Original

The Journal of the Korean Rheumatism Association 2006; 13(4): 299-305

Published online December 30, 2006

© Korean College of Rheumatology

아포지단백 E 유전자 다형성이 폐경 후 여성 류마티스관절염 환자의 골밀도에 미치는 영향

이상일·박진용·오수진*·나영균*·정치량*·최영훈*·윤희진*·류완희*

경상대학교 의과대학 내과학교실 건강과학연구원, 전북대학교 의과대학 내과학교실 임상의학연구소*

The Impact of Apolipoprotein E Genetic Polymorphism on Bone Mineral Density in Postmenopausal Women with Rheumatoid Arthritis

Sang-Il Lee, M.D., Jin-Yong Park, M.D., Su Jin Oh, M.D.*, Young Gyun Na, M.D.*, Chi Ryang Chung, M.D.*, Young Hun Choi, M.D.*, Hee Jin Yun*, Wan Hee Yoo, M.D.*

Department of Internal Medicine and Institute of Health Science, Gyeongsang National University College of Medicine, Jinju, Department of Internal Medicine and Research Institute of Clinical Medicine, Chonbuk National University Medical School*, Jeonju, Korea

Correspondence to : Wan Hee Yoo

Abstract

Objective: To evaluate the relationship between the presence of apolipoprotein E (Apo E) 4 allele and bone mineral density (BMD) and severity of joint destruction in postmenopausal women with rheumatoid arthritis (RA). Methods: Apo E genotypes were analyzed in 113 postmenopausal women who were first diagnosed with RA and had not receiving antiresorptive therapy for osteoporosis at the time of enrollment. BMD was measured using dual-energy X-ray absorptiometry (DEXA), and joint destruction was evaluated on plain radiographs according to 'Larsen score'. The differences in BMD and severity of joint destruction in groups with and without an Apo E4 allele were analyzed in 94 patients with clinical information available. Results: BMD (g/cm2) of the lumbar spine in the Apo E4 (⁣) group was 0.94⁑0.16 (n=67), whereas that in the Apo E4 (⁢) group was 0.87⁑0.14 (n=27; p=0.049). BMD of the femoral neck and great trochanter in the Apo E4 (⁣) group was 0.74⁑0.12 and 0.63⁑0.11, while that in the Apo E4 (⁢) group was 0.68⁑0.11 (p=0.039) and 0.57⁑0.11 (p=0.008). However, there were no significant differences in Larsen scores and erosive disease (%) between the Apo E4 (⁢) and Apo E4 (⁣) groups. Conclusion: The Apo E4 allele is associated with a reduced bone mass in postmenopausal RA patients. Therefore, Apo E4 allele is considered to be an independent risk factor for generalized osteoporosis in postmenopausal RA patients.

Keywords Rheumatoid arthritis, Apolipoprotein E, Osteoporosis

Article

Original

The Journal of the Korean Rheumatism Association 2006; 13(4): 299-305

Published online December 30, 2006

Copyright © Korean College of Rheumatology.

아포지단백 E 유전자 다형성이 폐경 후 여성 류마티스관절염 환자의 골밀도에 미치는 영향

이상일·박진용·오수진*·나영균*·정치량*·최영훈*·윤희진*·류완희*

경상대학교 의과대학 내과학교실 건강과학연구원, 전북대학교 의과대학 내과학교실 임상의학연구소*

The Impact of Apolipoprotein E Genetic Polymorphism on Bone Mineral Density in Postmenopausal Women with Rheumatoid Arthritis

Sang-Il Lee, M.D., Jin-Yong Park, M.D., Su Jin Oh, M.D.*, Young Gyun Na, M.D.*, Chi Ryang Chung, M.D.*, Young Hun Choi, M.D.*, Hee Jin Yun*, Wan Hee Yoo, M.D.*

Department of Internal Medicine and Institute of Health Science, Gyeongsang National University College of Medicine, Jinju, Department of Internal Medicine and Research Institute of Clinical Medicine, Chonbuk National University Medical School*, Jeonju, Korea

Correspondence to:Wan Hee Yoo

Abstract

Objective: To evaluate the relationship between the presence of apolipoprotein E (Apo E) 4 allele and bone mineral density (BMD) and severity of joint destruction in postmenopausal women with rheumatoid arthritis (RA). Methods: Apo E genotypes were analyzed in 113 postmenopausal women who were first diagnosed with RA and had not receiving antiresorptive therapy for osteoporosis at the time of enrollment. BMD was measured using dual-energy X-ray absorptiometry (DEXA), and joint destruction was evaluated on plain radiographs according to 'Larsen score'. The differences in BMD and severity of joint destruction in groups with and without an Apo E4 allele were analyzed in 94 patients with clinical information available. Results: BMD (g/cm2) of the lumbar spine in the Apo E4 (⁣) group was 0.94⁑0.16 (n=67), whereas that in the Apo E4 (⁢) group was 0.87⁑0.14 (n=27; p=0.049). BMD of the femoral neck and great trochanter in the Apo E4 (⁣) group was 0.74⁑0.12 and 0.63⁑0.11, while that in the Apo E4 (⁢) group was 0.68⁑0.11 (p=0.039) and 0.57⁑0.11 (p=0.008). However, there were no significant differences in Larsen scores and erosive disease (%) between the Apo E4 (⁢) and Apo E4 (⁣) groups. Conclusion: The Apo E4 allele is associated with a reduced bone mass in postmenopausal RA patients. Therefore, Apo E4 allele is considered to be an independent risk factor for generalized osteoporosis in postmenopausal RA patients.

Keywords: Rheumatoid arthritis, Apolipoprotein E, Osteoporosis

JRD
Oct 01, 2024 Vol.31 No.4, pp. 191~263
COVER PICTURE
Ancestry-driven pathways for SLE-risk SNP-associated genes. The ancestry-driven key signaling pathways in Asians, Europeans, and African Americans were analyzed by enrichr (https://maayanlab.cloud/Enrichr/#libraries) using non-HLA SNP-associated genes. SLE: systemic lupus erythematosus, SNP: single-nucleotide polymorphism, JAK–STAT: janus kinase–signal transducers and activators of transcription, IFN: interferon gamma. (J Rheum Dis 2024;31:200-211)

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