Evidence map›Paper›PMID 26666675›Full record

ArticleFoot & ankle international2016

Muscle and Joint Factors Associated With Forefoot Deformity in the Diabetic Neuropathic Foot.

Victor A Cheuy, Mary K Hastings, Paul K Commean, Michael J Mueller

Open access · greenAbstract read
In one paragraph

Article in Foot & ankle international, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 14% 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

24 citing papers in PubMed, 1 synthesis or guideline pooled it, 44 citations in OpenAlex.

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  18. The Role of Physical Therapists in Fighting the Type 2 Diabetes Epidemic.The Journal of orthopaedic and sports physical therapy · 2020
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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

4 authors at 3 institutions in 1 country.

Victor A CheuyPhysical Therapy Program, University of Colorado, Aurora, CO, USA victor.cheuy@ucdenver.edu.
Mary K HastingsProgram in Physical Therapy, Washington University School of Medicine, St. Louis, MO, USA.
Paul K CommeanMallinckrodt Institute of Radiology, Washington University School of Medicine, St. Louis, MO, USA.
Michael J MuellerProgram in Physical Therapy, Washington University School of Medicine, St. Louis, MO, USA.
Washington University in St. Louis · USMallinckrodt (United States) · USUniversity of Colorado Anschutz Medical Campus · US

Funding

MULTICENTER CAREER DEVELOPMENT PROGRAM FOR PHYSICAL AND OCCUPATIONAL THERAPYK12HD055931 · NICHD · WASHINGTON UNIVERSITY · PI HAYES, MARCIE HARRIS · 2007 to 2021
$12.7M
Washington University Institute of Clinical and Translational SciencesKL2TR000450 · NCATS · WASHINGTON UNIVERSITY · PI EVANOFF, BRADLEY A · 2012 to 2016
$8.8M
DOCTORAL TRAINING PROGRAM IN MOVEMENT SCIENCET32HD007434 · NICHD · WASHINGTON UNIVERSITY · PI Michael D Harris, Catherine Lang · 1993 to 2026
$4.2M
Contributing Factors to Forefoot Deformity in the Diabetic, Neuropathic FootF31DK101286 · NIDDK · WASHINGTON UNIVERSITY · PI CHEUY, VICTOR ADAM · 2014 to 2014
$27k
NCATS NIH HHS KL2 TR000450NICHD NIH HHS K12 HD055931NICHD NIH HHS T32 HD007434NIDDK NIH HHS F31 DK101286
6 · The paper itself

Abstract

backgroundDiabetic forefoot joint deformities are a known risk factor for skin breakdown and amputation, but the causes of deformity are not well understood. The purposes of this study were to determine the effects of intrinsic foot muscle deterioration and limited ankle joint mobility on the severity of metatarsophalangeal joint (MTPJ) deformity, and determine the relationships between these potential contributing factors and indicators of diabetic complications (peripheral neuropathy and advanced glycation end products).

methodsA total of 34 participants with diabetic neuropathy (average age, 59 years; range 41-73) were studied. MTPJ angle and intrinsic foot muscle deterioration were measured with computed tomography and magnetic resonance imaging, respectively. Maximum ankle dorsiflexion was measured using kinematics. Skin intrinsic fluorescence served as a proxy measure for advanced glycation end product accumulation.

resultsTotal forefoot lean muscle volume (r = -0.52, P < .01) and maximum ankle dorsiflexion (r = -0.42, P < .05) were correlated with severity of MTPJ deformity. Together they explained 35% of the variance of MTPJ angle. Neuropathy was correlated with forefoot muscle deterioration (ρ = 0.53, P < .01). Skin intrinsic fluorescence was correlated to severity of neuropathy (r = 0.50, P < .01) but not maximum ankle dorsiflexion, or forefoot deterioration when controlling for neuropathy.

conclusionThese results suggest that the interplay of intrinsic foot muscle deterioration and limited ankle mobility may be the primary contributor to the development of MTPJ deformity. Identifying these muscle and ankle motion impairments as risk factors for MTPJ deformity supports the need for targeted interventions early in the disease process to slow, or possibly stop the progression of deformity over time and reduce the risk of amputation. LEVEL OF EVIDENCE: Level IV, case series.

Indexed as

AdultAgedAnkle JointDiabetic FootFemaleFoot Deformities, AcquiredHumansMaleMetatarsophalangeal JointMiddle AgedMuscle, SkeletalRange of Motion, ArticularTomography, X-Ray Computedadvanced glycation end productshammertoeintermuscular adipose tissuemuscleneuropathy

Identifiers

PMID26666675
PMCPMC5111819
OpenAlexW2199076548

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.