Asian Spine J Search

CLOSE


Asian Spine J > Volume 9(5); 2015 > Article
Ghodsi, Rouhani, Abdollahzade, Khadivi, and Faghih Jouibari: Frequency of Vertebral Endplate Modic Changes in Patients with Unstable Lumbar Spine and Its Effect on Surgical Outcome

Abstract

Study Design

Prospective cohort study.

Purpose

In this study, we investigated the frequency of vertebral endplate Modic changes (MCs) and their effects on surgical outcomes in patients with unstable lumbar spines.

Overview of Literature

Signal changes in endplates have been classified into three types by Modic. The prognostic role of MCs has been investigated in various spinal disorders.

Methods

A series of 70 patients with clinical and radiographic unstable lumbar spine were included in the study. Endplate signal intensity was determined according to Modic classification. All patients underwent instrumented posterolateral fusion. Functional evaluation was made using the visual analog scale (VAS) and Oswestry disability index (ODI).

Results

Eighteen patients (26%) had normal endplate intensity, 31 patients (44%) had MC type I, 20 patients (28%) had MC type II, and one patient (1.4%) had MC type III. Pain level VAS and ODI decreased significantly from the preoperative evaluation to the six-month and one-year postoperative evaluations. The surgical outcome (VAS and ODI) was not significantly different between the various types of MC.

Conclusions

Posterolateral fusion is an effective treatment in patients with unstable lumbar spines. MC do not have a significant effect on the surgical outcome of these patients.

Introduction

Signal intensity changes of vertebral endplates and subchondral bone are often observed in the magnetic resonance imaging (MRI) of patients with spinal degenerative disorders and have been given increasing attention in recent years. In 1988, Modic summarized these changes and classified them into three types [12]: Modic change (MC) type I refers to an edema-like signal intensity (hypointense T1 and hyperintense T2 signal), MC II refers to fat-like signal intensity (hyperintense T1 and isointense or slightly hyperintense T2), and MC III refers to a sclerosislike signal intensity (hypointense T1 and T2). There are numerous studies evaluating the prognostic importance of MCs in different spinal disorders [345].
Segmental instability is a common cause of low back pain that has been regarded as a factor in developing MC [6]. It can cause the disruption of endplates and degeneration of the adjacent bone marrow. The standard of care for the surgical treatment of degenerative lumbar spine instability has long been spinal fusion.
The aim of this study was to investigate prevalence of MC in patients with radiographically unstable lumbar spines and its correlation with the severity of preoperative pain and outcome after posterolateral fusion. Such information could be used in the decision-making process prior to surgery.

Materials and Methods

From July 2010 to August 2013 a consecutive series of patients affected by chronic low back pain due to single-level degenerative lumbar instability and lasting over three or more months of continuous conservative care were recruited in our study. Sagittal segmental instability was measured using lateral radiographs at the extension and flexion positions. The amount of sagittal translation was obtained as the difference of the displacement between flexion and extension. Segmental angulation was also measured as the difference of the intervertebral angles from extension to flexion. Based on White and Panjabi method [7], translation ≥3 mm or angulation ≥10° were defined as instability. All patients underwent single-level pedicular fixation and posterolateral fusion.

1. Data collection

Preoperative MRI scans were evaluated by a neuroradiologist who was blinded to patient information other than the patient's name, sex, and age. MCs were evaluated according to the standardized evaluation protocol, "Nordic Modic Consensus Group classification" [8]. For each patient, the MRI findings were characterized into four groups; no MC, MC type I, MC type II, or MC type III.
The patients filled in the visual analog scale (VAS, 0-100 mm) and Oswestry disability index (ODI, 0-100) questionnaires before surgery, and at six months and one year post surgery.

2. Statistics

Continuous variables are expressed as mean±standard deviations. Categorical data are presented as frequencies and percentages. Differences of VAS and ODI between subgroups were analyzed by means of t-tests. Statistical analyses were carried out with the SAS ver. 9.1 (SAS Institute Inc., Cary, NC, USA).

