Metabolic syndrome and the progression of knee osteoarthritis on MRI.


Journal

Osteoarthritis and cartilage
ISSN: 1522-9653
Titre abrégé: Osteoarthritis Cartilage
Pays: England
ID NLM: 9305697

Informations de publication

Date de publication:
05 2023
Historique:
received: 14 09 2022
revised: 23 01 2023
accepted: 07 02 2023
medline: 2 5 2023
pubmed: 22 2 2023
entrez: 21 2 2023
Statut: ppublish

Résumé

Metabolic osteoarthritis (OA) is one of the proposed clinical phenotypes defined by the existence of metabolic syndrome (MetS). This study aimed to (1) investigate whether MetS and its components are associated with progression of knee OA magnetic resonance imaging (MRI) features, and (2) to evaluate the interaction of MetS with menopause and progression of MRI features. 682 women from the Rotterdam Study who participated in a sub-study with knee MRI data available and 5-year follow-up were included. Tibiofemoral (TF) and patellofemoral (PF) OA features were assessed with the MRI Osteoarthritis Knee Score. MetS was quantified by the MetS severity Z-score. Generalized estimating equations were used to evaluate associations between MetS and menopausal transition and progression of MRI features. MetS severity at baseline was associated with progression of osteophytes in all compartments, bone marrow lesions (BMLs) in the PF compartment, and cartilage defects in the medial TF compartment. Waist circumference was associated with progression of osteophytes in all compartments and cartilage defects in the medial TF compartment. High-density lipoprotein (HDL)-cholesterol levels were associated with progression of osteophytes in the medial and lateral TF compartment and glucose levels with osteophytes in the PF and medial TF compartment. No interactions were found between MetS with menopausal transition and MRI features. Women with higher MetS severity at baseline showed progression of osteophytes, BMLs, and cartilage defects, indicating more structural knee OA progression after 5 years. Further studies are required to understand whether targeting MetS components may prevent the progression of structural knee OA in women.

Identifiants

pubmed: 36801367
pii: S1063-4584(23)00613-1
doi: 10.1016/j.joca.2023.02.003
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

647-655

Informations de copyright

Copyright © 2023 The Author(s). Published by Elsevier Ltd.. All rights reserved.

Auteurs

N E J Jansen (NEJ)

Department of General Practice, Erasmus MC, University Medical Center, Rotterdam, the Netherlands. Electronic address: n.jansen@erasmusmc.nl.

E Molendijk (E)

Department of General Practice, Erasmus MC, University Medical Center, Rotterdam, the Netherlands. Electronic address: e.molendijk.1@erasmusmc.nl.

D Schiphof (D)

Department of General Practice, Erasmus MC, University Medical Center, Rotterdam, the Netherlands. Electronic address: d.schiphof@erasmusmc.nl.

J B J van Meurs (JBJ)

Department of Internal Medicine, Erasmus MC, University Medical Center, Rotterdam, the Netherlands. Electronic address: j.vanmeurs@erasmusmc.nl.

E H G Oei (EHG)

Department of Radiology & Nuclear Medicine, Erasmus MC, University Medical Center, Rotterdam, the Netherlands. Electronic address: e.oei@erasmusmc.nl.

M van Middelkoop (M)

Department of General Practice, Erasmus MC, University Medical Center, Rotterdam, the Netherlands. Electronic address: m.vanmiddelkoop@erasmusmc.nl.

S M A Bierma-Zeinstra (SMA)

Department of General Practice, Erasmus MC, University Medical Center, Rotterdam, the Netherlands; Department of Orthopaedics, Erasmus MC, University Medical Center, Rotterdam, the Netherlands. Electronic address: s.bierma-zeinstra@erasmusmc.nl.

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