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Original Article|Articles in Press

Quantitative evaluation of the lumbar ligamentum flavum using MRI T2-mapping: Efficacy of its clinical application in patients with lumbar spinal stenosis

Published:January 06, 2023DOI:https://doi.org/10.1016/j.jos.2022.12.013

      Abstract

      Obejective

      To perform a magnetic resonance imaging T2-mapping of the ligamentum flavum in healthy individuals and patients with lumbar spinal stenosis scheduled for surgery and compare the T2 relaxation times.

      Subjects and Methods

      The T2 relaxation time of the ligamentum flavum was compared among 3 groups, healthy young individuals (H group (age< 50)), healthy middle-aged and older individuals (H group (age≥50)), and patients with lumbar spinal stenosis (L group). Additionally, the thickness of the ligament was measured in the axial image plane, and the occupied area ratio of each fiber was measured by staining the surgically obtained ligament, and each was correlated with the T2 relaxation time. We also evaluated the adhesion of the ligamentum flavum with the dura mater during the surgery.

      Results

      The T2 relaxation times were significantly prolonged in H group (age ≥50) and L group (P < 0.001) compared to H group (age<50). The relationship between collagen fiber and T2 relaxation times was significantly positive (r = 0.720, P < 0.001). Moreover, the relaxation times were significantly prolonged in those with adhesion of the ligamentum flavum with the dura mater (P < 0.05). The cut-off for the relaxation time was 50 ms (sensitivity: 62.50%, false positive rate: 10.8%).

      Conclusion

      Healthy middle-aged and older individuals and patients with lumbar spinal stenosis and adhesion of the ligamentum flavum with the dura mater have prolonged T2 relaxation times. Hence, the adhesion between the ligamentum flavum and dura mater should be considered in cases with a relaxation time ≥50 ms.

