Degenerative Disk Disease

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Degenerative Disk Disease

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The intervertebral disk is a complex structure that has been the focus of much attention in clinical practice. The prevalence of low back and neck pain, which are thought to be associated with degenerative changes in the disk, represents a major epidemiologic problem. In the United States, back pain is the second leading symptom that prompts visits to physicians. As many as 80% of adults in the United States experience at least one episode of low back pain during their lifetime, and 5% experience chronic problems. [1]  An understanding of degenerative disk disease is important for managing these patients. (See the images below.)

The spine is composed of seven cervical vertebrae, 12 thoracic vertebrae, five lumbar vertebrae, and a fused set of sacral and vestigial coccygeal vertebrae. Spine stability is the result of three columns in one, as described by Dennis. Fracture or loss of two columns results in instability.

The anterior column consists of the anterior longitudinal ligament and the anterior portion of the vertebral body. The middle column consists of the posterior wall of the vertebral body and the posterior longitudinal ligament. The posterior column is formed by the posterior bony arch; this consists of transverse processes, facets, laminae, and spinous processes.

Intervertebral disks form one quarter of the total length of the spinal column. Each vertebra has the potential for 6° of freedom, translation in all thre axes of movement, and rotation around each axis. Not all vertebrae are created equal; the cervical vertebrae have the greatest freedom of flexion, extension, lateral rotation, and lateral flexion. This is because they are larger, they have concave lower and convex upper vertebral body surfaces, and they have transversely aligned facet joints.

Thoracic vertebrae have restricted flexion, extension, and rotation but freer lateral flexion because they are attached to the rib cage, are smaller, have flatter vertebral surfaces, have frontally aligned facet joints, and have larger overlapped spinous processes. The lumbar spine has good flexion and extension and free lateral flexion because its disks are large, the spinous processes are posteriorly directed, and the facet joints are sagittally directed. Lateral lumbar rotation is limited because of facet alignment.

The sensory of intervertebral discs is complex and varies according to their location within the spinal column. In the cervical spine, studies by Bogduk [2] and Mendel [3]  demonstrated the presence of both nerve fibers and mechanoreceptors within the anulus fibrosus. Impulses from these structures are transmitted via the sinuvertebral nerves and branches of the vertebral nerves. A another study by Bogduk [4]  found that the sensory innervation of the lumbar intervertebral disks, like that of the cervical disks, is derived from the sinuvertebral nerves but also from branches of the ventral primary rami and rami communicantes.

Of all connective tissues, the intervertebral disk undergoes the most serious age-related changes. By the third decade of life, the nucleus pulposus becomes replaced with fibrocartilage, and the distinction between the nucleus and the annulus becomes blurred. The proteoglycan, water, and noncollagenous protein concentrations decrease, while the collagen concentration increases. The increase in collagen concentration is more pronounced in the nucleus and in the posterior quadrants of the disk. It is more pronounced with age and moving caudally in the lumbar spine (similar to the Wolff law).

Biochemically, aging increases the ratio of keratin sulfate to chondroitin sulfate, and it also changes the proportion of chondroitin-4-sulfate to chondroitin-6-sulfate, with a parallel decrease in water content. Proteoglycan synthesis decreases, which decreases the osmotic swelling and the traffic of oxygen and nutrients to the disk. Because of this decreased traffic, breakdown products of link and noncollagenous proteins stagnate in the disk. Nonenzymatic glycosylation of these breakdown products accounts for the brown discoloration of the aging connective tissues.

Differentiating aging from degeneration is difficult. According to Pearce et al, “Aging and degeneration may represent successive stages within a single process that occurs in all individuals but at markedly different rates.” [5]  Aging and degeneration have in common decreased water and proteoglycan content in the disks, combined with increased collagen.

Whereas sagittal alignment, facet joint arthritis, and genetics potentially play a role in intervertebral disk degeneration, the results of one study suggest that the rate of degeneration may be associated with age. Those of African ethnicity also showed a faster rate of degeneration when compared with whites; sex did not show a significant effect on degeneration. [6]

One study demonstrated that the presence of juvenile disk degeneration was strongly associated with overweight and obesity, low back pain, increased low back pain intensity, and diminished physical and social functioning. An elevated body mass index was significantly associated with increased severity of disk degeneration. [7]

Another study found metabolic syndrome to be four times more prevalent in patients with radiographic evidence of severe degenerative disk disease as defined by degenerative spondylolisthesis or cervical or lumbar stenosis causing neurologic symptoms [8] .

