Background Osteoporosis is a common disorder with a strong geneticcomponent. One way in which the genetic component could be expressedis through polymorphism of COLIA1, the gene for collagen typeI1, a bone-matrix protein.
Methods We determined the COLIA1 genotypes SS, Ss, and ss ina population-based sample of 1778 postmenopausal women usinga polymerase-chain-reactionbased assay. We then relatedthe genotypes to bone mineral density and the occurrence ofosteoporotic fractures in these women.
Results As compared with the 1194 women with the SS genotype,the 526 women with the Ss genotype had 2 percent lower bonemineral density at the femoral neck (P = 0.003) and the lumbarspine (P = 0.02); the 58 women with the ss genotype had reductionsof 4 percent at the femoral neck (P = 0.05) and 6 percent atthe lumbar spine (P = 0.005). These differences increased withage (P = 0.01 for modification by age of the effect of COLIA1on femoral-neck bone density, and P = 0.004 for modificationof the effect on lumbar-spine bone density). Women with theSs and ss genotypes were overrepresented among the 111 womenwho had incident nonvertebral fractures (relative risk per copyof the s allele, 1.5; 95 percent confidence interval, 1.1 to2.1).
Conclusions The COLIA1 polymorphism is associated with reducedbone density and predisposes women to osteoporotic fractures.
Source Information
From the Departments of Internal Medicine III (A.G.U., J.P. T.M.L., H.A.P.P.) and Epidemiology and Biostatistics (A.G.U., H.B., Q.H., F.Y., A.H., H.A.P.P.), Erasmus University Medical School, Rotterdam, the Netherlands; and the Department of Medicine and Therapeutics, University of Aberdeen, Aberdeen, United Kingdom (F.E.A.M., S.F.A.G., S.H.R.).
Address reprint requests to Dr. Uitterlinden at the Department of Internal Medicine III, FGG-EUR, Erasmus University Medical School, P.O. Box 1738, 3000 DR Rotterdam, the Netherlands.
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