Evidence map›Paper›PMID 31938894›Full record

ArticleEuropean journal of orthopaedic surgery & traumatology : orthopedie traumatologie2020

The proton pump inhibitor, lansoprazole, prevents the development of non-traumatic osteonecrosis of the femoral head: an experimental and prospective clinical trial.

Ima Kosukegawa, Shunichiro Okazaki, Motohisa Yamamoto, Satoshi Nagoya, Chisako Suzuki, Junya Shimizu, Hiroki Takahashi, Toshihiko Yamashita

Open access · hybridAbstract read
In one paragraph

Article in European journal of orthopaedic surgery & traumatology : orthopedie traumatologie, 2020. 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
0.2field-weighted citation impact, top 55% 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, 2 citations in OpenAlex.

  1. Article
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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

8 authors at 3 institutions in 1 country.

Ima KosukegawaDepartment of Orthopedic Surgery, Sapporo Medical University School of Medicine, S1 W16, Chuo-ku, Sapporo, 060-8543, Japan. imakosukegawa@gmail.com.ORCID http://orcid.org/0000-0003-2385-6461
Shunichiro OkazakiDepartment of Orthopedic Surgery, Hokkaido Ohno Memorial Hospital, Sapporo, Japan.
Motohisa YamamotoDepartment of Rheumatology and Allergy, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan.
Satoshi NagoyaDepartment of Musculoskeletal Biomechanics and Surgical Development, Sapporo Medical University School of Medicine, Sapporo, Japan.
Chisako SuzukiDepartment of Rheumatology and Clinical Immunology, Sapporo Medical University School of Medicine, Sapporo, Japan.
Junya ShimizuDepartment of Orthopedic Surgery, Sapporo Medical University School of Medicine, S1 W16, Chuo-ku, Sapporo, 060-8543, Japan.
Hiroki TakahashiDepartment of Rheumatology and Clinical Immunology, Sapporo Medical University School of Medicine, Sapporo, Japan.
Toshihiko YamashitaDepartment of Orthopedic Surgery, Sapporo Medical University School of Medicine, S1 W16, Chuo-ku, Sapporo, 060-8543, Japan.
Sapporo Medical University · JPCardiovascular Center Hokkaido Ohno Hospital · JPThe University of Tokyo · JP

Funding

the Japanese Society for the Promotion of Science. 25861330the Japanese Society for the Promotion of Science. S.O.
6 · The paper itself

Abstract

backgroundAn effective prevention strategy for osteonecrosis of the femoral head (ONFH) has yet to be established. We previously reported that the innate immune system via the toll-like receptor (TLR) response induced by corticosteroids leads to the development of ONFH and that repression of IRF7 activity by an inhibitor could interfere with the development of ONFH while maintaining the therapeutic effect of the corticosteroids.

objectiveIn the present study, we hypothesize that lansoprazole has the potential to suppress IRF7 activity and prevent corticosteroid-induced ONFH in rats. Furthermore, we conducted a preliminary clinical trial to prevent corticosteroid-induced ONFH in autoimmune disease patients.

methodsMale Wistar rats were randomly divided into four groups. On Day 1, each rat was injected with TLR4 ligand (LPS) or TLR7 ligand (imiquimod), followed by methylprednisolone with or without lansoprazole on Day 2. They were killed at 1 or 14 days after the last injection.We prospectively recruited 30 patients requiring primary high-dose corticosteroid treatment for immune diseases. All patients were administered lansoprazole, starting the night before corticosteroid treatment began. MRI was performed before corticosteroid treatment, and at 4, 12 and 24 weeks afterward.

resultsIn rats, co-treatment of lansoprazole with corticosteroids significantly repressed both IRF7 activity and the development of ONFH. Moreover, in the human patients, the incidence of ONFH was significantly decreased from 53.4 to 13.3%.

conclusionsAlthough the present study is preliminary, the results show that co-treatment of lansoprazole with corticosteroids prevents ONFH development. Lansoprazole may be both safe and effective in preventing osteonecrosis of the femoral head in patients needing corticosteroid treatment.

Indexed as

Femur Head NecrosisAdrenal Cortex HormonesAnimalsAnti-Inflammatory AgentsDisease Models, AnimalFemaleFemur HeadHumansImmune System DiseasesLansoprazoleMagnetic Resonance ImagingMaleMiddle AgedProton Pump InhibitorsRatsToll-Like ReceptorsAdrenal Cortex HormonesAnti-Inflammatory AgentsLansoprazoleProton Pump InhibitorsToll-Like ReceptorsClinical trialExperimental animal modelLansoprazoleOsteonecrosis of the femoral headPrevention

Identifiers

PMID31938894
PMCPMC7181448
OpenAlexW2999802945

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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.