Extended reports
Allelic variation in the vitamin D receptor, lifestyle factors
and lumbar spinal degenerative disease
a Menzies Centre for Population Health
Research, GPO Box 252-23, Hobart, Tasmania, Australia, 7000, b Bone and Mineral Research Program, Garvan Institute of
Medical Research, Sydney, NSW, Australia, c Department of Rheumatology, Royal North Shore Hospital,
St Leonards, NSW, Australia
Correspondence to: Dr Jones.
Accepted for publication 15
December 1997
OBJECTIVE
To describe the relation between spinal
degenerative disease, allelic variation in the vitamin D receptor gene,
and lifestyle factors in a population-based association study.
METHODS
Random population-based sample of 110 men
and 172 women over 60 years of age participating in the Dubbo
Osteoporosis Epidemiology Study who had spinal radiographs (performed
according to a standardised approach), assessment of lifestyle factors,
bone densitometry as well as blood taken for genotyping.
RESULTS
Spinal degenerative disease of varying
severity was common in this sample. Multivariate analysis of genetic
and lifestyle factors simultaneously strengthened the statistical
significance of each indicating the presence of additive gene
environment interaction. Allelic variation in the vitamin D receptor
gene was associated with severity of osteophytosis (adjusted OR
"TT" v "tt" 0.41, 95% CI 0.17, 0.97), presence of
disc narrowing (adjusted OR "TT" v "tt" 0.45, 95%
CI 0.20, 0.99) and weakly with presence of osteophytosis (adjusted OR
"TT" v "tt" 0.47, 95% CI 0.19, 1.16) but not with severity of disc narrowing (OR "TT" v "tt" 1.05, 95% CI 0.40, 2.72) or apophyseal arthritis (OR "TT" v
"tt" 0.63, 95% CI 0.24, 1.59). Adjustment for femoral neck bone
density did not change these findings suggesting that the association
is not mediated through bone density. Presence and severity of spinal
degenerative disease increased with age at all sites. Current smoking
increased both the presence (adjusted OR 9.70, 95% CI 2.08, 45.1) and
severity (adjusted OR 2.91, 95% CI 1.16, 9.03) of spinal osteophytosis with intermediate values for past smokers. Severity of osteophytosis was also independently associated with body mass index and quadriceps strength consistent with a contributory effect of physical loading.
CONCLUSIONS
In this elderly sample, both genetic
and lifestyle factors were associated with the presence and severity
of spinal degenerative disease. There were site specific differences
in associations at the spine, which may be because of misclassification
of disease status or may indicate possible environmental and genetic
differences in the pathophysiology of spinal degenerative disease.
Further studies are required to confirm these findings in different
population samples and to further explore potential aetiological
mechanisms particularly gene environment interaction.
© 1998 by Annals of the Rheumatic Diseases
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