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Abstract Number: 1258

Association Between Low Vitamin D Levels and Indicators of Osteoporosis and Atherosclerosis

Barry J. Sheane1, Ruth Dunne2, Ken Scott3, Mary Hall4, Michelle O'Connor2, Martin Healy5, John Feely4, J.B. Walsh6 and Gaye Cunnane7, 1Dept. of Rheumatology, St. James's Hospital, Dublin, Ireland, 2Diagnostic Imaging Department, St James's Hospital, Dublin, Ireland, 3Department of Pharmacology and Therapeutics, Trinity College Dublin, Dublin 8, Ireland, 4Department of Pharmacology and Therapeutics, St James's Hospital, Dublin, Ireland, 5Central Pathology Laboratory, St James's Hospital, Dublin, Ireland, 6Medicine for the Elderly, St James's Hospital, Dublin, Ireland, 7Dept of Rheumatology, St James's Hospital, Dublin, Ireland

Meeting: 2012 ACR/ARHP Annual Meeting

Keywords: Atherosclerosis, Osteoporosis and rheumatoid arthritis (RA)

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Session Information

Title: Rheumatoid Arthritis - Clinical Aspects II: Clinical Features & Comorbidity/Cardiovascular Disease

Session Type: Abstract Submissions (ACR)

Background/Purpose:

Osteoporosis and cardiovascular disease are complications of chronic rheumatoid arthritis (RA). It is not known if these processes share pathogenetic mechanisms. Low levels of vitamin D predispose to bone fragility. Recent data suggest that they may also be linked to vascular disease.

Methods:

A cross-sectional study of RA patients and age-/sex-matched controls was carried out. None had any history of cardiovascular disease or diabetes mellitus. Levels of 25-hydroxy vitamin D were recorded and DXA scans were performed. Evidence of sub-clinical atherosclerosis was obtained with pulse wave analysis (PWA) and carotid intimal-medial thickness (CIMT). Serum markers of vascular disease (ICAM1, oxidized LDL, HSP60, IL6), a lipid profile and body mass index (BMI) were measured. Early RA was defined as those with disease duration less than 2 years. Data were analysed using SPSS 16.0.

Results:

99 people were included in this study (74 RA and 25 controls). Fifty-two (70%) of the RA group and 8 (31%) of the control group were taking calcium / vitamin D supplements (average vitamin D level 400iu/day). Only 12 (13%) had normal vitamin D levels (>80nmol/l). Vitamin D levels were deficient (<25nmol/l) in 21% and insufficient (>25 <80nmol/l) in 65%. All patients with early RA were vitamin D deplete (n = 18); 33% had insufficient levels and 67% deficient amounts. In contrast, 20% (n = 11) of those with established RA had normal vitamin D levels, while 65% had insufficient and 15% deficient levels. Mean vitamin D measurements were 38.5nmol/l in early RA versus 58nmol/l in established RA (p = 0.02).

Bone mineral density was similar between RA and controls. In the RA cohort, 29% had evidence of osteoporosis, while 46% had osteopenia and 25% had a normal DXA scan. In those with early RA, osteoporosis was present in 3 (18%) versus 16 (32%) patients with chronic RA (p = 0.3)

In RA, there was a negative correlation between vitamin D levels and DXA T-scores (p = 0.02), and BMI (p = 0.007). While RA patients had significantly greater levels of serum markers of vascular disease (IL6, ICAM1, oxidized LDL, HSP60) compared with controls, there was no correlation with vitamin D levels. CIMT measurements correlated negatively with vitamin D. (p=0.06). Using multiple linear regression controlling for age, CIMT and DXA T-scores, and calcium/vitamin D supplements, vitamin D levels were negatively correlated with PWV (p=0.04), across the entire study group. Triglyceride levels were inversely related to vitamin D across the study group (cc -0.3, p<0.01).

Conclusion:

Low levels of vitamin D were common in this population, particularly in those with early RA. Vitamin D supplementation at current dosages does not achieve normal vitamin D levels. The association between low vitamin D levels and markers of both osteoporosis and atherosclerosis needs to be further explored. In particular, a lack of sunlight in relation to insufficient exercise exposure may be relevant in exploring this link.


Disclosure:

B. J. Sheane,
None;

R. Dunne,
None;

K. Scott,
None;

M. Hall,
None;

M. O’Connor,
None;

M. Healy,
None;

J. Feely,
None;

J. B. Walsh,
None;

G. Cunnane,
None.

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