Resum
Idioma original | Anglès |
---|---|
Pàgines (de-a) | 1359-1369 |
Nombre de pàgines | 11 |
Revista | J. Infect. Dis. |
Volum | 207 |
Número | 9 |
DOIs | |
Estat de la publicació | Publicada - de maig 2013 |
SDG de les Nacions Unides
Aquest resultat contribueix als següents objectius de desenvolupament sostenible.
Accés al document
Altres arxius i enllaços
Fingerprint
Navegar pels temes de recerca de 'Association between antiretroviral exposure and renal impairment among HIV-positive persons with normal baseline renal function: The D:A:D Study a: Journal of Infectious Diseases'. Junts formen un fingerprint únic.Com citar-ho
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver
}
In: J. Infect. Dis., Vol. 207, Núm. 9, 05.2013, pàg. 1359-1369.
Producció científica: Contribució a revista › Article › Recerca › Avaluat per experts
TY - JOUR
T1 - Association between antiretroviral exposure and renal impairment among HIV-positive persons with normal baseline renal function: The D:A:D Study a
T2 - Journal of Infectious Diseases
AU - Ryom, L.
AU - Mocroft, A.
AU - Kirk, O.
AU - Worm, S.W.
AU - Kamara, D.A.
AU - Reiss, P.
AU - Ross, M.
AU - Fux, C.A.
AU - Morlat, P.
AU - Moranne, O.
AU - Smith, C.
AU - Lundgren, J.D.
AU - Torres, Ferran
N1 - Cited By :237 Export Date: 17 February 2022 CODEN: JIDIA Correspondence Address: Ryom, L.; Copenhagen HIV Program, Blegdamsvej 3B, 2200 Copenhagen N, Denmark; email: [email protected] Chemicals/CAS: abacavir, 136470-78-5, 188062-50-2; atazanavir, 198904-31-3; indinavir, 150378-17-9, 157810-81-6, 180683-37-8; lopinavir, 192725-17-0; proteinase inhibitor, 37205-61-1; ritonavir, 155213-67-5; tenofovir, 147127-19-3, 147127-20-6; Anti-Retroviral Agents Funding details: CT94-1637, CT97-2713 Funding details: FIS 99/0887 Funding details: 5U01AI042170-10, 5U01AI046362-03, FIPSE 3171/00 Funding details: CURE/97-46486 Funding details: National Institutes of Health, NIH Funding details: U.S. Food and Drug Administration, FDA Funding details: National Institute of Allergy and Infectious Diseases, NIAID, U01AI042170, U01AI046362, U01AI069907 Funding details: Boehringer Ingelheim, BI Funding details: amfAR, The Foundation for AIDS Research Funding details: Abbott Laboratories Funding details: Bristol-Myers Squibb, BMS Funding details: Pfizer Funding details: GlaxoSmithKline, GSK Funding details: Merck Funding details: Roche Funding details: Gilead Sciences Funding details: Janssen Pharmaceuticals Funding details: Merck Sharp and Dohme, MSD Funding details: ViiV Healthcare Funding details: European Commission, EC, QLK2-2000-00773 Funding details: Department of Health and Ageing, Australian Government Funding details: Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung, SNF Funding details: University of New South Wales, UNSW Funding details: Agence Nationale de Recherches sur le Sida et les Hépatites Virales, ANRS Funding text 1: Financial support. This work was supported by the Highly Active Antiretroviral Therapy Oversight Committee (HAART-OC), a collaborative committee with representation from academic institutions, the European Agency for the Evaluation of Medicinal Products, the US Food and Drug Administration, the patient community, and all pharmaceutical companies with licensed anti-HIV drugs in the European Union (Abbott Laboratories, Boehringer Ingelheim Pharmaceuticals, Bristol-Myers Squibb, Gilead Sciences, Viiv Healthcare, Merck, Pfizer, F. Hoffman- LaRoche, and Janssen Pharmaceuticals); the Health Insurance Fund Council, Amstelveen, the Netherlands (grant CURE/97-46486 to the ATHENA cohort); and the Agence Nationale de Recherches sur le SIDA (grant Action Coordonnée no. 7, Cohortes, to the Aquitaine