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Clinical and imaging findings associated with preservation of knee joint health over 8 years in individuals aged 65 and over: data from the OAI

Abstract

Objective

While risk factors for osteoarthritis (OA) are well known, it is not well understood why certain individuals maintain high mobility and joint health throughout their life while others demonstrate OA at older ages. The purpose of this study was to assess which demographic, clinical and MRI quantitative and semi-quantitative factors are associated with preserving healthy knees in older individuals.

Methods

This study analyzed data from the OA Initiative (OAI) cohort of individuals at the age of 65 years or above. Participants without OA at baseline (BL) (Kellgren-Lawrence (KL) ≤ 1) were followed and classified as incident cases (KL ≥ 2 during follow-up; n = 115) and as non-incident (KL ≤ 1 over 96-month; n = 391). Associations between the predictor-variables sex, age, BMI, race, clinical scoring systems, T2 relaxation times and Whole-Organ Magnetic Resonance Imaging-Score (WORMS) readings at BL and the preservation of healthy knees (KL ≤ 1) during a 96-month follow-up period were assessed using logistic regression models.

Results

Obesity and presence of pain showed a significant inverse association with maintaining radiographically normal joints in patients aged 65 and above. T2 relaxation times of the lateral femur and tibia as well as the medial femur were also significantly associated with maintaining radiographically normal knee joints. Additionally, absence of lesions of the lateral meniscus and absence of cartilage lesions in the medial and patellofemoral compartments were significantly associated with maintaining healthy knee joints.

Conclusion

Overall, this study provides protective clinical parameters as well as quantitative and semi-quantitative MR-imaging parameters associated with maintaining radiographically normal knee joints in an older population over 8 years.

Significance and innovations

Most protective parameters for osteoarthritis seem to be similar in the elderly as compared to mixed age cohorts. Nevertheless, some risk factors may be different in the elderly, especially regarding quantitative imaging parameters.

Peer Review reports

Introduction

Osteoarthritis (OA) is the most common form of arthritis and a major cause of physical disability and reduced quality of life in the elderly [1]. OA is most commonly located in the knee with an estimated prevalence of 27% at the age of 70 [2]. With an aging population, the economic burden and the loss in quality of life due to OA is expected to strongly increase within the next decades [3].

There are well known risk factors for OA in the general population. Nevertheless, it is unclear why certain individuals maintain high mobility and joint health at older ages while other individuals demonstrate cartilage breakdown and OA. The characteristics of patients above of the age of 65 who have and maintain radiographically normal joints have not been well investigated. On the other hand, there is some evidence suggesting that individuals who develop OA at older ages have different risk factors than those of younger age groups. For example, Driban et al. have shown that obese patients and patients at older age are at high risk of developing accelerated OA [4]. In addition, studies have demonstrated that physical activity, waist circumference and pain impact physical function or quality of life in older patients with OA [5,6,7].

Multiple of these studies are based on the Osteoarthritis Initiative (OAI), a longitudinal, multi-center cohort study that recruited 4796 individuals and is sponsored by the US National Institutes of Health (NIH) including clinical and imaging parameters during up to 8 years (OAI, https://oai.nih.gov).

In general, most studies on knee OA have focused on using radiographs with Kellgren-Lawrence (KL) scoring to define OA [1]. Nevertheless, MR imaging has been shown to give a more comprehensive understanding of structural OA development. The MR based Whole-Organ Magnetic Resonance Imaging Score (WORMS) of the knee provides a reliable multi-feature assessment tool in OA of the knee [8, 9]. Besides more granular analysis of meniscal, cartilage and bone marrow edema like lesions, MR imaging helps evaluate effusion and synovitis in the knee – an important mediator of OA [10]. Moreover, recent studies revealed associations between cartilage T2 relaxation times determined on MR images and the onset of cartilage lesions [11, 12], indicating the potential of MR imaging parameters to possibly predict morphologic OA. To date, however, there is only a limited number of studies investigating MRI findings in older patients with OA or risk factors for OA. One study, for example, has shown that full-thickness cartilage defects determined on MR images are an important predictive factor for the progression of OA to a total knee replacement in older patients [13]. A study by Sharma et al. in a mixed age group showed that worsening MRI lesions status was associated with concurrent incident radiographic OA and therefore proposed that these lesions represent early OA [14].

