The Journal of the Korean Rheumatism Association 2009; 16(2): 100-107
Published online June 30, 2009
© Korean College of Rheumatology
이정욱1ㆍ박영은2ㆍ조미라2ㆍ백승훈2ㆍ김근태3ㆍ이준희4ㆍ김성일2
부산성모병원 내과1, 부산대학교 의과대학 내과학교실2, 고신대학교 의과대학 내과학교실3, 춘해병원 내과4
Correspondence to : Sung-Il Kim
Objective: Rheumatoid arthritis (RA) is associated with an increased cardiovascular events. These may be related to insulin resistance (IR). We evaluated status of IR and analyzed the relationship between IR and clinical and laboratory characteristics in patients with RA. Methods: We examined 52 RA patients (43 females) and 52 age and sex matched healthy controls. We measured Homeostasis model assessment (HOMA) IR, calculated according to fasting serum glucose and insulin. Results: In patients, age was 50.8±10.2 years old, disease duration was 42.1±30.9 months. In controls, HOMA IR was 0.62±0.30 and in patients, it was 1.28±0.50. This difference was highly significant (p<0.001). Patients with early RA (disease duration is less than 36 months) were 28, and established RA (more than 36 months) were 24. HOMA IR was significantly higher in patients with established RA (1.42±0.45) than those with early RA (1.16±0.45) (p=0.03), and significantly correlated with disease duration (r=0.36, p=0.01), BMI (r=0.36, p<0.001), total cumulative prednisolon dose (r=0.34, p=0.01). Disease duration and BMI were independent predictors for HOMA IR (p<0.01, p=0.03). Conclusion: In patients with RA, IR measured by HOMA IR was more significantly increased than that of healthy control and significantly correlated with disease duration, BMI, and total cumulative prednisolon dose; however, the determinants of HOMA IR in RA patients were disease duration and BMI.
Keywords Rheumatoid arthritis, Insulin resistance, Homeostasis model assessment insulin resistance
The Journal of the Korean Rheumatism Association 2009; 16(2): 100-107
Published online June 30, 2009
Copyright © Korean College of Rheumatology.
이정욱1ㆍ박영은2ㆍ조미라2ㆍ백승훈2ㆍ김근태3ㆍ이준희4ㆍ김성일2
부산성모병원 내과1, 부산대학교 의과대학 내과학교실2, 고신대학교 의과대학 내과학교실3, 춘해병원 내과4
Joung-Wook Lee1, Young-Eun Park2, Mi-Ra Cho2, Seung-Hoon Baek2, Geun-Tae Kim3, Jun-Hee Lee4, Sung-Il Kim2
Department of Internal Medicine, Busan st. Mary's Medical Center1, Department of Internal Medicine, School of Medicine, Pusan National University2, Kosin University3, Department of Internal Medicine, Choonhae Hospital4, Busan, Korea
Correspondence to:Sung-Il Kim
Objective: Rheumatoid arthritis (RA) is associated with an increased cardiovascular events. These may be related to insulin resistance (IR). We evaluated status of IR and analyzed the relationship between IR and clinical and laboratory characteristics in patients with RA. Methods: We examined 52 RA patients (43 females) and 52 age and sex matched healthy controls. We measured Homeostasis model assessment (HOMA) IR, calculated according to fasting serum glucose and insulin. Results: In patients, age was 50.8±10.2 years old, disease duration was 42.1±30.9 months. In controls, HOMA IR was 0.62±0.30 and in patients, it was 1.28±0.50. This difference was highly significant (p<0.001). Patients with early RA (disease duration is less than 36 months) were 28, and established RA (more than 36 months) were 24. HOMA IR was significantly higher in patients with established RA (1.42±0.45) than those with early RA (1.16±0.45) (p=0.03), and significantly correlated with disease duration (r=0.36, p=0.01), BMI (r=0.36, p<0.001), total cumulative prednisolon dose (r=0.34, p=0.01). Disease duration and BMI were independent predictors for HOMA IR (p<0.01, p=0.03). Conclusion: In patients with RA, IR measured by HOMA IR was more significantly increased than that of healthy control and significantly correlated with disease duration, BMI, and total cumulative prednisolon dose; however, the determinants of HOMA IR in RA patients were disease duration and BMI.
Keywords: Rheumatoid arthritis, Insulin resistance, Homeostasis model assessment insulin resistance
Roshan Subedi, M.D., Afrah Misbah, M.D., Adnan Al Najada, M.D., Anthony James Ocon, M.D., Ph.D.
J Rheum Dis -0001; ():Hee Jun Kim, R.N., Ph.D., Ju-Yang Jung, M.D., Ph.D., Ji-Won Kim, M.D., Chang-Hee Suh, M.D., Ph.D., Hyoun-Ah Kim, M.D., Ph.D.
J Rheum Dis -0001; ():In-Woon Baek, M.D., Kyung-Su Park, M.D., Ph.D., Ki-Jo Kim, M.D., Ph.D.
J Rheum Dis -0001; ():