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Updated: Oct 10, 2026

Biomechanical Changes Related to Low Back Pain: An Innovative Tool for Movement Pattern Assessment and Treatment Evaluation in Rehabilitation
Published on: December 13, 2024
Distribution of lumbosacral transitional vertebrae subtypes and functional disability in patients with low back pain:
Merve Kök1, Şebnem Rumeli2, Hasan Hüsnü Yüksek3
1Department of Anesthesiology and Reanimation, Mersin University Faculty of Medicine, Mersin, Turkey.
Abstract:
BackgroundLumbosacral transitional vertebrae (LSTV) are a common congenital anomaly that often remain underrecognized in patients with low back pain (LBP), potentially leading to inappropriate management and disability.ObjectiveTo determine the prevalence and distribution of LSTV subtypes in a large LBP cohort and to evaluate functional disability and healthcare utilization in patients with LSTV.MethodsIn this single-center retrospective observational study, electronic records of 20,395 patients presenting with LBP between January 1, 2018 and January 1, 2024 were reviewed. Lumbar and lumbosacral imaging was evaluated and LSTV were classified according to the Castellvi system. Functional disability was assessed using the Oswestry Disability Index (ODI) in patients with LSTV. Associations between ODI scores, age, sex, Castellvi subtype and number of outpatient visits were analyzed.ResultsLSTV were identified in 405 patients (prevalence 1.98%; mean age 52.9 ± 15.2 years; 63% female). Castellvi Type 2a was the most frequent subtype (25.7%). More than half of the patients reported pain duration of 1-5 years and 67.7% had multiple outpatient visits. Patients with multiple visits had significantly higher ODI scores than those with a single visit (42.65 ± 17.30 vs. 29.53 ± 18.05, p < 0.001) whereas ODI scores did not differ significantly across LSTV subtypes (p > 0.05).ConclusionIn patients with LBP, LSTV were present in approximately 2%. Patients with LSTV demonstrated substantial disability and frequent healthcare utilization. Prospective controlled studies are needed to determine whether these findings are specifically attributable to LSTV and to clarify potential causal relationships.