Although some studies evaluated MR imaging criteria in OA and others focused on the correlation of clinical parameters and OA in patients of different age groups, so far it is unclear which factors help preserve healthy knees at higher ages and no study has been performed a combined investigation of demographic, clinical and imaging characteristics of individuals older than 65 years who maintain radiographically normal knees. In this study, we therefore aim (i) to analyze a cohort of participants from the OAI cohort with KL 0 and 1 knee radiographs over 8 years concerning demographic, clinical factors, and MRI quantitative and semi-quantitative parameters, which will serve as predictors and (ii) to compare this cohort with an age-matched cohort that develops radiographic OA above the age of 65 over 8 years.

The purpose of this study was to provide a comprehensive understanding of characteristics of knee joints in older individuals who maintain radiographically normal morphology over 8 years and the specific protective factors in this age group.

Patients and methods

Participant selection

The analyses in this study are based on data from the OAI (https://nda.nih.gov/oai), a longitudinal, observational multi-center study with a cohort size of n = 4796 individuals, designed to assess biomarkers in OA. This dataset includes clinical information with a symptom questionnaire and MRIs of both knees obtained at baseline (BL), 12-, 24, 36-, 48- 72- and 96-month follow-up. Institutional review boards of each center approved informed consent documentation, study protocols and amendments. All investigations were carried out in compliance with the Helsinki Declaration.

Figure 1 shows a flow chart illustrating the inclusion and exclusion criteria for this analysis. Our analysis focused on the right knee only as the full imaging complement was available for the right knee including T2 relaxation time measurements. From the 4796 participants in the OAI 1822 were at least 65 years of age at the baseline visit. Six participants were excluded due to rheumatoid arthritis at BL. In order to analyze features associated with the onset of OA, we excluded participants with radiographic OA at BL, which was defined as a KL score ≥ 2 as reported previously [15]. The remaining participants without OA at BL were classified into two outcome groups: A control group and an incidence group. Control group individuals were defined as those with a 96-month follow-up visit without OA demonstrated on knee radiographs (n = 391). The incidence group consisted of those individuals who showed OA (KL > 1) at any follow-up visit (n = 115).

Fig. 1
figure 1

Flow chart illustrating the inclusion and exclusion criteria for participant selection. Participants needed either an 8 year follow up visit without radiographic OA or radiographic incidence of OA at any other timepoint (then 8 year follow up radiograph was not required as OA is assumed to be irreversible). BL = Baseline; FU = Follow up; KL = Kellgren Lawrence; n = Number; OAI = Osteoarthritis Initiative; RA = Rheumatoid Arthritis; WORMS = Whole-Organ Magnetic Resonance Imaging Score; y = years

Image acquisition

MR images were acquired at four centers (Columbus, Ohio; Baltimore, Maryland; Pittsburgh, Pennsylvania and Pawtucket, Rhode Island), using four identical 3.0 Tesla scanners (Siemens Magnetom Trio, Erlangen, Germany). Acquired sequences of the knee used in this study included: (i) coronal 2D intermediate-weighted (IW) turbo spin-echo (TSE) [repetition time (TR) / echo time (TE); spatial resolution; field of view (FOV); slice thickness; gap] [3700 ms / 29 ms; 0.365 mm x 0.456 mm; 140 mm; 3.0 mm; 0 mm), (ii) sagittal, fat-saturated (FS) 2D IW TSE [3200 ms / 30 ms; 0.357 mm x 0.511 mm; 160 mm; 3 mm; 0 mm), (iii) coronal 3D fast low angle shot with water excitation (FLASH WE) [7.57 ms / 20 ms; 0.313 mm x 0.313 mm; 160 mm; 1.5 mm; 0 mm] and (iv) sagittal 3D dual-echo steady state sequence with water excitation (DESS WE) [4.7 ms / 16.3 ms; 0.365 mm x 0.456 mm; 140 mm; 1.5 mm; 0 mm] with axial and coronal reformations. To allow quantitative assessment of cartilage T2 relaxation times, a sagittal 2D multi slice multi echo sequence (MSME) was also included [2700 ms / 10–70 ms; 0.313 mm x 0.446 mm; 120 mm; 3.0 mm / 0.5 mm]. Detailed information on imaging protocols is available online (https://oai.epi-ucsf.org/datarelease/operationsManuals/MRI_ManualRev.pdf) [16].

