An Allele of COL9A2 Associated with Intervertebral Disc Disease

Author:

Annunen Susanna1,Paassilta Petteri1,Lohiniva Jaana1,Perälä Merja1,Pihlajamaa Tero1,Karppinen Jaro2,Tervonen Osmo3,Kröger Heikki4,Lähde Seppo3,Vanharanta Heikki2,Ryhänen Lasse5,Göring Harald H. H.6,Ott Jürg67,Prockop Darwin J.8,Ala-Kokko Leena18

Affiliation:

1. Collagen Research Unit, Biocenter and Department of Medical Biochemistry;

2. Department of Physical Medicine and Rehabilitation;

3. Diagnostic Radiology;

4. Department of Surgery, University of Kuopio, 70211 Kuopio, Finland.

5. Internal Medicine, University of Oulu, 90220 Oulu, Finland.

6. Department of Genetics and Development, Columbia University, New York, NY 10032, USA.

7. Laboratory of Statistical Genetics, Rockefeller University, New York, NY 10021, USA.

8. Center for Gene Therapy, MCP Hahnemann University, Philadelphia, PA 19102, USA.

Abstract

Intervertebral disc disease is one of the most common musculoskeletal disorders. A number of environmental and anthropometric risk factors may contribute to it, and recent reports have suggested the importance of genetic factors as well. The COL9A2 gene, which codes for one of the polypeptide chains of collagen IX that is expressed in the intervertebral disc, was screened for sequence variations in individuals with intervertebral disc disease. The analysis identified a putative disease-causing sequence variation that converted a codon for glutamine to one for tryptophan in six out of the 157 individuals but in none of 174 controls. The tryptophan allele cosegregated with the disease phenotype in the four families studied, giving a lod score (logarithm of odds ratio) for linkage of 4.5, and subsequent linkage disequilibrium analysis conditional on linkage gave an additional lod score of 7.1.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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