Royal Perth Hospital Unit, University of Western Australia, MRF Building, Level 3, Rear 50 Murray St, Perth, WA, 6000, Australia.
Vance B MatthewsDobney Hypertension Centre, School of Biomedical Science - Royal Perth Hospital Unit, University of Western Australia, MRF Building, Level 3, Rear 50 Murray St, Perth, WA, 6000, Australia. vance.matthews@uwa.edu.au.
The University of Western Australia · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purpose of reviewThe moderate glucose-lowering effect of sodium glucose co-transporter 2 (SGLT2) inhibitors is unlikely to explain SGLT2 inhibitor-mediated beneficial outcomes, and unravelling the underlying mechanisms is a high priority in the research community. Given the dominant pathophysiologic role of the sympathetic nervous system activation in conditions such as hypertension and perturbed glucose homeostasis, it is pertinent to postulate that SGLT2 inhibitors may exert their beneficial effects at least in part via sympathetic inhibition. RECENT

findingsSGLT2 inhibitors have shown enormous potential to improve cardiovascular outcomes in patients with type 2 diabetes, and their therapeutic potential is currently being investigated in a range of associated comorbidities such as heart failure and chronic kidney disease. Indeed, recent experimental data in relevant animal models highlight a bidirectional interaction between sympathetic nervous system activation and SGLT2 expression, and this facilitates several of the features associated with SGLT2 inhibition observed in clinical trials including improved glucose metabolism, weight loss, increased diuresis, and lowering of blood pressure. Currently available data highlight the various levels of interaction between the sympathetic nervous system and SGLT2 expression and explores the potential for SGLT2 inhibition as a therapeutic strategy in conditions commonly characterised by sympathetic activation.

Indexed as

Diabetes Mellitus, Type 2HypertensionMetabolic SyndromeSodium-Glucose Transporter 2 InhibitorsAnimalsGlucoseHumansHypoglycemic AgentsSodium-Glucose Transporter 2SympatholyticsGlucoseHypoglycemic AgentsSodium-Glucose Transporter 2Sodium-Glucose Transporter 2 InhibitorsSympatholyticsCardio-renal protectionHypertensionMetabolic syndromeSGLT2 inhibitionSympathetic nervous systemSympatho-inhibition

Identifiers

PMID35235172
PMCPMC8942945
OpenAlexW4214897721

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.