Clinical parameters

Influence of sex, age, BMI (normal vs. obese (≥ 30 kg/body height in m2)) and race (white vs. non-white) on the onset of OA were analyzed. Furthermore, the clinical scoring system “Western Ontario and McMaster Universities Osteoarthritis” (WOMAC) with subscales for stiffness, pain, and activity of daily life were included in the analysis as reported previously [17] [18]. , with scores ranging from 0 to 96 for the total WOMAC where 0 represents the best health status and 96 the worst possible status. Furthermore, the Physical Activity Scale for the Elderly (PASE), a scoring instrument that measures the level of physical activity in individuals aged 65 years and older on a scale of -400 to + 400 was evaluated [19].

Image analysis

Image analysis was performed on picture archiving communication system workstations (Agfa, Ridgefield Park, NJ, USA). Structural degenerative joint disease was semi-quantitatively graded for each exam using a modified version of the Whole-Organ Magnetic Resonance Imaging Score (WORMS) system in all participants, as previously described [8, 9]. Accordingly, cartilage lesions were graded in six locations (at the patella, trochlea, medial and lateral femoral condyle, medial and lateral tibial plateau, respectively). Meniscal lesions were also graded in six locations (anterior horn, body, and posterior horn, for medial and lateral meniscus, respectively). WORMS readings at baseline were available in a subset of participants: in 130 participants of the control group and in 78 participants of the incidence group. Intra-class correlation coefficients (ICC) demonstrating excellent inter- and intra-reader reproducibility for modified WORMS gradings of cartilage and menisci have previously been reported by our group (ICCinter-reader = 0.95–0.97 and ICCintra-reader = 0.97–0.98 respectively) [9].

Additionally, cartilage T2-relaxation times were included in this analysis. As reported previously, we developed a fully automatic method for reliable cartilage segmentation of knee MRI volumes on a T2 mapping sequence [11, 20, 21]. This algorithm was applied to all MR scans in the OAI dataset. The predicted cartilage compartments were then fully automatically subsegmented into lateral tibia (LT), medial tibia (MT), central lateral femur (cLF), central medial femur (cMF) and patella (P) compartments as reported previously [21]. The average T2-relaxation times in those regions were defined.

Selection of primary predictors

To reduce probability of error due to multiple testing, the predictor variables have been separated into primary, and secondary categories based on their importance for the proposed research and based on the preliminary data and previous research. As the predictor variables BMI and the WOMAC pain score are well established risk factors for OA in the general population, these clinical predictor variables were chosen as primary predictors [22, 23]. Age served as secondary predictor, as this study was performed in a subgroup of the OAI at older ages already. Race, due to the relatively small sample size, and the remaining clinical (sub-)scores (i.e. WOMAC stiffness) also served as secondary predictors as there is less evidence for association with OA incidence. From the semiquantitative imaging parameters, the sum score over all cartilage lesions was used as primary predictor as cartilage lesions have been shown to be associated with incidence of OA in a mixed age group [14]. The sum score over the lateral and medial meniscus as well as the cartilage lesions in the lateral, the medial, and the patellofemoral compartment were used as secondary predictors. From the quantitative imaging parameters, the mean T2 value over all regions was designated as a primary predictor, as it provides information on all compartments. Consequently, the T2 values of the lateral/medial femur/tibia and the patella were designated as secondary predictors.

Statistical analysis

All statistical analyses were performed using the statistical package R version 3.2.4 (R Foundation for Statistical Computing, Vienna, Austria), with a two-sided level of significance of α = 0.05. Descriptive statistics for participant age and sex at baseline were analyzed using crosstabs for sex and means and standard deviation (SD) for age. The outcome variable was a binary variable defined by whether an older individual developed radiographic OA within 96 months after the BL scan (yes/no). Associations between the predictor-variables at baseline (age, sex, BMI, race, WOMAC pain/total, PASE, WORMS, T2-values) and the onset of radiographic OA (yes/no) were assessed using logistic regression models and outcomes reported as odds ratios (OR) for developing OA during this timeframe. ORs are reported per standard deviation change of each predictor (labeled as sOR in the results section). Age, sex, and BMI adjustments were included in all analysis.

