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肥胖可能会保护接受肿瘤坏死因子抑制剂治疗的类风湿关节炎患者的系统性骨质流失。

Obesity potentially protects against systemic bone loss in patients with rheumatoid arthritis treated with tumour necrosis factor inhibitors.

机构信息

Division of Rheumatology, College of Medicine, Inha University, Incheon, Republic of Korea.

Occupational and Environmental Medicine, College of Medicine, Inha University, Incheon, Republic of Korea.

出版信息

Clin Exp Rheumatol. 2021 Jan-Feb;39(1):125-131. doi: 10.55563/clinexprheumatol/j6zhfm. Epub 2020 Apr 9.

DOI:10.55563/clinexprheumatol/j6zhfm
PMID:32301429
Abstract

OBJECTIVES

We aimed to investigate how systemic bone metabolism was affected after 1 year of treatment with tumour necrosis factor (TNF) inhibitors in rheumatoid arthritis (RA) patients.

METHODS

A total of 29 seropositive RA patients not treated for osteoporosis were enrolled and TNF inhibitors were administered for a year. Bone mineral density (BMD) at the lumbar spine, femur neck, and total hip was measured at baseline and 12 months after anti-TNF treatment. Blood samples were collected at baseline and 6 and 12 months after anti-TNF treatment and osteoclasts were cultured on bone slices. Weight was the strongest factor influencing systemic bone loss. Patients were categorised into two groups: obese (body mass index (BMI) ≥25 kg/m2) and non-obese (BMI <25 kg/m2).

RESULTS

All patients showed decreased BMD at all sites. The obese group showed relatively little change in BMD, although the non-obese group showed significant decreases in BMD at all sites after 1 year of treatment with TNF inhibitors. Resorption pits created by osteoclasts decreased at 6 months and increased at 12 months in the non-obese group, while the obese group presented with steadily decreasing sizes of resorption pits at all-time points. Levels of receptor activator of nuclear factor kappa B ligand were significantly decreased at 12 months compared to baseline in the obese group, while they were increased in the non-obese group.

CONCLUSIONS

One year of treatment with TNF inhibitors failed to halt systemic bone loss in RA patients, but obesity may have protective effects against bone loss.

摘要

目的

我们旨在研究类风湿关节炎(RA)患者接受肿瘤坏死因子(TNF)抑制剂治疗 1 年后全身骨代谢的变化。

方法

共纳入 29 例未经骨质疏松治疗的血清阳性 RA 患者,并接受 TNF 抑制剂治疗 1 年。在基线和抗 TNF 治疗 12 个月时测量腰椎、股骨颈和全髋关节的骨密度(BMD)。在基线和抗 TNF 治疗 6 个月和 12 个月时采集血样,并在骨切片上培养破骨细胞。体重是影响全身骨丢失的最强因素。患者分为两组:肥胖组(BMI≥25 kg/m2)和非肥胖组(BMI<25 kg/m2)。

结果

所有患者的所有部位 BMD 均降低。肥胖组 BMD 变化相对较小,而非肥胖组在接受 TNF 抑制剂治疗 1 年后所有部位的 BMD 均显著降低。在非肥胖组中,破骨细胞形成的吸收窝在 6 个月时减少,12 个月时增加,而肥胖组在所有时间点的吸收窝大小均呈持续减小趋势。与基线相比,肥胖组在 12 个月时的核因子κB 受体激活物配体水平显著降低,而非肥胖组则升高。

结论

TNF 抑制剂治疗 1 年未能阻止 RA 患者的全身骨丢失,但肥胖可能对骨丢失具有保护作用。

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