Assessment of age-related macroscopic changes in human lumbar intervertebral discs (IVD) and vertebral bodies.
To determine the sequence of macroscopic changes during aging/degeneration.
Descriptive studies on macroscopic alterations of the IVD during aging/degeneration are readily available, but quantitative analyses are sparse.
A total of 248 mid-/parasagittal sections of lumbar IVD and vertebral bodies from 41 routine autopsies (range, 7 months to 88 years) were semiquantitatively assessed for macroscopic parameters and correlated with age.
Nuclear fibrous transformation, anular disorganization, endplate, and vertebral body alterations progress predominantly in the first two and in the fifth to seventh decades. In the third and fourth decade, little progression occurs. Nuclear clefts and anular tears appear later, mostly starting in the second decade, with clefts preceding tear formation. Radial and concentric tears develop similarly over time, whereas rim lesions mostly develop after the sixth decade. Significant differences are observed between upper and lower lumbar spine.
Our data show that fibrous nuclear transformation during aging/degeneration precedes cleft formation. The temporal sequence suggests a strong correlation of cleft and tears formation starting with clefts in the second decade. Our results support the hypothesis that disc degeneration starts in the nucleus. Extensive macroscopic alterations already apparent in the second life decade present a challenge to any tissue engineering and repair attempt.
A total of 248 mid-/parasagittal slices of lumbar motion segments from 41 autopsies (range, 7 months to 88 years) were analyzed semiquantitatively for macroscopic parameters. The results suggest cleft formation as a result of fibrous transformation in the nucleus. A correlation of cleft and tears formation starting with nuclear clefts was found, supporting the concept that degeneration starts in the nucleus.
From the *Centre for Spinal Surgery, University of Zurich, Balgrist, Zurich, Switzerland; and †Institute of Pathology, Academic Hospital Munich-Bogenhausen, Germany.
Acknowledgment date: March 29, 2005. First revision date: July 8, 2005. Second revision date: September 6, 2005. Acceptance date: September 7, 2005.
Supported by a grant from the AO Spine (Grant No. SRN 02/103).
The manuscript submitted does not contain information about medical device(s)/drug(s).
Foundation funds were received in support of this work. No benefits in any form have been or will be received from a commercial party related directly or indirectly to the subject of this manuscript.
Address correspondence and reprint requests to Günther Paesold, PhD, Orthopedic Research, Centre for Spinal Surgery, University of Zurich, University Hospital Balgrist, Forchstrasse 340, CH-8008 Zurich, Switzerland; E-mail: firstname.lastname@example.org