Results

Participants demographics

Demographics are shown in Table 1. Overall, 506 participants were included in the analysis (115 older individuals with incident radiographic OA, and 391 without incident radiographic OA). Mean time before radiographic onset of OA was at 3.97 years with 34/20/18/9/30/14 patients showing onset of OA at 12/24/36/48/72/96-month follow-up. Mean age was at 70.3 ± 4.1 years for the incidence group and 70.5 ± 3.8 years for the non-incidence group with no significant difference between groups (p = 0.70). Also, no significant difference in sex was observed for the two groups (206 females in the incidence group (52.7%); 68 females in the non-incidence group (59.1%); p = 0.17). There was no significant difference between the average BMI of the incidence group at 28.22 [24.5-31.94] and the non-incidence group at 26.67 [23.0-30.34] (p = 0.21).

Table 1 Patient demographics at baseline

Primary predictors

Associations between primary predictor variables and maintaining radiographically normal joints are reported in Table 2. Obesity was significantly associated with a lower OR (per SD change in the predictor) of maintaining radiographically normal joints (standardized OR (sOR): 0.43, [95% CI = 0.23–0.79], p = 0.007). The pain-subscale for the WOMAC scoring system also was significantly associated with the OR of maintaining radiographically normal joints (sOR WOMAC pain: 0.69, [0.56–0.85], p < 0.001). Additionally, the overall sum score for all cartilage regions derived from the WORMS readings as well as average T2 values of all compartments of the knee were significantly associated with the OR of maintaining radiographically normal joints (sOR: 0.62, [0.46–0.82], p = 0.001; sOR: 0.72, [0.58–0.82], p = 0.003).

Table 2 Standardized odds ratios of primary predictors on maintaining radiographically normal joints

Secondary predictors

Associations between secondary predictor variables and maintaining radiographically normal joints are reported in Table 3. There was no significant association observed between sex, age, race and maintaining radiographically normal joints (p = 0.14/0.58/0.53). The total score of the clinical scoring system WOMAC significantly decreased the OR of maintaining radiographically normal joints (sOR: 0.68, [0.56–0.83], p = 0.001). Furthermore, there was no significant association between PASE score at baseline and the development of incident OA throughout an 8-year follow-up period (p = 0.97).

Table 3 Standardized odds ratios of secondary clinical, semiquantitative (WORMS) and quantitative predictors on maintaining radiographically normal joints

Regarding the WORMS readings, an elevated sum score for the lateral meniscus significantly decreased the OR for maintaining radiographically normal joints (sOR: 0.61, [0.45–0.81], p = 0.001), whereas the sum score of the medial meniscus did not show a significant association (p = 0.27). Regarding cartilage lesions, the sum score of the medial compartment (medial femur and tibia) and the patellofemoral compartment were significantly associated with a lower OR for maintaining radiographically normal joints (sOR medial compartment: 0.71, [0.54–0.93], p = 0.016; sOR patellofemoral compartment 0.67, [0.51–0.88], p = 0.004), whereas the sum score for the lateral compartment did not show any significant associations (p = 0.29).

Cartilage T2 values in both, the lateral femur and tibia showed a significant association with maintaining radiographically normal joints (sOR lateral tibia: 0.76 [0.62–0.94], p = 0.014; lateral femur: 0.7, [0.56–0.86], p = 0.001). Also, elevated cartilage T2 values in of the medial femur were significantly associated with lower odds of maintaining radiographically normal joints (sOR: 0.68, [0.54–0.84], p = 0.001). No significant associations between T2 values in the patella cartilage and incident OA were observed (p = 0.73).

Discussion

This study assessed the associations between demographic, clinical and imaging findings including WORMS readings (predictors) with maintaining radiographically normal knee joints (outcome) in OAI participants 65 years and above. Obesity, pain, functional impairment as well as high cartilage T2 relaxation times in the lateral compartment and of the medial femur significantly decreased the OR for maintaining radiographically normal joints. Moreover, WORMS readings demonstrated significant inverse associations between the sum scores for the lateral meniscus as well as the cartilage of the medial and the patellofemoral compartment and maintaining healthy knee joints.