      Keywords

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      References

        • Nieminen M.T.
        • Rieppo J.
        • Töyräs J.
        • Hakumäki J.M.
        • Silvennoinen J.
        • Hyttinen M.M.
        • et al.
        T2 relaxation reveals spatial collagen architecture in articular cartilage: a comparative quantitative MRI and polarized light microscopic study.
        Magn Reson Med. 2001 Sep; 46: 487-493
        • Watanabe A.
        • Benneker L.M.
        • Boesch C.
        • Watanabe T.
        • Obata T.
        • Anderson S.E.
        Classification of intervertebral disk degeneration with axial T2 mapping.
        AJR Am J Roentgenol. 2007 Oct; 189: 936-942
        • Takashima H.
        • Takebayashi T.
        • Yoshimoto M.
        • Terashima Y.
        • Ida K.
        • Shishido H.
        • et al.
        Investigation of intervertebral disc and facet joint in lumbar spondylolisthesis using T2 mapping.
        Magn Reson Med Sci. 2014; 13: 261-266
        • Ishimoto Y.
        • Yoshimura N.
        • Muraki S.
        • Yamada H.
        • Nagata K.
        • Hashizume H.
        • et al.
        Prevalence of symptomatic lumbar spinal stenosis and its association with physical performance in a population-based cohort in Japan: the Wakayama Spine Study.
        Osteoarthritis Cartilage. 2012 Oct; 20: 1103-1108
        • Boden S.D.
        • Davis D.O.
        • Dina T.S.
        • Patronas N.J.
        • Wiesel S.W.
        Abnormal magnetic-resonance scans of the lumbar spine in asymptomatic subjects. A prospective investigation.
        J Bone Joint Surg Am. 1990 Mar; 72: 403-408
        • Ju J.H.
        • Kim S.J.
        • Kim K.H.
        • Ryu D.S.
        • Park J.Y.
        • Chin D.K.
        • et al.
        Clinical relation among dural adhesion, dural ossification, and dural laceration in the removal of ossification of the ligamentum flavum.
        Spine J. 2018 May; 18: 747-754
        • Sato N.
        • Higashino K.
        • Sakai T.
        • Terai T.
        • Goel V.K.
        • Biyani A.
        • et al.
        Role of Epiligament in ligamentum flavum hypertrophy in patients with lumbar spinal canal stenosis:a pilot study.
        J Med Invest. 2018; 65: 85-89
        • Watanabe K.
        • Hosoya T.
        • Shiraishi T.
        • Matsumoto M.
        • Chiba K.
        • Toyama Y.
        Lumbar spinous process-splitting laminectomy for lumbar canal stenosis. Technical note [Technical note].
        J Neurosurg Spine. 2005 Nov; 3: 405-408
        • Sairyo K.
        • Biyani A.
        • Goel V.
        • Leaman D.
        • Booth R.
        • Thomas J.
        • et al.
        Pathomechanism of ligamentum flavum hypertrophy: a multidisciplinary investigation based on clinical, biomechanical, histologic, and biologic assessments.
        Spine (Phila Pa 1976). 2005 Dec 1; 30: 2649-2656
        • Nafziger H.C.
        • Inman V.
        • Saunders C.M.
        Lesions of the intervertebral disc and ligament flava: clinical and anatomical studies.
        Surg Gynecol Obstet. 1938; 66: 288-299
        • Ramsey R.H.
        The anatomy of the ligamenta flava.
        Clin Orthop Relat Res. 1966 Jan-Feb; 44: 129-140
        • Yoshida M.
        • Shima K.
        • Taniguchi Y.
        • Tamaki T.
        • Tanaka T.
        Hypertrophied ligamentum flavum in lumbar spinal canal stenosis. Pathogenesis and morphologic and immunohistochemical observation.
        Spine (Phila Pa 1976). 1992 Nov; 17: 1353-1360
        • Kosaka H.
        • Sairyo K.
        • Biyani A.
        • Leaman D.
        • Yeasting R.
        • Higashino K.
        • et al.
        Pathomechanism of loss of elasticity and hypertrophy of lumbar ligamentum flavum in elderly patients with lumbar spinal canal stenosis.
        Spine (Phila Pa 1976). 2007 Dec 1; 32: 2805-2811
        • Arnoldi C.C.
        • Brodsky A.E.
        • Cauchoix J.
        • Crock H.V.
        • Dommisse G.F.
        • Edgar M.A.
        • et al.
        Lumbar spinal stenosis and nerve root entrapment syndromes. Definition and classification.
        Clin Orthop Relat Res. 1976 Mar-Apr; : 4-5
        • Murphy M.E.
        • Kerezoudis P.
        • Alvi M.A.
        • McCutcheon B.A.
        • Maloney P.R.
        • Rinaldo L.
        • et al.
        Risk factors for dural tears: a study of elective spine surgery.
        Neurol Res. 2017 Feb; 39: 97-106
        • Miyakoshi N.
        • Shimada Y.
        • Suzuki T.
        • Hongo M.
        • Kasukawa Y.
        • Okada K.
        • et al.
        Factors related to long-term outcome after decompressive surgery for ossification of the ligamentum flavum of the thoracic spine.
        J Neurosurg. 2003 Oct; 99: 251-256
        • Saxler G.
        • Krämer J.
        • Barden B.
        • Kurt A.
        • Pförtner J.
        • Bernsmann K.
        The long-term clinical sequelae of incidental durotomy in lumbar disc surgery.
        Spine (Phila Pa 1976). 2005 Oct 15; 30: 2298-2302
        • Deyo R.A.
        • Cherkin D.C.
        • Loeser J.D.
        • Bigos S.J.
        • Ciol M.A.
        Morbidity and mortality in association with operations on the lumbar spine. The influence of age, diagnosis, and procedure.
        J Bone Joint Surg Am. 1992 Apr; 74: 536-543
        • Wang J.C.
        • Bohlman H.H.
        • Riew K.D.
        Dural tears secondary to operations on the lumbar spine. Management and results after a two-year-minimum follow-up of eighty-eight patients.
        J Bone Joint Surg Am. 1998 Dec; 80: 1728-1732