Background and objectives: It is known that difficulty sleeping after a fracture can have negative effects on both mental and physical health and may prolong the recovery process. The objective of this study is to explore how sleep quality and psychological health are linked in patients with pelvic and acetabulum fractures. Methods: A study was conducted on 265 patients between 2018 and 2022 who had suffered pelvic and acetabulum fractures. The study examined various factors, including age, gender, cause of injury, post-operative complications, and injury severity. The study employed ordinal logistic regression to examine the relationship between various pelvic fractures and seven subscales of the Majeed Pelvic Score (MPS), as well as the Sleep Disorder Questionnaire (SDQ) and Beck Depression Inventory (BDI). The study focused on the postoperative outcome one year after surgery, and each patient was assessed at the one-year mark after surgical intervention. Additionally, the study evaluated the functional outcome, sleep quality, and psychological disorders of the patients. Results: From 2018 to 2022, a total of 216 patients suffered from pelvic and acetabulum fractures. Among them, 6.6% experienced borderline clinical depression, and 45.2% reported mild mood disturbances. Anxiety was found to be mild to moderate in 46% of Tile C and posterior acetabulum wall fracture patients. About 24.8% of patients reported insomnia, while 23.1% reported sleep movement disorders. However, no significant correlation was found between fracture types and sleep disorders. The mean Majeed pelvic score (MPS) was 89.68. Conclusions: Patients with pelvic and acetabular fractures typically experience functional improvement, but may also be at increased risk for insomnia and sleep movement disorders, particularly for certain types of fractures. Psychological well-being varies between fracture groups, with signs of borderline clinical depression observed in some cases. However, anxiety levels do not appear to be significantly correlated with pelvic and acetabular fractures.

This study aimed to enhance the rehabilitation process for patients with unstable pelvic Tile C fractures resulting from polytrauma by integrating mechanotherapy using the Hocoma Lokomat robotic device with conventional rehabilitation methods. The goal was to improve functional recovery outcomes and minimize pain levels following surgical intervention. A total of 74 participants, aged 21 to 65 years, with severe unstable pelvic Tile C fractures were enrolled at Tongji Hospital’s Department of Rehabilitation from 2022 to 2024. They were randomly divided into two groups: Group A (34 patients) received comprehensive rehabilitation including mechanotherapy with the Hocoma Lokomat, while Group B (40 patients) underwent only conventional therapeutic exercises. Functional outcomes were assessed using the Majeed pelvic score, and pain were monitored over time. Group A demonstrated significantly better pelvic function scores compared to Group B throughout the rehabilitation period(91.53 ± 4.10vs. 88.17 ± 5.15). Additionally, at the six-month follow-up, Group A showed superior pain control benefits attributed to mechanotherapy(2.09 ± 1.10vs2.29 ± 1.12). Integrating the Hocoma Lokomat into rehab for unstable pelvic Tile C fractures improves function and pain control versus conventional care. The study supports robotic-assisted therapy’s benefits for polytrauma patients, advocating innovative rehab approaches.