It is well known that older people show a different set of risk factors for multiple diseases as compared to a younger population, especially in neurological diseases [24]. Comparable to younger participants, obesity increased the risk of developing incident radiographic OA, which is in line with a study by Driban et al. [4]. Although, female sex is a well-established risk factor for OA in the general population, results in the older participants of this study were not significant [22]. A lower WOMAC pain score as well as WOMAC total score were significantly associated with maintaining radiographically normal knee joints in the older group. Accordingly, previous studies showed a correlation of pain with the incidence of OA using cartilage volume loss and incident radiographic knee OA as outcomes [23, 25,26,27,28].

Edd et al. examined the longitudinal changes of knee cartilage T2 relaxation times and reported increases in T2 relaxation times of the medial compartment of the knee during radiographic progression of OA [29]. Liebl et al. showed in a middle-aged subgroup of the OAI (mean age 59 years), that early T2 changes predict the onset of radiographic knee OA [30]. Although they observed that effect in the entire lateral compartment and the medial femur, similar to our study, they did not observe a significant effect for the medial tibia. Nevertheless, different from our results, in their study, a highly significant correlation of the T2 relaxation times of the patella with the onset of OA was found using individual linear regression models. Heilmeier et al. showed that increased T2 relaxation times of the cartilage in the lateral compartment significantly increased the risk of total knee arthroplasty within 4–7 years [31]. This allows the conclusion that T2 values of the lateral compartment may be an important predictor of OA progression in all age groups, whereas the cartilage of the patella may be more important in younger patients as compared to older patients in maintaining healthy knees.

The WORMS system used in this study provides a multi-feature, whole-organ assessment of the knee in OA using conventional MR images [8]. The absence of focal lesions of the patellofemoral cartilage was a significant predictor for maintaining healthy knees in this older participant group. Cartilage lesions in the medial compartment were associated with developing OA, whereas lesions in the lateral compartment did not show such an association. Hafezi-Nejad et al. also demonstrated a significant increase in the hazard ratio for future knee replacement through increased cartilage lesions scores of WORMS in a subset of the OAI including all age-groups [32]. Sharma et a. showed in a mixed age group that worsening MRI lesions status was associated with concurrent incident radiographic OA. Nevertheless, these studies were performed in a mixed age group and did not examine the individual knee compartments separately. Comparable to our results, a study by Yang et al. based on 88 patients found that the medial compartment and the patellofemoral joint degenerate more severely in early stage knee OA [33]. Interestingly, absence of lesions of the lateral meniscus and not the medial meniscus was associated with maintaining healthy knees in the elderly. These results are in line with a study by Badlani et al. in a younger cohort, who also found that lesions of the medial but not the lateral meniscus are more frequent in patients who develop OA as compared to those who maintain healthy knees [34].

This study has some limitations: Firstly, radiographic KL scores are used as outcome measurements, although studies have shown that KL does not fully correlate with disease severity and alternative endpoints have been proposed for OA [35, 36]. Nevertheless, KL is still the most commonly used grading system for OA. Secondly, although the analyzed group of 506 OAI participants and 208 WORMS readings was relatively large as compared to previous studies, some associations remained borderline significant. Studies investigating a larger cohort may resolve this limitation. A further limitation involves the nature of the study design: The study examined statistically significant associations of clinical parameters, imaging parameters and WORMS readings with the development of OA. This does not allow for conclusions on causal relationships or generate concrete clinical implications. Lastly, no head-to-head comparison between older and younger patients has been performed as this was beyond the scope of this study. Overall, further studies are needed to overcome these limitations and confirm our observations, especially regarding a head-to-head comparison of risk factors for OA in different age groups.

In summary, this study describes significant protective factors for maintaining radiographically normal knee joints in an older population, including clinical parameters as well as quantitative and semi-quantitative MR-imaging parameters. Although results of this study suggest that most protective parameters seem to be similar in the elderly as compared to mixed age cohorts, some risk factors may be different in the elderly, especially regarding secondary quantitative parameters of the patella cartilage.

Data availability

The underlying data is publicly available (OAI, https://oai.nih.gov).

