Insights and implications of sexual dimorphism in osteoporosis
Yuan-Yuan Zhang,
Na Xie,
Xiao-Dong Sun,
Edouard C. Nice,
Yih-Cherng Liou,
Canhua Huang,
Huili Zhu,
Zhisen Shen
Affiliations
Yuan-Yuan Zhang
Key Laboratory of Drug-Targeting and Drug Delivery System of the Education Ministry and Sichuan Province, Sichuan Research Center for Drug Precision Industrial Technology, West China School of Pharmacy, Sichuan University
Na Xie
West China School of Basic Medical Sciences & Forensic Medicine, Sichuan University
Xiao-Dong Sun
West China School of Basic Medical Sciences & Forensic Medicine, Sichuan University
Edouard C. Nice
Department of Biochemistry and Molecular Biology, Monash University
Yih-Cherng Liou
Department of Biological Sciences, Faculty of Science, National University of Singapore
Canhua Huang
Department of Biotherapy, Cancer Center and State Key Laboratory of Biotherapy, West China Hospital, and West China School of Basic Medical Sciences & Forensic Medicine, Sichuan University
Huili Zhu
Key Laboratory of Birth Defects and Related Diseases of Women and Children of Ministry of Education, Department of Reproductive Medicine, West China Second University Hospital of Sichuan University
Zhisen Shen
Department of Otorhinolaryngology and Head and Neck Surgery, The Affiliated Lihuili Hospital, Ningbo University
Abstract Osteoporosis, a metabolic bone disease characterized by low bone mineral density and deterioration of bone microarchitecture, has led to a high risk of fatal osteoporotic fractures worldwide. Accumulating evidence has revealed that sexual dimorphism is a notable feature of osteoporosis, with sex-specific differences in epidemiology and pathogenesis. Specifically, females are more susceptible than males to osteoporosis, while males are more prone to disability or death from the disease. To date, sex chromosome abnormalities and steroid hormones have been proven to contribute greatly to sexual dimorphism in osteoporosis by regulating the functions of bone cells. Understanding the sex-specific differences in osteoporosis and its related complications is essential for improving treatment strategies tailored to women and men. This literature review focuses on the mechanisms underlying sexual dimorphism in osteoporosis, mainly in a population of aging patients, chronic glucocorticoid administration, and diabetes. Moreover, we highlight the implications of sexual dimorphism for developing therapeutics and preventive strategies and screening approaches tailored to women and men. Additionally, the challenges in translating bench research to bedside treatments and future directions to overcome these obstacles will be discussed.