Evidence map›Paper›PMID 25893475›Full record

ReviewCurrent hypertension reports2015

Are SGLT2 inhibitors reasonable antihypertensive drugs and renoprotective?

J A Lovshin, R E Gilbert

Abstract readReview
PubMed Publisher
In one paragraph

Review in Current hypertension reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Trial
  2. Review
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  4. Review
  5. Review
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  7. Review
  8. Review
  9. Review
  10. Article
  11. Article
  12. Pharmacological Agents Utilized in Patients With Type-2 Diabetes: Beyond Lowering A1c.P & T : a peer-reviewed journal for formulary management · 2018
    Article
  13. Review
  14. Sodium-Glucose Cotransporter 2 Inhibitors and Euglycemic Diabetic Ketoacidosis: Metabolic Acidosis With a Twist.Clinical diabetes : a publication of the American Diabetes Association · 2016
    Article
  15. Impact of sodium-glucose cotransporter 2 inhibitors on blood pressure.Vascular health and risk management · 2016 · on this map
    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

2 authors.

J A LovshinMt. Sinai Hospital, Division of Endocrinology and Metabolism, University of Toronto, Toronto, ON, Canada, lovshin@lunenfeld.ca.
R E Gilbert

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

By eliminating glucose in the urine, the sodium-glucose-linked cotransporter-2 (SGLT2) inhibitors act as osmotic diuretics to lower blood pressure in addition to reducing plasma glucose and assisting with weight loss. While not approved as antihypertensive agents, the ability of this new class of antihyperglycemic agents to lower blood pressure is not insubstantial, and while not used primarily for this indication, they may assist diabetic individuals in attaining currently recommended blood pressure targets. In addition to lowering systemic pressure, preclinical and exploratory human studies suggest that SGLT2 inhibitors may also lower intraglomerular pressure, potentially reducing the rate of GFR decline in patients with diabetic nephropathy. However, given the lack of clinically meaningful endpoint data, the use of SGLT2 inhibitors, primarily, as either antihypertensive or renoprotective agents would, at present, be premature. Fortunately, further insight will be garnered from large, randomized controlled trials that will assess the effects of various SGLT2 inhibitors on cardiovascular and renal outcomes.

Indexed as

CytoprotectionSodium-Glucose Transporter 2 InhibitorsAntihypertensive AgentsDiabetes ComplicationsHumansHypertensionKidneySodium-Glucose Transporter 2Antihypertensive AgentsSodium-Glucose Transporter 2Sodium-Glucose Transporter 2 Inhibitors

Identifiers

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.