Abstract

This exploratory study aimed to examine the impact of abatacept treatment on bone structure in patients with rheumatoid arthritis (RA) using high-resolution peripheral quantitative computed tomography (HR-pQCT). RA patients initiating either abatacept or newly introduced csDMARDs were enrolled in this prospective, non-randomized, two-group study. Bone structure in the 2nd and 3rd metacarpal heads was assessed using HR-pQCT at 0, 6, and 12 months after enrollment. Synovitis was evaluated using musculoskeletal ultrasound and MRI. The adjusted mean between-group differences (abatacept–csDMARDs group) were estimated using a mixed-effect model. Thirty-five patients (abatacept group: n = 15; csDMARDs group: n = 20) were analyzed. Changes in erosion volume, depth and width were numerically smaller in the abatacept group compared to the csDMARDs group (adjusted mean between-group differences: − 1.86 mm3, − 0.02 mm, and − 0.09 mm, respectively). Over a 12-month period, 5 erosions emerged in the csDMARDs group, while only 1 erosion appeared in the abatacept group. Compared to csDMARDs, abatacept better preserved bone microarchitecture; several components of bone microarchitecture were significantly worsened at 6 months in the csDMARDs group, but were not deteriorated at 6 months in the abatacept group. Changes in synovitis scores were similar between the two treatment groups. Our results indicate that abatacept prevented the progression of bone erosion including new occurrence, and also prevented worsening of bone strength independently with synovitis compared to csDMARDs including MTX. Thus, abatacept treatment may provide benefits not only in inhibiting the progress of bone erosion but also in preventing bone microarchitectural deterioration.

Details

Title
Preferable effect of CTLA4-Ig on both bone erosion and bone microarchitecture in rheumatoid arthritis revealed by HR-pQCT
Author
Iwamoto, Naoki 1 ; Chiba, Ko 2 ; Sato, Shuntaro 3 ; Tashiro, Shigeki 3 ; Shiraishi, Kazuteru 2 ; Watanabe, Kounosuke 2 ; Ohki, Nozomi 4 ; Okada, Akitomo 5 ; Koga, Tomohiro 1 ; Kawashiri, Shin-ya 6 ; Tamai, Mami 1 ; Osaki, Makoto 2 ; Kawakami, Atsushi 1 

 Nagasaki University Graduate School of Biomedical Sciences, Division of Advanced Preventive Medical Sciences, Department of Immunology and Rheumatology, Nagasaki, Japan (GRID:grid.174567.6) (ISNI:0000 0000 8902 2273) 
 Nagasaki University Graduate School of Biomedical Sciences, Department of Orthopedic Surgery, Nagasaki, Japan (GRID:grid.174567.6) (ISNI:0000 0000 8902 2273) 
 Nagasaki University Hospital, Clinical Research Center, Nagasaki, Japan (GRID:grid.411873.8) (ISNI:0000 0004 0616 1585) 
 Nagasaki University Graduate School of Biomedical Sciences, Department of Radiological Sciences, Nagasaki, Japan (GRID:grid.174567.6) (ISNI:0000 0000 8902 2273) 
 National Hospital Organization Nagasaki Medical Center, Department of Rheumatology, Omura, Japan (GRID:grid.415640.2) 
 Nagasaki University Graduate School of Biomedical Sciences, Division of Advanced Preventive Medical Sciences, Department of Immunology and Rheumatology, Nagasaki, Japan (GRID:grid.174567.6) (ISNI:0000 0000 8902 2273); Nagasaki University Institute of Biomedical Sciences, Center for Collaborative Medical Education and Development, Nagasaki, Japan (GRID:grid.174567.6) (ISNI:0000 0000 8902 2273) 
Pages
27673
Publication year
2024
Publication date
2024
Publisher
Nature Publishing Group
e-ISSN
20452322
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
3127428809
Copyright
© The Author(s) 2024. This work is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.