Abstract
| Original language | English |
|---|---|
| Pages (from-to) | 1396-1404 |
| Number of pages | 9 |
| Journal | Osteoarthritis Cartilage |
| Volume | 31 |
| Issue number | 10 |
| DOIs | |
| Publication status | Published - 2023 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
-
SDG 3 Good Health and Well-being
Keywords
- Knee
- Meniscus extrusion
- MRI
- Osteoarthritis
- Progression
- biological marker
- adult
- Article
- case control study
- clinical feature
- controlled study
- disease exacerbation
- female
- human
- knee osteoarthritis
- knee radiography
- major clinical study
- male
- medial meniscal extrusion
- middle aged
- musculoskeletal system parameters
- nuclear magnetic resonance imaging
- quantitative study
- risk factor
- Western Ontario and McMaster Universities Osteoarthritis Index
- diagnostic imaging
- knee
- knee meniscus
- tibia
- Disease Progression
- Humans
- Knee Joint
- Magnetic Resonance Imaging
- Menisci, Tibial
- Meniscus
- Osteoarthritis, Knee
- Tibia
Classification according to Österreichische Systematik der Wissenschaftszweige (ÖFOS 2012)
- 303012 Health sciences
Applied Research Level (ARL)
- Not applicable
Research focus/foci
- Applied Health Innovation
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In: Osteoarthritis Cartilage, Vol. 31, No. 10, 2023, p. 1396-1404.
Research output: Contribution to journal › Article › peer-review
TY - JOUR
T1 - Association of quantitative measures of medial meniscal extrusion with structural and symptomatic knee osteoarthritis progression – Data from the OAI FNIH biomarker study
AU - Sharma, K.
AU - Eckstein, F.
AU - Maschek, S.
AU - Roth, M.
AU - Hunter, D.J.
AU - Wirth, W.
N1 - Export Date: 14 December 2023 CODEN: OSCAE Correspondence Address: Wirth, W.; Institute of Anatomy and Cell Biology, Strubergasse 21, Austria; email: [email protected] Funding details: National Institutes of Health, NIH, HHSN2682010000, N01-AR-2-2258, N01-AR-2-2259, N01-AR-2-2260, N01-AR-2-2261, N01-AR-2-2262 Funding details: Foundation for the National Institutes of Health, FNIH Funding details: U.S. Department of Health and Human Services, HHS Funding details: Arthritis Foundation, AF Funding details: Pfizer Funding details: GlaxoSmithKline, GSK Funding details: Osteoarthritis Research Society International, OARSI Funding text 1: Scientific and financial support for the FNIH OA Biomarkers Consortium were made possible through grants, direct and in-kind contributions provided by: AbbVie; Amgen Inc.; Arthritis Foundation; Bioiberica S.A.; DePuyMitek, Inc.; Flexion Therapeutics, Inc.; GlaxoSmithKline; Merck Serono; Rottapharm | Madaus; Sanofi; Stryker; The Pivotal OAI MRI Analyses (POMA) Study, NIH HHSN2682010000. We thank the Osteoarthritis Research Society International (OARSI) for their leadership and expertise on the FNIH OA Biomarker Consortium project. The OAI, a public-private partnership comprised of five contracts (N01-AR-2-2258; N01-AR-2-2259; N01-AR-2-2260; N01-AR-2-2261; N01-AR-2-2262), was funded by the National Institutes of Health, a branch of the Department of Health and Human Services, and conducted by the OAI Study Investigators. Private funding partners of the OAI 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. The Ph.D. project of Kalpana Sharma is funded by a grant from the Rotary Club Salzburg-Paracelsus. Funding text 2: Scientific and financial support for the FNIH OA Biomarkers Consortium were made possible through grants, direct and in-kind contributions provided by: AbbVie; Amgen Inc.; Arthritis Foundation; Bioiberica S.A.; DePuyMitek, Inc.; Flexion Therapeutics, Inc.; GlaxoSmithKline; Merck Serono; Rottapharm | Madaus; Sanofi; Stryker; The Pivotal OAI MRI Analyses (POMA) Study, NIH HHSN2682010000 . We thank the Osteoarthritis Research Society International (OARSI) for their leadership and expertise on the FNIH OA Biomarker Consortium project. The OAI, a public-private partnership comprised of five contracts ( N01-AR-2-2258 ; N01-AR-2-2259 ; N01-AR-2-2260 ; N01-AR-2-2261 ; N01-AR-2-2262 ), was funded by the National Institutes of Health , a branch of the Department of Health and Human Services, and conducted by the OAI Study Investigators. Private funding partners of the OAI 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. The Ph.D. project of Kalpana Sharma is funded by a grant from the Rotary Club Salzburg-Paracelsus. 