Lodewyckx Liesbet, Lories Rik J U
Department of Musculoskeletal Sciences, Division of Rheumatology, Laboratory for Skeletal Development and Joint Disorders, Katholieke Universiteit Leuven, Leuven, Belgium.
Curr Rheumatol Rep. 2009 Feb;11(1):23-30. doi: 10.1007/s11926-009-0004-6.
Osteoporosis and osteoarthritis are common musculoskeletal disorders in which cause and outcome are determined by genetic and environmental factors. The WNT signaling pathway plays an important role in skeletal development and growth. Polymorphisms in a number of genes that belong to this pathway are associated with osteoarthritis and/or osteoporosis. This suggests a role for this molecular signaling pathway in postnatal joint and bone homeostasis and pathology. Increased activity of WNT signaling strengthens the bone but may have adverse effects on the articular cartilage. Frizzled related protein (FRZB) plays a role in both bone and cartilage. Better understanding of the WNT pathway and its modulators may lead to specific therapeutics for both osteoarthritis and osteoporosis. This review focuses on recent studies in human genetics and animal models and highlights the potential clinical relevance of this rapidly evolving field of research.
骨质疏松症和骨关节炎是常见的肌肉骨骼疾病,其病因和后果由遗传和环境因素决定。WNT信号通路在骨骼发育和生长中起重要作用。属于该通路的许多基因中的多态性与骨关节炎和/或骨质疏松症相关。这表明该分子信号通路在出生后关节和骨骼稳态及病理过程中发挥作用。WNT信号活性增加可增强骨骼,但可能对关节软骨产生不利影响。卷曲相关蛋白(FRZB)在骨骼和软骨中均起作用。更好地理解WNT通路及其调节剂可能会带来针对骨关节炎和骨质疏松症的特异性疗法。本综述重点关注人类遗传学和动物模型的最新研究,并强调了这一快速发展的研究领域的潜在临床相关性。