Evidence map›Paper›PMID 34558835›Full record

Trial reportHepatology communications2022

Ipragliflozin Improves the Hepatic Outcomes of Patients With Diabetes with NAFLD.

Hirokazu Takahashi, Takaomi Kessoku, Miwa Kawanaka, Michihiro Nonaka, Hideyuki Hyogo, Hideki Fujii, Tomoaki Nakajima, Kento Imajo, Kenichi Tanaka, Yoshihito Kubotsu and 14 more

Open access · goldAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Hepatology communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 88 papers, 7 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
88citing papers in PubMed, 7 pooled it
14.8field-weighted citation impact, top 1% 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

88 citing papers in PubMed, 7 syntheses or guidelines pooled it, 141 citations in OpenAlex.

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

24 authors at 9 institutions in 1 country.

Hirokazu TakahashiDivision of Metabolism and Endocrinology, Faculty of Medicine, Saga University, Saga, Japan.ORCID 0000-0002-2374-2889
Takaomi KessokuDepartment of Gastroenterology and Hepatology, Graduate School of Medicine, Yokohama City University, Yokohama, Japan.
Miwa KawanakaDepartment of General Internal Medicine Kawasaki Medical Center, Kawasaki Medical School, Okayama, Japan.
Michihiro NonakaDepartment of Gastroenterology and Hepatology, JA Hiroshima General Hospital, Hatsukaichi, Japan.
Hideyuki HyogoDepartment of Gastroenterology and Hepatology, JA Hiroshima General Hospital, Hatsukaichi, Japan.
Hideki FujiiDepartment of Gastroenterology and Hepatology, Osaka City Juso Hospital, Osaka, Japan.ORCID 0000-0003-1267-9623
Tomoaki NakajimaDepartment of Hepatology, Sapporo Kosei General Hospital, Sapporo, Japan.
Kento ImajoDepartment of Gastroenterology and Hepatology, Graduate School of Medicine, Yokohama City University, Yokohama, Japan.
Kenichi TanakaDivision of Metabolism and Endocrinology, Faculty of Medicine, Saga University, Saga, Japan.
Yoshihito KubotsuDivision of Metabolism and Endocrinology, Faculty of Medicine, Saga University, Saga, Japan.
Hiroshi IsodaLiver Center, Saga University Hospital, Faculty of Medicine, Saga University, Saga, Japan.
Satoshi OedaLiver Center, Saga University Hospital, Faculty of Medicine, Saga University, Saga, Japan.
Osamu KuraiDepartment of Gastroenterology and Hepatology, Osaka City Juso Hospital, Osaka, Japan.
Masato YonedaDepartment of Gastroenterology and Hepatology, Graduate School of Medicine, Yokohama City University, Yokohama, Japan.
Masafumi OnoInternal Medicine, Tokyo Women's Medical University Medical Center East, Tokyo, Japan.
Yoichiro KitajimaDivision of Metabolism and Endocrinology, Faculty of Medicine, Saga University, Saga, Japan.
Ryo TajiriClinical Research Center, Saga University Hospital, Saga, Japan.
Ayako TakamoriClinical Research Center, Saga University Hospital, Saga, Japan.
Atsushi KawaguchiEducation and Research Center for Community Medicine, Faculty of Medicine, Saga University, Saga, Japan.
Shinichi AishimaDepartment of Pathology and Microbiology, Faculty of Medicine, Saga University, Saga, Japan.
Masayoshi KageKurume University Research Center for Innovative Cancer Therapy, Kurume, Japan.
Atsushi NakajimaDepartment of Gastroenterology and Hepatology, Graduate School of Medicine, Yokohama City University, Yokohama, Japan.
Yuichiro EguchiLiver Center, Saga University Hospital, Faculty of Medicine, Saga University, Saga, Japan.
Keizo AnzaiDivision of Metabolism and Endocrinology, Faculty of Medicine, Saga University, Saga, Japan.
Saga University · JPYokohama City University · JPHiroshima General Hospital · JPKawasaki Medical School · JPKurume University · JPOsaka City University · JPOsaka Hospital · JPSapporo Kosei General Hospital · JPTokyo Women's Medical University Adachi Medical Center · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sodium glucose cotransporter-2 inhibitors (SGLT2is) are now widely used to treat diabetes, but their effects on nonalcoholic fatty liver disease (NAFLD) remain to be determined. We aimed to evaluate the effects of SGLT2is on the pathogenesis of NAFLD. A multicenter, randomized, controlled trial was conducted in patients with type 2 diabetes with NAFLD. The changes in glycemic control, obesity, and liver pathology were compared between participants taking ipragliflozin (50 mg/day for 72 weeks; IPR group) and participants being managed without SGLT2is, pioglitazone, glucagon-like peptide-1 analogs, or insulin (CTR group). In the IPR group (n = 25), there were significant decreases in hemoglobin A1c (HbA1c) and body mass index (BMI) during the study (HbA1c, -0.41%, P < 0.01; BMI, -1.06 kg/m

Indexed as

AgedBody Mass IndexDiabetes Mellitus, Type 2FemaleGlucosidesGlycated HemoglobinGlycemic ControlHumansMaleMiddle AgedNon-alcoholic Fatty Liver DiseaseSodium-Glucose Transporter 2 InhibitorsThiophenesGlucosidesGlycated Hemoglobinhemoglobin A1c protein, humanipragliflozinSodium-Glucose Transporter 2 InhibitorsThiophenes

Identifiers

PMID34558835
PMCPMC8710792
OpenAlexW3174290103

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.