Krela-Kaźmierczak Iwona, Szymczak-Tomczak Aleksandra, Łykowska-Szuber Liliana, Wysocka Ewa, Michalak Michał, Stawczyk-Eder Kamila, Waszak Katarzyna, Linke Krzysztof, Eder Piotr
Department of Gastroenterology, Dietetics and Internal Medicine, Poznan University of Medical Sciences, Poland.
Department of Laboratory Diagnostics, Poznan University of Medical Sciences, Poland.
Adv Clin Exp Med. 2018 Apr;27(4):449-453. doi: 10.17219/acem/75675.
Cytokines are mediators of inflammatory processes in the course of inflammatory bowel disease (IBD) and participate in the bone metabolism. Interleukin 6 (IL-6) initiates osteoclastogenesis by modulating the activity of soluble receptor activator of nuclear factor kappa B ligand (sRANKL) and osteoprotegerin.
The aim of the study was to evaluate bone mineral density (BMD) by densitometry and the concentration of interleukin 6, osteoprotegerin (OPG) and sRANKL protein (sRANKL) by ELISA in patients with IBD in relation to the control group; to assess the relationship between IL-6, OPG, sRANKL and BMD; and to assess the impact of disease duration and number hospitalization on BMD.
The studied group included 37 patients with Crohn's disease (I - CD), 37 patients with ulcerative colitis (II - UC) and 37 healthy subjects - control group (III - CG).
The prevalence of osteoporosis and osteopenia was as follows: in I - CD, 18.92% and 32.43% in L2-L4; 13.51% and 35.13% in the neck, and in II - UC, 2.7% and 37.84% in L2-L4; 2.7%, and 29.73% in the femoral neck. The concentration of IL-6 correlated negatively with T-scores in the neck for the whole group, and in group I - CD, there was a significant positive correlation between serum OPG and IL-6.
The incidence of osteopenia and osteoporosis in patients with IBD is high and increases with the duration of the disease and the number of hospitalizations. Patients with CD are at a higher risk of skeletal pathology than patients with UC. IL-6 can modulate bone mineral density in the femoral neck especially in the course of CD.
细胞因子是炎症性肠病(IBD)炎症过程的介质,并参与骨代谢。白细胞介素6(IL-6)通过调节核因子κB配体可溶性受体激活剂(sRANKL)和骨保护素的活性来启动破骨细胞生成。
本研究旨在通过骨密度测定评估IBD患者的骨矿物质密度(BMD),并通过酶联免疫吸附测定(ELISA)评估IL-6、骨保护素(OPG)和sRANKL蛋白(sRANKL)的浓度,与对照组进行比较;评估IL-6、OPG、sRANKL与BMD之间的关系;评估疾病持续时间和住院次数对BMD的影响。
研究组包括37例克罗恩病患者(I - CD)、37例溃疡性结肠炎患者(II - UC)和37例健康受试者——对照组(III - CG)。
骨质疏松症和骨质减少症的患病率如下:在I - CD组中,L2-L4椎体分别为18.92%和32.43%;股骨颈分别为13.51%和35.13%。在II - UC组中,L2-L4椎体分别为2.7%和37.84%;股骨颈分别为2.7%和29.73%。IL-6浓度与全组股骨颈T值呈负相关,在I - CD组中,血清OPG与IL-6之间存在显著正相关。
IBD患者骨质减少症和骨质疏松症的发生率较高,且随着疾病持续时间和住院次数的增加而升高。CD患者比UC患者发生骨骼病变的风险更高。IL-6可调节股骨颈的骨矿物质密度,尤其是在CD病程中。