Modic MT, Ross JS. Lumbar degenerative disk disease. Radiology. 2007 Oct. 245(1):43-61. [Medline].

Bogduk N, Windsor M, Inglis A. The innervation of the cervical intervertebral discs. Spine (Phila Pa 1976). 1988 Jan. 13(1):2-8. [Medline].

Mendel T, Wink CS, Zimny ML. Neural elements in human cervical intervertebral discs. Spine (Phila Pa 1976). 1992 Feb. 17(2):132-5. [Medline].

Bogduk N, Tynan W, Wilson AS. The nerve supply to the human lumbar intervertebral discs. J Anat. 1981 Jan. 132:39-56. [Medline]. [Full Text].

Pearce RH, Grimmer BJ, Adams ME. Degeneration and the chemical composition of the human lumbar intervertebral disc. J Orthop Res. 1987. 5(2):198-205. [Medline].

Siemionow K, An H, Masuda K, Andersson G, Cs-Szabo G. The effects of age, sex, ethnicity, and spinal level on the rate of intervertebral disc degeneration: a review of 1712 intervertebral discs. Spine (Phila Pa 1976). 2011 Aug 1. 36(17):1333-9. [Medline]. [Full Text].

Samartzis D, Karppinen J, Mok F, Fong DY, Luk KD, Cheung KM. A population-based study of juvenile disc degeneration and its association with overweight and obesity, low back pain, and diminished functional status. J Bone Joint Surg Am. 2011 Apr. 93(7):662-70. [Medline].

Gandhi R, Woo KM, Zywiel MG, Rampersaud YR. Metabolic syndrome increases the prevalence of spine osteoarthritis. Orthop Surg. 2014 Feb. 6 (1):23-7. [Medline].

Heuck A, Glaser C. Basic aspects in MR imaging of degenerative lumbar disk disease. Semin Musculoskelet Radiol. 2014 Jul. 18 (3):228-39. [Medline].

Gundry CR, Heithoff KB. Lumbar spine imaging. Kirkaldy-Willis WH, Burton CV, eds. Managing Low Back Pain. New York: Churchill Livingstone; 1992. 171.

Malfair D, Beall DP. Imaging the degenerative diseases of the lumbar spine. Magn Reson Imaging Clin N Am. 2007 May. 15(2):221-38, vi. [Medline].

Anderberg L, Annertz M, Brandt L, Säveland H. Selective diagnostic cervical nerve root block–correlation with clinical symptoms and MRI-pathology. Acta Neurochir (Wien). 2004 Jun. 146 (6):559-65; discussion 565. [Medline].

Carreon LY, Glassman SD, Howard J. Fusion and nonsurgical treatment for symptomatic lumbar degenerative disease: a systematic review of Oswestry Disability Index and MOS Short Form-36 outcomes. Spine J. 2008 Sep-Oct. 8(5):747-55. [Medline].

Jacobs W, Willems PC, van Limbeek J, Bartels R, Pavlov P, Anderson PG, et al. Single or double-level anterior interbody fusion techniques for cervical degenerative disc disease. Cochrane Database Syst Rev. 2011 Jan 19. CD004958. [Medline].

DiPaola CP, Molinari RW. Posterior lumbar interbody fusion. J Am Acad Orthop Surg. 2008 Mar. 16(3):130-9. [Medline].

Coric D, Mummaneni PV. Nucleus replacement technologies. J Neurosurg Spine. 2008 Feb. 8(2):115-20. [Medline].

Bertagnoli R, Yue JJ, Fenk-Mayer A, et al. Treatment of symptomatic adjacent-segment degeneration after lumbar fusion with total disc arthroplasty by using the prodisc prosthesis: a prospective study with 2-year minimum follow up. J Neurosurg Spine. 2006 Feb. 4(2):91-7. [Medline].

