Evidence map›Paper›PMID 27351380›Full record

Trial reportPLoS medicine2016

The Effect of Sitagliptin on Carotid Artery Atherosclerosis in Type 2 Diabetes: The PROLOGUE Randomized Controlled Trial.

Jun-Ichi Oyama, Toyoaki Murohara, Masafumi Kitakaze, Tomoko Ishizu, Yasunori Sato, Kazuo Kitagawa, Haruo Kamiya, Masayoshi Ajioka, Masaharu Ishihara, Kazuoki Dai and 16 more

Open access · goldAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in PLoS medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 4 pooled it
8.2field-weighted citation impact, top 2% 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

40 citing papers in PubMed, 4 syntheses or guidelines pooled it, 67 citations in OpenAlex.

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  17. Sex-Related Differences in Sitagliptin Treatment in Type 2 Diabetes: Results from the PROLOGUE Trial.Medical science monitor : international medical journal of experimental and clinical research · 2022
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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

26 authors at 19 institutions in 1 country.

Jun-Ichi OyamaDepartment of Cardiovascular Medicine, Saga University, Saga, Japan.
Toyoaki MuroharaDepartment of Cardiology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Masafumi KitakazeDepartment of Clinical Medicine and Development, National Cerebral and Cardiovascular Center, Osaka, Japan.
Tomoko IshizuDepartment of Clinical Laboratory Medicine, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan.
Yasunori SatoDepartment of Global Clinical Research, Graduate School of Medicine, Chiba University, Chiba, Japan.
Kazuo KitagawaDepartment of Neurology, Tokyo Women's Medical University, Tokyo, Japan.
Haruo KamiyaDivision of Cardiology, Japanese Red Cross Nagoya Daiichi Hospital, Nagoya, Japan.
Masayoshi AjiokaDepartment of Cardiovascular Internal Medicine, Tosei General Hospital, Seto, Japan.
Masaharu IshiharaDivision of Cardiovascular Medicine and Coronary Heart Disease, Hyogo College of Medicine, Nishinomiya, Japan.
Kazuoki DaiDepartment of Cardiology, Hiroshima City Hospital, Hiroshima, Japan.
Mamoru NanasatoCardiovascular Center, Japanese Red Cross Nagoya Daini Hospital, Nagoya, Japan.ORCID http://orcid.org/0586-9181-7500-7156
Masataka SataDepartment of Cardiovascular Medicine, Institute of Biomedical Sciences, Tokushima University Graduate School, Tokushima, Japan.
Koji MaemuraDepartment of Cardiovascular Medicine, Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki, Japan.
Hirofumi TomiyamaDepartment of Cardiology, Tokyo Medical University, Tokyo, Japan.
Yukihito HigashiDepartment of Cardiovascular Regeneration and Medicine, Research Institute for Radiation Biology and Medicine, Hiroshima University, Hiroshima, Japan.
Kohei KakuDepartment of Internal Medicine, Kawasaki Medical School, Kurashiki, Japan.
Hirotsugu YamadaDepartment of Cardiovascular Medicine, Tokushima University Hospital, Tokushima, Japan.ORCID http://orcid.org/0000-0003-3741-5560
Munehide MatsuhisaDiabetes Therapeutics and Research Center, Tokushima University, Tokushima, Japan.
Kentaro YamashitaDepartment of Cardiology, Nagoya University Graduate School of Medicine and National Hospital Organization Nagoya Medical Center, Nagoya, Japan.
Yasuko K BandoDepartment of Cardiology, Nagoya University Graduate School of Medicine and National Hospital Organization Nagoya Medical Center, Nagoya, Japan.
Naoki KashiharaDepartment of Nephrology and Hypertension, Kawasaki Medical School, Kurashiki, Japan.
Shinichiro UedaDepartment of Clinical Pharmacology and Therapeutics, University of the Ryukyus, Nishihara, Japan.
Teruo InoueDepartment of Cardiovascular Medicine, Dokkyo Medical University, Mibu, Japan.
Atsushi TanakaDepartment of Cardiovascular Medicine, Saga University, Saga, Japan.
Koichi NodeDepartment of Cardiovascular Medicine, Saga University, Saga, Japan.
PROLOGUE Study Investigators
Saga University · JPKawasaki Medical School · JPNational Hospital Organization · JPTokushima University · JPChiba University · JPDokkyo Medical University · JPHiroshima University · JPHyogo Medical University · JPJapanese Red Cross Nagoya Daiichi Hospital · JPJapanese Red Cross Nagoya Daini Hospital · JPNagasaki University · JPNagoya University · JPNational Cerebral and Cardiovascular Center · JPTokushima University Hospital · JPTokyo Medical University · JPTokyo Women's Medical University · JPTosei General Hospital · JPUniversity of the Ryukyus · JPUniversity of Tsukuba · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundExperimental studies have suggested that dipeptidyl peptidase-4 (DPP-4) inhibitors provide cardiovascular protective effects. We performed a randomized study to evaluate the effects of sitagliptin added on to the conventional therapy compared with conventional therapy alone (diet, exercise, and/or drugs, except for incretin-related agents) on the intima-media thickness (IMT) of the carotid artery, a surrogate marker for the evaluation of atherosclerotic cardiovascular disease, in people with type 2 diabetes mellitus (T2DM). METHODS AND

findingsWe used a multicenter PROBE (prospective, randomized, open label, blinded endpoint) design. Individuals aged ≥30 y with T2DM (6.2% ≤ HbA1c < 9.4%) were randomly allocated to receive either sitagliptin (25 to 100 mg/d) or conventional therapy. Carotid ultrasound was performed at participating medical centers, and all parameters were measured in a core laboratory. Of the 463 enrolled participants with T2DM, 442 were included in the primary analysis (sitagliptin group, 222; conventional therapy group, 220). Estimated mean (± standard error) common carotid artery IMT at 24 mo of follow-up in the sitagliptin and conventional therapy groups was 0.827 ± 0.007 mm and 0.837 ± 0.007 mm, respectively, with a mean difference of -0.009 mm (97.2% CI -0.028 to 0.011, p = 0.309). HbA1c level at 24 mo was significantly lower with sitagliptin than with conventional therapy (6.56% ± 0.05% versus 6.72% ± 0.05%, p = 0.008; group mean difference -0.159, 95% CI -0.278 to -0.041). Episodes of serious hypoglycemia were recorded only in the conventional therapy group, and the rate of other adverse events was not different between the two groups. As it was not a placebo-controlled trial and carotid IMT was measured as a surrogate marker of atherosclerosis, there were some limitations of interpretation.

conclusionsIn the PROLOGUE study, there was no evidence that treatment with sitagliptin had an additional effect on the progression of carotid IMT in participants with T2DM beyond that achieved with conventional treatment.

trial registrationUniversity Hospital Medical Information Network Clinical Trials Registry UMIN000004490.

Indexed as

AdultAgedAtherosclerosisCarotid ArteriesCarotid Intima-Media ThicknessDiabetes Mellitus, Type 2Dipeptidyl-Peptidase IV InhibitorsFemaleHumansMaleMiddle AgedProspective StudiesSitagliptin PhosphateDipeptidyl-Peptidase IV InhibitorsSitagliptin Phosphate

Identifiers

PMID27351380
PMCPMC4924847
OpenAlexW2461388886

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.