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Identification of lumbar disc disease hallmarks: a large cross-sectional study

BACKGROUND: Lumbar disc disease has a disabling impact on global people with heavy burden on society, mainly consisting of lumbar disc degeneration (LDD) and lumbar disc herniation (LDH). The recently released lumbar disc nomenclature version 2.0 deepens our understandings on the diseases. Consequen...

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Autores principales: Zhang, Jun, Zhao, Fei, Wang, Feng-Liang, Yang, Yong-Feng, Zhang, Chen, Cao, Yue, Wang, You-Lin, Shi, Xiao-Juan, Wan, Yi, Zhang, Min, Liu, Meng-Qiao, Zuo, Chun-Guang, Wang, Hai-Qiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5108747/
https://www.ncbi.nlm.nih.gov/pubmed/27917347
http://dx.doi.org/10.1186/s40064-016-3662-7
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author Zhang, Jun
Zhao, Fei
Wang, Feng-Liang
Yang, Yong-Feng
Zhang, Chen
Cao, Yue
Wang, You-Lin
Shi, Xiao-Juan
Wan, Yi
Zhang, Min
Liu, Meng-Qiao
Zuo, Chun-Guang
Wang, Hai-Qiang
author_facet Zhang, Jun
Zhao, Fei
Wang, Feng-Liang
Yang, Yong-Feng
Zhang, Chen
Cao, Yue
Wang, You-Lin
Shi, Xiao-Juan
Wan, Yi
Zhang, Min
Liu, Meng-Qiao
Zuo, Chun-Guang
Wang, Hai-Qiang
author_sort Zhang, Jun
collection PubMed
description BACKGROUND: Lumbar disc disease has a disabling impact on global people with heavy burden on society, mainly consisting of lumbar disc degeneration (LDD) and lumbar disc herniation (LDH). The recently released lumbar disc nomenclature version 2.0 deepens our understandings on the diseases. Consequently, there is an urgent need to clarify the occurrence and distribution features of LDD and LDH in a large-scale sample in terms of the novel version. QUESTION/PURPOSES: We asked: (1) Is there a difference in the occurrence and distribution hallmarks of LDD and LDH in a population-based large-scale sample? (2) Does the novel nomenclature version bring novel vision on lumbar disc disease? METHODS: Five thousand two hundred eighty-eight consecutive cases (26,440 lumbar discs) undergoing lumbar spine MRI were retrospectively included from Jan 2008 to Dec 2010 in a territory university hospital. Five hundred nine cases were excluded. There were 2727 males (51.57%) and 2561 females (48.43%) with a mean age of 43.73 years. Both T1 and T2 weighted lumbar MRI images from L1/2 to L5/S1 were profoundly analyzed in axial and sagittal planes. We classified lumbar discs in terms of version 2.0. RESULTS: The occurrence of LDH and LDD was 14.18 and 44.23% in average, respectively. Notably, lumbar spine discs were more prone to LDD than LDH. L4/5 was the most frequent level in terms of LDH (26.08%) and LDD (56.09%), followed by L5/S1 (LDH: 24.09%; LDD: 55.33%), then L3/4, L2/3 and L1/2 in ranking order. The prevalence of LDH and LDD in upper lumbar discs from L1/2 to L3/4 was significant lower than the average prevalence rate (P < 0.05). The mean age was 24.70 (±14.81) years for normal lumbar discs; 49.76 (±14.95) years for LDD; 37.01 (±12.91) years for LDH; 51.31(±15.00) years for LDD and LDH (P < 0.05). Modic changes, HIZ, spondylosis deformans and decreased disc height were linked with older age; whereas Schmorl node and lumbar disc sequestration were not associated with age (P < 0.05). CONCLUSIONS: The prevalence of LDD is 44.23%, higher than LDH as 14.18%. L4/5 and L5/S1 are the most frequent involved segments for the majority of lumbar disc diseases. Schmorl node occurs (1.6%) more frequently in upper lumbar spine, independent of age. Modic changes (0.87%) are closely related with older age. CLINICAL RELEVANCE: When diagnosing and treating lumbar disc disease, it might be important to consider the updated nomenclature of LDD and LDH. Our study provides additional novel vision on the features of LDD and LDH in a large-scale sample based on the nomenclature of novel version.
