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Paraspinal musculature impairment is associated with spinopelvic and spinal malalignment in patients undergoing lumbar fusion surgery
Affiliation:1. Spine Care Institute, Hospital for Special Surgery, Weill Cornell Medicine, 535 East 70th St, New York City, NY 10021, USA;2. Center for Musculoskeletal Surgery, Charité – Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, Berlin, Germany;3. Department of Spine Surgery, Lucerne Cantonal Hospital, Lucerne, Switzerland;4. Department of Radiology and Imaging, Hospital for Special Surgery, Weill Cornell Medicine, New York City, NY, USA;5. Biostatistics Core, Hospital for Special Surgery, New York City, NY, USA;1. Department of Rheumatology, Østfold Hospital Trust, PB 300, 1714 Grålum, Norway;2. Department of Physical Medicine and Rehabilitation, Østfold Hospital Trust, PB 300, 1714 Grålum, Norway;1. Joint Research, Department of Orthopaedic Surgery, OLVG Amsterdam, Amsterdam, The Netherlands;2. Department of Orthopaedic Surgery, Amsterdam University Medical Center, Amsterdam, The Netherlands;1. Department of Orthopaedics and Rehabilitation, Yale School of Medicine, 800 Howard Ave, New Haven, CT, 06510, USA;2. Harvard Combined Orthopaedic Residency Program, 55 Fruit St, Boston, MA, 02114, USA;3. Nuvasive Clinical Services 10275 Little Patuxent Pkwy Ste 300 Columbia, MD 21044, USA;4. UConn Main Campus 2131 Hillside Road, Unit 3088 Storrs, CT 06269-3088;1. Michael Ogon Laboratory for Orthopaedic Research, Orthopaedic Hospital Speising, Vienna, Austria;2. Second Department, Orthopaedic Hospital Speising, Vienna, Austria;3. Third Department, Orthopaedic Hospital Speising, Vienna, Austria;1. Department of Orthopaedics & Rehabilitation Robert T. Stafford Hall, University of Vermont Medical Center, 4th Floor, 95 Carrigan Drive, Burlington, VT 05405, USA;2. The Robert Larner, M.D. College of Medicine at The University of Vermont Given Medical Building, E-126, 89 Beaumont Ave, Burlington, VT 05405, USA;3. Department of Anesthesiology, University of Vermont Medical Center, West Pavilion Level 2, 111 Colchester Ave, Burlington, VT 05401, USA
Abstract:BACKGROUND CONTEXTThe concept of sagittal spinal malalignment is well established in spinal surgery. However, the effect of musculature on its development has not been fully considered and the position of the pelvis is mostly seen as compensatory and not necessarily a possible cause of sagittal imbalance.PURPOSEThis study aimed to investigate the influence of the posterior paraspinal muscles (PPM, erector spinae, and multifidus) and the psoas muscle on spinopelvic and spinal alignment.STUDY DESIGN/SETTINGRetrospective cross-sectional study.PATIENT SAMPLEPatients undergoing posterior lumbar fusion between 2014 and 2021 for degenerative conditions at a tertiary care center, with preoperative lumbar magnetic resonance imaging (MRI) within 12 months prior the surgery and a preoperative whole spine radiograph were included.OUTCOME MEASURESPPM and psoas muscle measurements including the cross-sectional area (CSA), the functional cross-sectional area (fCSA), the amount of intramuscular fat (FAT), and the percentage of fat infiltration (FI). Spinopelvic measurements including lumbar lordosis (LL), pelvic tilt (PT), sacral slope (SS), pelvic incidence (PI), and sagittal vertical axis (SVA).METHODSA T2-weighted MRI-based quantitative assessment of the CSA, the fCSA and the amount FAT was conducted, and FI was further calculated. The regions of interest included the psoas muscle and the PPM on both sides at the L4 level that were summarized and normalized by the patient's height (cm2/m2). LL, PT, SS, PI, and SVA were determined on standing lateral radiographs. Spearman correlation was used to calculate the crude relationship between spinopelvic and muscle parameters. Multiple linear regression models with age, sex, LL, PT, SS, and SVA set as independent variables were established to determine the association with spinal muscle outcome measures.RESULTSA total of 150 patients (53.3% female) were included in the final analysis with a median age of 65.6 years and a median BMI of 28.2 kg/m2. Significant positive correlations were observed between PT (ρ=0.327), SVA (ρ=0.256) and PI (ρ=0.202) and the FIPPM. Significant negative correlations were detected for the PT and the fCSAPPM (ρ=-0.202) and PT and the fCSAPsoas (ρ=-0.191). Furthermore, a negative correlation was seen for PI and SVA and FIPsoas. PT (β=0.187; p=.006), SVA (β=0.155; p=.035), age (β=0.468; p<.001) and sex (β=0.235; p<.001) significantly predict FIPPM (corrected R2=0.393) as independent variables.CONCLUSIONSThis study demonstrated the potential role of posterior paraspinal muscles and psoas muscle on pelvic retroversion and elucidated the relation to sagittal spinal malalignment. Although we cannot establish causality, we propose that increasing FIPPM, representing loss of muscular strength, may lead to increased pelvic retroversion and thus might be the initiating point for the development of the sagittal imbalance. These findings might challenge the well-known theory of increased pelvic retroversion being a compensatory mechanism for sagittal spinal balance. Thus, muscular weakness might be a factor involved in the development of sagittal spinal malalignment.
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