Ratajczak-Pawłowska Alicja Ewa, Szymczak-Tomczak Aleksandra, Hryhorowicz Szymon, Zawada Agnieszka, Skoracka Kinga, Rychter Anna Maria, Skrzypczak-Zielińska Marzena, Słomski Ryszard, Dobrowolska Agnieszka, Krela-Kaźmierczak Iwona
Department of Gastroenterology, Dietetics and Internal Diseases, Poznan University of Medical Sciences, Poznan, Poland.
Laboratory of Nutrigenetics, Department of Gastroenterology, Dietetics and Internal Diseases, Poznan University of Medical Sciences, Poznan, Poland.
Front Immunol. 2025 Mar 18;16:1533955. doi: 10.3389/fimmu.2025.1533955. eCollection 2025.
Inflammatory bowel disease (IBD) is an increasingly prevalent condition in developed countries. Alongside the growing number of patients, there is a rising incidence of disease-related complications, including osteoporosis. While well-established risk factors for low bone mineral density in IBD-such as low body mass or steroid therapy-are widely recognized, other contributing factors warrant further investigation. One such factor is visfatin, a proinflammatory adipokine encoded by the gene.
This review aimed to explore the association between visfatin level, bone health, and obesity among patients with inflammatory bowel disease.
Although visfatin is primarily associated with metabolic syndrome, it may also influence bone mineral density by affecting osteoblast and osteoclast differentiation and function. Additionally, some studies have identified a correlation between visfatin levels and bone mineral density. A deeper understanding of visfatin's role in osteoporosis development may contribute to the identification of novel therapeutic strategies. Therefore, lower bone mineral density in inflammatory bowel disease may be associated with obesity and visfatin levels. However, visfatin concentrations depend on many factors, including genetics, immunology, and nutritional factors, which may affect visfatin levels.
Current research highlights visfatin as both a potential biomarker and a therapeutic target for osteoporosis treatment. Nevertheless, limited studies have specifically examined the relationship between visfatin and bone mineral density in IBD. Further research is required to clarify this association and to explore how variations in visfatin levels impact bone density in IBD patients.
炎症性肠病(IBD)在发达国家的患病率日益上升。随着患者数量的增加,包括骨质疏松症在内的疾病相关并发症的发生率也在上升。虽然IBD中公认的低骨矿物质密度风险因素,如低体重或类固醇治疗,已广为人知,但其他促成因素仍需进一步研究。内脂素就是这样一个因素,它是一种由 基因编码的促炎脂肪因子。
本综述旨在探讨炎症性肠病患者内脂素水平、骨骼健康与肥胖之间的关联。
虽然内脂素主要与代谢综合征相关,但它也可能通过影响成骨细胞和破骨细胞的分化及功能来影响骨矿物质密度。此外,一些研究已经确定了内脂素水平与骨矿物质密度之间的相关性。更深入地了解内脂素在骨质疏松症发展中的作用可能有助于确定新的治疗策略。因此,炎症性肠病中较低的骨矿物质密度可能与肥胖和内脂素水平有关。然而,内脂素浓度取决于许多因素,包括遗传学、免疫学和营养因素,这些因素可能会影响内脂素水平。
目前的研究强调内脂素既是骨质疏松症治疗的潜在生物标志物,也是治疗靶点。然而,仅有有限的研究专门探讨了IBD中内脂素与骨矿物质密度之间的关系。需要进一步的研究来阐明这种关联,并探索内脂素水平的变化如何影响IBD患者的骨密度。