The vertebral column supports our body’s physical structure and nervous system, enabling movement and sensation. Pathology of the spine can lead to debilitating outcomes on quality of life. The vertebral column (spine) defines the animal subphylum Vertebra, or vertebrates, of the phylum Chordata. In humans, it is composed of 33 individual vertebrae grouped into the cervical, thoracic, lumbar, sacral, and coccygeal regions. There are 7 cervical, 12 thoracic, 5 lumbar, 5 sacral, and 4 coccygeal vertebrae. Along with the skull, ribs, and sternum, these vertebrae make up the axial skeletal system.
The function of the spinal cord and spinal nerves includes:
The human skeleton begins to develop soon after conception. The notochordal process starts to form around day 17. The floor of the notochordal processes forms the notochordal plate after fusion of the roof of the yolk sac (of the underlying endoderm). The notochordal plate then folds inward to create the notochord. The notochord helps maintain the structure of the embryo and is the location of the development of the vertebral column. Parts of the notochord persist in adults to form the nucleus pulposus. Furthermore, the notochord stimulates the overlying ectoderm to form neuroectoderm, creating the neural plate. The neural plate gives rise to the neural tube, the rostral part becomes the adult brain, and the caudal end becomes the spinal cord.[1]
When the embryo begins gastrulation around 3 weeks, the sclerotome of somites, specifically the mesodermal portion, grows around the neural tube and notochord to form vertebral bodies and arches as well as the ribs. Each vertebral body is formed in a process called resegmentation from the fusion of 2 adjacent sclerotomes (caudal and cranial halves).
The vertebrae develop through endochondral ossification. Cartilage is formed first around week 6, and it is replaced with bone starting around week 7 to 8. Complete endochondral ossification occurs around age 26. Bony remodeling (degeneration and regeneration) occur throughout the lifespan.
Congenital Anomalies of the Spine
VACTERL (vertebral defects, anal atresia, cardiac defects, trachea-esophageal fistula, renal anomalies, limb anomalies): Defects of the spine in this association include fused vertebrae, missing or extra vertebrae, or misshapen vertebrae. While only 3 of these features are required for the diagnosis of this condition, 60% to 80% of patients with VACTERL have vertebral defects.[2]
Spina Bifida: incomplete closure of the vertebral column and meninges known as a neural tube defect. There are 3 types, and in order of increasing severity, they are spina bifida occulta, meningocele, and myelomeningocele. Myelomeningocele is often associated with Arnold-Chiari malformation and tethered spinal cord.
Spinal arteries originate from branches of larger arteries that supply the internal organs. The subclavian arteries of the neck branch into the vertebral arteries and ascending cervical arteries of the spine. The posterior intercostal arteries of the spine branch from the thoracic aorta while the lumbar arteries of the spine originate from the abdominal aorta. The lateral sacral arteries branch from the internal iliac arteries in the pelvis. Each of these arteries supplying the spine divides into an anterior and a posterior branch. The anterior branch supplies the vertebral body, and the posterior branch supplies the vertebral arch. Radicular arteries course along the middle, supplying the interior of the vertebral canal and vertebral column.
Radicular veins drain the smaller veins of the spinal cord and the internal and external vertebral veins. They empty into segmental and intervertebral veins. Blood flows from these vessels into 1 of 3 large vessels depending on the location. The superior vena cava drains the area of the cervical spine. The azygous and hemiazygous veins drain the thoracic area, and the inferior vena cava drains the lower regions of the lumbar and sacral spine.
The central nervous system (CNS) is composed of the brain and spinal cord, while the peripheral nervous system consists of spinal nerves, cranial nerves, and their ganglia. The spinal cord is contained within the vertebral column. It extends from the base of the brain to the base of the spine where it comes to an end at the conus medullaris and filum terminale. The conus medullaris is the tapering, cone-shaped end of the spinal cord. It usually terminates at L1-L2 in adults but may extend further as an anatomical variant. In newborns, the conus medullaris is as low as L3-L4. The ending location is relevant for procedures such as the lumbar puncture to reduce the risk of cord trauma. The filum terminale is a delicate extension of the spinal cord from the conus medullaris that anchors to the dorsum of the coccyx. The cauda equina (“horse’s tail”) extend from the conus medullaris below.
Thirty-one pairs of spinal nerves exit the spinal cord and pass through the intervertebral foramen to innervate the periphery. Meningeal branches of spinal nerves innervate the vertebrae.
As the central weight-bearing bony structure, the spine undergoes tremendous force. The muscles that attach to the spine help maintain posture and distribute the uneven force of the body’s weight. They are divided into the extrinsic and intrinsic back muscle groups.
The extrinsic muscles are further divided into superficial (trapezius, latissimus dorsi, levator scapulae, and the major and minor rhomboids) and intermediate (serratus posterior superior and serratus posterior inferior) groups. The superficial extrinsic muscles are involved in the movement of the upper limbs including movements of the scapula and humerus. The intermediate extrinsic muscles are involved in rib movement to aid respiration.
The intrinsic back muscles are separated into 3 layers: superficial, intermediate, and deep. These muscles aid in the movement of the spine and maintain postures. The superficial layer is made of the splenius capitis and splenius cervicis. These are involved in neck flexion, rotation, and extension. The intermediate layer is mostly made of the paraspinal or erector spinae muscles, the iliocostalis, longissimus, and spinalis. As the name implies, the erector spinae are important in extending and maintaining the central curvature of the spine.
