J Rheum Dis 2012; 19(1): 30-38
Published online February 29, 2012
© Korean College of Rheumatology
김지훈1ㆍ강종완1ㆍ김나리1ㆍ배기범1ㆍ이수곤2ㆍ임철현1ㆍ남언정1ㆍ강영모1
경북대학교 의학전문대학원 류마티스내과학교실1, 연세대학교 의과대학 류마티스내과학교실2
Correspondence to : Young Mo Kang
Objective. This study sought to investigate independent predictive factors for subclinical atherosclerosis in Korean patients with rheumatoid arthritis (RA).
Methods. We used high-resolution B-mode ultrasonography to measure the carotid artery intima-media thickness (IMT) and carotid plaque in 367 patients with RA. Detailed information on the demographic characteristics, cardiovascular (CV) risk factors, and RA disease characteristics were collected on all subjects. The relationship of the carotid artery IMT and carotid plaque to relevant clinical and laboratory variables were examined.
Results. Old age and male sex had the most significant association with increased IMT and presence of plaque than other factors. Erythrocyte sedimentation rate (ESR), C-reactive protein (CRP), and mKHAQ (Korean version of modified health assessment questionnaire) were significantly associated with both increased IMT and presence of plaque after univariate analysis adjusting for age and sex. A multivariable logistic regression analysis revealed that ESR and TJC68 were independent factors associated with the presence of plaque (p<0.001 and p=0.019, respectively). There was a significant linear correlation between the number of plaques and ESR (p<0.001 and R2=0.07).
Conclusion. Our results indicated that markers of systemic inflammation contributed significantly to subclinical atherosclerosis in patients with RA. We emphasize the need for aggressive control of RA disease activity in patients who persistently demonstrate highly elevated ESR levels.
Keywords Rheumatoid arthritis, Atherosclerosis, Cardiovascular disease, Inflammation, Erythrocyte sedimentation rate
J Rheum Dis 2012; 19(1): 30-38
Published online February 29, 2012
Copyright © Korean College of Rheumatology.
김지훈1ㆍ강종완1ㆍ김나리1ㆍ배기범1ㆍ이수곤2ㆍ임철현1ㆍ남언정1ㆍ강영모1
경북대학교 의학전문대학원 류마티스내과학교실1, 연세대학교 의과대학 류마티스내과학교실2
Ji Hun Kim1, Jong Wan Kang1, Na Ri Kim1, Gi Bum Bae1, Soo-Kon Lee2, Churl Hyun Im1, Eon Jeong Nam1, Young Mo Kang1
Division of Rheumatology, Department of Internal Medicine, Kyungpook National University School of Medicine1, Daegu, Yonsei University College of Medicine2, Seoul, Korea
Correspondence to:Young Mo Kang
Objective. This study sought to investigate independent predictive factors for subclinical atherosclerosis in Korean patients with rheumatoid arthritis (RA).
Methods. We used high-resolution B-mode ultrasonography to measure the carotid artery intima-media thickness (IMT) and carotid plaque in 367 patients with RA. Detailed information on the demographic characteristics, cardiovascular (CV) risk factors, and RA disease characteristics were collected on all subjects. The relationship of the carotid artery IMT and carotid plaque to relevant clinical and laboratory variables were examined.
Results. Old age and male sex had the most significant association with increased IMT and presence of plaque than other factors. Erythrocyte sedimentation rate (ESR), C-reactive protein (CRP), and mKHAQ (Korean version of modified health assessment questionnaire) were significantly associated with both increased IMT and presence of plaque after univariate analysis adjusting for age and sex. A multivariable logistic regression analysis revealed that ESR and TJC68 were independent factors associated with the presence of plaque (p<0.001 and p=0.019, respectively). There was a significant linear correlation between the number of plaques and ESR (p<0.001 and R2=0.07).
Conclusion. Our results indicated that markers of systemic inflammation contributed significantly to subclinical atherosclerosis in patients with RA. We emphasize the need for aggressive control of RA disease activity in patients who persistently demonstrate highly elevated ESR levels.
Keywords: Rheumatoid arthritis, Atherosclerosis, Cardiovascular disease, Inflammation, Erythrocyte sedimentation rate
Yong-Beom Park, M.D., Soo-Kon Lee, M.D.
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