Bertagnoli R, Yue JJ, Nanieva R, et al. Lumbar total disc arthroplasty in patients older than 60 years of age: a prospective study of the ProDisc prosthesis with 2-year minimum follow-up period. J Neurosurg Spine. 2006 Feb. 4(2):85-90. [Medline].

Reed Abelson. Financial Ties Are Cited as Issue in Spine Study. The New York Times. January 30, 2008. Available at http://www.nytimes.com/2008/01/30/business/30spine.html.

Hellum C, Johnsen LG, Storheim K, et al. Surgery with disc prosthesis versus rehabilitation in patients with low back pain and degenerative disc: two year follow-up of randomised study. BMJ. 2011 May 19. 342:d2786. [Medline]. [Full Text].

Tropiano P, Huang RC, Girardi FP, et al. Lumbar total disc replacement. Surgical technique. J Bone Joint Surg Am. 2006 Mar. 88 Suppl 1 Pt 1:50-64. [Medline].

Siepe CJ, Heider F, Wiechert K, Hitzl W, Ishak B, Mayer MH. Mid- to long-term results of total lumbar disc replacement: a prospective analysis with 5- to 10-year follow-up. Spine J. 2014 Aug 1. 14 (8):1417-31. [Medline].

Lu SB, Hai Y, Kong C, Wang QY, Su Q, Zang L, et al. An 11-year minimum follow-up of the Charite III lumbar disc replacement for the treatment of symptomatic degenerative disc disease. Eur Spine J. 2015 Sep. 24 (9):2056-64. [Medline].

Zigler J, Garcia R. ISASS Policy Statement – Lumbar Artificial Disc. Int J Spine Surg. 2015 Mar 12. 9:7. [Medline]. [Full Text].

Kaiser MG, Haid RW Jr, Subach BR, et al. Anterior cervical plating enhances arthrodesis after discectomy and fusion with cortical allograft. Neurosurgery. 2002 Feb. 50(2):229-36; discussion 236-8. [Medline].

Lawton CD, Smith ZA, Lam SK, Habib A, Wong RH, Fessler RG. Clinical outcomes of microendoscopic foraminotomy and decompression in the cervical spine. World Neurosurg. 2014 Feb. 81 (2):422-7. [Medline].

Jackson R, Johnson DE. 159 Neurological Outcomes of Two-Level Total Disk Replacement Versus Anterior Discectomy and Fusion: 7-Year Results From a Prospective, Randomized, Multicenter Trial. Neurosurgery. 2016 Aug. 63 Suppl 1:164. [Medline].

Chen BH, Natarajan RN, An HS, Andersson GB. Comparison of biomechanical response to surgical procedures used for cervical radiculopathy: posterior keyhole foraminotomy versus anterior foraminotomy and discectomy versus anterior discectomy with fusion. J Spinal Disord. 2001 Feb. 14(1):17-20. [Medline].

Silveri CP, Simpson JM, Simeone FA, Balderston RA. Cervical disk disease and the keyhole foraminotomy: proven efficacy at extended long-term follow up. Orthopedics. 1997 Aug. 20(8):687-92. [Medline].

Li Z, Yu S, Zhao Y, Hou S, Fu Q, Li F, et al. Clinical and radiologic comparison of dynamic cervical implant arthroplasty versus anterior cervical discectomy and fusion for the treatment of cervical degenerative disc disease. J Clin Neurosci. 2014 Jun. 21 (6):942-8. [Medline].

Yee AJ, Yoo JU, Marsolais EB, Carlson G, Poe-Kochert C, Bohlman HH, et al. Use of a postoperative lumbar corset after lumbar spinal arthrodesis for degenerative conditions of the spine. A prospective randomized trial. J Bone Joint Surg Am. 2008 Oct. 90(10):2062-8. [Medline].

Chin KR, Tomlinson DT, Auerbach JD, Shatsky JB, Deirmengian CA. Success of lumbar microdiscectomy in patients with modic changes and low-back pain: a prospective pilot study. J Spinal Disord Tech. 2008 Apr. 21(2):139-44. [Medline].

