单位:[1]Fudan Univ, Shanghai Hua Dong Hosp, Ctr Osteoporosis, Shanghai 200433, Peoples R China[2]Shanghai Jiao Tong Univ, People Hosp 9, Dept Orthoped, Shanghai 200030, Peoples R China[3]Jilin Univ, Dept Orthoped, Hosp 1, Changchun 130023, Ji Lin Province, Peoples R China[4]Capital Med Univ, Beijing Sino Japan Friendship Hosp, Beijing, Peoples R China[5]Chinese Univ Hong Kong, Dept Orthopaed & Traumatol, Hong Kong, Hong Kong, Peoples R China[6]INSERM, Res Unit 664, F-69008 Lyon, France[7]Synarc Clin Res Ctr, San Francisco, CA USA[8]Ji Nan Univ, Inst Tradit Chinese Med & Nat Prod, Guangzhou, Guangdong, Peoples R China[9]Chinese Acad Sci, Translat Med Res & Dev Ctr, Inst Biomed & Hlth Engn, Shenzhen Inst Adv Technol, Shenzhen, Peoples R China[10]Synarc Clin Res Ctr, Stanford, CA 94305 USA[11]Synarc Biochem Marker Div, Lyon, France
This multicenter and randomized clinical trial showed that daily oral herbal formula Xian Ling Gu Bao (XLGB) was safe in postmenopausal women over a 1-year treatment. Those patients (n similar to aEuro parts per thousand 50) treated with XLGB at the conventional dose demonstrated a statistically significant increase in dual-energy X-ray absorptiometry (DXA) bone mineral density (BMD) at lumbar spine at 6 months and a numerically increased BMD at 12 months. The aim of this study was to examine the safety and efficacy of a herbal formula XLGB in postmenopausal women (ChiCTR-TRC-00000347). One hundred eighty healthy postmenopausal women (a parts per thousand yen60 years old) with BMD T-score a parts per thousand currency signaEuro parts per thousand a'2.0 (lumbar spine or femoral neck) were recruited from four clinical centers to receive low-dose (conventional dose) XLGB (L-XLGB group, 3 g/day, n = 61) or high-dose XLGB (H-XLGB group, 6 g/day, n = 58) or placebo (CON group, n = 61). Women received daily calcium (500 mg) and vitamin D (200 IU) supplementation. Primary endpoints were lumbar spine BMD and safety; secondary endpoints were femoral neck BMD and bone turnover markers measured at baseline and at 6 and 12 months. Of 180 women recruited, 148 completed the study. The compliance in each group was comparable. Prominent adverse events were not observed in either group. In the L-XLGB group at 6 months, lumbar spine BMD by DXA increased significantly from baseline (+2.11% versus CON +0.58%, p < 0.05), but femoral neck BMD did not; at 12 months, BMD in the L-XLGB group decreased from 6-month levels yet remained higher than baseline, but without difference from the CON group. There was no dose-dependent response. Bone turnover marker levels declined during the first 6 months after XLGB treatment. There was no significant difference in the overall incidence of side effects among treatment and control groups. XLGB over 1-year treatment at the conventional dose demonstrated safe and only a statistically significant increase in BMD at lumbar spine at 6 months in postmenopausal women.
第一作者单位:[1]Fudan Univ, Shanghai Hua Dong Hosp, Ctr Osteoporosis, Shanghai 200433, Peoples R China
通讯作者:
推荐引用方式(GB/T 7714):
Zhu H. M.,Qin L.,Garnero P.,et al.The first multicenter and randomized clinical trial of herbal Fufang for treatment of postmenopausal osteoporosis[J].OSTEOPOROSIS INTERNATIONAL.2012,23(4):1317-1327.doi:10.1007/s00198-011-1577-2.
APA:
Zhu, H. M.,Qin, L.,Garnero, P.,Genant, H. K.,Zhang, G....&Zhao, S. J..(2012).The first multicenter and randomized clinical trial of herbal Fufang for treatment of postmenopausal osteoporosis.OSTEOPOROSIS INTERNATIONAL,23,(4)
MLA:
Zhu, H. M.,et al."The first multicenter and randomized clinical trial of herbal Fufang for treatment of postmenopausal osteoporosis".OSTEOPOROSIS INTERNATIONAL 23..4(2012):1317-1327