Decreased catalase expression is associated with ligamentum flavum hypertrophy due to lumbar spinal canal stenosis

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Background: This is an immunohistologic study of gene expression between patients and controls. This study aims to evaluate expression of the catalase gene in hypertrophied ligamentum flavum (LF) specimens obtained from patients with lumbar spinal canal stenosis (LSCS). LSCS is one of the most common spinal disorders. It is well known that LF hypertrophy plays an important role in the onset of LSCS. Although degenerative changes, aging, and mechanical stress are all thought to contribute to hypertrophy and fibrosis of the LF, the precise pathogenesis of LF hypertrophy remains unknown. Previous genetic studies have tried to determine the mechanism of LF hypertrophy. However, the association between catalase gene expression and LF hypertrophy has not yet been explored. Methods: LF specimens were surgically obtained from 30 patients with spinal stenosis (LSCS group) and from 30 controls with lumbar disc herniation (LDH group). LF thickness was measured at the thickest point using calipers to an accuracy of 0.01 mm during surgical intervention. The extent of LF elastin degradation and fibrosis were graded (grades 0–4) by hematoxylin and eosin staining and Masson trichrome staining, respectively. The resulting LF measurements, histologic data, and immunohistologic results were then compared between the 2 groups. Results: The average LF thickness was significantly higher in the LSCS group than in the LDH group (5.99 and 2.95 mm, respectively, P = .004). Elastin degradation and fibrosis of the LF were significantly more severe in spinal stenosis samples than in the disc herniation samples (3.04 ± 0.50 vs 0.79 ± 0.60, P = .007; 3.01 ± 0.47 vs 0.66 ± 0.42, P = .009, respectively). Significantly lower expression of catalase was observed in the perivascular area of LF samples obtained from patients with LSCS compared with controls (61.80 ± 31.10 vs 152.80 ± 41.13, respectively, P = .009). Conclusion: Our findings suggest that decreased expression of catalase is associated with LF hypertrophy in patients with LSCS. Copyright © 2019 the Author(s). Published by Wolters Kluwer Health, Inc.

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RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/ebyu/13565Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.1097/md.0000000000015192Yayıncı resmi DOI adresi
Tam Kayıt
AlanDeğerDil
dc.contributor.authorYücetaş, Şeyho Cem
dc.contributor.authorÇakır, Tayfun
dc.date.accessioned2026-10-18T20:28:23.966742366Z
dc.date.available2026-10-18T20:28:23.966742366Z
dc.date.issued2019
dc.description.abstractBackground: This is an immunohistologic study of gene expression between patients and controls. This study aims to evaluate expression of the catalase gene in hypertrophied ligamentum flavum (LF) specimens obtained from patients with lumbar spinal canal stenosis (LSCS). LSCS is one of the most common spinal disorders. It is well known that LF hypertrophy plays an important role in the onset of LSCS. Although degenerative changes, aging, and mechanical stress are all thought to contribute to hypertrophy and fibrosis of the LF, the precise pathogenesis of LF hypertrophy remains unknown. Previous genetic studies have tried to determine the mechanism of LF hypertrophy. However, the association between catalase gene expression and LF hypertrophy has not yet been explored. Methods: LF specimens were surgically obtained from 30 patients with spinal stenosis (LSCS group) and from 30 controls with lumbar disc herniation (LDH group). LF thickness was measured at the thickest point using calipers to an accuracy of 0.01 mm during surgical intervention. The extent of LF elastin degradation and fibrosis were graded (grades 0–4) by hematoxylin and eosin staining and Masson trichrome staining, respectively. The resulting LF measurements, histologic data, and immunohistologic results were then compared between the 2 groups. Results: The average LF thickness was significantly higher in the LSCS group than in the LDH group (5.99 and 2.95 mm, respectively, P = .004). Elastin degradation and fibrosis of the LF were significantly more severe in spinal stenosis samples than in the disc herniation samples (3.04 ± 0.50 vs 0.79 ± 0.60, P = .007; 3.01 ± 0.47 vs 0.66 ± 0.42, P = .009, respectively). Significantly lower expression of catalase was observed in the perivascular area of LF samples obtained from patients with LSCS compared with controls (61.80 ± 31.10 vs 152.80 ± 41.13, respectively, P = .009). Conclusion: Our findings suggest that decreased expression of catalase is associated with LF hypertrophy in patients with LSCS. Copyright © 2019 the Author(s). Published by Wolters Kluwer Health, Inc.
dc.identifier.doi10.1097/md.0000000000015192
dc.identifier.eissn1536-5964
dc.identifier.issn0025-7974
dc.identifier.issue15
dc.identifier.pmcidPMC6485878
dc.identifier.pmid30985713
dc.identifier.scopus2-s2.0-85064853080
dc.identifier.startpagee15192
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/13565
dc.identifier.volume98
dc.identifier.wosWOS:000467331500074
dc.language.isoen
dc.publisherLippincott Williams and Wilkins
dc.relation.ispartofMedicine (United States)
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectcatalase
dc.subjectelastin degradation
dc.subjectfibrosis
dc.subjectligamentum flavum hypertrophy
dc.subjectlumbar spinal canal stenosis
dc.subjectAdult
dc.subjectAged
dc.subjectElastin
dc.subjectFemale
dc.subjectGene Expression
dc.subjectHumans
dc.subjectHypertrophy
dc.subjectIntervertebral Disc Displacement
dc.subjectLigamentum Flavum
dc.subjectLumbar Vertebrae
dc.subjectMale
dc.subjectMiddle Aged
dc.subjectOrgan Size
dc.subjectRetrospective Studies
dc.subjectSpinal Stenosis
dc.subjectenzymology
dc.subjecthuman
dc.subjectintervertebral disk hernia
dc.subjectlumbar vertebra
dc.subjectmetabolism
dc.subjectpathology
dc.subjectretrospective study
dc.subjectvertebral canal stenosis
dc.titleDecreased catalase expression is associated with ligamentum flavum hypertrophy due to lumbar spinal canal stenosis
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus15
rdl.citation.wos12
rdl.departmentDepartment of Neurosurgery, Erzincan Binali Yildirim University Medical Faculty, Başbağlar Mah, Center of City Erzincan, Turkey.
rdl.oa.statusgold
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)