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Abstract Number: 388

Vitamin D Levels and Inflammation In The Aortic Wall Of Patients With Inflammatory Rheumatic Disease and Coronary Artery Disease

Ingvild Oma1, Jacqueline Kirsti Andersen2, Torstein Lyberg3, Øyvind Molberg4, Jon Elling Whist1, Ingjerd Lien Kvelstad1, Terje Veel5, Morten Fagerland6, Sven M. Almdahl7, Knut Mikkelsen8 and Ivana Hollan9, 1Innlandet Hospital Trust, Lillehammer, Norway, 2Gjøvik University College, Gjøvik, Norway, 3Oslo University Hospital, Oslo, Norway, 4Institute of Clinical Medicine, University of Oslo, Oslo, Norway, 5Feiringklinikken, Feiring, Norway, 6Department of Biostatistics, Oslo University Hospital, Oslo, Norway, 7Cardiothoracic surgery, University Hospital of North Norway, Tromsø, Norway, 8Lillehammer Hospital for Rheumatic Diseases, Lillehammer, Norway, 9Rheumatology, Lillehammer Hospital for Rheumatic Diseases, Lillehammer, Norway

Meeting: 2013 ACR/ARHP Annual Meeting

Keywords: biopsies, Cardiovascular disease, inflammation and rheumatic disease, Vitamin D

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Session Information

Title: Rheumatoid Arthritis - Clinical Aspects I: Comorbidities in Rheumatoid Arthritis

Session Type: Abstract Submissions (ACR)

Background/Purpose: Vitamin D is involved in immune reactions, and vitamin D deficiency is associated with autoimmune diseases and with cardiovascular diseases. In Feiring Heart Biopsy Study (FHBS), we previously demonstrated a high occurrence of mononuclear cell infiltrates (MCIs) in subintimal layers of the aorta, related to inflammatory rheumatic disease (IRD). In theory, vitamin D deficiency might contribute to vascular inflammation involved in the pathogenesis of cardiovascular disease (CVD) along with the premature and accelerated CVD in IRD.

We looked for differences in plasma levels of 25(OH)D3 and 1,25(OH)2D3 in patients with coronary arterial disease (CAD) and CAD+IRD, and examined if the levels of 25(OH)D3 and 1,25(OH)2D3 were related to inflammation in subintimal aortic layers in terms of MCIs.

Methods: Plasma levels of 25(OH)D3 were examined by radioimmunoassay and 1,25(OH)2D3 by immunoassay in 53 patients with CAD and 68 patients with CAD and IRD from FHBS. The D vitamin levels were then correlated to the number of MCI previously identified in the subintimal aortic layers of these patients (I. Hollan et.al., Arthritis Rheum, 56 (2007), 2072-9).

Results: From our univariate analysis, we observed no differences in 25(OH)D3 and 1,25(OH)2D3 levels between patients with CAD+IRD and patients with CAD only (see Table). Nor did we observe any relationships between vitamin D levels and occurrence of MCIs in the subintimal aortic layers. However, after adjustment for variables with p<0,20 (CRP, glucocorticosteroids, daily vitamin and mineral supplementation, group, MCI) and age and sex, there was a significant inverse relationship between 1,25(OH)2D3and the occurrence of MCIs in the subintimal aortic layers (B=-17, p=0.019, CI= -31.3, -2.8).

 

CAD-IRD (n=68)

CAD-nonIRD (n=53)

P value

Age – years

67±10

68±10

0.601

Women – no. (%)

26 (38)

19 (36)

0.851

25(OH)D3 – nmol/l

59±20

59±14

0.930

1,25(OH)2D3 – pmol/l

108±46

96±23

0.055

MCI in aortic adventitia – no. (%)

30 (48)

10 (20)

0.002

Conclusion: Our study does not support the hypothesis that vitamin D deficiency contributes to the premature and accelerated CVD in IRD. However, based on multivariate analyses, low 1,25(OH)2D3 might  be related to the presence inflammation in the subintimal layers of the aorta.  This fact needs more exploration in future studies. If there is a causal relationship, vitamin d supplementation might represent a simple and cheap treatment for vascular inflammation.


Disclosure:

I. Oma,
None;

J. K. Andersen,
None;

T. Lyberg,
None;

Molberg,
None;

J. E. Whist,
None;

I. Lien Kvelstad,
None;

T. Veel,
None;

M. Fagerland,
None;

S. M. Almdahl,
None;

K. Mikkelsen,
None;

I. Hollan,
None.

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