Evidence map›Paper›PMID 35059247›Full record

ArticleDiabetology international2022

Two-year administration of sodium-glucose co-transporter 2 inhibitor brought about marked reduction of body fat independent of skeletal muscle amount or glycemic improvement in Japanese patients with type 2 diabetes.

Moeko Sakamoto, Yuka Goto, Ayako Nagayama, Mamiko Yano, Shuichi Sato, Yuji Tajiri, Masatoshi Nomura

Open access · greenAbstract read
In one paragraph

Article in Diabetology international, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 2 pooled it
1.3field-weighted citation impact, top 19% 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

6 citing papers in PubMed, 2 syntheses or guidelines pooled it, 13 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Article
  5. Article
  6. 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

7 authors at 2 institutions in 1 country.

Moeko SakamotoDivision of Endocrinology and Metabolism, Kurume University School of Medicine, Kurume, Japan.
Yuka GotoDivision of Endocrinology and Metabolism, Kurume University School of Medicine, Kurume, Japan.
Ayako NagayamaDivision of Endocrinology and Metabolism, Kurume University School of Medicine, Kurume, Japan.
Mamiko YanoDivision of Endocrinology and Metabolism, Kurume University School of Medicine, Kurume, Japan.
Shuichi SatoYame General Hospital, Yame, Japan.
Yuji TajiriDivision of Endocrinology and Metabolism, Kurume University School of Medicine, Kurume, Japan.ORCID 0000-0001-8266-2080
Masatoshi NomuraDivision of Endocrinology and Metabolism, Kurume University School of Medicine, Kurume, Japan.
Kurume University · JPOno Clinic · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimTo investigate long-term effects of sodium-glucose co-transporter 2 inhibitor (SGLT2i) on anthropometric and metabolic factors in Japanese patients with type 2 diabetes (T2DM). PATIENTS AND

methodsThis is a retrospective observation study. Forty-six outpatients with T2DM (32 men and 14 women, 51 ± 13 years old, BMI 27.9 ± 4.8, means ± S.D.) who had been treated by SGLT2i for 2 years were selected and their metabolic and anthropometric data were retrieved from medical records retrospectively. Regular instruction for diet and exercise had been performed throughout the administration of SGLT2i in outpatient clinic basis.

resultsBy the administration of SGLT2i for 2 years, body weight and body fat amount were significantly reduced (

conclusionSGLT2i can effectively reduce body weight and body fat mass independent of the blood glucose improvement or the renal function. Under the periodical instruction for nutrition and exercise this oral hypoglycemic agent can be safely administered for a long term without a risk for sarcopenia.

Indexed as

Body fat massHbA1cLong-term administrationSGLT2 inhibitorWeight reduction

Identifiers

PMID35059247
PMCPMC8733087
OpenAlexW3164445252

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.