Cohort). AHOD is funded as part of the Asia Pacific HIV Observational Database, a program of the Foundation for AIDS Research, amfAR, and is supported in part by the National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH; grant U01-AI069907) and by unconditional grants from Merck Sharp and Dohme, Gilead Sciences, Bristol-Myers Squibb, Boehringer Ingelheim Pharmaceuticals, Roche, Pfizer, GlaxoSmithKline, and Janssen Pharmaceuticals. The Kirby Institute is funded by the Australian Government Department of Health and Ageing and is affiliated with the Faculty of Medicine, the University of New South Wales. The BASS is funded by the Fondo de Investigación Sanitaria (grant FIS 99/0887) and the Fundación para la Investigación y la Prevención del SIDA en Espanã (grant FIPSE 3171/00). The Terry Beirn Community Programs for Clinical Research on AIDS (CPCRA) is funded by the NIAID, NIH (grants 5U01AI042170-10 and 5U01AI046362-03). The EuroSIDA study is funded by the BIOMED 1 (grant CT94-1637) and BIOMED 2 (grant CT97-2713) programs, by the Fifth Framework Program of the European Commission (grant QLK2-2000-00773), and by grants from Bristol-Myers Squibb, GlaxoSmithKline, Boehringer Ingel-heim Pharmaceuticals, and Roche. The ICONA Foundation is funded by unrestricted educational grants from Abbott Laboratories, Bristol-Myers Squibb, Gilead Sciences, GSK, Pfizer, and Janssen Pharmaceutical. The SHCS is funded by the Swiss National Science Foundation. References: Mocroft, A., Kirk, O., Reiss, P., Estimated glomerular filtration rate, chronic kidney disease and antiretroviral drug use in HIV-positive patients (2010) AIDS, 24, pp. 1667-1678; Flandre, P., Pugliese, P., Cuzin, L., Risk factors of chronic kidney disease in HIV-infected patients (2011) Clinical Journal of the American Society of Nephrology:CJASN, 6, pp. 1700-1707; Scherzer, R., Estrella, M., Li, Y., Association of tenofovir exposure with kidney disease risk in HIV infection (2012) AIDS, 26, pp. 867-875; Sax, P.E., Tierney, C., Collier, A.C., Abacavir/lamivudine versus tenofovir DF/emtricitabine as part of combination regimens for initial treatment of HIV: Final results (2011) The Journal of Infectious Diseases, 204, pp. 1191-1201; Ibrahim, F., Hamzah, L., Jones, R., Nitsch, D., Sabin, C., Post, F.A., Baseline kidney function as predictor of mortality and kidney disease progression in HIV-Positive patients (2012) American Journal of Kidney Diseases: The Official Journal of the National Kidney Foundation, 60, pp. 539-547; Friis-Moller, N., Sabin, C.A., Weber, R., Combination antiretroviral therapy and the risk of myocardial infarction (2003) The New England Journal of Medicine, 349, pp. 1993-2003; Levey, A.S., Coresh, J., Balk, E., National Kidney Foundation practice guidelines for chronic kidney disease: Evaluation, classification, and stratification (2003) Annals of Internal Medicine, 139, pp. 137-147; Cockcroft, D.W., Gault, M.H., Prediction of creatinine clearance from serum creatinine (1976) Nephron, 16, pp. 31-41; Mosteller, R.D., Simplified calculation of body-surface area (1987) The New England Journal of Medicine, 317, p. 1098; Vrouenraets, S.M., Fux, C.A., Wit, F.W., A comparison of measured and estimated glomerular filtration rate in successfully treated HIV-patients with preserved renal function (2012) Clinical Nephrology, 77, pp. 311-320; Boehringer Ingelheim Pharmaceuticals I. Highlights of Prescribing Information, , http://bidocs.boehringer-ingelheim.com/BIWebAccess/ViewServlet.ser? docBase=renetnt&folderPath=/Prescribing+Information/PIs/Aptivus/ 10003515+US+01.pdf, Accessed 24 May 2012; ViiV. Highlights of Prescribing