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维生素K2单独或与依替膦酸或利塞膦酸联合使用对类风湿性关节炎患者破骨细胞的抑制作用:2年结果

Osteoclast inhibitory effects of vitamin K2 alone or in combination with etidronate or risedronate in patients with rheumatoid arthritis: 2-year results.

作者信息

Morishita Minoru, Nagashima Masakazu, Wauke Koichi, Takahashi Hiroshi, Takenouchi Kenji

机构信息

Department of Joint Disease and Rheumatism, Nippon Medical School, Tokyo, Japan.

出版信息

J Rheumatol. 2008 Mar;35(3):407-13. Epub 2008 Feb 1.

Abstract

OBJECTIVE

To investigate the effects of vitamin K2 (Vit K2) alone or in combination with etidronate and risedronate on bone loss, osteoclast induction, and inflammation in patients with rheumatoid arthritis (RA).

METHODS

Subjects comprised 79 patients with RA who were receiving prednisolone, divided into 3 groups: Group K, Vit K2 alone; Group KE, Vit K2 plus etidronate; and Group KR, Vit K2 plus risedronate. During a 24-month treatment and followup period, levels of N-terminal telopeptide of type I collagen (NTx) and bone alkaline phosphatase were measured. Bone mineral density (BMD) of the 3 groups was measured using dual-energy x-ray absorptiometry. Damage score to fingers on radiographic findings were measured according to the Larsen method. Serum levels of receptor activator of nuclear factor-kappaB ligand (RANKL) and osteoprotegerin (OPG) were measured.

RESULTS

Falls in rate of change of BMD decreased after 18 months in groups KR and KE. Larsen damage scores indicated a significant difference between Group KE and other groups. Significant decreases in serum NTx were observed in groups KE and KR at all timepoints, but not in Group K. Levels of RANKL decreased significantly in all 3 groups.

CONCLUSION

Vit K2 alone or in combination with bisphosphonates for treatment of osteoporosis in patients with RA may inhibit osteoclast induction via decreases in levels of RANKL.

摘要

目的

研究维生素K2(Vit K2)单独使用或与依替膦酸和利塞膦酸联合使用对类风湿关节炎(RA)患者骨质流失、破骨细胞诱导和炎症的影响。

方法

研究对象包括79例正在接受泼尼松龙治疗的RA患者,分为3组:K组,单独使用Vit K2;KE组,Vit K2加依替膦酸;KR组,Vit K2加利塞膦酸。在24个月的治疗和随访期间,测量I型胶原N端肽(NTx)和骨碱性磷酸酶水平。使用双能X线吸收法测量3组的骨密度(BMD)。根据Larsen方法测量X线片上手指的损伤评分。测量血清核因子κB受体活化剂配体(RANKL)和骨保护素(OPG)水平。

结果

KR组和KE组在18个月后骨密度变化率下降。Larsen损伤评分显示KE组与其他组之间存在显著差异。KE组和KR组在所有时间点血清NTx均显著下降,但K组未下降。所有3组的RANKL水平均显著下降。

结论

Vit K2单独使用或与双膦酸盐联合使用治疗RA患者的骨质疏松症可能通过降低RANKL水平来抑制破骨细胞诱导。

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