References

  1. Kellgren JH, Lawrence JS. Radiological assessment of osteo-arthrosis. Ann Rheum Dis. 1957;16(4):494–502.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  2. Felson DT, Naimark A, Anderson J, Kazis L, Castelli W, Meenan RF. The prevalence of knee osteoarthritis in the elderly. The Framingham Osteoarthritis Study. Arthritis Rheum. 1987;30(8):914–8.

    Article  CAS  PubMed  Google Scholar 

  3. Global regional. National incidence, prevalence, and years lived with disability for 354 diseases and injuries for 195 countries and territories, 1990–2017: a systematic analysis for the global burden of Disease Study 2017. Lancet. 2018;392(10159):1789–858.

    Article  Google Scholar 

  4. Driban JB, Eaton CB, Lo GH, Price LL, Lu B, Barbe MF, et al. Overweight older adults, particularly after an injury, are at high risk for accelerated knee osteoarthritis: data from the Osteoarthritis Initiative. Clin Rheumatol. 2016;35(4):1071–6.

    Article  PubMed  Google Scholar 

  5. Batsis JA, Germain CM, Vásquez E, Zbehlik AJ, Bartels SJ. Physical activity predicts higher physical function in older adults: the Osteoarthritis Initiative. J Phys Act Health. 2016;13(1):6–16.

    Article  PubMed  Google Scholar 

  6. Bindawas SM, Vennu V, Auais M. Health-related quality of life in older adults with bilateral knee pain and back pain: data from the Osteoarthritis Initiative. Rheumatol Int. 2015;35(12):2095–101.

    Article  PubMed  PubMed Central  Google Scholar 

  7. Batsis JA, Zbehlik AJ, Barre LK, Mackenzie TA, Bartels SJ. The impact of waist circumference on function and physical activity in older adults: longitudinal observational data from the osteoarthritis initiative. Nutr J. 2014;13:81.

    Article  PubMed  PubMed Central  Google Scholar 

  8. Peterfy CG, Guermazi A, Zaim S, Tirman PF, Miaux Y, White D, et al. Whole-organ magnetic resonance imaging score (WORMS) of the knee in osteoarthritis. Osteoarthritis Cartilage. 2004;12(3):177–90.

    Article  CAS  PubMed  Google Scholar 

  9. Joseph GB, Baum T, Alizai H, Carballido-Gamio J, Nardo L, Virayavanich W, et al. Baseline mean and heterogeneity of MR cartilage T2 are associated with morphologic degeneration of cartilage, meniscus, and bone marrow over 3 years–data from the Osteoarthritis Initiative. Osteoarthritis Cartilage. 2012;20(7):727–35.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  10. Ramezanpour S, Kanthawang T, Lynch J, McCulloch CE, Nevitt MC, Link TM et al. Impact of sustained synovitis on knee joint structural degeneration: 4-Year MRI Data from the Osteoarthritis Initiative. J Magn Reson Imaging. 2022.

  11. Kretzschmar M, Nevitt MC, Schwaiger BJ, Joseph GB, McCulloch CE, Link TM. Spatial distribution and temporal progression of T2 relaxation time values in knee cartilage prior to the onset of cartilage lesions - data from the Osteoarthritis Initiative (OAI). Osteoarthritis Cartilage. 2019;27(5):737–45.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  12. Crema MD, Roemer FW, Marra MD, Burstein D, Gold GE, Eckstein F, et al. Articular cartilage in the knee: current MR imaging techniques and applications in clinical practice and research. Radiographics. 2011;31(1):37–61.

    Article  PubMed  Google Scholar 

  13. Everhart JS, Abouljoud MM, Kirven JC, Flanigan DC. Full-thickness cartilage defects are important independent predictive factors for progression to total knee arthroplasty in older adults with minimal to moderate osteoarthritis: data from the Osteoarthritis Initiative. J Bone Joint Surg Am. 2019;101(1):56–63.

    Article  PubMed  Google Scholar 

  14. Sharma L, Nevitt M, Hochberg M, Guermazi A, Roemer FW, Crema M, et al. Clinical significance of worsening versus stable preradiographic MRI lesions in a cohort study of persons at higher risk for knee osteoarthritis. Ann Rheum Dis. 2016;75(9):1630–6.

