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本文引用的文献

1
Short-term bone loss in HIV-infected premenopausal women.HIV 感染的绝经前妇女的短期骨丢失。
J Acquir Immune Defic Syndr. 2010 Feb;53(2):202-8. doi: 10.1097/QAI.0b013e3181bf6471.
2
Continuous antiretroviral therapy decreases bone mineral density.持续抗逆转录病毒疗法会降低骨密度。
AIDS. 2009 Jul 31;23(12):1519-29. doi: 10.1097/QAD.0b013e32832c1792.
3
Loss of bone mineral density after antiretroviral therapy initiation, independent of antiretroviral regimen.开始抗逆转录病毒治疗后骨矿物质密度的丧失,与抗逆转录病毒治疗方案无关。
J Acquir Immune Defic Syndr. 2009 Aug 15;51(5):554-61. doi: 10.1097/QAI.0b013e3181adce44.
4
First line zidovudine/lamivudine/lopinavir/ritonavir leads to greater bone loss compared to nevirapine/lopinavir/ritonavir.与奈韦拉平/洛匹那韦/利托那韦相比,一线治疗药物齐多夫定/拉米夫定/洛匹那韦/利托那韦会导致更多的骨质流失。
AIDS. 2009 Jul 17;23(11):1367-76. doi: 10.1097/QAD.0b013e32832c4947.
5
Greater decrease in bone mineral density with protease inhibitor regimens compared with nonnucleoside reverse transcriptase inhibitor regimens in HIV-1 infected naive patients.在初治的HIV-1感染患者中,与非核苷类逆转录酶抑制剂方案相比,蛋白酶抑制剂方案导致的骨矿物质密度下降幅度更大。
AIDS. 2009 Apr 27;23(7):817-24. doi: 10.1097/QAD.0b013e328328f789.
6
Evolution and predictors of change in total bone mineral density over time in HIV-infected men and women in the nutrition for healthy living study.“健康生活营养研究”中感染HIV的男性和女性随时间推移骨矿物质密度总量变化的演变及预测因素
J Acquir Immune Defic Syndr. 2008 Nov 1;49(3):298-308. doi: 10.1097/QAI.0b013e3181893e8e.
7
Fracture prevalence among human immunodeficiency virus (HIV)-infected versus non-HIV-infected patients in a large U.S. healthcare system.美国一个大型医疗系统中感染人类免疫缺陷病毒(HIV)的患者与未感染HIV的患者之间的骨折患病率。
J Clin Endocrinol Metab. 2008 Sep;93(9):3499-504. doi: 10.1210/jc.2008-0828. Epub 2008 Jul 1.
8
The safety and efficacy of tenofovir DF in combination with lamivudine and efavirenz through 6 years in antiretroviral-naïve HIV-1-infected patients.替诺福韦酯与拉米夫定及依非韦伦联合应用于初治的HIV-1感染患者6年的安全性和疗效。
HIV Clin Trials. 2007 May-Jun;8(3):164-72. doi: 10.1310/hct0803-164.
9
Decreased bone mineral density and increased fracture risk in aging men with or at risk for HIV infection.感染HIV或有感染风险的老年男性骨矿物质密度降低,骨折风险增加。
AIDS. 2007 Mar 12;21(5):617-23. doi: 10.1097/QAD.0b013e3280148c05.
10
Low bone density in patients receiving methadone maintenance treatment.接受美沙酮维持治疗患者的低骨密度
Drug Alcohol Depend. 2006 Dec 1;85(3):258-62. doi: 10.1016/j.drugalcdep.2006.05.027. Epub 2006 Jul 21.

中年 HIV 感染和未感染女性的骨密度前瞻性评估:美沙酮使用与骨丢失的关系。

Prospective evaluation of bone mineral density among middle-aged HIV-infected and uninfected women: Association between methadone use and bone loss.

机构信息

Department of Medicine, Division of Infectious Diseases, SUNY Downstate Medical Center, Brooklyn, NY, USA.

出版信息

Maturitas. 2011 Nov;70(3):295-301. doi: 10.1016/j.maturitas.2011.08.003. Epub 2011 Sep 25.

DOI:10.1016/j.maturitas.2011.08.003
PMID:21944566
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3189307/
Abstract

OBJECTIVE

We undertook a prospective study to assess the impact of HIV infection on BMD in a cohort of HIV-infected and uninfected women that included illicit drug users, and to measure the contribution of traditional risk factors as well as HIV-related factors to loss of BMD over time.

METHODS

We analyzed BMD at baseline and after ≥18 months in 245 middle-aged HIV-infected and 219 uninfected women, and conducted linear regression analysis to determine factors associated with annual BMD change at the femoral neck, total hip and lumbar spine.

RESULTS

HIV-infected women had lower baseline BMD at the femoral neck and total hip compared with controls; unadjusted rates of BMD change did not differ by HIV status at any site. In multivariable analyses, we found that HIV seropositivity without protease inhibitor (PI) use was associated with BMD decline at the lumbar spine (-.009g/cm(2) per year, p=.03). Additional factors associated with BMD decline were: postmenopausal status, lower BMI, and methadone use at the lumbar spine; postmenopausal status and hepatitis C seropositivity at the femoral neck; and postmenopausal status, age, smoking, and lower BMI at the total hip (all p<.05). Among HIV-infected women, ≥3 years of PI use was associated with an increase in lumbar spine BMD (.013g/cm(2) per year, p=.008).

CONCLUSIONS

Bone loss among HIV-infected middle-aged women was modest, and possibly mitigated by PI use. Methadone use was associated with BMD decline, and should be considered when evaluating women for osteoporosis risk.

摘要

目的

我们进行了一项前瞻性研究,以评估 HIV 感染对包括吸毒者在内的 HIV 感染和未感染女性的骨密度的影响,并测量传统危险因素以及与 HIV 相关的因素对随时间推移骨密度丧失的贡献。

方法

我们分析了 245 名中年 HIV 感染和 219 名未感染女性在基线时和≥18 个月时的骨密度,并进行线性回归分析,以确定与股骨颈、全髋和腰椎骨密度每年变化相关的因素。

结果

与对照组相比,HIV 感染女性的股骨颈和全髋关节的基线骨密度较低;在任何部位,未调整的骨密度变化率均不因 HIV 状态而异。在多变量分析中,我们发现未使用蛋白酶抑制剂(PI)的 HIV 血清阳性与腰椎骨密度下降有关(每年-.009g/cm²,p=.03)。与骨密度下降相关的其他因素包括:绝经后状态、较低的 BMI 和腰椎的美沙酮使用;绝经后状态和股骨颈的丙型肝炎血清阳性;以及绝经后状态、年龄、吸烟和全髋关节较低的 BMI(均 p<.05)。在 HIV 感染女性中,≥3 年的 PI 使用与腰椎骨密度增加有关(每年.013g/cm²,p=.008)。

结论

中年 HIV 感染女性的骨质流失适度,可能通过使用 PI 得到缓解。美沙酮使用与骨密度下降有关,在评估女性骨质疏松风险时应予以考虑。