Scrutinizing the cut-off for "pathological" meniscal body extrusion on knee MRI.


Journal

European radiology
ISSN: 1432-1084
Titre abrégé: Eur Radiol
Pays: Germany
ID NLM: 9114774

Informations de publication

Date de publication:
May 2019
Historique:
received: 28 05 2018
accepted: 23 11 2018
revised: 24 10 2018
pubmed: 12 1 2019
medline: 29 5 2019
entrez: 12 1 2019
Statut: ppublish

Résumé

Medial meniscal body extrusion ≥ 3 mm on MRI is often considered "pathologic." The aims of this study were to (1) assess the adequacy of 3 mm as cut-off for "pathological" extrusion and (2) find an optimal cut-off for meniscal extrusion cross-sectionally associated with radiographic knee osteoarthritis, bone marrow lesions (BMLs), and cartilage damage. Nine hundred fifty-eight persons, aged 50-90 years from Framingham, MA, USA, had readable 1.5 T MRI scans of the right knee for meniscal body extrusion (measured in mm). BMLs and cartilage damage were read using the whole organ magnetic resonance imaging score (WORMS). Knee X-rays were read according to the Kellgren and Lawrence (KL) scale. We evaluated the performance of the 3-mm cut-off with respect to the three outcomes and estimated a new cut-off maximizing the sum of sensitivity and specificity. The study persons had mean age of 62.2 years, 57.0% were women and the mean body mass index was 28.5 kg/m The 4-mm cut-off may be used as an alternative cut-off for denoting pathological meniscal extrusion. • Medial meniscal body extrusion is strongly associated with osteoarthritis. • The 3-mm cut-off for medial meniscal body extrusion has high sensitivity but low specificity with respect to bone marrow lesions, cartilage damage, and radiographic osteoarthritis. • The 4-mm cut-off maximizes the sensitivity and specificity with respect to all three osteoarthritis features.

Identifiants

pubmed: 30631922
doi: 10.1007/s00330-018-5914-0
pii: 10.1007/s00330-018-5914-0
pmc: PMC6443617
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2616-2623

Subventions

Organisme : NIAMS NIH HHS
ID : P30 AR072571
Pays : United States
Organisme : NIH HHS
ID : AR47785
Pays : United States
Organisme : NIH HHS
ID : AG18393
Pays : United States

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Auteurs

F Svensson (F)

Faculty of Medicine, Department of Clinical Sciences Lund, Orthopedics, Clinical Epidemiology Unit, Lund University, Lund, Sweden. fredrik.svensson@med.lu.se.

D T Felson (DT)

Clinical Epidemiology Research & Training Unit, Boston University School of Medicine, Boston, MA, USA.

A Turkiewicz (A)

Faculty of Medicine, Department of Clinical Sciences Lund, Orthopedics, Clinical Epidemiology Unit, Lund University, Lund, Sweden.

A Guermazi (A)

Department of Radiology, Boston University School of Medicine, Boston, MA, USA.

F W Roemer (FW)

Department of Radiology, Boston University School of Medicine, Boston, MA, USA.
Department of Radiology, University of Erlangen-Nuremberg, Erlangen, Germany.

P Neuman (P)

Faculty of Medicine, Department of Clinical Sciences Lund, Orthopedics, Clinical Epidemiology Unit, Lund University, Lund, Sweden.

M Englund (M)

Faculty of Medicine, Department of Clinical Sciences Lund, Orthopedics, Clinical Epidemiology Unit, Lund University, Lund, Sweden.
Clinical Epidemiology Research & Training Unit, Boston University School of Medicine, Boston, MA, USA.

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