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] .
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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
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