The most inspiring finding of the present study is that the TT-TG distances measured by PCRL and/or transepicondylar axis on MRI are reliable no matter how severe trochlear dysplasia is. In patients with PD, the TT-TG distance measured by PCRL is larger than that measured by transepicondylar axis, indicating that such previously recorded TT-TG distance may be over-evaluated. Each TT-TG distance is correlated with the OBC of trochlear dysplasia and also has fair to good diagnostic capacity for PD. The pathological value of each TT-TG distance has been identified, which helps with TTO decision making.
As an important risk factor affecting patellar stability, the TT-TG distance can reflect the lateralization of the tibial tubercle and has been attached much importance by lots of researchers, with a value greater than 20mm indicating pathological 8. However, the TT-TG distance measured on axial CT images was inaccurate, because it was greatly affected by dysplastic femoral trochlea 12. On the other hand, previous literature showed that the measurement of the TT-TG distance on MRI slices was reliable 14, 23. The results of our study showed that the three TT-TG distances were reliable in different types of the OBC, even in patients with severe trochlear dysplasia.
Previous studies focus on identifying a reference point that can avoid the influence of the femoral trochlea to assess the lateralization of the tibial tubercle, such as the TT-PCL distance and TT-RA distance 15, 16. PCRL was depicted as the reference line in most measurements. Yang et al. 18 suggested that the dysplastic distal femoral condyle was composed of anterior and posterior femoral condylar dysplasia. In accordance with previous studies on CT images 17, 20, 22, the results of our study by MRI showed that patients with PD was in the presence of posterior femoral condylar dysplasia: longer medial and shorter lateral posterior condyle, and larger PCA. We hypothesized that although the TT-TG distance measured by PCRL on MRI had a good consistency, there could be deviations in the recorded TT-TGp distance due to the PCRL itself was affected by posterior femoral morphology.
In this study, we found that the TT-TG distances were larger in patients with PD than in healthy individuals, which was consistent with previous studies 15, 28. The mean difference between the TT-TGp distance and the TT-TGs or TT-TGa distance was 0.7 mm in patients with PD, but such difference in healthy individuals was not significant. This to some extent suggests that the measuring method using PCRL as reference line could contribute to an over-evaluated TT-TG distance preoperatively. The TT-TG distances were not statistically correlated with PCA or the ratio of LPD/MPD in patients with PD based on our data. However, in this study, the fact is that the TT-TGp distance is greater than the TT-TGs or the TT-TGa distance in patients with PD. This may attribute to the influence of the limited parameters included in this study regarding posterior condylar morphologies, or other factors affecting the measurement of the TT-TG distance (potential measurement errors or the inclusion of the study group). Whether this 0.7 mm deviation has an impact on TTO decision making or on postoperative outcomes is still unknown.
Trochlear dysplasia was considered as a significant risk factor for PD, which can change the interaction between the patella and the femoral trochlea and contribute to patellar instability. Researchers used to evaluate trochlear dysplasia via the Dejour classification and some specific parameters, like sulcus angle and lateral trochlear facet inclination (LTI) 6. Dejour classification has been performed on MRI, but poor inter- and intra-observer agreements have been reported 29. Sharma et al. 26 depicted the OBC to grade the severity of trochlear dysplasia with the superiority of simplicity and good consistency. Our study also confirmed that the four-part classification system was reliable. He also reported that, based on the OBC, 28% patients were classified as ‘normal’ to ‘mild’, 62% as ‘moderate’ to ‘severe’. In our study, among the patients with PD, 28 (32.5%) patients have normal to shallow femoral trochlea, 58 (67.5%) patients are in the presence of moderate to severe trochlear dysplasia. A large proportion of patients were accompanied by trochlear dysplasia 6. In this study we found that each TT-TG distance increased with the severity of trochlear dysplasia, which was in accordance with previous study 9. It informed the orthopedic surgeons of the existence of excessive TT-TG distance when severe trochlear dysplasia was presented in patients with PD. After normalizing the TT-TG distances by TEW, the ratio of the TT-TG distances/TEW showed similar results.
We also analyzed the diagnostic efficacy of each TT-TG distance for PD and found that the TT-TGp distance had a good diagnostic capacity, with an AUC of 0.811, which was almost equivalent to the results reported by Xu et al. (AUC = 0.820) 14. While the TT-TGs and TT-TGa distance had a fair capacity, with an AUC of 0.777 and 0.768, respectively. The discrepancies might attribute to the larger TT-TGp distance or caused by the participants included in this study. Similar to the previous literature that the normalized TT-TG distance had a stronger ability to predict PD 30, 31, the ratios of the TT-TG distances/TEW in our study had stronger diagnostic capacities than the TT-TG distances alone. The TT-TGp distance greater than 20mm measured on CT images was considered the indication for TTO and good postoperative outcomes following TTO had been reported 10. However, since the measuring method of the TT-TG distance differs from CT images to MRI slices, the recorded value of the TT-TG distance measured on such two different images are not equivalent in the same patient 14. So, it is worthy of identifying the pathological threshold value of each TT-TG distance measured on MRI cuts.
We set the pathological value of all the three TT-TG distances measured on MRI slices at 13.0 mm in our study. And 0.6 mm discrepancy was identified when compared with previous literature (13.6 mm) 14, which may had been caused by the inclusion of the control group. And the pathological value of the TT-TG distances/TEW was set at 17.0% based on our data. It does not mean that the TTO is needed when the TT-TG distance or TT-TG distances/TEW manifests pathology. We expected to establish a “data base” regarding the indication for TTO based on MRI slices to help with surgical decision making. Whether the 13.0mm of the TT-TG distance was an appropriate indication for TTO and its postoperative outcomes are still needed to be investigated.
Previous studies have shown that when a pathological TT-TGp distance is presented, the risk of PD would increase 5–14 times 11, 14, 30, 31. In our study, all the three TT-TG distances were verified as risk factors for PD, and the risk was 18.7, 11.1, and 14.8-fold higher in patients with pathological TT-TGp, TT-TGs, and TT-TGa distance, respectively. This discrepancy may have been caused by the different cutoff values and methods used for logistic regression analysis. we set the cutoff value at 13.0 mm and established simple regression model, but previous studies set the pathological value at 13.6 or 20 mm.