Evidence map›Paper›PMID 38840664›Full record

ArticleResearch and practice in thrombosis and haemostasis2024

Mitral regurgitation is associated with similar loss of von Willebrand factor large multimers but lower frequency of anemia compared with aortic stenosis.

Hiroshi Takiguchi, Mizuki Miura, Shin-Ichi Shirai, Yoshimitsu Soga, Michiya Hanyu, Genichi Sakaguchi, Yoshiharu Soga, Yoshio Arai, Shin Watanabe, Takeshi Kimura and 24 more

Abstract read
In one paragraph

Article in Research and practice in thrombosis and haemostasis, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Bleeding in valvular heart disease: is von Willebrand factor the culprit?Research and practice in thrombosis and haemostasis · 2024
    Article
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

34 authors.

Hiroshi TakiguchiDepartment of Cardiology, Kokura Memorial Hospital, Kitakyushu, Japan.
Mizuki MiuraDepartment of Cardiology, Kokura Memorial Hospital, Kitakyushu, Japan.
Shin-Ichi ShiraiDepartment of Cardiology, Kokura Memorial Hospital, Kitakyushu, Japan.
Yoshimitsu SogaDepartment of Cardiology, Kokura Memorial Hospital, Kitakyushu, Japan.
Michiya HanyuDepartment of Cardiovascular Surgery, Kokura Memorial Hospital, Kitakyushu, Japan.
Genichi SakaguchiDepartment of Cardiovascular Surgery, Kokura Memorial Hospital, Kitakyushu, Japan.
Yoshiharu SogaDepartment of Cardiovascular Surgery, Kokura Memorial Hospital, Kitakyushu, Japan.
Yoshio AraiDepartment of Cardiovascular Surgery, Kokura Memorial Hospital, Kitakyushu, Japan.
Shin WatanabeDepartment of Cardiovascular Medicine, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Takeshi KimuraDepartment of Cardiovascular Medicine, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Hiroyuki TakahamaCardiovascular Department, National Cerebral and Cardiovascular Center, Suita, Japan.
Satoshi YasudaCardiovascular Department, National Cerebral and Cardiovascular Center, Suita, Japan.
Takaharu NakayoshiDivision of Cardiovascular Medicine, Department of Internal Medicine, Kurume University School of Medicine, Kurume, Japan.
Yoshihiro FukumotoDivision of Cardiovascular Medicine, Department of Internal Medicine, Kurume University School of Medicine, Kurume, Japan.
Nobuhiro YaoitaDepartment of Cardiovascular Medicine, Tohoku University Graduate School of Medicine, Sendai, Japan.
Hiroaki ShimokawaDepartment of Cardiovascular Medicine, Tohoku University Graduate School of Medicine, Sendai, Japan.
Ko SakatsumeDivision of Cardiovascular Surgery, Tohoku University Graduate School of Medicine, Sendai, Japan.
Yoshikatsu SaikiDivision of Cardiovascular Surgery, Tohoku University Graduate School of Medicine, Sendai, Japan.
Koichi KaikitaDepartment of Cardiovascular Medicine, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.
Kenichi TsujitaDepartment of Cardiovascular Medicine, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.
Toshihiro TamuraDepartment of Cardiology, Tenri Hospital, Tenri, Japan.
Tsuyoshi DomanDepartment of Molecular and Cellular Biology, Institute of Development, Aging and Cancer, Tohoku University Graduate School of Medicine, Sendai, Japan.
Mihoko YamashitaDepartment of Molecular and Cellular Biology, Institute of Development, Aging and Cancer, Tohoku University Graduate School of Medicine, Sendai, Japan.
Misako SuzukiDepartment of Molecular and Cellular Biology, Institute of Development, Aging and Cancer, Tohoku University Graduate School of Medicine, Sendai, Japan.
Yuka EuraDepartment of Molecular Pathogenesis, National Cerebral and Cardiovascular Center, Suita, Japan.
Koichi KokameDepartment of Molecular Pathogenesis, National Cerebral and Cardiovascular Center, Suita, Japan.
Masaki HayakawaDepartment of Blood Transfusion Medicine, Nara Medical University, Kashihara, Japan.
Masanori MatsumotoDepartment of Blood Transfusion Medicine, Nara Medical University, Kashihara, Japan.
Noriyuki OkuboDepartment of Clinical Laboratory Medicine, Tohoku University Hospital, Sendai, Japan.
Shingo SugawaraDepartment of Clinical Laboratory Medicine, Tohoku University Hospital, Sendai, Japan.
Shin-Ichi FujimakiDepartment of Clinical Laboratory Medicine, Tohoku University Hospital, Sendai, Japan.
Yasunori KawateMedical Affairs 2, Medical & Scientific Affairs, Sysmex Corporation, Kobe, Japan.
Kenji AndoDepartment of Cardiology, Kokura Memorial Hospital, Kitakyushu, Japan.
Hisanori HoriuchiDepartment of Molecular and Cellular Biology, Institute of Development, Aging and Cancer, Tohoku University Graduate School of Medicine, Sendai, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Various cardiovascular diseases cause acquired von Willebrand syndrome (AVWS), which is characterized by a decrease in high-molecular-weight (large) von Willebrand factor (VWF) multimers. Mitral regurgitation (MR) has been reported as a cause of AVWS. However, much remains unclear about AVWS associated with MR. Objectives: To evaluate VWF multimers in MR patients and examine their impact on clinical characteristics. Methods: Moderate or severe MR patients ( Results: At baseline, the mean hemoglobin level was 12.9 ± 1.9 g/dL and 58 patients (69.0%) showed loss of VWF large multimers defined as VWF-LMI < 80%. VWF-LMI in patients with degenerative MR was lower than in those with functional MR. VWF-LMI appeared to be restored the day after mitral valve intervention, and the improvement was maintained 1 month after the intervention. Seven patients (8.3%) had a history of bleeding, 6 (7.1%) of whom had gastrointestinal bleeding. Gastrointestinal endoscopy was performed in 23 patients (27.4%) to investigate overt gastrointestinal bleeding, anemia, etc. Angiodysplasia was detected in 2 of the 23 patients (8.7%). Conclusion: Moderate or severe MR is frequently associated with loss of VWF large multimers, and degenerative MR may cause more severe loss compared with functional MR. Mitral valve intervention corrects the loss of VWF large multimers. Gastrointestinal bleeding may be relatively less frequent and hemoglobin level remains stable in MR patients.

Indexed as

angiodysplasiagastrointestinal hemorrhagemitral valve insufficiencyvon Willebrand diseasesvon Willebrand factor

Identifiers

PMID38840664
PMCPMC11152679

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