    Article  PubMed  Google Scholar 

  15. Lo GH, Musa SM, Driban JB, Kriska AM, McAlindon TE, Souza RB, et al. Running does not increase symptoms or structural progression in people with knee osteoarthritis: data from the osteoarthritis initiative. Clin Rheumatol. 2018;37(9):2497–504.

    Article  PubMed  PubMed Central  Google Scholar 

  16. Peterfy CG, Schneider E, Nevitt M. The osteoarthritis initiative: report on the design rationale for the magnetic resonance imaging protocol for the knee. Osteoarthritis Cartilage. 2008;16(12):1433–41.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  17. Bellamy N, Buchanan WW, Goldsmith CH, Campbell J, Stitt LW. Validation study of WOMAC: a health status instrument for measuring clinically important patient relevant outcomes to antirheumatic drug therapy in patients with osteoarthritis of the hip or knee. J Rheumatol. 1988;15(12):1833–40.

    CAS  PubMed  Google Scholar 

  18. Lawrence RC, Felson DT, Helmick CG, Arnold LM, Choi H, Deyo RA, et al. Estimates of the prevalence of arthritis and other rheumatic conditions in the United States. Part II. Arthritis Rheum. 2008;58(1):26–35.

    Article  PubMed  PubMed Central  Google Scholar 

  19. Washburn RA, Smith KW, Jette AM, Janney CA. The physical activity scale for the Elderly (PASE): development and evaluation. J Clin Epidemiol. 1993;46(2):153–62.

    Article  CAS  PubMed  Google Scholar 

  20. Razmjoo A, Caliva F, Lee J, Liu F, Joseph GB, Link TM, et al. T(2) analysis of the entire osteoarthritis initiative dataset. J Orthop Res. 2021;39(1):74–85.

    Article  PubMed  Google Scholar 

  21. Iriondo C, Liu F, Calivà F, Kamat S, Majumdar S, Pedoia V. Towards understanding mechanistic subgroups of osteoarthritis: 8-year cartilage thickness trajectory analysis. J Orthop Res. 2021;39(6):1305–17.

    Article  PubMed  Google Scholar 

  22. Felson DT, Lawrence RC, Dieppe PA, Hirsch R, Helmick CG, Jordan JM, et al. Osteoarthritis: new insights. Part 1: the disease and its risk factors. Ann Intern Med. 2000;133(8):635–46.

    Article  CAS  PubMed  Google Scholar 

  23. Wang Y, Teichtahl AJ, Abram F, Hussain SM, Pelletier JP, Cicuttini FM, et al. Knee pain as a predictor of structural progression over 4 years: data from the Osteoarthritis Initiative, a prospective cohort study. Arthritis Res Ther. 2018;20(1):250.

    Article  PubMed  PubMed Central  Google Scholar 

  24. Balduino E, de Melo BAR, de Silva S, Martinelli L, Cecato JE. JF. The SuperAgers construct in clinical practice: neuropsychological assessment of illiterate and educated elderly. Int Psychogeriatr. 2020;32(2):191-8.

  25. Pelletier JP, Raynauld JP, Berthiaume MJ, Abram F, Choquette D, Haraoui B, et al. Risk factors associated with the loss of cartilage volume on weight-bearing areas in knee osteoarthritis patients assessed by quantitative magnetic resonance imaging: a longitudinal study. Arthritis Res Ther. 2007;9(4):R74.

    Article  PubMed  PubMed Central  Google Scholar 

  26. Spector TD, Dacre JE, Harris PA, Huskisson EC. Radiological progression of osteoarthritis: an 11 year follow up study of the knee. Ann Rheum Dis. 1992;51(10):1107–10.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  27. Wolfe F, Lane NE. The longterm outcome of osteoarthritis: rates and predictors of joint space narrowing in symptomatic patients with knee osteoarthritis. J Rheumatol. 2002;29(1):139–46.

    PubMed  Google Scholar 

  28. Driban JB, Price LL, Eaton CB, Lu B, Lo GH, Lapane KL, et al. Individuals with incident accelerated knee osteoarthritis have greater pain than those with common knee osteoarthritis progression: data from the Osteoarthritis Initiative. Clin Rheumatol. 2016;35(6):1565–71.

