Background: Vitamin D has been associated in observational studies with multiple sclerosis, diabetes, cardiovascular disease, cancers, autoimmunity and allergy. Whether there is a causal link is however not known. In a similar vein, recent studies have provided conflicting results regarding a possible role for vitamin D in the pathophysiology of OA. In particular, its impact on disease progression in patients with established OA is uncertain. We investigated whether vitamin D level predicted the rate of structural progression of OA. Methods: 396 men and women (59.1-70.7 years) from the Hertfordshire Cohort Study underwent knee radiographs in 1999- 2003 and again a mean of 10.3 years later. Tibiofemoral joint K&L score and joint space (medial and lateral) were assessed by an experienced reader at both time points in both the left and right knee. At baseline, 25(OH)vitamin D was assayed using a DiaSorin Liason automated chemiluminescent assay (CoV <15%). Results: The mean (S.D.) age of participants was 64.8(2.7) years. OA progression (an increase in K&L score of ≥1) occurred in 51.4% of knees (395 of 768). In 276 knees, the K&L grade increased by 1, in 109 it increased by 2, and in 10 by 3. There was no difference in geometric mean vitamin D level in those that progressed and those that did not (left knee 43.6 and 42.9 nmol/l, P=0.725; right knee 42.5 and 44.3 nmol/l, P=0.409). Vitamin D levels did not differ by magnitude of change in K&L grade from baseline (0, 1, 2, or 3). There was no evidence of a relationship between vitamin D level and tibiofemoral joint space narrowing in either the medial or lateral compartment. Conclusion: Baseline serum vitamin D was not shown to be associated with rate of OA progression in older men and women. Larger prospective studies are required to confirm these findings.
CITATION STYLE
Jagannath, D., Edwards, M. H., Parsons, C., Litwic, A., Cooper, C., & Dennison, E. (2014). 186. Serum Vitamin D Does Not Influence Rate of Progression of Knee Osteoarthritis Over 10 Years: Results from the Hertfordshire Cohort Study. Rheumatology, 53(suppl_1), i129–i129. https://doi.org/10.1093/rheumatology/keu110.001
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