Evidence map›Paper›PMID 31193597›Full record

ArticleEClinicalMedicine

Cardiovascular Outcomes in Patients With Previous Myocardial Infarction and Mild Diabetes Mellitus Following Treatment With Pioglitazone: Reports of a Randomised Trial From The Japan Working Group for the Assessment Whether

Masanori Asakura, Jiyoong Kim, Hiroshi Asanuma, Yasuharu Nakama, Kengo Tsukahara, Yorihiko Higashino, Tetsuya Ishikawa, Shinji Koba, Mitsuru Tsujimoto, Hideo Himeno and 38 more

Open access · goldAbstract read
In one paragraph

Article in EClinicalMedicine. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.1field-weighted citation impact, top 20% 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

2 citing papers in PubMed, 10 citations in OpenAlex.

  1. 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

48 authors at 20 institutions in 1 country.

Masanori AsakuraDepartment of Clinical Medicine and Development, National Cerebral and Cardiovascular Center, Osaka, Japan.
Jiyoong KimDepartment of Clinical Medicine and Development, National Cerebral and Cardiovascular Center, Osaka, Japan.
Hiroshi AsanumaDepartment of Internal Medicine, Meiji University of Integrative Medicine, Kyoto, Japan.
Yasuharu NakamaDepartment of Cardiology, Hiroshima City Hospital, Hiroshima, Japan.
Kengo TsukaharaDivision of Cardiology, Yokohama City University Medical Center, Kanagawa, Japan.
Yorihiko HigashinoDepartment of Cardiology, Higashi Takarazuka Satoh Hospital, Hyogo, Japan.
Tetsuya IshikawaDepartment of Cardiology, Saitama Prefecture Cardiovascular and Respiratory Center, Saitama, Japan.
Shinji KobaDivision of Cardiology, Department of Medicine, Showa University Hospital, Tokyo, Japan.
Mitsuru TsujimotoDepartment of Cardiology, Cardiovascular Center, Veritas Hospital, Hyogo, Japan.
Hideo HimenoDivision of Cardiology, Fujisawa City Hospital, Kanagawa, Japan.
Yasuyuki MaruyamaDepartment of Cardiology, Iwatsuki-Minami Hospital, Saitama, Japan.
Takanori OokusaDepartment of Cardiology, Hokko Memorial Hospital, Hokkaido, Japan.
Shunichi YodaDivision of Cardiology, Department of Internal Medicine, Nihon University School of Medicine, Tokyo, Japan.
Hiroshi SuzukiDivision of Cardiology, Showa University Fujigaoka Hospital, Kanagawa, Japan.
Shinji OkuboDepartment of Cardiovascular Medicine, Tokyo Medical University Ibaraki Medical Center, Ibaraki, Japan.
Makoto ShimizuDepartment of Cardiology, International Goodwill Hospital, Kanagawa, Japan.
Yuji HashimotoDepartment of Cardiology, Kameda Medical Center, Chiba, Japan.
Kazuo SatakeDepartment of Cardiology, Fukui General Clinic, Fukui, Japan.
Susumu FujinoDepartment of Cardiology, Fukui Prefectural Hospital, Fukui, Japan.
Hiroyasu UzuiDepartment of Cardiology, University of Fukui Hospital, Fukui, Japan.
Yoshiyuki NagaiDepartment of Cardiology, Rinku General Medical Center, Osaka, Japan.
Tohru KohnoDepartment of Cardiology, Tokyo Rinkai Hospital, Tokyo, Japan.
Sumio MizunoDepartment of Internal Medicine, Fukui Cardiovascular Center, Fukui, Japan.
Makoto NakahamaDepartment of Cardiology, Fukuyama City Hospital, Hiroshima, Japan.
Hounin KanayaDivision of Cardiology, Ishikawa Prefectural Central Hospital, Ishikawa, Japan.
Toyoaki MuroharaDepartment of Cardiology, Nagoya University, Aichi, Japan.
Kazuki FukuiDepartment of Cardiology, Kanagawa Cardiovascular and Respiratory Center, Kanagawa, Japan.
Hiroyuki TakaseDepartment of Internal Medicine, Enshu Hospital, Shizuoka, Japan.
Nobuyuki OhteDepartment of Cardio-Renal Medicine and Hypertension, Nagoya City University Graduate School of Medical Sciences, Aichi, Japan.
Takaaki ShionoDepartment of Cardiology, Kitasato University Medical Center, Saitama, Japan.
Masatake FukunamiDivision of Cardiology, Osaka General Medical Center, Osaka, Japan.
Tsutomu EndoDepartment of Cardiology, Saiseikai Yokohama City Southern Hospital, Kanagawa, Japan.
Reimin SawadaDepartment of Cardiology, Hadano Red Cross Hospital, Kanagawa, Japan.
Kenshi FujiiDepartment of Cardiology, Fukui Prefectural Hospital, Fukui, Japan.
Motoshi TakeuchiDepartment of Internal Medicine, Takeuchi Clinic, Hyogo, Japan.
Shuntaro IkedaDivision of Cardiology, Uwajima City Hospital, Ehime, Japan.
Koichi MizunoDepartment of Cardiology, Kawasaki Municipal Tama Hospital, Kanagawa, Japan.
Masaaki UematsuCardiovascular Center, Kansai Rosai Hospital, Hyogo, Japan.
Taku MatsubaraDepartment of Cardiovascular Medicine, Shinrakuen Hospital, Niigata, Japan.
Shoji YanoDepartment of Cardiovascular Medicine, Almeida Memorial Hospital, Oita, Japan.
Jun TakahashiDepartment of Cardiovascular Medicine, Tohoku University Graduate School of Medicine, Miyagi, Japan.
Kousei UedaDivision of Cardiology, Komatsu Municipal Hospital, Ishikawa, Japan.
Yoshihiko KinoshitaDepartment of Cardiology, Kinoshita Clinic, Hiroshima, Japan.
Koichi TamitaDepartment of Cardiology, Nishinomiya Watanabe Cardiovascular Center, Hyogo, Japan.
Hideki HayashiDepartment of Internal Medicine, Hoetsu Hospital, Tokushima, Japan.
Toshimitsu HamasakiDepartment of Data Science, National Cerebral and Cardiovascular Center, Osaka, Japan.
Masafumi KitakazeDepartment of Clinical Medicine and Development, National Cerebral and Cardiovascular Center, Osaka, Japan.
PPAR investigators
National Cerebral and Cardiovascular Center · JPFukui CardioVascular Center · JPFukui Prefectural Hospital · JPAlmeida Memorial Hospital · JPFujisawa City Hospital · JPFukuyama City Hospital · JPHigashi Takarazuka Satoh Hospital · JPHokko Memorial Hospital · JPHyogo Brain and Heart Center · JPInternational Goodwill Hospital · JPIshikawa Prefectural Central Hospital · JPJapanese Red Cross Hadano Hospital · JPJA Shizuoka Koseiren ENSHU hospital · JPKameda Medical Center · JPKanagawa Cardiovascular and Respiratory Center · JPKansai Rosai Hospital · JPKawasaki Municipal Hospital · JPKitasato University Medical Center · JPKomatsu (Japan) · JPMeiji University of Integrative Medicine · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSecondary prevention in patients with myocardial infarction (MI) is critically important to prevent ischaemic heart failure and reduce social burden. Pioglitazone improves vascular dysfunction and prevents coronary atherosclerosis, mainly via anti-inflammatory and antiatherogenic effects by enhancing adiponectin production in addition to antihyperglycemic effects, thus suggesting that pioglitazone attenuates cardiovascular events in patients with mild (HbA1c levels < 6·5%) diabetes mellitus (DM). Therefore, we evaluated the effects of pioglitazone on cardiovascular events in patients with both previous MI and mild DM.

