Evidence map›Paper›PMID 28940110›Full record

ArticleAnnals of biomedical engineering2017

Are DXA/aBMD and QCT/FEA Stiffness and Strength Estimates Sensitive to Sex and Age?

Asghar Rezaei, Hugo Giambini, Timothy Rossman, Kent D Carlson, Michael J Yaszemski, Lichun Lu, Dan Dragomir-Daescu

Abstract readComparative StudyEvaluation Study
In one paragraph

Article in Annals of biomedical engineering, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
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  8. Imaging Modalities to Assess Fracture Healing.Current osteoporosis reports · 2020
    Review
  9. Article
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  11. 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

7 authors.

Asghar RezaeiDepartment of Physiology and Biomedical Engineering, Mayo Clinic, 200 First Street, S.W., Rochester, MN, 55905, USA.
Hugo GiambiniDepartment of Orthopedic Surgery, Mayo Clinic, Rochester, MN, USA.
Timothy RossmanDivision of Engineering, Mayo Clinic, Rochester, MN, USA.
Kent D CarlsonDepartment of Physiology and Biomedical Engineering, Mayo Clinic, 200 First Street, S.W., Rochester, MN, 55905, USA.
Michael J YaszemskiDepartment of Orthopedic Surgery, Mayo Clinic, Rochester, MN, USA.
Lichun LuDepartment of Physiology and Biomedical Engineering, Mayo Clinic, 200 First Street, S.W., Rochester, MN, 55905, USA.
Dan Dragomir-DaescuDepartment of Physiology and Biomedical Engineering, Mayo Clinic, 200 First Street, S.W., Rochester, MN, 55905, USA. dragomirdaescu.dan@mayo.edu.

Funding

Mayo Clinic Center for Translational Science ActivitiesUL1TR000135 · NCATS · MAYO CLINIC ROCHESTER · PI KHOSLA, SUNDEEP · 2012 to 2015
$41.2M
EXTRAMURAL RES FACIL IMPROVEMENT PROG: POLYCYSTIC KIDNEY DISEASE, RENAL STUDIES,C06RR018898 · NCRR · MAYO CLINIC · PI BURNETT, JOHN C · 2004 to 2004
$2.3M
Grainger Foundation Grainger Innovation FundNCATS NIH HHS UL1 TR000135NCRR NIH HHS C06 RR018898NIH HHS RR018898
6 · The paper itself

Abstract

Dual X-ray absorptiometry (DXA) measures areal bone mineral density (aBMD) by simplifying a complex 3D bone structure to a 2D projection and is not equally effective for explaining fracture strength in women and men. Unlike DXA, subject-specific quantitative computed tomography-based finite element analysis (QCT/FEA) estimates fracture strength using 3D bone mineral distribution and geometry. By using experimentally-measured femoral stiffness and strength from a one hundred sample cadaveric cohort that included variations in sex and age, we wanted to determine if QCT/FEA estimates were able to better predict the experimental variations than DXA/aBMD. For each femur, DXA/aBMD was assessed and a QCT/FEA model was developed to estimate femoral stiffness and strength. Then, the femur was mechanically tested to fracture in a sideways fall on the hip position to measure stiffness and strength. DXA/aBMD and QCT/FEA estimates were compared for their sensitivity to sex and age with multivariate statistical analyses. When comparing the measured data with DXA/aBMD predictions, both age and sex were significant (p ≤ 0.0398) for both femoral stiffness and strength. However, QCT/FEA predictions of stiffness and strength showed sex was insignificant (p ≥ 0.23). Age was still significant (p ≤ 0.0072). These results indicate that QCT/FEA, unlike DXA/aBMD, accounted for bone differences due to sex.

Indexed as

Models, BiologicalAbsorptiometry, PhotonAdultAgedAged, 80 and overAgingCadaverCalcification, PhysiologicCompressive StrengthComputer SimulationElastic ModulusFemaleFemurFinite Element AnalysisHumansMaleAgingBone biomechanicsFinite element analysisHip fractureSex differences

Identifiers

PMID28940110
PMCPMC5890422

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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.