Results

During the observation period, 70 patients who met the inclusion criteria were admitted to our center and underwent pedicular fixation and posterolateral fusion. The mean patient age on admission was 58±14 years (range, 15-74 years); 53 patients (76%) were female and 17 patients (24%) were male. Segmental instability involved the L2-L3 level in 5 patients, L3-L4 level in 7 patients, L4-L5 level in 44 patients, and L5-S1 level in 14 patients. Eighteen patients (26%) had normal endplate intensity in the unstable segment. MCs were found in 52 patients (74%). Thirty-one patients (44%) had MC type I, 20 patients (28%) had MC type II, and 1 patient (1.4%) had MC type III.
In L2-L3 level patients, 1 had no MC, 2 had type I, and 2 had type II. In L3-L4 level patients, 2 had no MC, 4 had type I and 1 had type II. In L4-L5 level patients, 9 had no MC, 21 had type I, 13 had type II and 1 had type III. In L5-S1 level patients, 6 had no MC, 4 had type I and 4 had type II.
The mean intensity of pain according to the VAS obtained prior to surgical intervention was 6.1±3.4. Pain level decreased progressively by the sixth month (4.2±3.9) and first year (3.8±3.3) after surgery. Clinical outcomes evaluated using ODI decreased significantly from the preoperative evaluation (mean, 43; range, 10-66) to the sixth month (mean, 20.3; range, 0-26) and first year (mean, 16.2; range, 0-58) postoperative evaluations (p<0.001). There was no association between the type of MC and VAS before surgery. Also, clinical outcomes (VAS and ODI) six months and one year postoperatively were not significantly different between the various types of MC.

Discussion

Instability is one of the main causes of low back pain and a common reason for surgical treatment. Decreased structural integrity of intervertebral discs [910], ligaments, and facets [1112] is responsible for the genesis of spinal instability. Degenerative changes can cause instability by loss of disc height, posterior facet joint subluxation, and abnormal patterns of motion [113]. So, it is a common problem in old age, and most of our patients were older. The number of female patients were three times greater than the number of male patients in the present study, which may be related to their susceptibility to degenerative changes, hormonal status, or lifestyle [14151617].
Abnormal MRI signals in endplates have been classified to Modic types. Biomechanical [18] and biochemical [19202122] causes, are possible mechanisms in the pathogenesis of MC [23]. Instability as a biomechanical abnormality can predispose the affected segments to MC. There are numerous studies [345] investigating the prevalence of MC in patients with low back pain and its effect on surgical outcomes after fusion. We specifically studied a subgroup of patients with lumbar instability and evaluated the prognostic role of MC. MCs were found in 74% of our patients, which is higher than most studies investigating patients with nonspecific low back pain [2425]. This underlines the probable role of instability in the pathogenesis of MCs. On the other hand, 25% of patients did not show MC in their respective unstable segments. So, instability can happen without MC and an abnormal signal in the endplates is not a prerequisite for segmental instability. It seems informative to design another study to evaluate any correlation between the severity of instability and prevalence of MC.
Low back pain, which is aggravated by movement, is the typical presentation of unstable lumbar spine. Different mechanisms can be responsible for pain generation in lumbar instability, such as neural compression, traction and tear of spinal ligaments, spasm in paravertebral muscles, inflammation of facet joints, and pathologic changes in the disc and endplates [262728]. MCs, which reflect endplate abnormalities, have been considered to be risk factors for back pain in some studies [182930]. In our study, the severity of preoperative pain was not higher in patients with MCs or in type I than in type II. We think that abnormal changes of endplates in unstable segments does not play a prominent role among other more powerful mechanisms of pain generation.
Arthrodesis is the preferred method of treatment in most patients with unstable lumbar spines. It can improve symptoms by alleviating abnormal motion and reducing distress on endplates, ligaments, and neural elements. In our study, posterolateral fusion significantly improved symptoms according to the VAS and ODI. There was no significant difference in outcome among patients with MC type I and type II. It can be concluded that spinal fusion improves symptoms effectively by restricting the abnormal segmental movement and probably by reducing the repeated injury to ligaments, paravertebral muscles, and neural structures in different types of MC. Endplate changes do not play a notable role in predicting surgical outcome.

