Table of Contents Author Guidelines Submit a Manuscript
BioMed Research International
Volume 2016, Article ID 7870925, 7 pages
http://dx.doi.org/10.1155/2016/7870925
Research Article

Serum Heme Oxygenase-1 and BMP-7 Are Potential Biomarkers for Bone Metabolism in Patients with Rheumatoid Arthritis and Ankylosing Spondylitis

1Department of Rheumatology and Immunology, West China Hospital, Sichuan University, Chengdu 610041, China
2Department of Health Statistics, West China School of Public Health, Sichuan University, Chengdu 610041, China
3Division of Allergy, Immunology and Rheumatology, Chung Shan Medical University Hospital, Taichung 40201, Taiwan
4Institute of Medicine, Chung Shan Medical University, Taichung 40201, Taiwan
5Institute of Integrative Medicine, China Medical University, Taichung 40201, Taiwan
6Department of Internal Medicine 3, University of Erlangen-Nuremberg, 91054 Erlangen, Germany

Received 12 April 2016; Revised 4 May 2016; Accepted 5 May 2016

Academic Editor: Hai-Feng Pan

Copyright © 2016 Tong-ling Yuan et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Backgrounds. Heme oxygenase-1 (HO-1) has been reported to play a regulatory role in osteoclastogenesis. Bone morphogenetic protein (BMP) pathways induce osteoblastic differentiation and bone remodeling. Aims. To identify serum levels of HO-1, BMP-7, and Runt related-transcription factor 2 (Runx2) in patients with rheumatoid arthritis (RA) and ankylosing spondylitis (AS) and to investigate the relationships between HO-1, BMP-7, Runx2, and other common biomarkers for bone metabolism. Results. Serum levels of HO-1 and BMP-7 were revealed to be significantly higher in patients with RA or AS than in healthy controls (). In RA group, HO-1 was positively correlated with BMP-7, Runx2, and tartrate-resistant acid phosphatase-5b (TRAP-5b) (, resp.), BMP-7 was positively correlated with Runx2 and TRAP-5b (, resp.), and Runx2 was negatively correlated with N-terminal midfragment of osteocalcin (NMID) (). In AS group, we observed identical correlation between HO-1 and BMP-7, but opposite correlations between BMP-7 and TRAP-5b and between Runx2 and NMID, when comparing with the RA cohort. Conclusion. Our findings suggest that HO-1 and BMP-7 are potential biomarkers for bone metabolism in patients with RA and AS. The different correlations between the bone markers point to distinct differences in bone remodeling pathways in the two types of arthritis.