TY - JOUR
T1 - Bone phenotypes in rheumatology - there is more to bone than just bone
AU - Thudium, Christian S
AU - Nielsen, Signe Holm
AU - Sardar, Samra
AU - Mobasheri, Ali
AU - van Spil, Willem Evert
AU - Lories, Rik
AU - Henriksen, Kim
AU - Bay-Jensen, Anne-Christine
AU - Karsdal, Morten A
N1 - Publisher Copyright:
© 2020, The Author(s).
PY - 2020/12
Y1 - 2020/12
N2 - Osteoarthritis, rheumatoid arthritis, psoriatic arthritis, and ankylosing spondylitis, all have one clear common denominator; an altered turnover of bone. However, this may be more complex than a simple change in bone matrix and mineral turnover. While these diseases share a common tissue axis, their manifestations in the area of pathology are highly diverse, ranging from sclerosis to erosion of bone in different regions. The management of these diseases will benefit from a deeper understanding of the local versus systemic effects, the relation to the equilibrium of the bone balance (i.e., bone formation versus bone resorption), and the physiological and pathophysiological phenotypes of the cells involved (e.g., osteoblasts, osteoclasts, osteocytes and chondrocytes). For example, the process of endochondral bone formation in chondrocytes occurs exists during skeletal development and healthy conditions, but also in pathological conditions. This review focuses on the complex molecular and cellular taxonomy of bone in the context of rheumatological diseases that alter bone matrix composition and maintenance, giving rise to different bone turnover phenotypes, and how biomarkers (biochemical markers) can be applied to potentially describe specific bone phenotypic tissue profiles.
AB - Osteoarthritis, rheumatoid arthritis, psoriatic arthritis, and ankylosing spondylitis, all have one clear common denominator; an altered turnover of bone. However, this may be more complex than a simple change in bone matrix and mineral turnover. While these diseases share a common tissue axis, their manifestations in the area of pathology are highly diverse, ranging from sclerosis to erosion of bone in different regions. The management of these diseases will benefit from a deeper understanding of the local versus systemic effects, the relation to the equilibrium of the bone balance (i.e., bone formation versus bone resorption), and the physiological and pathophysiological phenotypes of the cells involved (e.g., osteoblasts, osteoclasts, osteocytes and chondrocytes). For example, the process of endochondral bone formation in chondrocytes occurs exists during skeletal development and healthy conditions, but also in pathological conditions. This review focuses on the complex molecular and cellular taxonomy of bone in the context of rheumatological diseases that alter bone matrix composition and maintenance, giving rise to different bone turnover phenotypes, and how biomarkers (biochemical markers) can be applied to potentially describe specific bone phenotypic tissue profiles.
KW - Ankylosing spondylitis
KW - Biochemical marker
KW - Biomarker
KW - Bone
KW - Endochondral
KW - Endotype
KW - Matrix
KW - Osteoarthritis
KW - Phenotype
KW - Psoriatic arthritis
KW - Remodeling
KW - Rheumatoid arthritis
KW - Therapeutic
UR - http://www.scopus.com/inward/record.url?scp=85096848777&partnerID=8YFLogxK
U2 - 10.1186/s12891-020-03804-2
DO - 10.1186/s12891-020-03804-2
M3 - Review article
C2 - 33248451
SN - 1471-2474
VL - 21
JO - BMC Musculoskeletal Disorders
JF - BMC Musculoskeletal Disorders
IS - 1
M1 - 789
ER -