The summary of PVF values for all four limbs under sound (control) and lame conditions is presented in Table 1. Statistical significance was confirmed. Mean PVF values (expressed as % body weight) did not differ between the two forelimbs or between the two hind limbs (contralateral forelimb: 103.72±22.64%; ipsilateral forelimb: 101.89± 20.96%; contralateral hind limb: 75.11±15.17%; ipsilateral hind limb: 74.00±15.26%; p
>0.05; Fig 3). When lameness was induced in the right forelimb, PVF of the ipsilateral forelimb decreased to 91.33±26.39% body weight (p = 0.012), whereas PVF of the contralateral forelimb increased to 121.72±26.44% body weight (p = 0.008); PVF values in the contralateral and ipsilateral hind limbs changed only slightly (86.50±19.65% and 73.67±13.36% body weight, respectively) and these differences were not statistically significant (p = 0.27 and p = 0.81, respectively; Fig 3).
For SI, no significant asymmetry was detected between the two forelimbs or between the two hind limbs under the sound (control) condition during leash walking (forelimbs SI: 8.19±4.88, p = 0.35; hindlimbs SI: 8.43±8.16, p = 0.42). After induction of lameness in the right forelimb, SI increased to 34.24±20.26 for the forelimbs (p = 0.004) and to 16.54±11.83 for the hindlimbs (p = 0.018), indicating a marked increase in asymmetry despite the absence of significant changes in hindlimb PVF (p = 0.29; Fig 4).
Force platform gait analysis was more sensitive than visual observation in detecting subtle lameness and assessing compensatory load redistribution
(Evans et al., 2005). These findings are consistent with previous research on lameness in dogs, which has shown that compensatory mechanisms often involve increased loading on the contralateral limbs
(Waxman et al., 2008). Using the variables of PVF and SI, the study was conducted about induced right forelimb’s lameness to evaluate compensatory changes in the other limbs and recorded and analyzed the compensatory changes, while also evaluating and analyzing objective information such as kinetics using a gait analysis system on six healthy small dogs.
Fig 3 results show that during the lame condition, the PVF in the ipsilateral forelimb decreased significantly to 91.33±26.39, while the contralateral forelimb exhibited an increase to 121.72±26.44. In the gait of dogs affected by elbow osteoarthritis, mean vertical force was measured to be higher on the unaffected side compared to the affected side. Similarly, in the evaluation of forelimb function after arthrotomy using an approach to the shoulder joint, the mean vertical force was higher on the unaffected side than on the affected side
(Bockstahler et al., 2009). As demon-strated in the results of this study, the contralateral forelimb, where lameness was intentionally induced, showed a significant increase compared to the sound condition. In the evaluation of the ipsilateral forelimb, a significant increase was also observed in the sound condition, indicating that unilateral lameness leads to compensatory changes in the contralateral limb.
Furthermore, no compensatory alterations in PVF were identified in the contralateral hindlimb, where PVF was 86.50±19.65, or in the ipsilateral hindlimb, which showed a PVF of 73.67±13.36. However, a notable reduction in PVF was observed in the ipsilateral forelimb, alongside a significant increase in the contralateral hind limb. In contrast, no PVF changes were detected in the contralateral forelimb and ipsilateral hind limb in a study involving 24 dogs clinically diagnosed with elbow joint osteoarthritis.
These results may be linked to the severity of the traumatic injury, as superficial and acute injuries tend to trigger less pronounced compensatory responses compared to deep and chronic injuries. Additionally, variations in the affected joints, such as the elbow versus the carpus, may influence the degree of weight redistribution and compensatory mechanisms during movement.
In our study, although induced lameness, differences found significant increases and decreases in both sound and lameness in the contralateral forelimb and ipsilateral forelimb in the forelimb, but no significant changes in the hindlimb. The difference is that the previous study was conducted on medium-sized dogs weighing 27.2±5.5 kg, while the present study was conducted on small dogs weighing 4.3±1.5 kg. It can be speculated that small dogs may be able to compensate for contralateral forelimb gait during induced lameness without clearly detectable effects on hindlimb PVF. In this small-sized dog group, distinct compensatory changes were observed between the forelimbs, whereas corresponding changes in hindlimb PVF were not apparent within the sensitivity of the present analysis. This may highlight the role of the hindlimbs in maintaining stability and balance during gait. This study did not directly evaluate the effects of morphometric measures (
e.g., body weight, withers height and speed) on GRF. However, according to previous literature, these variables are likely to influence GRF not as isolated factors but through their interactions. Future studies should include such morphometric variables to provide a more comprehensive assessment of the variability in GRF.
SI measures the differences in force application between the ipsilateral (same side as the induced lameness) and contralateral (opposite side) limbs. For the sound condition (before lameness induction), there was no significant asymmetry between the left and right forelimbs, indicating a balanced load distribution. However, after lameness was induced, a significant asymmetry was observed in all variables. The increased hindlimb SI suggests that the pelvic limbs contribute to maintaining dynamic postural control during induced forelimb lameness
(Abdelhadi et al., 2012; Abdelhadi et al., 2013). In this study, SI results, as shown in Fig 4, provide further evidence of asymmetry during lameness. For the forelimbs, the SI in sound dogs was 8.19±4.88, but this value increased to 34.24±20.26 in lame dogs, indicating a significant imbalance between the left and right forelimbs during lameness. Similarly, the hindlimb SI was 8.43±8.16 in the sound condition and rose to 16.54±11.83 in the lame condition, reflecting the compensatory load redistribution to the contralateral hindlimb. In the hindlimbs, SI increased significantly despite the absence of significant changes in PVF. This pattern suggests that fore-hind compensation may involve subtle left-right redistribution or timing adjustments in the pelvic limbs that are captured by SI but not by limb specific PVF alone, highlighting the comple-mentary value of SI for detecting compensatory gait changes.
The limitations of this study include, first, the very small number of participating dogs (n = 6), which restricts the statistical power and the generalizability of the findings. In addition, the experimental lameness model induced by attaching a stopper to the paw has not been fully validated in terms of reproducing the gait patterns and pain behaviors observed in naturally occurring orthopedic diseases and the degree of lameness may have varied between individuals, potentially introducing additional variability into the results.
Nevertheless, this study demonstrates that induced forelimb lameness in dogs’ results in significant load redistribution to the contralateral forelimb and hindlimb, as evidenced by changes in PVF and SI. These findings contribute to our understanding of the biomechanical adaptations that occur in response to lameness and highlight the importance of comprehensive gait analysis in the diagnosis and treatment of lameness in dogs. From a broader welfare perspective, integrating objective kinetic variables with information on housing and husbandry practices or structured need indices, as proposed for pet dogs in Kerala, may provide a more comprehensive assessment of canine welfare in future studies
(Vijayakumar et al., 2003; Vijayakumar et al., 2006).