BackgroundBone marrow lesion (BML) is an important magnetic resonance finding (MRI) finding that predicts knee osteoarthritis. The purpose of this study was to investigate the influence of proximal tibial morphology on BML, including the spreading root sign (SRS), in women without radiographic knee osteoarthritis (OA). It was hypothesized that varus alignment and a greater posterior tibial slopes (PTS) are associated with BML.Materials and methodsA total of 359 female volunteers without knee OA who were participants in the Iwaki Health Promotion Project in 2017 or 2019 were enrolled. Participants were divided into the non-OA and early knee OA (EKOA) groups based on the Luyten's classification criteria. The presence of pathological cartilage lesions, BMLs, attritions, meniscal lesions and effusions was scored on T2-weighted fat-suppressed magnetic resonance imaging (MRI) according to the Whole-Organ MRI Scoring system. The medial proximal tibial angle (MPTA) and medial and lateral PTS (MPTS and LPTS, respectively) were measured. Regression and receiver operating characteristic (ROC) analyses were performed to reveal the relationship between BMLs and proximal tibial morphological parameters.ResultsOf the 359 participants, 54 (15%) were classified as having EKOA. The prevalence of cartilage lesions, BMLs, attritions, meniscal lesions and effusions was higher in the EKOA group than in the non-OA group. The two groups had no significant difference in the proximal tibial parameters. Regression analysis revealed that age and a smaller MPTA were associated with BML in both groups. Attrition (p = 0.029) and the MPTS (p = 0.025) were positively associated with BML in the EKOA group.ConclusionThe prevalence of BMLs was higher in women with EKOA and correlated with the varus and greater posterior slopes in those without radiographic knee OA.Level of evidenceLevel III, retrospective case-control study.
机构:
Anhui Med Univ, Affiliated Hosp 1, Dept Rheumatol & Immunol, Arthrit Res Inst, Hefei, Peoples R China
Univ Tasmania, Menzies Inst Med Res, Private Bag 23, Hobart, Tas 7000, AustraliaAnhui Med Univ, Affiliated Hosp 1, Dept Rheumatol & Immunol, Arthrit Res Inst, Hefei, Peoples R China
Wang, Kang
Xu, Jianhua
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Anhui Med Univ, Affiliated Hosp 1, Dept Rheumatol & Immunol, Arthrit Res Inst, Hefei, Peoples R ChinaAnhui Med Univ, Affiliated Hosp 1, Dept Rheumatol & Immunol, Arthrit Res Inst, Hefei, Peoples R China
Xu, Jianhua
Cai, Jingyu
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Anhui Med Univ, Affiliated Hosp 1, Dept Rheumatol & Immunol, Arthrit Res Inst, Hefei, Peoples R ChinaAnhui Med Univ, Affiliated Hosp 1, Dept Rheumatol & Immunol, Arthrit Res Inst, Hefei, Peoples R China
Cai, Jingyu
Zheng, Shuang
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Anhui Med Univ, Affiliated Hosp 1, Dept Rheumatol & Immunol, Arthrit Res Inst, Hefei, Peoples R China
Univ Tasmania, Menzies Inst Med Res, Private Bag 23, Hobart, Tas 7000, AustraliaAnhui Med Univ, Affiliated Hosp 1, Dept Rheumatol & Immunol, Arthrit Res Inst, Hefei, Peoples R China
Zheng, Shuang
Yang, Xueqing
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Anhui Med Univ, Affiliated Hosp 1, Dept Rheumatol & Immunol, Arthrit Res Inst, Hefei, Peoples R ChinaAnhui Med Univ, Affiliated Hosp 1, Dept Rheumatol & Immunol, Arthrit Res Inst, Hefei, Peoples R China
Yang, Xueqing
Ding, Changhai
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Anhui Med Univ, Affiliated Hosp 1, Dept Rheumatol & Immunol, Arthrit Res Inst, Hefei, Peoples R China
Univ Tasmania, Menzies Inst Med Res, Private Bag 23, Hobart, Tas 7000, AustraliaAnhui Med Univ, Affiliated Hosp 1, Dept Rheumatol & Immunol, Arthrit Res Inst, Hefei, Peoples R China