ArticleEuropean spine journal : official publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society2026
Local fragility index and Radiomics-lite modeling of CT-Derived Hounsfield units for osteoporosis risk assessment in spine surgery patients.
Article in European spine journal : official publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
STUDY
designRetrospective cohort study. PURPOSE: To develop and validate the Local Fragility Index (LFI), a novel CT-derived measure that integrates the lowest vertebral Hounsfield Unit (HU) (Min HU), inter-level variability (SD), and cranio-caudal slope to quantify vertebral heterogeneity and improve osteoporosis risk assessment.
methodsWe retrospectively analyzed 172 patients who underwent spinal surgery. Severe adult spinal deformity (Cobb angle > 30°) was excluded to ensure measurement consistency. HU values from L1-L4 were obtained on preoperative CT. Min HU was inverted (- Min HU) to emphasize fragility, SD was calculated across levels, and the cranio-caudal slope of HU values was estimated by linear regression across L1-L4. Each parameter was standardized using Z-scores, and LFI was defined as z(- Min HU) + z(SD) + z(- Slope). The composite score was then further standardized to generate a normalized index (LFI_z), which was used for all statistical analyses. Osteoporosis was defined as the lowest DXA T-score ≤ - 2.5. Diagnostic performance was assessed by ROC analysis, logistic regression, decision curve analysis (DCA), and category-free net reclassification improvement (cfNRI).
resultsMin HU was significantly lower in osteoporotic patients (p < 0.001) and correlated with the lowest DXA T-score (r = 0.52). LFI_z showed comparable discrimination to Mean HU (AUC 0.664 vs. 0.690), while their combination achieved higher accuracy (AUC 0.701). In adjusted models, LFI_z remained an independent predictor of osteoporosis (OR 1.9 per SD, p < 0.01), with improved reclassification (cfNRI + 0.19, 95% CI 0.05-0.32). The Radiomics-lite + Clinical model (HU quantiles, variability metrics, and demographics) provided the best performance (AUC 0.824) and the greatest net clinical benefit across 10-40% thresholds.
conclusionsThe LFI captures vertebral heterogeneity and complements mean HU, thereby enhancing osteoporosis risk stratification. Building on this framework, a simplified Radiomics-lite + Clinical model further improved discriminative performance and decision-analytic utility, offering a scalable approach for CT-based assessment in patients undergoing spine surgery. This approach may directly inform surgical planning (e.g., screw augmentation, extended fusion levels) and perioperative management of osteoporosis. As this outcome-agnostic, hypothesis-generating analysis was benchmarked to DXA rather than clinical endpoints, prospective validation against fractures and instrumentation-related complications is needed before clinical use.
Indexed as
Identifiers
41261238What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.