    Article  PubMed  Google Scholar 

  29. Edd SN, Omoumi P, Jolles BM, Favre J. Longitudinal femoral cartilage T2 relaxation time and thickness changes with fast sequential Radiographic progression of medial knee osteoarthritis-data from the Osteoarthritis Initiative (OAI). J Clin Med. 2021;10(6).

  30. Liebl H, Joseph G, Nevitt MC, Singh N, Heilmeier U, Subburaj K, et al. Early T2 changes predict onset of radiographic knee osteoarthritis: data from the osteoarthritis initiative. Ann Rheum Dis. 2015;74(7):1353–9.

    Article  PubMed  Google Scholar 

  31. Heilmeier U, Wamba JM, Joseph GB, Darakananda K, Callan J, Neumann J, et al. Baseline knee joint effusion and medial femoral bone marrow edema, in addition to MRI-based T2 relaxation time and texture measurements of knee cartilage, can help predict incident total knee arthroplasty 4–7 years later: data from the Osteoarthritis Initiative. Skeletal Radiol. 2019;48(1):89–101.

    Article  PubMed  Google Scholar 

  32. Hafezi-Nejad N, Zikria B, Eng J, Carrino JA, Demehri S. Predictive value of semi-quantitative MRI-based scoring systems for future knee replacement: data from the osteoarthritis initiative. Skeletal Radiol. 2015;44(11):1655–62.

    Article  PubMed  Google Scholar 

  33. Yang GY, Guo HL, Li T, Shang HB, Zhao YF, Shi YY. The medial compartment and patellofemoral joint degenerate more severely in early stage knee osteoarthritis: a cross-sectional study. Eur Rev Med Pharmacol Sci. 2020;24(19):9815–23.

    PubMed  Google Scholar 

  34. Badlani JT, Borrero C, Golla S, Harner CD, Irrgang JJ. The effects of meniscus injury on the development of knee osteoarthritis: data from the osteoarthritis initiative. Am J Sports Med. 2013;41(6):1238–44.

    Article  PubMed  Google Scholar 

  35. Kim Y, Levin G, Nikolov NP, Abugov R, Rothwell R. Concept End points informing design considerations for confirmatory clinical trials in Osteoarthritis. Arthritis Care Res (Hoboken). 2022;74(7):1154–62.

    Article  CAS  PubMed  Google Scholar 

  36. Abdelaziz H, Balde OM, Citak M, Gehrke T, Magan A, Haasper C. Kellgren-Lawrence scoring system underestimates cartilage damage when indicating TKA: preoperative radiograph versus intraoperative photograph. Arch Orthop Trauma Surg. 2019;139(9):1287–92.

    Article  PubMed  Google Scholar 

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Acknowledgements

No acknowledgments.

Funding

This study was funded by NIH R01-AR064771, NIH R01-AR078917 and R01-AG070647. The OAI is 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) 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 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.

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Authors and Affiliations

Authors

Contributions

Conception and design: FGG, GBJ, JAL, TML. Analysis and interpretation of the data: GBJ, JAL, JL, MCN, CEM, NEL, SM, TML. Drafting of the article: FGG. Critical revision of the article for important intellectual content: GBJ, JAL, JL, MCN, CEM, NEL, SM, TML. Final approval of the article: FGG, GBJ, JAL, JL, MCN, CEM, NEL, SM, TML. Statistical expertise: FGG, GBJ, CEM, MCN. Obtaining of funding: SM.

Corresponding author

Correspondence to Felix G. Gassert.

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Human ethics and consent to participate declaration

Not applicable. Consent to participate is covered by the Osteoarthritis Initiative. The analyses in this study are based on data from the Osteoarthritis Initiative (OAI, https://nda.nih.gov/oai). Institutional review boards of each center approved informed consent documentation, study protocols and amendments. All investigations were carried out in compliance with the Helsinki Declaration.

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Not applicable.

Competing interests

The authors declare no competing interests.

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Gassert, F.G., Joseph, G.B., Lynch, J.A. et al. Clinical and imaging findings associated with preservation of knee joint health over 8 years in individuals aged 65 and over: data from the OAI. BMC Musculoskelet Disord 25, 495 (2024). https://doi.org/10.1186/s12891-024-07590-z

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