methodsIn this multicentre, prospective, randomised, open, blinded-endpoint trial, we randomly assigned 630 patients with mild DM with a history of MI to undergo either DM therapy with (pioglitazone group) or without (control group) pioglitazone. DM was diagnosed using the 75-g oral glucose tolerance test, and mild DM was defined if HbA1c level was < 6·5%. The primary endpoint was the composite of cardiovascular death and hospitalisation caused by acute MI, unstable angina, coronary revascularisation (including percutaneous coronary intervention and cardiac bypass surgery), and stroke.

findingsHbA1C levels were 5·9 and 5·8% (p = 0·71) at baseline and 6·0 and 5·8% (p < 0·01) at 2 years for the control and pioglitazone groups, respectively.The primary endpoint was observed in 14·2% and 14·1% patients in the control and pioglitazone groups during two years (95% confidential interval (CI):0.662-1·526, p = 0·98), respectively; the incidence of MI and cerebral infarction was 0·3% and 2·2% (95%CI: 0·786-32·415, p = 0·09) and 1·0% and 0·3% (95%CI: 0·051-3·662, p = 0·44), respectively. Post-hoc analyses of the 7-year observation period showed that these trends were comparable (21·9% and 19·2% in the control and pioglitazone groups, 95%CI: 0.618-1·237, p = 0·45).

interpretationPioglitazone could not reduce the occurrence of cardiovascular events in patients with mild DM and previous MI.

Indexed as

Blood glucose-loweringCardiovascular eventsDiabetes mellitusMyocardial infarctionPioglitazonePROBE study

Identifiers

PMID31193597
PMCPMC6537525
OpenAlexW2896399430

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