Evidence map›Paper›PMID 27611858›Full record

Trial reportScientific reports2016

Sodium-Glucose Cotransporter 2 (SGLT2) Inhibitor Increases Circulating Zinc-Α2-Glycoprotein Levels in Patients with Type 2 Diabetes.

Xin Liao, Xuemei Wang, Haopeng Li, Ling Li, Guohao Zhang, Mengliu Yang, Lei Yuan, Hua Liu, Gangyi Yang, Lin Gao

Open access · goldAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
3.7field-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

26 citing papers in PubMed, 1 synthesis or guideline pooled it, 51 citations in OpenAlex.

  1. Pooled it
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  5. Review
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  14. Changes of Serum Zinc-Journal of diabetes research · 2021
    Article
  15. Zinc.Advances in food and nutrition research · 2021
    Review
  16. Article
  17. Article
  18. Article
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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

10 authors at 5 institutions in 2 countries.

Xin LiaoDepartment of Endocrinology, the Affiliated Hospital, Zunyi Medical University, 563003 Guizhou, China.
Xuemei WangDepartment of Endocrinology, the Affiliated Hospital, Zunyi Medical University, 563003 Guizhou, China.
Haopeng LiDepartment of Endocrinology, the Affiliated Hospital, Zunyi Medical University, 563003 Guizhou, China.
Ling LiKey Laboratory of Diagnostic Medicine (Ministry of Education) and Department of Clinical Biochemistry, College of Laboratory Medicine, Chongqing Medical University, 400016, China.
Guohao ZhangDepartment of Endocrinology, the Affiliated Hospital, Zunyi Medical University, 563003 Guizhou, China.
Mengliu YangDepartment of Endocrinology, the Second Affiliated Hospital, Chongqing Medical University, 400010 Chongqing, China.
Lei YuanDepartment of Endocrinology, the Second Affiliated Hospital, Chongqing Medical University, 400010 Chongqing, China.
Hua LiuDepartment of Pediatrics, University of Mississippi Medical Center, Jackson, Mississippi 39216, USA.
Gangyi YangDepartment of Endocrinology, the Affiliated Hospital, Zunyi Medical University, 563003 Guizhou, China.
Lin GaoDepartment of Endocrinology, the Affiliated Hospital, Zunyi Medical University, 563003 Guizhou, China.
Zunyi Medical University · CNDalian Medical University · CNAffiliated Hospital of Guizhou Medical University · CNChongqing Medical University · CNUniversity of Mississippi Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

ZAG has recently been characterized as a potent metabolic regulator, but the effect of anti-diabetic agents on ZAG in humans remains unknown. Our aim was to study the effects of SGLT2 inhibitor on circulating ZAG and ADI in nT2DM. 162 subjects with nT2DM were treated by a placebo or DAPA. After 3-months of DAPA therapy, HbA1c, FBG, 2h-PBG, FFA, TG, blood pressure, BMI, WHR, body weight, FAT%, FINS, and HOMA-IR in T2DM patients decreased significantly, whereas HDL-C was significantly increased. Importantly, circulating ZAG and ADI levels in these patients were also significantly increased after DAPA therapy. Basal ZAG levels were associated with changes in BMI, FAT%, TC, HbA1c, HDL-C and ADI at post-treatment, whereas basal ADI levels were associated with changes in FAT%, TC, HbA1c, FFA and HDL-c. In vitro, DAPA treatment showed increased ZAG expression and secretion in HepG2 cells. When combined with a PPAR-γinhibitor GW9662, the effect of DAPA on ZAG was abrogated. These findings suggest that circulating ZAG can be regulated by DAPA, and DAPA promotes the expression and secretion of ZAG in the liver via the activation of PPAR-γ. The changes in ZAG induced by DAPA may play a physiologic role in enhancing insulin sensitivity.

Indexed as

Sodium-Glucose Transporter 2 InhibitorsAdipokinesAdultCarrier ProteinsDiabetes Mellitus, Type 2FemaleGene Expression RegulationGlycoproteinsHumansLiverMaleMiddle AgedPPAR gammaProspective StudiesSodium-Glucose Transporter 2Zn-Alpha-2-GlycoproteinAdipokinesAZGP1 protein, humanCarrier ProteinsGlycoproteinsPPAR gammaSLC5A2 protein, humanSodium-Glucose Transporter 2Sodium-Glucose Transporter 2 InhibitorsZn-Alpha-2-Glycoprotein

Identifiers

PMID27611858
PMCPMC5017191
OpenAlexW2508112571

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.