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Abstract Number: 62

Severe Spine Osteoarthritis in Older Men Is Associated with the Risk of Incident Fragility Fracture

Roland Chapurlat1, Charline Estublier2 and Pawel Szulc3, 1Pavillon F Rheumatology, Hopital Edouard Herriot, Lyon, France, 2Rheumatology, Hôpital Edouard Herriot, Pavillon F, Lyon, France, 3Epidemiology of Osteoporosis, INSERM UMR 1033, Lyon, France

Meeting: 2014 ACR/ARHP Annual Meeting

Keywords: Bone density, fracture risk and osteoarthritis

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Session Information

Title: Epidemiology and Public Health: Osteoporosis, Non-Inflammatory Arthritis and More

Session Type: Abstract Submissions (ACR)

Background/Purpose:

Data on the association of osteoarthritis (OA) with bone fragility are limited. In particular, data on the fracture risk in older men with spine OA are scarce. Our aim was to study the association of baseline severity of spine OA with bone mineral density (BMD), bone loss and risk of fragility fracture in a prospective study of a cohort of older men.

Methods: Men aged >50 (n=766) had lateral spine radiographs at baseline. Spine OA was assessed by Lane’s score (J Rheumatol, 1993). We calculated the total osteophyte score by adding up osteophyte scores for 6 intervertebral levels. We calculated total disc narrowing score (DSN) and total overall grade score similarly. BMD was measured by DXA using a HOLOGIC QDR1500 device. Abdominal aortic calcification (AAC) was assessed by Kauppila’s semiquantitative score (Atherosclerosis, 1997).  Men were followed up for 7.5 yr to assess bone loss (every 18 mo) and incident vertebral fractures. Incident peripheral fractures were assessed for 10 yr.

Results:

Moderate and severe osteophytes were found in 85% of men, 72% of men had DSN. After adjustment for age and weight, BMD (hip, forearm, whole body) was 2-7% higher (p<0.05 to <0.001) in men with severe spine OA in comparison with men with or without mild spine OA. For instance, men with severe DSN (total score>4, highest quartile) had 5% (0.4SD, p<0.001) higher total hip BMD compared with men without DSN. The rate of bone loss did not differ according to the severity of spine OA regardless of the measure of the spine OA (DSN, osteophytosis) and regardless of the skeletal site (p>0.4).

During the follow-up, 27 men sustained radiographic vertebral fractures. After adjustment for age, BMI, lumbar spine BMD, AAC, prior falls and fractures, risk of vertebral fracture increased with the DSN severity (HR= 1.15 per increase by 1 unit, 95%CI: 1.01-1.31, p<0.05). In this multivariable model, the risk of vertebral fracture was higher in the highest quartile of total DSN score vs. the three lower quartiles combined (HR= 2.47, 95%CI: 1.04-5.86, p<0.05).

During the follow-up, 61 men sustained non-vertebral fragility fractures. The incidence of non-vertebral fracture was lower above the median of total DSN score (4.6 vs 10.2%, p<0.005). After adjustment for the confounders (including hip BMD and leg disability), the risk of peripheral fracture was lower in men above the median total DSN score vs. below the median (HR= 0.44, 95%CI: 0.24-0.80, p<0.01).

Other measures of spine OA were not associated with the risk of fracture.

Conclusion: Men with severe spine OA have fewer non vertebral fractures but more vertebral fractures. This may be due to better bone quality but abnormal spine biomechanics.


Disclosure:

R. Chapurlat,
None;

C. Estublier,
None;

P. Szulc,
None.

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