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Kao, et al: RA and calcification risks
Personal non-commercial use only. The Journal of Rheumatology Copyright © 2008. All rights reserved.
Subclinical Coronary Artery Calcification and
Relationship to Disease Duration in Women with
Rheumatoid Arthritis
AMY H. KAO, SHANTHI KRISHNASWAMI,AMYLYNN CUNNINGHAM, DANIEL EDMUNDOWICZ,
PENELOPEA. MOREL, LEWIS H. KULLER, and MARY CHESTER M. WASKO
ABSTRACT. Objective. To examine the association between disease duration of rheumatoid arthritis (RA) and the
presence and extent of coronary artery calcification (CAC) in women with RA.
Methods. In this cross-sectional study, 185 women with RA duration of at least 2 years and no clinical
cardiovascular disease completed electron-beam tomography (EBT) scans and risk factor assessment.
Multivariable logistic regression was used to associate RA duration quartiles with subclinical CAC and
extent of CAC.
Results. Age was similar across the quartiles of RA duration. Patients with RA > 23 years had signifi-
cant increased odds (unadjusted OR 2.60, 95% CI 1.21–5.53) of having more extensive CAC compared
to the referent group, those with RA for 2–7 years. This association remained significant after adjust-
ment for traditional coronary heart disease (CHD) risk factors and RA-related covariates. Patients with
intermediate RA duration (8–13 yrs) were more likely to have presence of any CAC (OR 3.03, 95% CI
1.06–8.66) compared to the referent group only after adjusting for age, race, and traditional CHD risk
factors. Patients with longer RA duration were more likely to have cumulative joint damage, manifest-
ed as prior joint surgery, joint deformity, and greater functional disability. Lower body mass index also
was associated with longer RA duration.
Conclusion. Patients with longstanding RA have more extensive subclinical atherosclerosis or CAC
compared to patients of the same age, independent of other CHD risk factors. RA duration may be a
surrogate for factors related to the disease process or its treatment that may promote coronary athero-
genesis. (First Release Nov 15 2007; J Rheumatol 2008;35:61–9)
Key Indexing Terms:
RHEUMATOIDARTHRITIS CORONARYARTERYCALCIFICATION RISK FACTORS
DISEASE DURATION ELECTRON BEAM TOMOGRAPHY CARDIOVASCULARDISEASE
From the Division of Rheumatology and Clinical Immunology,
Department of Medicine, and Department of Immunology, University of
Pittsburgh; University of Pittsburgh Cardiovascular Institute; Department
of Epidemiology, University of Pittsburgh Graduate School of Public
Health, Pittsburgh, Pennsylvania; the Division of Rheumatology and
Immunology, Department of Medicine, Vanderbilt University, Nashville,
Tennessee; and the Department of Psychology, LaSalle University,
Philadelphia, Pennsylvania, USA.
Supported by NIH/NCRR/GCRC Grant MO1-RR000056, American Heart
Association Established Investigator Award 0040149N, Arthritis
Foundation, Western PAChapter, NIH K23AR47571,American College
of Rheumatology/REF Physician Scientist DevelopmentAward, NIH K23
AR051044, and NIH/NCRR/GCRC Grant M01 RR000056.
A.H. Kao, MD, MPH; M.C.M. Wasko, MD, MSc, Division of
Rheumatology and Clinical Immunology, Department of Medicine,
University of Pittsburgh; S. Krishnaswami, MBBS, MPH, Division of
Rheumatology and Immunology, Department of Medicine, Vanderbilt
University; A. Cunningham, BS, Department of Psychology, LaSalle
University; D. Edmundowicz, MS, MD, University of Pittsburgh
Cardiovascular Institute; P.A. Morel, MD, Division of Rheumatology and
Clinical Immunology; L.H. Kuller, MD, DrPH, Department of
Epidemiology, University of Pittsburgh Graduate School of
Public Health.
Address reprint requests to Dr.A.H. Kao, S721 Biomedical Science Tower,
3500 Terrace Street, Pittsburgh, PA15261. E-mail: ahk7@pitt.edu
Accepted for publication September 10, 2007.
Rheumatoid arthritis (RA) is a chronic inflammatory disease
associated with increased morbidity and mortality from car-
diovascular events
1-4
, particularly ischemic heart disease
5
.
Patients with RA have higher prevalence and severity of sur-
rogate measures of coronary atherosclerosis compared to con-
trols
6-8
. Disease duration in RA has been reported as an inde-
pendent risk factor for myocardial infarction
9
and indicators
of subclinical atherosclerosis detected by noninvasive testing.
Specifically, the associations of arterial stiffness
7
, presence of
carotid plaque
10
, more extensive carotid plaque
11
, increased
carotid intima-media thickness
12,13
, and increase in coronary
artery calcification (CAC)
14
with increasing RA duration sug-
gest that the cumulative effect of the disease process and/or its
treatment may potentiate cardiovascular risk.
Electron-beam computed tomography (EBT) is a surrogate
measure of atherosclerosis. This noninvasive technique has a
high degree of accuracy and reproducibility and can assess the
presence and extent of CAC, reflecting calcium deposits in
atherosclerotic plaque
15,16
. CAC as measured by EBT has
been shown to be a strong predictor of subsequent coronary
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