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(2006) Arthritis Rheum, 54 (8), pp. 2488-2495; Hunter, D.J., Zhang, Y.Q., Niu, J.B., Tu, X., Amin, S., Clancy, M., The association of meniscal pathologic changes with cartilage loss in symptomatic knee osteoarthritis (2006) Arthritis Rheum, 54 (3), pp. 795-801; Liu, Y., Joseph, G.B., Foreman, S.C., Li, X., Lane, N.E., Nevitt, M.C., Determining a threshold of medial meniscal extrusion for prediction of knee pain and cartilage damage progression over 4 years: data from the osteoarthritis initiative (2021) Am J Roentgenol, 216 (5), pp. 1318-1328; Xu, D., van der Voet, J., Waarsing, J.H., Oei, E.H., Klein, S., Englund, M., Are changes in meniscus volume and extrusion associated to knee osteoarthritis development? A structural equation model (2021) Osteoarthr Cartil, 29 (10), pp. 1426-1431; Wirth, W., Frobell, R.B., Souza, R.B., Li, X., Wyman, B.T., Hellio Le Graverand, M.-P., A three-dimensional quantitative method to measure meniscus shape, position, and signal intensity using MR Images: a pilot study and preliminary results in knee osteoarthritis (2010) Magn Reson Med, 63 (5); Wenger, A., Englund, M., Wirth, W., Hudelmaier, M., Kwoh, K., Eckstein, F., Relationship of 3D meniscal morphology and position with knee pain in subjects with knee osteoarthritis: a pilot study (2012) Eur Radiol, 22 (1), pp. 211-220; Gao, K.T., Xie, E., Chen, V., Iriondo, C., Calivà, F., Souza, R.B., Large-scale analysis of meniscus morphology as risk factor for knee osteoarthritis (2023) Arthritis Rheumatol; Sharma, K., Eckstein, F., Wirth, W., Emmanuel, K., Meniscus position and size in knees with versus without structural knee osteoarthritis progression: data from the osteoarthritis initiative (2022) Skeletal Radiol, 51 (5), pp. 997-1006; Ghouri, A., Robinson, E., Muzumdar, S., Barr, A., Murdoch, C., Kingsbury, S.R., A systematic review of the relationship between imaging-assessed meniscal pathologies, cartilage loss, joint replacement and pain in knee osteoarthritis (2022) Osteoarthr Cartil, 30 (10), pp. 1287-1327; Hunter, D.J., Nevitt, M., Losina, E., Kraus, V., Biomarkers for osteoarthritis: current position and steps towards further validation (2014) Best Pract Res Clin Rheumatol, 28 (1), pp. 61-71; Ornetti, P., Brandt, K., Hellio-Le Graverand, M.P., Hochberg, M., Hunter, D.J., Kloppenburg, M., OARSI-OMERACT definition of relevant radiological progression in hip/knee osteoarthritis (2009) Osteoarthr Cartil, 17 (7), pp. 856-863; Angst, F., Aeschlimann, A., Stucki, G., Smallest detectable and minimal clinically important differences of rehabilitation intervention with their implications for required sample sizes using WOMAC and SF-36 quality of life measurement instruments in patients with osteoarthritis of the lower ex (2001) Arthritis Rheum, 45 (4), pp. 384-391; Peterfy, C.G., Schneider, E., Nevitt, M., The osteoarthritis initiative: report on the design rationale for the magnetic resonance imaging protocol for the knee (2008) Osteoarthr Cartil, 16 (12), pp. 1433-1441; Schneider, E., NessAiver, M., White, D., Purdy, D., Martin, L., Fanella, L., The osteoarthritis initiative (OAI) magnetic resonance imaging quality assurance methods and results (2008) Osteoarthr Cartil, 16 (9), pp. 994-1004; Siorpaes, K., Wenger, A., Bloecker, K., Wirth, W., Hudelmaier, M., Eckstein, F., Interobserver reproducibility of quantitative meniscus analysis using coronal multiplanar DESS and IWTSE MR imaging (2012) Magn Reson Med, 67 (5), pp. 1419-1426; Kraus, V.B., Collins, J.E., Charles, H.C., Pieper, C.F., Whitley, L., Losina, E., Predictive validity of radiographic trabecular bone texture in knee osteoarthritis: the Osteoarthritis Research Society International/Foundation for the National Institutes of Health osteoarthritis biomarkers consortium (2018) Arthritis Rheumatol, 70 (1), pp. 80-87; Kraus, V.B., Collins, J.E., Hargrove, D., Losina, E., Nevitt, M., Katz, J.N., Predictive validity of biochemical biomarkers in knee osteoarthritis: data from the FNIH OA biomarkers consortium (2017) Ann Rheum Dis, 76 (1), pp. 186-195; Eckstein, F., Collins, J.E., Nevitt, M.C., Lynch, J.A., Kraus, V., Katz, J.N., Cartilage thickness change as an imaging biomarker of knee osteoarthritis progression - data from the fnih OA biomarkers consortium (2015) Arthritis Rheumatol; Hunter, D.J., Deveza, L.A., Collins, J.E., Losina, E., Nevitt, M.C., Roemer, F.W., Multivariable modeling of biomarker data from the phase 1 foundation for the NIH osteoarthritis biomarkers consortium (2022) Arthritis Care Res, 74 (7), pp. 1142-1153; Collins, J.E., Losina, E., Nevitt, M.C., Roemer, F.W., Guermazi, A., Lynch, J.A., Semi-quantitative imaging biomarkers of knee osteoarthritis progression: data from the FNIH OA biomarkers consortium (2016) Arthritis Rheumatol, 68 (10), pp. 2422-2431; Hunter, D., Nevitt, M., Lynch, J., Kraus, V.B., Katz, J.N., Collins, J.E., Longitudinal validation of periarticular bone area and 3D shape as biomarkers for knee OA progression? 