Information, , http://www.accessdata.fda.gov/drugsat.fda_docs/label/2009/021548s021, 022116s005lbl.pdf, Accessed 24 May 2012; Eriksen, B.O., Ingebretsen, O.C., The progression of chronic kidney disease: A 10-year population-based study of the effects of gender and age (2006) Kidney International, 69 (2), pp. 375-382. , DOI 10.1038/sj.ki.5000058, PII 5000058; Hanratty, R., Chonchol, M., Miriam Dickinson, L., Incident chronic kidney disease and the rate of kidney function decline in individuals with hypertension (2010) Nephrology Dialysis Transplantation : Official Publication of the European Dialysis and Transplant Association-European Renal Association, 25, pp. 801-807; Alves, T.P., Hulgan, T., Wu, P., Race, kidney disease progression, and mortality risk in HIV-infected persons (2010) Clinical Iournal of the American Society of Nephrology : CJASN, 5, pp. 2269-2275; Ryom, L., Kamara, D.A., Worm, S.W., Development of a definition for rapid progression of renal disease in HIV-positive persons (2011) 13th International Workshop on Adverse Drug Reactions and Co-Morbidities in HIV, , for the D:A:D Study Group Rome, Italy 14-16 July; Young, J., Schafer, J., Fux, C.A., Renal function in patients with HIV starting therapy with tenofovir and either efavirenz, lopinavir or atazanavir (2012) AIDS, 26, pp. 567-575; Goicoechea, M., Liu, S., Best, B., Sun, S., Jain, S., Kemper, C., Witt, M., Louie, S., Greater tenofovir-associated renal function decline with protease inhibitor-based versus nonnucleoside reverse-transcriptase inhibitor-based therapy (2008) Journal of Infectious Diseases, 197 (1), pp. 102-108. , DOI 10.1086/524061; Brewster, U.C., Perazella, M.A., Acute interstitial nephritis associated with atazanavir, a new protease inhibitor (2004) American Journal of Kidney Diseases, 44 (5), pp. E81-E84. , DOI 10.1053/j.ajkd.2004.07.017, PII S0272638604010935; Schmid, S., Opravil, M., Moddel, M., Huber, M., Pfammatter, R., Keusch, G., Ambuhl, P., Varga, Z., Acute interstitial nephritis of HIV-positive patients under atazanavir and tenofovir therapy in a retrospective analysis of kidney biopsies (2007) Virchows Archiv, 450 (6), pp. 665-670. , DOI 10.1007/s00428-007-0418-3; Izzedine, H., M'Rad, M.B., Bardier, A., Daudon, M., Salmon, D., Atazanavir crystal nephropathy (2007) AIDS, 21, pp. 2357-2358; Chang, H.R., Pella, P.M., Atazanavir urolithiasis (2006) The New England Journal of Medicine, 355, pp. 2158-2159; Hamada, Y., Nishijima, T., Watanabe, K., High incidence of renal stones among HIV-Infected patients on ritonavir-boosted atazanavir than in those receiving other protease inhibitor-containing antiretroviral therapy (2012) Clinical Infectious Diseases : An Official Publication of the Infectious Diseases Society of America, 55, pp. 1262-1269; Albini, L., Cesana, B.M., Motta, D., A randomized, pilot trial to evaluate glomerular filtration rate by creatinine or cystatin c in naive hiv-infected patients after tenofovir/emtricitabine in combination with atazanavir/ritonavir or efavirenz (2012) J Acquir Immune Defic Syndr, 59, pp. 18-30; Dauchy, F.A., Lawson-Ayayi, S., De La Faille, R., Increased risk of abnormal proximal renal tubular function with HIV infection and antiretroviral therapy (2011) Kidney International, 80, pp. 302-309; Rockwood, N., Mandalia, S., Bower, M., Gazzard, B., Nelson, M., Ritonavirboosted atazanavir exposure is associated with an increased rate of renal stones compared with efavirenz, ritonavir-boosted lopinavir and ritonavir-boosted darunavir (2011) AIDS, 25, pp. 1671-1673; Doco-Lecompte, T., Garrec, A., Thomas, L., Trechot, P., May, T., Rabaud, C., Lopinavir-ritonavir (Kaletra) and lithiasis: Seven cases [4] (2004) AIDS, 18 (4), pp. 705-706. , DOI 