Evidence map›Paper›PMID 42592373›Full record

ArticleGout, urate, and crystal deposition disease2024

SGLT2 Inhibitors and Uric Acid Homeostasis.

Ava M Zapf, Owen M Woodward

Abstract read
In one paragraph

Article in Gout, urate, and crystal deposition disease, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Observational
  2. Review
  3. Review
  4. Review
  5. 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

2 authors.

Ava M ZapfDepartment of Physiology, University of Maryland School of Medicine, Baltimore, MD 21201, USA.ORCID 0000-0002-5642-3585
Owen M WoodwardDepartment of Physiology, University of Maryland School of Medicine, Baltimore, MD 21201, USA.ORCID 0000-0001-9514-2180

Funding

PKD Innovation and Resource Development CoreU54DK126114 · NIDDK · UNIVERSITY OF MARYLAND BALTIMORE · PI OWEN M WOODWARD · 2020 to 2026
$7.3M
Diabetes, Obesity, and Metabolic ComplicationsT32DK098107 · NIDDK · UNIVERSITY OF MARYLAND BALTIMORE · PI TAYLOR, SIMEON I. · 2015 to 2025
$2.4M
Molecular Mechanisms of Uric Acid HomeostasisR01DK114091 · NIDDK · UNIVERSITY OF MARYLAND BALTIMORE · PI WOODWARD, OWEN M · 2017 to 2020
$1.4M
NIDDK NIH HHS R01 DK114091NIDDK NIH HHS T32 DK098107NIDDK NIH HHS U54 DK126114
6 · The paper itself

Abstract

A relationship between metabolic disorders and hyperuricemia is well established. The nature of the relationship-risk factor, causal agent, or byproduct-remains unclear. Recent studies of sodium-glucose transporter 2 inhibitors (SGLT2i's) have established that this pharmacological intervention is beneficial to patients with hyperglycemia and type 2 diabetes mellitus (T2D) and also against the common cardio and renal comorbidities associated with diabetes. Hyperuricemia, or high plasma uric acid levels, is one of the comorbidities mitigated with SGLT2i treatment, raising the potential for using SGLT2i's as part of the treatment for gout and hyperuricemia. However, the mechanisms underlying the lower plasma urate levels and increased uricosuria produced with SGLT2i's remains poorly understood. Here, we review the renal physiology of glucose and uric acid transport, the renal consequences of hyperglycosuria and diabetes, the benefits and physiology of SGLT2i use, and discuss several potential mechanisms that may be responsible for the favorable uricosuric effect observed in those treated with SGLT2i's.

Indexed as

glucosegoutkidneySGLT2SGLT2 inhibitorsurateuric acid

Identifiers

PMID42592373
PMCPMC13464547

What Socratic 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 Socratic graph.