Evidence map›Paper›PMID 26893835›Full record

ArticleBiomedical reports2016

Efficacy of alogliptin in preventing non-alcoholic fatty liver disease progression in patients with type 2 diabetes.

Tsuyoshi Mashitani, Ryuichi Noguchi, Yasushi Okura, Tadashi Namisaki, Akira Mitoro, Hitoshi Ishii, Toshiya Nakatani, Eiryo Kikuchi, Hiroto Moriyasu, Masami Matsumoto and 11 more

Open access · bronzeAbstract read
In one paragraph

Article in Biomedical reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
5.7field-weighted citation impact, top 4% 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

16 citing papers in PubMed, 42 citations in OpenAlex.

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  12. Dipeptidyl Peptidase-4 at the Interface Between Inflammation and Metabolism.Clinical medicine insights. Endocrinology and diabetes · 2020
    Review
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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

21 authors at 8 institutions in 1 country.

Tsuyoshi MashitaniThird Department of Internal Medicine, Nara Medical University, Kashihara, Nara 634-8521, Japan; Department of Diabetology, Nara Medical University, Kashihara, Nara 634-8521, Japan.
Ryuichi NoguchiThird Department of Internal Medicine, Nara Medical University, Kashihara, Nara 634-8521, Japan.
Yasushi OkuraThird Department of Internal Medicine, Nara Medical University, Kashihara, Nara 634-8521, Japan.
Tadashi NamisakiThird Department of Internal Medicine, Nara Medical University, Kashihara, Nara 634-8521, Japan.
Akira MitoroThird Department of Internal Medicine, Nara Medical University, Kashihara, Nara 634-8521, Japan.
Hitoshi IshiiDepartment of Diabetology, Nara Medical University, Kashihara, Nara 634-8521, Japan.
Toshiya NakataniDepartment of Gastroenterology, Nara Prefecture General Medical Center, Nara 631-846, Japan.
Eiryo KikuchiDepartment of Gastroenterology, Nara Prefecture General Medical Center, Nara 631-846, Japan.
Hiroto MoriyasuDepartment of Gastroenterology, Nara Prefectural Gojo Hospital, Gojo, Nara 637-8511, Japan.
Masami MatsumotoDepartment of Gastroenterology, Nara Prefectural Gojo Hospital, Gojo, Nara 637-8511, Japan.
Shinya SatoDepartment of Gastroenterology, Belland General Hospital, Sakai, Osaka 599-8247, Japan.
Tatsuichi AnDepartment of Gastroenterology, Belland General Hospital, Sakai, Osaka 599-8247, Japan.
Hiroshi MoritaDepartment of Internal Medicine, Takamiya Hospital, Tenri, Nara 632-0052, Japan.
Sigeyuki AizawaDepartment of Gastroenterology, Nara Prefecture Western Medical Center, Nara 636-0802, Japan.
Yasunori TokuokaDepartment of Internal Medicine, Kokuho Chuo Hospital, Nara 636-0302, Japan.
Masatoshi IshikawaDepartment of Gastroenterology, Ishinkai Yao General Hospital, Yao, Osaka 581-0036, Japan.
Yoshinobu MatsumuraDepartment of Gastroenterology, Ishinkai Yao General Hospital, Yao, Osaka 581-0036, Japan.
Hiromasa OhiraDepartment of Gastroenterology and Rheumatology, School of Medicine, Fukushima Medical University, Fukushima 960-1295, Japan.
Atsuko KogureDepartment of Gastroenterology, Fujita General Hospital, Fukusima 969-1793, Japan.
Kazuhiro NoguchiDepartment of Gastroenterology, Fujita General Hospital, Fukusima 969-1793, Japan.
Hitoshi YoshijiThird Department of Internal Medicine, Nara Medical University, Kashihara, Nara 634-8521, Japan.
Nara Medical University · JPBerurando General Hospital · JPNara City Hospital · JPNara Prefecture General Medical CenterYao Tokushukai General Hospital · JPFukushima Medical University · JPGunma Chuo Hospital · JPTenri Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Non-alcoholic fatty liver disease (NAFLD) represents one of the most common causes of chronic liver disease worldwide and is characterized by chronic liver inflammation and fibrosis leading to cirrhosis and increased risk of liver cancer in a proportion of patients. Effective anti-fibrotic agents have yet to be approved for the treatment of NAFLD. The present study aimed to evaluate the efficacy of dipeptidyl peptidase 4 inhibitors (DPP4-I) in the prevention of NAFLD progression in NAFLD patients with type 2 diabetes. The study was a single arm, multi-centre, non-randomised study of NAFLD patients with type 2 diabetes. NAFLD was diagnosed according to ultrasonographic findings. All the patients received 25 mg/day of alogliptin for 12 months. The efficacy of alogliptin in preventing NAFLD progression was assessed using overall NAFIC scores [non-alcoholic steatohepatitis (NASH), ferritin, insulin and type IV collagen 7S] and individual component scores according to baseline haemoglobin A1c (HbA1c) levels. Of the 39 patients enrolled in the study, 16 patients (40.3%) had NAFIC scores >2 points, indicating the presence of NASH. NAFIC scores markedly decreased following 12 months of alogliptin administration, but remained >2 points in 10 patients, indicating that NASH may have persisted in these patients. The relative risks for persistent NASH were 4.92 (95% confidence interval, 0.61-40.0) in the highest HbA1c tertile group compared with those in the lowest group. However, no statistically significant linear trend was observed across all HbA1c categories (P=0.145). DPP4-I may have efficacy against NAFLD progression in patients with type 2 diabetes with relatively lower HbA1c levels. DPP4-I may represent a potential new therapeutic strategy for the prevention of disease progression in NAFLD patients with type 2 diabetes.

Indexed as

diabetesdipeptidyl peptidase 4 inhibitornon-alcoholic fatty liver disease

Identifiers

PMID26893835
PMCPMC4734121
OpenAlexW2225535009

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.