Evidence map›Paper›PMID 32768598›Full record

ArticleOsteoarthritis and cartilage2020

The relation of oral bisphosphonates to bone marrow lesion volume among women with osteoarthritis.

P Ballal, M Sury, N Lu, J Duryea, Y Zhang, C Ratzlaff, T Neogi

Open access · greenAbstract read
In one paragraph

Article in Osteoarthritis and cartilage, 2020. 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
2.5field-weighted citation impact, top 12% 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

6 citing papers in PubMed, 16 citations in OpenAlex.

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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

7 authors at 5 institutions in 2 countries.

P BallalBoston Medical Center, Boston, MA, USA. Electronic address: priyankaballal@gmail.com.
M SuryBrigham and Women's Hospital, Harvard Medical School, Boston, MA, USA. Electronic address: meera.sury@gmail.com.
N LuArthritis Research Canada, British Columbia, Canada. Electronic address: llu@arthritisresearch.ca.
J DuryeaBrigham and Women's Hospital, Harvard Medical School, Boston, MA, USA. Electronic address: jduryea@bwh.harvard.edu.
Y ZhangMassachusetts General Hospital, Harvard Medical School, Boston, MA, USA. Electronic address: yzhang108@mgh.harvard.edu.
C RatzlaffBrigham and Women's Hospital, Harvard Medical School, Boston, MA, USA. Electronic address: chuck.ratzlaff@ubc.ca.
T NeogiBoston University School of Medicine, Boston, MA, USA. Electronic address: tneogi@bu.edu.
Brigham and Women's Hospital · USBoston Medical Center · USBoston University · USHarvard University · USResearch Canada · CA

Funding

Research and Evaluation Support Core Unit (RESCU Core)P30AR072571 · NIAMS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI Michael Paul Lavalley · 2019 to 2026
$6.9M
The Role of Urate in Knee Osteoarthritis-Related Inflammation, Pathology and PainK24AR070892 · NIAMS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI TUHINA NEOGI · 2017 to 2026
$1.1M
NIAMS NIH HHS K24 AR070892NIAMS NIH HHS P30 AR072571
6 · The paper itself

Abstract

objectiveBone marrow lesions (BMLs) contribute to pain and progression of knee OA. Bisphosphonates may be a potential disease-modifier through amelioration of BMLs. We sought to determine the effect of oral bisphosphonates on BML volume over 12 months.

designWomen in the Osteoarthritis Initiative who newly initiated an oral bisphosphonate were propensity-score matched to non-initiators. BML volume was assessed using sagittal turbo spin echo fat-suppressed intermediate-weighted MR images at the index date and 12 months later. A validated semi-automated process was used to segment subchondral OA-related BMLs to determine total volume of BMLs based on number of voxels within the outlined area of interest. Mean change in BML volume over 12 months among bisphosphonate initiators was compared with non-initiators using multiple linear regression.

results145 bisphosphonate initiators were identified, who were well-matched to their comparators. The difference in mean change in total BML volume between the two groups, regardless of presence of baseline BMLs, was not significant (P = 0.4, 95% CI -156.6 to +354.2). The proportion of participants with decreased, increased, or unchanged BML volumes over the 12 months were similar in both groups. Among those with baseline BMLs, bisphosphonate initiators had a greater proportion with a decrease in BML volume compared with stable or increased BML volume than non-initiators (P = 0.03).

conclusionsIn this 'real-world' setting of women starting bisphosphonates, we found no clear evidence of benefit on BML volume over a 12-month period, though a trend towards a decrease in BML volume was noted.

Indexed as

AgedAlendronateBone Density Conservation AgentsBone MarrowDiphosphonatesFemaleHumansIbandronic AcidLongitudinal StudiesMagnetic Resonance ImagingMiddle AgedOsteoarthritis, KneePropensity ScoreRisedronic AcidAlendronateBone Density Conservation AgentsDiphosphonatesIbandronic AcidRisedronic AcidBisphosphonateBone marrow lesionsMRIOsteoarthritis

Identifiers

PMID32768598
PMCPMC7530037
OpenAlexW3047498705

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.