Evidence map›Paper›PMID 33641442›Full record

ReviewExperimental biology and medicine (Maywood, N.J.)2021

Emerging evidence that adaptive bone formation inhibition by non-steroidal anti-inflammatory drugs increases stress fracture risk.

Jeffery S Staab, Alexander L Kolb, Ryan E Tomlinson, Paola Divieti Pajevic, Ronald W Matheny, Julie M Hughes

Registry-linked trialOpen access · greenAbstract readReview
In one paragraph

Review in Experimental biology and medicine (Maywood, N.J.), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05512013 (The Effects of Non-steroidal Anti-inflammatory Drugs on Circulating Markers of Bone Metabolism Following Plyometric Exercise in Humans), which is not on this map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.0field-weighted citation impact, top 24% 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.

NCT05512013 phase1completednot on this mapstarted 2022, after this paper: background citation

The Effects of Non-steroidal Anti-inflammatory Drugs on Circulating Markers of Bone Metabolism Following Plyometric Exercise in Humans

TypeinterventionalSponsorUnited States Army Research Institute of Environmental MedicineRan2022 to 2023Enrolled12ConditionsBone Resorption, Stress Fracture, Bone InjuryArmsIbuprofen 800 mg, Celecoxib 200mg, Flurbiprofen 100 mg, Placebo
3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. 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

6 authors at 4 institutions in 1 country.

Jeffery S StaabMilitary Performance Division, United States Army Research Institute of Environmental Medicine, Natick, MA 01760, USA.ORCID 0000-0003-0080-1441
Alexander L KolbMilitary Performance Division, United States Army Research Institute of Environmental Medicine, Natick, MA 01760, USA.
Ryan E TomlinsonDepartment of Orthopaedic Surgery, Thomas Jefferson University, Philadelphia, PA 19107, USA.
Paola Divieti PajevicGoldman School of Dental Medicine, Boston University, Boston, MA 02118, USA.
Ronald W MathenyMilitary Operational Medicine Research Program, Fort Detrick, MD 21702, USA.
Julie M HughesMilitary Performance Division, United States Army Research Institute of Environmental Medicine, Natick, MA 01760, USA.
U.S. Army Research Institute of Environmental Medicine · USBoston University · USThomas Jefferson University · USUnited States Army Medical Research and Development Command · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There is mounting evidence suggesting that the commonly used analgesics, non-steroidal anti-inflammatory drugs (NSAIDs), may inhibit new bone formation with physical training and increase risk of stress fractures in physically active populations. Stress fractures are thought to occur when bones are subjected to repetitive mechanical loading, which can lead to a cycle of tissue microdamage, repair, and continued mechanical loading until fracture. Adaptive bone formation, particularly on the periosteal surface of long bones, is a concurrent adaptive response of bone to heightened mechanical loading that can improve the fatigue resistance of the skeletal structure, and therefore may play a critical role in offsetting the risk of stress fracture. Reports from animal studies suggest that NSAID administration may suppress this important adaptive response to mechanical loading. These observations have implications for populations such as endurance athletes and military recruits who are at risk of stress fracture and whose use of NSAIDs is widespread. However, results from human trials evaluating exercise and bone adaptation with NSAID consumption have been less conclusive. In this review, we identify knowledge gaps that must be addressed to further support NSAID-related guidelines intended for at-risk populations and individuals.

Indexed as

Fractures, StressAnimalsAnti-Inflammatory Agents, Non-SteroidalBone RemodelingHumansOsteogenesisAnti-Inflammatory Agents, Non-Steroidalbonecyclooxygenasemechanical loadingNon-steroidal anti-inflammatory drugsprostaglandinsstress fracture

Identifiers

PMID33641442
PMCPMC8113733
OpenAlexW3135216037

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.