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(2004) Am J Roentgenol; Crema, M.D., Roemer, F.W., Felson, D.T., Englund, M., Wang, K., Jarraya, M., Factors associated with meniscal extrusion in knees with or at risk for osteoarthritis: the multicenter osteoarthritis study (2012) Radiology, 264 (2), pp. 494-503; Lee, D.H., Lee, B.S., Kim, J.M., Yang, K.S., Cha, E.J., Park, J.H., Predictors of degenerative medial meniscus extrusion: radial component and knee osteoarthritis (2011) Knee Surg Sports Traumatol Arthrosc, 19 (2), pp. 222-229; Roth, M., Wirth, W., Emmanuel, K., Culvenor, A.G., Eckstein, F., The contribution of 3D quantitative meniscal and cartilage measures to variation in normal radiographic joint space width—data from the osteoarthritis initiative healthy reference cohort (2017) Eur J Radiol, 87, pp. 90-98; Roth, M., Emmanuel, K., Wirth, W., Kwoh, C.K., Hunter, D.J., Eckstein, F., Sensitivity to change and association of three-dimensional meniscal measures with radiographic joint space width loss in rapid clinical progression of knee osteoarthritis (2018) Eur Radiol, 28, pp. 1844-1853; Roemer, F.W., Guermazi, A., Collins, J.E., Losina, E., Nevitt, M.C., Lynch, J.A., Semi-quantitative MRI biomarkers of knee osteoarthritis progression in the FNIH biomarkers consortium cohort − methodologic aspects and definition of change (2016) BMC Musculoskelet Disord, 17 (1), p. 466; Collins, J.E., Losina, E., Nevitt, M.C., Roemer, F.W., Guermazi, A., Lynch, J.A., Semiquantitative imaging biomarkers of knee osteoarthritis progression: data from the foundation for the National Institutes of Health osteoarthritis biomarkers consortium (2016) Arthritis Rheumatol, 68 (10), pp. 2422-2431
PY - 2023
Y1 - 2023
N2 - Objective: To study the association of quantitative medial meniscal position measures with radiographic and symptomatic knee osteoarthritis (OA) progression over 2–4 years. Methods: The FNIH OAI Biomarkers study comprised 600 participants in four subgroups: 194 case knees with combined structural (medial minimum joint space width (minJSW) loss ≥0.7 mm) and symptomatic (persistent Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) pain subscale increase ≥9 [0–100 scale]) progression; 200 knees with neither structural nor symptomatic progression; 103 knees with isolated structural and 103 with isolated symptomatic progression. Coronal double echo at steady state (DESS) MRIs were used for segmenting five central slices of the medial meniscus. Associations with progression were examined using logistic regression (adjusted for demographic and clinical data). Results: Greater baseline medial meniscal extrusion was associated with combined structural/symptomatic progression (OR 1.59; 95%CI: [1.25,2.04]). No relationship was observed for tibial plateau coverage or meniscal overlap distance. The two-year increase in meniscal extrusion (OR 1.48 [1.21, 1.83]), and reduction in tibial plateau coverage (OR 0.70 [0.58,0.86]) and overlap distance (OR 0.73 [0.60,0.89]) were associated with combined progression. Greater baseline extrusion was associated with isolated structural and less extrusion with isolated symptomatic progression. The longitudinal increase in meniscal extrusion, and reduction in tibial plateau coverage and overlap distance were associated with structural, but not with symptomatic progression. Conclusion: Baseline measures of medial meniscal extrusion were consistently positively associated with combined radiographic/symptomatic progression and with isolated structural, but not with isolated symptomatic progression. These measures may therefore allow one to assess the risk of structural knee OA progression and to monitor interventions restoring meniscal position and function.
