First line zidovudine/lamivudine/lopinavir/ritonavir leads to greater bone loss compared to nevirapine/lopinavir/ritonavir

被引:86
|
作者
van Vonderen, Marit G. A. [1 ]
Lips, Paul [1 ]
van Agtmael, Michiel A. [1 ]
Hassink, Elly A. M. [2 ]
Brinkman, Kees [3 ]
Geerlings, Suzanne E. [4 ,5 ]
Sutinen, Jussi [6 ]
Ristola, Matti [6 ]
Danner, Sven A. [1 ]
Reiss, Peter [4 ,5 ]
机构
[1] Vrije Univ Amsterdam, Med Ctr, Dept Internal Med, NL-1007 MB Amsterdam, Netherlands
[2] Int Antiviral Therapy Evaluat Ctr, Amsterdam, Netherlands
[3] Onze Lieve Vrouw Hosp, Dept Internal Med, Amsterdam, Netherlands
[4] Univ Amsterdam, Acad Med Ctr, Dept Infect Dis Trop Med & AIDS, NL-1105 AZ Amsterdam, Netherlands
[5] Univ Amsterdam, Acad Med Ctr, Ctr Infect & Immun, NL-1105 AZ Amsterdam, Netherlands
[6] Univ Helsinki, Cent Hosp, Dept Internal Med, Helsinki, Finland
关键词
acquired immune deficiency syndrome; HIV; nucleoside reverse transcriptase inhibitors bone mineral density; osteoporosis; HUMAN-IMMUNODEFICIENCY-VIRUS; HIV-INFECTED PATIENTS; ACTIVE ANTIRETROVIRAL THERAPY; MINERAL DENSITY; PROTEASE INHIBITORS; BODY-COMPOSITION; MARKERS; OSTEOCLASTOGENESIS; PREVALENCE; METABOLISM;
D O I
10.1097/QAD.0b013e32832c4947
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Objective: We studied changes in bone mineral density (BMD) and bone turnover after initiation of combination antiretroviral therapy (CART) and the contribution of zidovudine/lamivudine (ZDV/3TC) in particular. Design: Randomized clinical trial comparing lopinavir/ritonavir(LPV/r)+ZDV/3TC with LPV/r+nevirapine (NVP) in 50 cART-naive men. Methods: Dual energy X-ray absorptiometry (DXA) and quantitative computed tomography scans (QCT) were performed at baseline and 3, 12, and 24 months after CART initiation. Serum 25-hydroxy-vitamin D3, parathyroid hormone (PTH), osteocalcin, and urine deoxypyridinoline (DPD)/creatinine ratio were measured. Results: BMD decreased rapidly in both femoral neck and lumbar spine after cART initiation. BMD loss during 24 months measured by DXA, but not by QCT, was greater in the ZDV/3TC/LPV/r group compared to the NVP/LPV/r group [femoral neck: -6.3% +/- 1.0% (P<0.0001) compared to -2.3% +/- 0.9% (P=0.01), between-group P=0.0006); lumbar spine: -5.1% +/- 0.8% (P<0.0001) compared to -2.6% +/- 0.7% (P=0.0006), between-group P=0.071. Osteocalcin 1.+1.60 +/- 0.32 (P<0.0001) and +1.81 +/- 0.29 (P< 0.0001) nmol/l] and the urine DPD/creatinine ratio [+1.35 +/- 0.44 (P=0.0029) and +1.19 +/- 3=0.38 nmol/mmol (P=0.0024)] increased in both groups over 24 months, with no significant difference between groups. PTH increased to a greater degree in the NVP/LPV/r group [+2.0 +/- 0.31 pmol/l (P<0.0001)] compared to [+0.81 +/- 0.33 pmol/l (P=0.021) in the ZDV/3TC/LPV/r group]. Conclusion: BMD in both femoral neck and lumbar spine decreased rapidly after initiation of CART, in parallel to an increase in bone turnover. The greater bone loss in the ZDV/3TC/LPV/r group compared to the NVP/LPV/r group suggests that ZDV/3TC contributes to this process. The PTH increase does not explain this greater bone loss. (C) 2009 Wolters Kluwer Health | Lippincott Williams & Wilkins
引用
收藏
页码:1367 / 1376
页数:10
相关论文
共 50 条
  • [1] Protease gene mutations in a trial comparing first-line lopinavir/ritonavir monotherapy to lopinavir/ritonavir plus zidovudine/lamivudine (MONARK Trial)
    Delaugerre, C.
    Flandre, P.