Mannion AF, Leivseth G, Brox JI, Fritzell P, Hägg O, Fairbank JC. ISSLS Prize winner: Long-term follow-up suggests spinal fusion is associated with increased adjacent segment disc degeneration but without influence on clinical outcome: results of a combined follow-up from 4 randomized controlled trials. Spine (Phila Pa 1976). 2014 Aug 1. 39 (17):1373-83. [Medline].

Stephen Kishner, MD, MHA Professor of Clinical Medicine, Physical Medicine and Rehabilitation Residency Program Director, Louisiana State University School of Medicine in New Orleans

Stephen Kishner, MD, MHA is a member of the following medical societies: American Academy of Physical Medicine and Rehabilitation, American Association of Neuromuscular and Electrodiagnostic Medicine

Disclosure: Nothing to disclose.

Grant Stone, DO, MBA Resident Physician, Department of Physical Medicine and Rehabilitation, Louisiana State University School of Medicine in New Orleans

Disclosure: Nothing to disclose.

Edward Babigumira, MD Interventional Spine and Pain Medicine Specialist, Lewes Medical and Surgical Associates, Delaware

Edward Babigumira, MD is a member of the following medical societies: American Academy of Physical Medicine and Rehabilitation, American Association of Neuromuscular and Electrodiagnostic Medicine, International Spine Intervention Society

Disclosure: Nothing to disclose.

James Monroe Laborde, MD, MS Clinical Assistant Professor, Department of Orthopedics, Louisiana State University Health Sciences Center and Tulane Medical School; Board of Advisors, Department of Biomedical Engineering, Tulane University; Adjunct Assistant Professor, Department of Physical Medicine and Rehabilitation, Louisiana State University Medical School

James Monroe Laborde, MD, MS is a member of the following medical societies: American Academy of Orthopaedic Surgeons

Disclosure: Nothing to disclose.

Michael R Voorhies, Jr, MD Resident Physician, Department of Physical Medicine and Rehabilitation, Louisiana State University Health Sciences Center

Disclosure: Nothing to disclose.

Francisco Talavera, PharmD, PhD Adjunct Assistant Professor, University of Nebraska Medical Center College of Pharmacy; Editor-in-Chief, Medscape Drug Reference

Disclosure: Received salary from Medscape for employment. for: Medscape.

William O Shaffer, MD Orthopedic Spine Surgeon, Northwest Iowa Bone, Joint, and Sports Surgeons

William O Shaffer, MD is a member of the following medical societies: American Academy of Orthopaedic Surgeons, American Orthopaedic Association, Kentucky Medical Association, North American Spine Society, Kentucky Orthopaedic Society, International Society for the Study of the Lumbar Spine, Southern Medical Association, Southern Orthopaedic Association

Disclosure: Received royalty from DePuySpine 1997-2007 (not presently) for consulting; Received grant/research funds from DePuySpine 2002-2007 (closed) for sacropelvic instrumentation biomechanical study; Received grant/research funds from DePuyBiologics 2005-2008 (closed) for healos study just closed; Received consulting fee from DePuySpine 2009 for design of offset modification of expedium.

Jeffrey A Goldstein, MD Clinical Professor of Orthopedic Surgery, New York University School of Medicine; Director of Spine Service, Director of Spine Fellowship, Department of Orthopedic Surgery, NYU Hospital for Joint Diseases, NYU Langone Medical Center

Jeffrey A Goldstein, MD is a member of the following medical societies: American Academy of Orthopaedic Surgeons, American College of Surgeons, American Orthopaedic Association, AOSpine, Cervical Spine Research Society, International Society for the Advancement of Spine Surgery, International Society for the Study of the Lumbar Spine, Lumbar Spine Research Society, North American Spine Society, Scoliosis Research Society, Society of Lateral Access Surgery

Disclosure: Serve(d) as a director, officer, partner, employee, advisor, consultant or trustee for: Medtronic, Nuvasive, NLT Spine, RTI, Magellan Health<br/>Received consulting fee from Medtronic for consulting; Received consulting fee from NuVasive for consulting; Received royalty from Nuvasive for consulting; Received consulting fee from K2M for consulting; Received ownership interest from NuVasive for none.

Degenerative Disk Disease

Research & References of Degenerative Disk Disease|A&C Accounting And Tax Services
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Degenerative Disk Disease

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