Evidence mapPaperPMID 12748858Full record

ReviewPflugers Archiv : European journal of physiology2004

The sodium/glucose cotransport family SLC5.

Ernest M Wright, Eric Turk

Erratum issued Registry-linked trialAbstract readReview
PubMed Publisher
In one paragraph

Review in Pflugers Archiv : European journal of physiology, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. It is linked to trial NCT02887677 (A Study of the Effects of Dapagliflozin on Ambulatory Aortic Pressure, Arterial Stiffness and Urine Albumin Excretion in Patients With Type 2 Diabetes), which is not on this map. Cited by 193 papers.

0numbers the graph read from it
0cells of the map it votes in
193citing papers in PubMed
3.1field-weighted citation impact, top 8% 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.

NCT02887677 phase4terminatedstarted 2016, after this paper: background citation

A Study of the Effects of Dapagliflozin on Ambulatory Aortic Pressure, Arterial Stiffness and Urine Albumin Excretion in Patients With Type 2 Diabetes

Ran2016Enrolled85Registered outcomes9Posted comparisons0ConditionsDiabetes MellitusArmsdapagliflozin, Placebo
Open the trial in the graph
3 · Its place in the literature

Who cites it

193 citing papers in PubMed, 236 citations in OpenAlex.

  1. Trial
  2. Article
  3. ChREBP-β Exacerbates Renal Tubular Disorders Caused by Fructose via ATF4.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
  4. Revisiting vSGLT: Non-Radioactive Characterization of the Vibrio NaInternational journal of molecular sciences · 2026
    Article
  5. Review
  6. Article
  7. Molecular therapy. Nucleic acids · 2025
    Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Handling the sugar rush: the role of the renal proximal tubule.American journal of physiology. Renal physiology · 2024
    Review
  15. Article
  16. Article
  17. Review
  18. Review
  19. Review
  20. SGLT2 Inhibitors in Aging-Related Cardiovascular Disease: A Review of Potential Mechanisms.American journal of cardiovascular drugs : drugs, devices, and other interventions · 2023
    Review

133 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Ernest M WrightDepartment of Physiology, David Geffen School of Medicine at UCLA, Los Angeles, CA 90095-1751, USA. ewright@mednet.ucla.edu
Eric Turk
University of California, Los Angeles · US

Funding

MOLECULAR MECHANISMS OF INTESTINAL TRANSPORTR01DK019567 · UNIVERSITY OF CALIFORNIA LOS ANGELES · 1986 to 2005
$1.8M
MOLECULAR ARCHITECTURE OF THE NA/GLUCOSE COTRANSPORTERR01DK044602 · UNIVERSITY OF CALIFORNIA LOS ANGELES · 1992 to 2005
$1.5M
FAMILIAL GLUCOSE/GALACTOSE MALABSORPTIONR01DK044582 · UNIVERSITY OF CALIFORNIA LOS ANGELES · 1992 to 2001
$555k
NIDDK NIH HHS DK19567NIDDK NIH HHS DK44582NIDDK NIH HHS DK44602
6 · The paper itself

Abstract

The sodium/glucose cotransporter family (SLCA5) has 220 or more members in animal and bacterial cells. There are 11 human genes expressed in tissues ranging from epithelia to the central nervous system. The functions of nine have been revealed by studies using heterologous expression systems: six are tightly coupled plasma membrane Na(+)/substrate cotransporters for solutes such as glucose, myo-inositol and iodide; one is a Na(+)/Cl(-)/choline cotransporter; one is an anion transporter; and another is a glucose-activated ion channel. The exon organization of eight genes is similar in that each comprises 14-15 exons. The choline transporter (CHT) is encoded in eight exons and the Na(+)-dependent myo-inositol transporter (SMIT) in one exon. Mutations in three genes produce genetic diseases (glucose-galactose malabsorption, renal glycosuria and hypothyroidism). Members of this family are multifunctional membrane proteins in that they also behave as uniporters, urea and water channels, and urea and water cotransporters. Consequently it is a challenge to determine the role(s) of these genes in human physiology and pathology.

Indexed as

Amino Acid SequenceBiological TransportGlucoseHumansMembrane GlycoproteinsMolecular Sequence DataMonosaccharide Transport ProteinsMultigene FamilySodiumSodium-Glucose Transporter 1GlucoseMembrane GlycoproteinsMonosaccharide Transport ProteinsSLC5A1 protein, humanSodiumSodium-Glucose Transporter 1

Identifiers

PMID12748858
OpenAlexW2147693969

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

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.