Increased bone resorption during tenofovir plus lopinavir/ritonavir therapy in Chinese individuals with HIV

被引:12
|
作者
Hsieh, E. [1 ,2 ]
Fraenkel, L. [2 ]
Xia, W. [3 ]
Hu, Y. Y. [4 ]
Han, Y. [1 ]
Insogna, K. [5 ]
Yin, M. T. [6 ]
Xie, J. [1 ]
Zhu, T. [1 ]
Li, T. [1 ,7 ]
机构
[1] Peking Union Med Coll Hosp, Dept Infect Dis, Beijing 100730, Peoples R China
[2] Yale Univ, Sch Med, Rheumatol Sect, New Haven, CT 06520 USA
[3] Peking Union Med Coll Hosp, Dept Endocrinol, Key Lab Endocrinol, Beijing 100730, Peoples R China
[4] Peking Union Med Coll Hosp, Clin Lab, Beijing 100730, Peoples R China
[5] Yale Univ, Endocrinol Sect, Sch Med, New Haven, CT 06520 USA
[6] Columbia Univ, Div Infect Dis, Med Ctr, New York, NY 10032 USA
[7] Peking Union Med Coll Hosp, Peking Union Med Coll, Dept Infect Dis, Beijing 100730, Peoples R China
关键词
Bone turnover; Chinese; HIV; Resorption; Tenofovir; MINERAL DENSITY; ANTIRETROVIRAL THERAPY; DISOPROXIL FUMARATE; VITAMIN-D; PARATHYROID-HORMONE; ABACAVIR-LAMIVUDINE; INFECTED PATIENTS; FRACTURE RISK; MARKERS; METABOLISM;
D O I
10.1007/s00198-014-2874-3
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
A Summary We sought to evaluate the effects of antiretroviral therapy on skeletal metabolism in Chinese individuals with human immunodeficiency virus. Patients switched to tenofovir/lamivudine + lopinavir/ritonavir after treatment failure had an increase in bone resorption marker levels by nearly 60 %, which is greater than the magnitude previously described in non-Chinese populations. Introduction Few studies have evaluated the effects of antiretroviral therapy on skeletal metabolism in Asian populations infected with human immunodeficiency virus (HIV). Methods We performed a secondary analysis of bone turnover markers (BTM) at baseline and 2 years in stored plasma samples collected from 2/2009 to 1/2013 as part of a multi-center trial. Two groups were compared: (1) treatment-na < ve patients initiated on zidovudine (AZT)/lamivudine (3TC) plus nevirapine (NVP) and (2) patients who failed first-line therapy and were switched to tenofovir (TDF)/3TC plus lopinavir/ritonavir (LPVr). Tests included the bone resorption marker, C-terminal cross-linking telopeptide of type-1 collagen (CTX), and the bone formation marker procollagen type 1 N-terminal propeptide (P1NP). Results In the TDF/3TC + LPVr group, samples were available from 59 patients at baseline and 56 patients at 2 years. Of these, 36 patients had samples available from both time points. In the AZT/3TC + NVP group, plasma samples were analyzed from 82 participants at baseline and of those, 61 had samples at 2 years. Median change over 2 years was greater in the TDF/3TC + LPVr group for both CTX (+0.24 ng/mL, interquartile ranges (IQR) 0.10-0.43 vs. +0.09 ng/mL, IQR -0.03 to 0.18, p = 0.001) and P1NP (+25.5 ng/mL, IQR 2.4-51.3 vs. +7.11 ng/mL, IQR -4.3 to 21.6, p = 0.012). Differences remained after adjusting for potential confounders in the multivariable analysis. Conclusions Switching to TDF/3TC + LPVr after treatment failure resulted in greater increases in BTMs than initiation with AZT/3TC + NVP in Chinese patients with HIV. Following this change, bone resorption marker levels increased by nearly 60 %, which is greater than the 25-35 % increase from baseline described previously in non-Chinese populations. Further studies are warranted to elucidate these findings.
引用
收藏
页码:1035 / 1044
页数:10
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