The deep layer of the intrinsic back muscles includes muscles that lie between the transverse and spinous processes of the vertebrae. They are sometimes called the paravertebral muscles and include three groups of muscles. The semispinalis is the most superficial; it is prominent in the thoracic and cervical region. The multifidus is deep to semispinalis and most prominent in the lumbar region. Finally, the rotatores muscles are deepest and most prominent in the thoracic region.
The suboccipital muscles are located deep in the back of the neck. They attach to the skull and are involved in the movement of the head. These include the muscles that make up the suboccipital triangle: the rectus capitis posterior major, obliquus capitis superior, and obliquus capitis inferior. The importance of this triangle is that this is the location of the vertebral artery’s loop from the transverse foramen of the atlas to enter the foramen magnum of the skull where it supplies the brainstem.
Surgery may be done for fractures, dislocations, tumors, scoliosis, or other mechanical defects. Care must be taken regarding a patient’s age, weight, and medical comorbidities. Complications may include neurological damage, incomplete relief of pain, vertebral fracture, and infection. [3]
Osteoarthritis: The progressive erosion of joint cartilage. This is the most common form of arthritis and often affects the spine. Advanced osteoarthritis may lead to hyperextension of the cervical spine and compression of spinal nerves causing pain.
Osteoporosis: Demineralization of the bones. Current USPSTF guidelines recommend screening for osteoporosis in all women aged 65 and older as well younger women with increased risk factors (assess using the FRAX tool). Severe osteoporosis increases the risk of developing a vertebral compression fracture.[4]
Seronegative spondyloarthropathies: Disease of the vertebral column that is typically associated with lack of the serum markers ANA and rheumatoid arthritis and has an increased incidence of HLA-B27. Conditions include ankylosing spondylitis, reactive arthritis, psoriatic arthritis, juvenile idiopathic arthritis, and spondylitis associated with inflammatory bowel disease.
Spinal cord injury: Trauma to the vertebral column may lead to spinal cord damage with serious consequences such as paraplegia.
Spinal disc herniation: The intervertebral discs act as shock absorbers for load bearing and relaxing. Over time, or with injury, the discs may tear at the periphery along the annulus fibrosus leading to herniation of the internal nucleus pulposus. This can cause symptoms of pain, numbness, weakness, and decreased reflexes.
Spinal stenosis: Narrowing of the central spinal canal that can cause symptoms of numbness, weakness, or pain in the upper or lower extremities. This condition may be secondary to osteoarthritis, rheumatoid arthritis, Paget disease of the bone, or trauma. Symptoms classically improve with bending forwards.
Spondylolisthesis: Complete dislocation with anterior displacement of one vertebra on another. This may increase pressure on spinal nerves, leading to pain in the nerve’s distribution.
Tuberculous spondylitis: Also known as Pott Disease, this is osteomyelitis of the vertebral bodies along with intervertebral discitis caused by advanced tuberculosis. Symptoms may include weakness of the lower limbs, kyphosis, back pain, fever, and weight loss.
The adult spine is normally curved slightly with cervical lordosis, thoracic kyphosis, and lumbar lordosis. This curvature originates during embryogenesis and further develops during childhood. Thoracic kyphosis and sacral curvature are formed during fetal development: the “fetal position.” Cervical curvature develops when babies begin to support the weight of their heads. Lumbar lordosis develops when children begin to stand and support their body weight. This curvature may become exaggerated or abnormal due to various pathological processes.
[1] | Kaplan KM,Spivak JM,Bendo JA, Embryology of the spine and associated congenital abnormalities. The spine journal : official journal of the North American Spine Society. 2005 Sep-Oct [PubMed PMID: 16153587] |
[2] | Passias PG,Poorman GW,Jalai CM,Diebo BG,Vira S,Horn SR,Baker JF,Shenoy K,Hasan S,Buza J,Bronson W,Paul JC,Kaye I,Foster NA,Cassilly RT,Oren JH,Moskovich R,Line B,Oh C,Bess S,LaFage V,Errico TJ, Incidence of Congenital Spinal Abnormalities Among Pediatric Patients and Their Association With Scoliosis and Systemic Anomalies. Journal of pediatric orthopedics. 2017 Oct 9 [PubMed PMID: 29016431] |
[3] | Nasser R,Yadla S,Maltenfort MG,Harrop JS,Anderson DG,Vaccaro AR,Sharan AD,Ratliff JK, Complications in spine surgery. Journal of neurosurgery. Spine. 2010 Aug [PubMed PMID: 20672949] |
[4] | Curry SJ,Krist AH,Owens DK,Barry MJ,Caughey AB,Davidson KW,Doubeni CA,Epling JW Jr,Kemper AR,Kubik M,Landefeld CS,Mangione CM,Phipps MG,Pignone M,Silverstein M,Simon MA,Tseng CW,Wong JB, Screening for Osteoporosis to Prevent Fractures: US Preventive Services Task Force Recommendation Statement. JAMA. 2018 Jun 26 [PubMed PMID: 29946735] |