Evidence map›Paper›PMID 29605381›Full record

ArticleOsteoarthritis and cartilage2018

Type 2 diabetes patients have accelerated cartilage matrix degeneration compared to diabetes free controls: data from the Osteoarthritis Initiative.

J Neumann, F C Hofmann, U Heilmeier, W Ashmeik, K Tang, A S Gersing, B J Schwaiger, M C Nevitt, G B Joseph, N E Lane and 2 more

Open access · bronzeAbstract readComparative StudyMulticenter Study
In one paragraph

Article in Osteoarthritis and cartilage, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
6.1field-weighted citation impact, top 3% 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

30 citing papers in PubMed, 64 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

12 authors at 3 institutions in 2 countries.

J NeumannMusculoskeletal Quantitative Imaging Research Group, Department of Radiology & Biomedical Imaging, University of California San Francisco, San Francisco, USA. Electronic address: Jan.Neumann@ucsf.edu.
F C HofmannMusculoskeletal Quantitative Imaging Research Group, Department of Radiology & Biomedical Imaging, University of California San Francisco, San Francisco, USA. Electronic address: Felix.Hofmann@tum.de.
U HeilmeierMusculoskeletal Quantitative Imaging Research Group, Department of Radiology & Biomedical Imaging, University of California San Francisco, San Francisco, USA. Electronic address: Ursula.Heilmeier@ucsf.edu.
W AshmeikMusculoskeletal Quantitative Imaging Research Group, Department of Radiology & Biomedical Imaging, University of California San Francisco, San Francisco, USA. Electronic address: Walid.Ashmeik@ucsf.edu.
K TangMusculoskeletal Quantitative Imaging Research Group, Department of Radiology & Biomedical Imaging, University of California San Francisco, San Francisco, USA. Electronic address: Kennethtang1216@gmail.com.
A S GersingMusculoskeletal Quantitative Imaging Research Group, Department of Radiology & Biomedical Imaging, University of California San Francisco, San Francisco, USA; Department of Diagnostic and Interventional Radiology, Technical University of Munich, Munich, Germany. Electronic address: Alexandra.Gersing@ucsf.edu.
B J SchwaigerMusculoskeletal Quantitative Imaging Research Group, Department of Radiology & Biomedical Imaging, University of California San Francisco, San Francisco, USA; Department of Diagnostic and Interventional Radiology, Technical University of Munich, Munich, Germany. Electronic address: bschwaiger@gmx.com.
M C NevittDepartment of Epidemiology and Biostatistics, University of California San Francisco, San Francisco, USA. Electronic address: MNevitt@psg.ucsf.edu.
G B JosephMusculoskeletal Quantitative Imaging Research Group, Department of Radiology & Biomedical Imaging, University of California San Francisco, San Francisco, USA. Electronic address: Gabby.Joseph@ucsf.edu.
N E LaneDepartment of Medicine and Center for Musculoskeletal Health, University of California at Davis, Sacramento, CA, USA. Electronic address: nelane@ucdavis.edu.
C E McCullochDepartment of Epidemiology and Biostatistics, University of California San Francisco, San Francisco, USA. Electronic address: Charles.McCulloch@ucsf.edu.
T M LinkMusculoskeletal Quantitative Imaging Research Group, Department of Radiology & Biomedical Imaging, University of California San Francisco, San Francisco, USA. Electronic address: Thomas.Link@ucsf.edu.
University of California, San Francisco · USTechnical University of Munich · DEUniversity of California, Davis · US

Funding

Translation of Quantitative Imaging in OsteoarthritisP50AR060752 · NIAMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI SOUZA, RICHARD BRIAN · 2011 to 2015
$6.2M
UCSF Core Center for Musculoskeletal Biology and MedicineP30AR066262 · NIAMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI LOTZ, JEFFREY C. · 2014 to 2018
$3.0M
Impact of Weight loss on Knee Joint Biochemical and Structural DegenerationR01AR064771 · NIAMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI LINK, THOMAS M · 2014 to 2019
$1.6M
NIAMS NIH HHS P30 AR066262NIAMS NIH HHS P50 AR060752NIAMS NIH HHS R01 AR064771
6 · The paper itself

Abstract

purposeOsteoarthritis (OA) and diabetes mellitus (DM) share common risk factors with a potential underlying relationship between both diseases. The purpose of this study was to investigate the longitudinal effects of DM on cartilage deterioration over 24-months with MR-based T2 relaxation time measurements.

methodsFrom the Osteoarthritis Initiative (OAI) cohort 196 diabetics were matched in small sets for age, sex, BMI and Kellgren-Lawrence score with 196 non-diabetic controls. Knee cartilage semi-automatic segmentation was performed on 2D multi-slice multi-echo spin-echo sequences. Texture of cartilage T2 maps was obtained via grey level co-occurrence matrix analysis. Linear regression analysis was used to compare cross-sectional and changes in T2 and texture parameters between the groups.

resultsBoth study groups were similar in age (63.3 vs 63.0 years, P = 0.70), BMI (30.9 vs 31.2 kg/m

conclusionCartilage T2 values in diabetics show a faster increase with a consistently more heterogeneous cartilage texture composition. DM seems to be a risk factor for developing early OA with an accelerated degeneration of the articular cartilage in the knee.

Indexed as

Cartilage, ArticularDiabetes ComplicationsDiabetes Mellitus, Type 2Disease ProgressionFemaleHumansLongitudinal StudiesMaleMiddle AgedOsteoarthritis, KneeProspective StudiesBiomarkersCartilage imagingDiabetes mellitusKnee osteoarthritisMagnetic resonance imaging

Identifiers

PMID29605381
PMCPMC5962437
OpenAlexW2794615236

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.