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
Efficacy of low-dose Escherichia coli-derived recombinant human bone morphogenetic protein-2 in minimally invasive transforaminal lumbar interbody fusion.
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. Cited by 2 papers.
What it found
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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.
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Who cites it
2 citing papers in PubMed.
- Total and Hidden Blood Loss in Biportal Endoscopic Versus Tubular-Based Minimally Invasive Transforaminal Lumbar Interbody Fusion.Clinics in orthopedic surgery · 2026Article
- Clinical and radiologic outcomes of expandable versus static cages in biportal endoscopic TLIF: focus on endplate injury and subsidence.Journal of orthopaedic surgery and research · 2026Article
Corrections and comments
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Authors and funding
4 authors.
Funding
Abstract
purposeMinimally invasive transforaminal lumbar interbody fusion (MIS-TLIF) offers advantages over open procedures but is limited by the reduced availability of autologous bone. Escherichia coli-derived recombinant human bone morphogenetic protein-2 (E.BMP-2) has emerged as a scalable osteoinductive alternative, though its application in MIS-TLIF remains unstudied. This study aimed to evaluate the efficacy and safety of E.BMP-2 combined with hydroxyapatite (HA) carriers in the context of MIS-TLIF.
methodsSeventy patients (85 fusion levels) who underwent one- or two-level MIS-TLIF for degenerative lumbar conditions between 2016 and 2024 were included, with a minimum follow-up of one year. The E.BMP-2 group (34 patients, 39 levels) received local bone graft and allogenic cancellous bone graft along with a fixed dose of 1 mg E.BMP-2. The control group (36 patients, 46 levels) received local bone graft and allogenic cancellous bone graft only. Fusion was assessed using dynamic radiographs and CT imaging. Solid fusion on radiographs was defined as segmental motion < 3°, and on CT as continuous trabecular bone bridging between the upper and lower endplates. Clinical outcomes were evaluated using the visual analog scale (VAS) for back and leg pain, the Oswestry Disability Index (ODI), and the Functional Rating Index (FRI). Perioperative and delayed complications-including fever, elevated inflammatory markers, seroma formation, heterotopic ossification, and cage subsidence-were assessed via imaging and medical records.
resultsThe E.BMP-2 group demonstrated significantly higher fusion rates (radiographs: 97.4% vs. 78.3%, p = 0.001; CT: 89.7% vs. 63.0%, p = 0.005) without an increase in complications. No cases of seroma, heterotopic ossification, or reoperation were observed in the E.BMP-2 group. A standardized application protocol using 1 mg of E.BMP-2 per patient, combined with a containment technique, likely contributed to these favorable outcomes. Although clinical improvements were similar between groups, the rate of cage subsidence was significantly lower in the E.BMP-2 group at 6 and 12 months.
conclusionLow-dose E.BMP-2 appears to be a safe and effective osteoinductive adjunct for MIS-TLIF, particularly in cases with limited autologous bone. Appropriate carrier selection, dosing, and containment techniques are key to optimizing outcomes.
Indexed as
Identifiers
41315069What Socratic 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 Socratic graph.