    Chaix, M. L.
    Dellamonica, P.
    Raffi, F.
    Jueger, H.
    Schuermann, D.
    NgoVan
    Norton, M.
    Codar, I. Cohen
    Delfraissy, J. F.
    Rouzioux, C.
    ANTIVIRAL THERAPY, 2007, 12 (05) : S84 - S84
  • [2] Predictors of Loss of Virologic Response in Subjects Who Simplified to Lopinavir/Ritonavir Monotherapy from Lopinavir/Ritonavir Plus Zidovudine/Lamivudine
    Campo, Rafael E.
    Da Silva, Barbara A.
    Cotte, Laurent
    Gathe, Joseph C.
    Gazzard, Brian
    Hicks, Charles B.
    Klein, Cheri E.
    Chiu, Yi-Lin
    King, Martin S.
    Bernstein, Barry M.
    AIDS RESEARCH AND HUMAN RETROVIRUSES, 2009, 25 (03) : 269 - 275
  • [3] Zidovudine/lamivudine but not nevirapine in combination with lopinavir/ritonavir decreases subcutaneous adipose tissue mitochondrial DNA
    Feeney, Eoin R.
    van Vonderen, Marit G. A.
    Wit, Ferdinand
    Danner, Sven A.
    van Agtmael, Michiel A.
    Villarroya, Francesc
    Domingo, Pere
    Capeau, Jacqueline
    Reiss, Peter
    Mallon, Patrick W. G.
    AIDS, 2012, 26 (17) : 2165 - 2174
  • [4] Plasma lopinavir trough levels in a group of pregnant women on lopinavir, ritonavir, zidovudine, and lamivudine
    Manavi, Kaveh
    McDonald, Amy
    Al-Sharqui, Ali
    AIDS, 2007, 21 (05) : 643 - 645
  • [5] Protease Inhibitor Resistance Analysis in the MONARK Trial Comparing First-Line Lopinavir-Ritonavir Monotherapy to Lopinavir-Ritonavir plus Zidovudine and Lamivudine Triple Therapy
    Delaugerre, Constance
    Flandre, Philippe
    Chaix, Marie Laure
    Ghosn, Jade
    Raffi, Francois
    Dellamonica, Pierre
    Jaeger, H.
    Shuermann, D.
    Cohen-Codar, Isabelle
    Van, Philippe Ngo
    Norton, Michael
    Taburet, Anne-Marie
    Delfraissy, Jean-Francois
    Rouzioux, Christine
    ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2009, 53 (07) : 2934 - 2939
  • [7] Switching to lopinavir/ritonavir with or without abacavir/lamivudine in lipoatrophic patients treated with zidovudine/abacavir/lamivudine
    Bernardino, J. I.
    Pulido, F.
    Martinez, E.
    Arrizabalaga, J.
    Domingo, P.
    Portilla, J.
    Ocampo, A.
    Munoz, J.
    Torres, R.
    Arribas, J. R.
    JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2013, 68 (06) : 1373 - 1381
  • [8] Changes in bone biomarkers in antiretroviral naive HIV-infected men randomised to nevirapine/lopinavir/ritonavir (NVP/LPV/R) or zidovudine/lamivudine/lopinavir/ritonavir (AZT/3TC/LPV/R) help explain limited loss of bone mineral density over first 12 months
    Murray, B. F.
    van Vonderen, M. G.
    Mallon, P. W.
    Doran, P.
    van Agtmael, M. A.
    Danner, S. A.
    Lips, P.
    Reiss, P.
    BONE, 2012, 50 : S167 - S167
  • [9] Exploratory study comparing the metabolic toxicities of a lopinavir/ritonavir plus saquinavir dual protease inhibitor regimen versus a lopinavir/ritonavir plus zidovudine/lamivudine nucleoside regimen
    Cameron, D. William
    Becker, Stephen
    King, Martin S.
    da Silva, Barbara
    Klein, Cheri
    Tokimoto, Debbie
    Foit, Cheryl
    Calhoun, Deborah
    Bernstein, Barry
    Hanna, George J.
    JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2007, 59 (05) : 957 - 963
  • [10] Tolerability of postexposure prophylaxis with the combination of zidovudine-lamivudine and lopinavir-ritonavir for HIV infection
    Rabaud, C
    Burty, C
    Grandidier, M
    Christian, B
    Penalba, C
    Béguinot, I
    Jeanmaire, H
    May, T
    CLINICAL INFECTIOUS DISEASES, 2005, 40 (02) : 303 - 305