Conclusions

Posterolateral fusion is an effective treatment in patients with radiographically unstable lumbar spine regardless of Modic type. MCs do not have a significant effect on the severity of preoperative pain or the surgical outcome of these patients.

Conflict of Interest

Conflict of Interest: No potential conflict of interest relevant to this article was reported.

References

1. Modic MT, Steinberg PM, Ross JS, Masaryk TJ, Carter JR. Degenerative disk disease: assessment of changes in vertebral body marrow with MR imaging. Radiology 1988 166:193–199. PMID: 3336678.
crossref pmid
2. Modic MT, Masaryk TJ, Ross JS, Carter JR. Imaging of degenerative disk disease. Radiology 1988 168:177–186. PMID: 3289089.
crossref pmid
3. Jensen RK, Leboeuf-Yde C, Wedderkopp N, Sorensen JS, Jensen TS, Manniche C. Is the development of Modic changes associated with clinical symptoms? A 14-month cohort study with MRI. Eur Spine J 2012 21:2271–2279. PMID: 22526703.
crossref pmid pmc
4. Keller A, Boyle E, Skog TA, Cassidy JD, Bautz-Holter E. Are Modic changes prognostic for recovery in a cohort of patients with non-specific low back pain? Eur Spine J 2012 21:418–424. PMID: 21837412.
crossref pmid
5. Sorlie A, Moholdt V, Kvistad KA, et al. Modic type I changes and recovery of back pain after lumbar microdiscectomy. Eur Spine J 2012 21:2252–2258. PMID: 22842978.
crossref pmid pmc
6. Toyone T, Takahashi K, Kitahara H, Yamagata M, Murakami M, Moriya H. Vertebral bone-marrow changes in degenerative lumbar disc disease. An MRI study of 74 patients with low back pain. J Bone Joint Surg Br 1994 76:757–764. PMID: 8083266.
crossref pmid
7. White AA III, Panjabi MM. Clinical biomechanics of the spine. 2nd ed. Philadelphia: Lippincott Williams & Wilkins; 1990.