Tile C pelvic fractures present significant therapeutic challenges, especially in obese and osteoporotic patients, where traditional techniques (Modified Stoppa approach, minimally invasive percutaneous plate osteosynthesis [MIPPO]) are limited by poor precision and high complication rates. Robotic-assisted navigation (RAN) with patient-specific implants (PSI) may improve outcomes, but gaps remain in understanding its performance in multicenter settings (e.g., surgeon skill variability), nonlinear BMI effects on functional recovery, and cost-effectiveness stratified by BMI-bone mineral density (BMD) interactions. This study aimed to compare RAN + PSI with traditional methods in operative efficiency, functional outcomes, and cost-effectiveness, while addressing multicenter bias and validating the optimal BMI for functional recovery. This was a multicenter prospective observational cohort study conducted at tertiary trauma centers in China (January 2022-2025), enrolling 220 patients with Tile C pelvic fractures. Patients were stratified by center and fracture subtype (Tile C1/C3) before allocation to three groups: RAN + PSI (n = 110), Modified Stoppa (n = 55), and MIPPO (n = 55)-this stratification minimized bias from intercenter surgeon skill differences and uneven case distribution. For RAN + PSI, preoperative CT scans generated 3D pelvic reconstructions to design custom implants and plan screw trajectories; intraoperative robotic calibration (TianJi Robot system) ensured submillimeter precision. Traditional techniques followed standardized protocols (Modified Stoppa: open anterior pelvic exposure with precontoured plates; MIPPO: fluoroscopy-guided percutaneous plate/screw placement). Primary outcomes included Matta reduction grade, Majeed Pelvic Score (12 months), and cost-effectiveness (incremental cost-effectiveness ratio [ICER], Chinese RMB/quality-adjusted life-year [QALY]). Polynomial regression modeled nonlinear BMI effects, and stratified analyses validated BMI-BMD interactions. RAN + PSI outperformed traditional methods in key metrics: (1) Implant precision: mean deviation 1.2 ± 0.5 mm vs. 2.7 ± 1.1 mm (Modified Stoppa) and 2.4 ± 0.9 mm (MIPPO, p < 0.001); (2) Operative efficiency: 98 ± 22 min vs. 145 ± 35 min (Modified Stoppa) and 138 ± 30 min (MIPPO, p < 0.001); (3) Complications: 10% vs. 25.5% (Modified Stoppa) and 23.6% (MIPPO, p = 0.003). Polynomial regression identified a peak Majeed Score (89.2 ± 5.8) at BMI ~ 26.5 kg/m² (p = 0.041), with declining outcomes in underweight (BMI < 18.5) and obese (BMI ≥ 30) subgroups. Obese osteoporotic patients (BMI ≥ 30 + BMD T ≤ -2.5) had a 2.9-fold higher risk of screw loosening (p < 0.001) and higher ICER (¥250,000/QALY), though RAN + PSI remained more cost-effective than traditional methods (¥400,000-500,000/QALY). Stratified allocation by center ensured balanced case distribution across techniques (no single center dominated RAN + PSI cases), eliminating intercenter skill bias. RAN + PSI surpasses Modified Stoppa and MIPPO in precision, efficiency, and functional recovery for Tile C pelvic fractures. The optimal BMI for functional outcomes is ~ 26.5 kg/m², and BMI-BMD interactions necessitate personalized strategies (e.g., bone cement augmentation for obese osteoporotic patients). Multicenter stratification by center and fracture subtype effectively mitigates bias from surgeon skill variability, confirming the reliability of results. RAN + PSI is most cost-effective in normal-weight, nonosteoporotic patients and remains clinically valuable in high-risk subgroups.

Background and objective: Osteosarcopenia, a comorbidity of osteoporosis and sarcopenia in the elderly, involves bone-muscle crosstalk, but its core molecular mechanism remains unclear. miR-206 is traditionally considered muscle-specific; this study explores miR-206-3p’s expression in musculoskeletal tissue and correlation with clinical parameters. Methods: A prospective cohort of 158 elderly hip fracture patients (79 osteosarcopenia, 79 controls) was enrolled. qRT-PCR, in situ hybridization, and scRNA-seq were used to analyze miR-206-3p’s expression, distribution, and cell specificity. Correlations with grip strength, gait speed, and BMD were assessed. Results: miR-206-3p was significantly downregulated in both tissues of the osteosarcopenia group (P < 0.001), highly expressed in Myod1⁺ muscle satellite cells and Runx2⁺ osteoprogenitor cells (> 82%), and weakly in mature cells (< 12%). It positively correlated with grip strength, gait speed, and BMD (r = 0.562–0.682, P < 0.001). Conclusion: miR-206-3p is co-expressed in bone-muscle progenitor cells, with synchronous downregulation linked to functional decline, challenging its "muscle-specific" notion and serving as a key molecular hub for bone-muscle crosstalk.