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spelling pubmed-51087472016-12-02 Identification of lumbar disc disease hallmarks: a large cross-sectional study Zhang, Jun Zhao, Fei Wang, Feng-Liang Yang, Yong-Feng Zhang, Chen Cao, Yue Wang, You-Lin Shi, Xiao-Juan Wan, Yi Zhang, Min Liu, Meng-Qiao Zuo, Chun-Guang Wang, Hai-Qiang Springerplus Research BACKGROUND: Lumbar disc disease has a disabling impact on global people with heavy burden on society, mainly consisting of lumbar disc degeneration (LDD) and lumbar disc herniation (LDH). The recently released lumbar disc nomenclature version 2.0 deepens our understandings on the diseases. Consequently, there is an urgent need to clarify the occurrence and distribution features of LDD and LDH in a large-scale sample in terms of the novel version. QUESTION/PURPOSES: We asked: (1) Is there a difference in the occurrence and distribution hallmarks of LDD and LDH in a population-based large-scale sample? (2) Does the novel nomenclature version bring novel vision on lumbar disc disease? METHODS: Five thousand two hundred eighty-eight consecutive cases (26,440 lumbar discs) undergoing lumbar spine MRI were retrospectively included from Jan 2008 to Dec 2010 in a territory university hospital. Five hundred nine cases were excluded. There were 2727 males (51.57%) and 2561 females (48.43%) with a mean age of 43.73 years. Both T1 and T2 weighted lumbar MRI images from L1/2 to L5/S1 were profoundly analyzed in axial and sagittal planes. We classified lumbar discs in terms of version 2.0. RESULTS: The occurrence of LDH and LDD was 14.18 and 44.23% in average, respectively. Notably, lumbar spine discs were more prone to LDD than LDH. L4/5 was the most frequent level in terms of LDH (26.08%) and LDD (56.09%), followed by L5/S1 (LDH: 24.09%; LDD: 55.33%), then L3/4, L2/3 and L1/2 in ranking order. The prevalence of LDH and LDD in upper lumbar discs from L1/2 to L3/4 was significant lower than the average prevalence rate (P < 0.05). The mean age was 24.70 (±14.81) years for normal lumbar discs; 49.76 (±14.95) years for LDD; 37.01 (±12.91) years for LDH; 51.31(±15.00) years for LDD and LDH (P < 0.05). Modic changes, HIZ, spondylosis deformans and decreased disc height were linked with older age; whereas Schmorl node and lumbar disc sequestration were not associated with age (P < 0.05). CONCLUSIONS: The prevalence of LDD is 44.23%, higher than LDH as 14.18%. L4/5 and L5/S1 are the most frequent involved segments for the majority of lumbar disc diseases. Schmorl node occurs (1.6%) more frequently in upper lumbar spine, independent of age. Modic changes (0.87%) are closely related with older age. CLINICAL RELEVANCE: When diagnosing and treating lumbar disc disease, it might be important to consider the updated nomenclature of LDD and LDH. Our study provides additional novel vision on the features of LDD and LDH in a large-scale sample based on the nomenclature of novel version. Springer International Publishing 2016-11-14 /pmc/articles/PMC5108747/ /pubmed/27917347 http://dx.doi.org/10.1186/s40064-016-3662-7 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Research
Zhang, Jun
Zhao, Fei
Wang, Feng-Liang
Yang, Yong-Feng
Zhang, Chen
Cao, Yue
Wang, You-Lin
Shi, Xiao-Juan
Wan, Yi
Zhang, Min
Liu, Meng-Qiao
Zuo, Chun-Guang
Wang, Hai-Qiang
Identification of lumbar disc disease hallmarks: a large cross-sectional study
title Identification of lumbar disc disease hallmarks: a large cross-sectional study
title_full Identification of lumbar disc disease hallmarks: a large cross-sectional study
title_fullStr Identification of lumbar disc disease hallmarks: a large cross-sectional study
title_full_unstemmed Identification of lumbar disc disease hallmarks: a large cross-sectional study
title_short Identification of lumbar disc disease hallmarks: a large cross-sectional study
title_sort identification of lumbar disc disease hallmarks: a large cross-sectional study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5108747/
https://www.ncbi.nlm.nih.gov/pubmed/27917347
http://dx.doi.org/10.1186/s40064-016-3662-7
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