8. Jensen TS, Sorensen JS, Kjaer P. Intra- and interobserver reproducibility of vertebral endplate signal (modic) changes in the lumbar spine: the Nordic Modic Consensus Group classification. Acta Radiol 2007 48:748–754. PMID: 17729006.
crossref pmid
9. Kirkaldy-Willis WH, Farfan HF. Instability of the lumbar spine. Clin Orthop Relat Res 1982 (165): 110–123. PMID: 6210480.
crossref
10. Fujiwara A, Lim TH, An HS, et al. The effect of disc degeneration and facet joint osteoarthritis on the segmental flexibility of the lumbar spine. Spine (Phila Pa 1976) 2000 25:3036–3044. PMID: 11145815.
crossref pmid
11. Haher TR, O'Brien M, Dryer JW, Nucci R, Zipnick R, Leone DJ. The role of the lumbar facet joints in spinal stability. Identification of alternative paths of loading. Spine (Phila Pa 1976) 1994 19:2667–2670. PMID: 7899961.
pmid
12. Fujiwara A, Tamai K, An HS, et al. The relationship between disc degeneration, facet joint osteoarthritis, and stability of the degenerative lumbar spine. J Spinal Disord 2000 13:444–450. PMID: 11052356.
crossref pmid
13. Gruber HE, Hanley EN Jr. Recent advances in disc cell biology. Spine (Phila Pa 1976) 2003 28:186–193. PMID: 12544938.
crossref pmid
14. Wang YX, Griffith JF. Menopause causes vertebral endplate degeneration and decrease in nutrient diffusion to the intervertebral discs. Med Hypotheses 2011 77:18–20. PMID: 21440996.
crossref pmid
15. Wang YX, Griffith JF, Zeng XJ, et al. Prevalence and sex difference of lumbar disc space narrowing in elderly chinese men and women: osteoporotic fractures in men (Hong Kong) and osteoporotic fractures in women (Hong Kong) studies. Arthritis Rheum 2013 65:1004–1010. PMID: 23335175.
crossref pmid pmc
16. Teraguchi M, Yoshimura N, Hashizume H, et al. Prevalence and distribution of intervertebral disc degeneration over the entire spine in a population-based cohort: the Wakayama Spine Study. Osteoarthritis Cartilage 2014 22:104–110. PMID: 24239943.
crossref pmid
17. Manson NA, Goldberg EJ, Andersson GB. Sexual dimorphism in degenerative disorders of the spine. Orthop Clin North Am 2006 37:549–553. PMID: 17141011.
crossref pmid
18. Modic MT. Modic type 1 and type 2 changes. J Neurosurg Spine 2007 6:150–151. PMID: 17330582.
crossref pmid
19. Albert HB, Kjaer P, Jensen TS, Sorensen JS, Bendix T, Manniche C. Modic changes, possible causes and relation to low back pain. Med Hypotheses 2008 70:361–368. PMID: 17624684.
crossref pmid
20. Crock HV. A reappraisal of intervertebral disc lesions. Med J Aust 1970 1:983–989. PMID: 5427658.
crossref pmid
21. Crock HV. Internal disc disruption. A challenge to disc prolapse fifty years on. Spine (Phila Pa 1976) 1986 11:650–653. PMID: 3787337.
crossref pmid
22. Braithwaite I, White J, Saifuddin A, Renton P, Taylor BA. Vertebral end-plate (Modic) changes on lumbar spine MRI: correlation with pain reproduction at lumbar discography. Eur Spine J 1998 7:363–368. PMID: 9840468.
crossref pmid pmc
23. Zhang YH, Zhao CQ, Jiang LS, Chen XD, Dai LY. Modic changes: a systematic review of the literature. Eur Spine J 2008 17:1289–1299. PMID: 18751740.
crossref pmid pmc
24. Villarreal-Arroyo M, Mejia-Herrera JC, Larios-Forte MC. Incidence of Modic degenerative changes in patients with chronic lumbar pain at Monterrey Regional ISSSTE Hospital. Acta Ortop Mex 2012 26:180–184. PMID: 23320314.
pmid
25. Jensen TS, Karppinen J, Sorensen JS, Niinimaki J, Leboeuf-Yde C. Vertebral endplate signal changes (Modic change): a systematic literature review of prevalence and association with non-specific low back pain. Eur Spine J 2008 17:1407–1422. PMID: 18787845.
crossref pmid pmc
26. Macnab I. The traction spur: an indicator of segmental instability. J Bone Joint Surg Am 1971 53:663–670. PMID: 5580025.
crossref pmid
27. Lettin AW. Diagnosis and treatment of lumbar instability. J Bone Joint Surg Br 1967 49:520–529. PMID: 6037565.
crossref pmid
28. Morgan FP, King T. Primary instability of lumbar vertebrae as a common cause of low back pain. J Bone Joint Surg Br 1957 39:6–22. PMID: 13405944.
crossref pmid
29. Albert HB, Manniche C. Modic changes following lumbar disc herniation. Eur Spine J 2007 16:977–982. PMID: 17334791.
crossref pmid pmc
30. Kuisma M, Karppinen J, Niinimaki J, et al. Modic changes in endplates of lumbar vertebral bodies: prevalence and association with low back and sciatic pain among middle-aged male workers. Spine (Phila Pa 1976) 2007 32:1116–1122. PMID: 17471095.
crossref pmid


ABOUT
ARTICLE CATEGORY

Browse all articles >

BROWSE ARTICLES
EDITORIAL POLICY
FOR CONTRIBUTORS
Editorial Office
Department of Orthopedic Surgery, Asan Medical Center, University of Ulsan College of Medicine
88, Olympic-ro 43-gil, Songpa-gu, Seoul 05505, Korea
Tel: +82-2-3010-3530    Fax: +82-2-3010-8555    E-mail: asianspinejournal@gmail.com                
Korean Society of Spine Surgery
27, Dongguk-ro, Ilsandong-gu, Goyang-si 10326, Korea
Tel: +82-31-966-3413    Fax: +82-2-831-3414    E-mail: office@spine.or.kr                

Copyright © 2024 by Korean Society of Spine Surgery.

Developed in M2PI

Close layer
prev next