AB - Objective: To study the association of quantitative medial meniscal position measures with radiographic and symptomatic knee osteoarthritis (OA) progression over 2–4 years. Methods: The FNIH OAI Biomarkers study comprised 600 participants in four subgroups: 194 case knees with combined structural (medial minimum joint space width (minJSW) loss ≥0.7 mm) and symptomatic (persistent Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) pain subscale increase ≥9 [0–100 scale]) progression; 200 knees with neither structural nor symptomatic progression; 103 knees with isolated structural and 103 with isolated symptomatic progression. Coronal double echo at steady state (DESS) MRIs were used for segmenting five central slices of the medial meniscus. Associations with progression were examined using logistic regression (adjusted for demographic and clinical data). Results: Greater baseline medial meniscal extrusion was associated with combined structural/symptomatic progression (OR 1.59; 95%CI: [1.25,2.04]). No relationship was observed for tibial plateau coverage or meniscal overlap distance. The two-year increase in meniscal extrusion (OR 1.48 [1.21, 1.83]), and reduction in tibial plateau coverage (OR 0.70 [0.58,0.86]) and overlap distance (OR 0.73 [0.60,0.89]) were associated with combined progression. Greater baseline extrusion was associated with isolated structural and less extrusion with isolated symptomatic progression. The longitudinal increase in meniscal extrusion, and reduction in tibial plateau coverage and overlap distance were associated with structural, but not with symptomatic progression. Conclusion: Baseline measures of medial meniscal extrusion were consistently positively associated with combined radiographic/symptomatic progression and with isolated structural, but not with isolated symptomatic progression. These measures may therefore allow one to assess the risk of structural knee OA progression and to monitor interventions restoring meniscal position and function.
KW - Knee
KW - Meniscus extrusion
KW - MRI
KW - Osteoarthritis
KW - Progression
KW - biological marker
KW - adult
KW - Article
KW - case control study
KW - clinical feature
KW - controlled study
KW - disease exacerbation
KW - female
KW - human
KW - knee osteoarthritis
KW - knee radiography
KW - major clinical study
KW - male
KW - medial meniscal extrusion
KW - middle aged
KW - musculoskeletal system parameters
KW - nuclear magnetic resonance imaging
KW - quantitative study
KW - risk factor
KW - Western Ontario and McMaster Universities Osteoarthritis Index
KW - diagnostic imaging
KW - knee
KW - knee meniscus
KW - tibia
KW - Disease Progression
KW - Humans
KW - Knee Joint
KW - Magnetic Resonance Imaging
KW - Menisci, Tibial
KW - Meniscus
KW - Osteoarthritis, Knee
KW - Tibia
UR - https://www.mendeley.com/catalogue/ccb723a1-ce1e-381f-9750-93d36df12e2c/
U2 - 10.1016/j.joca.2023.07.007
DO - 10.1016/j.joca.2023.07.007
M3 - Article
SN - 1063-4584
VL - 31
SP - 1396
EP - 1404
JO - Osteoarthritis Cartilage
JF - Osteoarthritis Cartilage
IS - 10
ER -