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Association between Patellofemoral and medial Tibiofemoral compartment osteoarthritis progression: exploring the effect of body weight using longitudinal data from osteoarthritis initiative (OAI)

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Abstract

Objectives

To investigate the associations of medial and lateral patellofemoral osteoarthritis (PF-OA) at baseline with symptomatic and radiographic OA outcomes in the medial tibiofemoral compartment (MTFC) over 4 years, according to baseline overweight status.

Methods

Data and MRI images of 600 subjects in the FNIH-OA biomarkers consortium were used. Symptomatic worsening and radiographic progression of MTFC-OA were defined using Western Ontario and McMaster Universities Arthritis Index (WOMAC) pain scores and MTFC joint space narrowing (JSN) from baseline to 4-year follow-up. Baseline MRIs were read to establish PF-OA diagnosis. The association between baseline regional PF-OA pattern and odds for MTFC-OA progression was evaluated using regression models (adjusted for relevant confounding covariates including body mass index (BMI), age, sex, PF alignment measurements, KL grade, and knee alignment). To evaluate the effect modifying role for overweight status, stratification analysis was performed (BMI ≥ 25 vs. < 25 kg/m2).

Results

At baseline, 340 (56.7%), 255 (42.5%), and 199 (33.2%) subjects had OA in the medial, lateral, and both PF compartments. Baseline medial PF-OA was associated with WOMAC pain score and MTFC JSN progression at 4 years (Adjusted OR:1.56[95%CI:1.09–2.23] and 1.59[1.11–2.28], respectively) but not lateral PF-OA. In stratification analysis, overweight status was found to be an effect modifier for medial PF-OA and WOMAC pain (OR in overweight vs. non-overweight subjects:1.65[1.13–2.42] vs. 0.50[0.12–1.82]) as well as MTFC-JSN progression (1.63[1.12–2.4] vs. 0.75[0.19–2.81]).

Conclusions

In addition to the known confounding effect of BMI for PF-OA and MTFC-OA, the overweight status may also play an effect modifier role in the association between baseline medial PF-OA and MTFC-OA progression, which is amenable to secondary prevention.

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Abbreviations

(BMI):

Body mass index

(BML):

Bone marrow lesion

(CI):

Confidence interval

(DESS):

Dual-echo at steady state

(FNIH):

Foundation for the National Institutes of Health

(ISR):

Insall-Salvati ratio

(IW):

Intermediate-weighted

(JSN):

Joint space narrowing

(JSW):

Joint space width

(KLG):

Kellgren Lawrence grade

(LPT):

Lateral patellar tilt

(LTFC):

Lateral tibiofemoral compartments

(MRI):

Magnetic resonance imaging

(MTFC):

Medial tibiofemoral compartments

(MOAKS):

MRI osteoarthritis knee scoring

(MPRs):

Multiplane reconstructions

(OR):

Odds ratio

(OA):

Osteoarthritis

(OAI):

Osteoarthritis Initiative

(PF):

Patellofemoral

(SD):

Standard deviation

(TT-TG):

Tibial tuberosity to trochlear groove

(TF):

Tibiofemoral

(TGD):

Trochlear groove depth

(TSE):

Turbo spino-echo

(WE):

Water-excitation

(WOMAC):

Western Ontario and McMaster universities osteoarthritis

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Acknowledgments

The OAI was a public-private partnership comprised of several contracts (N01-AR-2-2258; N01-AR-2-2259; N01-AR-2-2260; N01-AR-2-2261; N01-AR-2-2262) funded by the National Institutes of Health (NIH), a branch of the Department of Health and Human Services, and conducted by the Osteoarthritis Initiative (OAI) Study Investigators. Private funding partners include Merck Research Laboratories; Novartis Pharmaceuticals Corporation, GlaxoSmithKline; and Pfizer, Inc. Private sector funding for the OAI is managed by the Foundation for the National Institutes of Health. This manuscript was prepared using an OAI public-use dataset and does not necessarily reflect the opinions or views of the OAI investigators, the NIH, or the private funding partners.

Moreover, several grants and direct or in-kind contributions provide the publicly available data from the FNIH OA Biomarkers Consortium, including AbbVie, Amgen, Arthritis Foundation, Artialis; Bioiberica, BioVendor, DePuy, Flexion Therapeutics, GSK, IBEX, IDS, Merck Serono, Quidel, Rottapharm | Madaus, Sanofi, Stryker, the Pivotal OAI MRI Analyses (POMA) study, NIH HHSN2682010000 21C, and the Osteoarthritis Research Society International.

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Correspondence to Farhad Pishgar.

Ethics declarations

The institutional review boards of the University of California, San Francisco (OAI Coordinating Center; Approval Number: 10–00532), and all other OAI clinical centers approved the OAI study. All subjects have given informed consent before participating in the OAI project. All procedures performed in studies involving human participants were following the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards.

Conflict of interest

None of the authors have any conflicting personal or financial relationships that could have influenced the results of this study.

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Pishgar, F., Guermazi, A., Ashraf-ganjouei, A. et al. Association between Patellofemoral and medial Tibiofemoral compartment osteoarthritis progression: exploring the effect of body weight using longitudinal data from osteoarthritis initiative (OAI). Skeletal Radiol 50, 1845–1854 (2021). https://doi.org/10.1007/s00256-021-03749-0

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