10.1097/00002030-200403050-00022; Zimmermann, A.E., Pizzoferrato, T., Bedford, J., Morris, A., Hoffman, R., Braden, G., Tenofovir-associated acute and chronic kidney disease: A case of multiple drug interactions (2006) Clinical Infectious Diseases, 42 (2), pp. 283-290. , DOI 10.1086/499048; Rollot, F., Nazal, E.M., Chauvelot-Moachon, L., Tenofovir-related Fanconi syndrome with nephrogenic diabetes insipidus in a patient with acquired immunodeficiency syndrome: The role of lopinavirritonavir-didanosine (2003) Clinical Infectious Diseases : An Official Publication of the Infectious Diseases Society of America, 37, pp. e174-e176; Lastours, D.V., Silva, E., Daudon, M., Porcher, R., Sauvageon, H., Molina, J., Atazanavir (ATV) and darunavir (DRV) cristalluria and high ATV and DRV concentrations in urine of asymptomatic patients receiving ATV and DRV based regimens (2012) 52nd ICAAC Interscience Conference on Antimicrobial Agents and Chemotherapy, , San Francisco, CA 9-12 September; Kohler, J.J., Hosseini, S.H., Green, E., Tenofovir renal proximal tubular toxicity is regulated by OAT1 and MRP4 transporters (2011) Laboratory Investigation; A Journal of Technical Methods and Pathology, 91, pp. 852-858; Van Rompay, K.K.A., Brignolo, L.L., Meyer, D.J., Jerome, C., Tarara, R., Spinner, A., Hamilton, M., Bischofberger, N., Biological Effects of Short-Term or Prolonged Administration of 9-[2-(Phosphonomethoxy)Propyl]Adenine (Tenofovir) to Newborn and Infant Rhesus Macaques (2004) Antimicrobial Agents and Chemotherapy, 48 (5), pp. 1469-1487. , DOI 10.1128/AAC.48.5.1469-1487.2004; Lebrecht, D., Venhoff, A.C., Kirschner, J., Wiech, T., Venhoff, N., Walker, U.A., Mitochondrial tubulopathy in tenofovir disoproxil fumaratetreated rats (2009) J Acquir Immune Defic Syndr, 51, pp. 258-263; Lee, J.C., Marosok, R.D., Acute tubular necrosis in a patient receiving tenofovir [1] (2003) AIDS, 17 (17), pp. 2543-2544. , DOI 10.1097/00002030-200311210-00021; Karras, A., Lafaurie, M., Furco, A., Bourgarit, A., Droz, D., Sereni, D., Legendre, C., Molina, J.-M., Tenofovir-related nephrotoxicity in human immunodeficiency virus-infected patients: Three cases of renal failure, fanconi syndrome, and nephrogenic diabetes insipidus (2003) Clinical Infectious Diseases, 36 (8), pp. 1070-1073. , DOI 10.1086/368314; Menezes, A.M., Torelly Jr., J., Real, L., Bay, M., Poeta, J., Sprinz, E., Prevalence and risk factors associated to chronic kidney disease in hivinfected patients on HAART and undetectable viral load in brazil (2011) PloS One, 6, pp. e26042; Gallant, J.E., Parish, M.A., Keruly, J.C., Moore, R.D., Changes in renal function associated with tenofovir disoproxil fumarate treatment, compared with nucleoside reverse-transcriptase inhibitor treatment (2005) Clinical Infectious Diseases, 40 (8), pp. 1194-1198. , DOI 10.1086/428840; Overton, E.T., Nurutdinova, D., Freeman, J., Seyfried, W., Mondy, K.E., Factors associated with renal dysfunction within an urban HIVinfected cohort in the era of highly active antiretroviral therapy (2009) HIV Medicine, 10, pp. 343-350; Cooper, R.D., Wiebe, N., Smith, N., Keiser, P., Naicker, S., Tonelli, M., Systematic review and meta-analysis: Renal safety of tenofovir disoproxil fumarate in HIV-infected patients (2010) Clinical Infectious Diseases : An Official Publication of the Infectious Diseases Society of America, 51, pp. 496-505; Arribas, J.R., Pozniak, A.L., Gallant, J.E., DeJesus, E., Gazzard, B., Campo, R.E., Chen, S.