Int J Rheum Dis. 2019;00:1–16. wileyonlinelibrary.com/journal/apl
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1 © 2019 Asia Pacific League of Associations for
Rheumatology and John Wiley & Sons Australia, Ltd
Received: 17 September 2017
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Revised: 2 June 2019
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Accepted: 5 August 2019
DOI: 10.1111/1756-185X.13685
ORIGINAL ARTICLE
Coronary artery calcium score in female rheumatoid arthritis
patients: Associations with apolipoproteins and disease
biomarkers
Miguel Bernardes
1,2
| António Madureira
2,3
| Ana Oliveira
4
| Maria João Martins
5,6
|
Raquel Lucas
7,8
| Lúcia Costa
1
| Jorge G. Pereira
4
| Francisco Ventura
9
|
Isabel Ramos
2,3
| Elisabete Martins
2,6,10
1
Department of Rheumatology, São João
Hospital Center, Porto, Portugal
2
Department of Medicine, Faculty of
Medicine, University of Porto, Porto,
Portugal
3
Department of Radiology, São João
Hospital Center, Porto, Portugal
4
Department of Nuclear Medicine, São João
Hospital Center, Porto, Portugal
5
Departamento de Biomedicina,
Unidade de Bioquímica, Faculdade de
Medicina, Universidade do Porto, Porto,
Portugal
6
Instituto de Investigação e Inovação em
Saúde (i3s), Universidade do Porto, Porto,
Portugal
7
EPI Unit-Institute of Public
Health, University of Porto, Porto, Portugal
8
Department of Clinical Epidemiology,
Predictive Medicine and Public Health,
Faculty of Medicine, University of Porto,
Porto, Portugal
9
Faculty of Medicine, University of Porto,
Porto, Portugal
10
Department of Cardiology, São João
Hospital Center, Porto, Portugal
Correspondence
Miguel Bernardes, Department of
Rheumatology, São João Hospital Center,
Porto, Portugal; Department of Medicine,
Faculty of Medicine, University of Porto,
Alameda Prof. Hernâni Monteiro, 4200-319
Porto, Portugal.
Email: mbernardes09@gmail.com
Funding information
This study was supported by Associação
Nacional de Reumatologia, Portugal.
Abstract
Aims and methods: In rheumatoid arthritis (RA), cardiovascular (CV) comorbidities
are a major cause of mortality. Coronary Calcium Score (CCS) assessed by computed
tomography has been associated with RA prognosis. In this work, we aimed to as-
sess CCS in female RA patients and determine CCS association with different clinical,
laboratory and imaging disease parameters.
Results: We evaluated 60 female patients, with a mean age of 53.6 ± 10.4 years,
a mean Disease Activity Score of 28 joints (DAS28) (4v) and Health Assessment
Questionnaire (HAQ) of 4.542 ± 1.317 and 1.488 ± 0.631, respectively, and a disease
duration of 14.7 ± 10.3 years. Mean CCS value was 35.192 ± 117.786. CCS > 10 was
significantly associated with CV risk factors (age: odds ratio [OR] = 1.120; P = .002,
body mass index [BMI] ≥ 25 kg/m
2
: OR = 0.271; P = .025, high-density lipoprotein
[HDL]: OR = 0.011; P = .025, low-density lipoprotein/ HDL ratio: OR = 2.084; P = .030,
apolipoprotein A1 [ApoA1]: OR = 0.965; P = .014, apolipoprotein B/ApoA1 [ApoB/
ApoA1] ratio: OR = 59.834; P = .011, homocysteine: OR = 1.287; P = .045, diabetes:
OR = 10.400; P = .043, and anti-diabetic therapy: OR = 10.667, P = .041), disease
parameters (C-reactive protein [CRP]: OR = 1.038; P = .046, DAS[4v]: OR = 1.900;
P = .009, DAS28[4v; CRP]: OR = 1.700; P = .019, DAS[3v]: OR = 1.947; P = .010,
DAS28[3v; CRP]: OR = 1.696; P = .022, HAQ: OR = 3.299; P = .023, erosion score:
OR = 1.015; P = .012, and total modified Sharp/van der Heijde Score: OR = 1.008;
P = .035), biomarkers (osteoprotegerin: OR = 1.505; P = .022), and bone mineral den-
sity (femoral: OR = 0.005; P = .018, lumbar spine: OR = 0.001; P = .002, left hand:
OR = 7.9 × 10
−9
; P = .005, and osteoporosis: OR = 6.628; P = .007). After adjustment
for age and BMI, significant associations were maintained with ApoA1, ApoB/ApoA1
ratio, homocysteine, CRP, DAS(4v), DAS(4v; CRP), DAS(3v) and DAS(3v; CRP). A sen-
sitivity analysis undertaken after excluding the 6 diabetics yielded similar results.
Conclusions: Our work reinforces the hypothesis that in RA, CCS may be a useful tool
in CV risk assessment, particularly valuable in poorer controlled patients with certain
lipoprotein profiles.