-S., Cheng, A.K., Tenofovir disoproxil fumarate, emtricitabine, and efavirenz compared with zidovudine/lamivudine and efavirenz in treatment-naive patients: 144-Week analysis (2008) Journal of Acquired Immune Deficiency Syndromes, 47 (1), pp. 74-78. , DOI 10.1097/QAI.0b013e31815acab8, PII 0012633420080101000009; Izzedine, H., Hulot, J.S., Vittecoq, D., Gallant, J.E., Staszewski, S., Launay-Vacher, V., Cheng, A., Deray, G., Long-term renal safety of tenofovir disoproxil fumarate in antiretroviral-naïve HIV-1-infected patients. Data from a double-blind randomized active-controlled multicentre study (2005) Nephrology Dialysis Transplantation, 20 (4), pp. 743-746. , DOI 10.1093/ndt/gfh658; Squires, K., Pozniak, A.L., Pierone Jr., G., Tenofovir disoproxil fumarate in nucleoside-resistant HIV-1 infection: A randomized trial (2003) Annals of Internal Medicine, 139, pp. 313-320; Gallant, J.E., Staszewski, S., Pozniak, A.L., DeJesus, E., Suleiman, J.M.A.H., Miller, M.D., Coakley, D.F., Cheng, A.K., Efficacy and safety of tenofovir DF vs stavudine in combination therapy in antiretroviral-naive patients: A 3-year randomized trial (2004) Journal of the American Medical Association, 292 (2), pp. 191-201. , DOI 10.1001/jama.292.2.191; Wyatt, C.M., Klotman, P.E., Antiretroviral therapy and the kidney: Balancing benefit and risk in patients with HIV infection (2006) Expert Opinion on Drug Safety, 5 (2), pp. 275-287. , DOI 10.1517/14740338.5.2.275; Ahmad, M., Abacavir-induced reversible Fanconi syndrome with nephrogenic diabetes insipidus in a patient with acquired immunodeficiency syndrome (2006) Journal of Postgraduate Medicine, 52 (4), pp. 296-297; Mallal, S., Phillips, E., Carosi, G., HLA-B*5701 screening for hypersensitivity to abacavir (2008) The New England Journal of Medicine, 358, pp. 568-579; Crum-Cianflone, N., Ganesan, A., Teneza-Mora, N., Prevalence and factors associated with renal dysfunction among HIV-infected patients (2010) AIDS Patient Care and STDs, 24, pp. 353-360; Deti, E.K., Thiebaut, R., Bonnet, F., Prevalence and factors associated with renal impairment in HIV-infected patients, ANRS C03 Aquitaine Cohort, France (2010) HIV Medicine, 11, pp. 308-317; Jotwani, V., Li, Y., Grunfeld, C., Choi, A.I., Shlipak, M.G., Risk factors for ESRD in HIV-Infected individuals: Traditional and HIV-related factors (2011) American Journal of Kidney Diseases : The Official Journal of the National Kidney Foundation; Peters, L., Grint, D., Lundgren, J.D., HCV viremia increases the incidence of chronic kidney disease in HIV-infected patients (2012) AIDS, , in press
PY - 2013/5
Y1 - 2013/5
N2 - Background. Several antiretroviral agents (ARVs) are associated with chronic renal impairment, but the extent of such adverse events among human immunodeficiency virus (HIV)-positive persons with initially normal renal function is unknown.Methods. D:A:D study participants with an estimated glomerular filtration rate (eGFR) of ≥90 mL/min after 1 January 2004 were followed until they had a confirmed eGFR of ≤70 mL/min (the threshold below which we hypothesized that renal interventions may begin to occur) or ≤60 mL/min (a value indicative of moderately severe chronic kidney disease [CKD]) or until the last eGFR measurement during follow-up. An eGFR was considered confirmed if it was detected at 2 consecutive measurements ≥3 months apart. Predictors and eGFR-related ARV discontinuations were identified using Poisson regression.Results. Of 22 603 persons, 468 (2.1%) experienced a confirmed eGFR of ≤70 mL/min (incidence rate, 4.78 cases/1000 person-years of follow-up [95% confidence interval "CI", 4.35-5.22]) and 131 (0.6%) experienced CKD (incidence rate, 1.33 cases/1000 person-years of follow-up [95% CI, 1.10-1.56]) during a median follow-up duration of 4.5 years (interquartile range [IQR], 2.7-6.1 years). A current eGFR of 60-70 mL/min caused significantly higher rates of discontinuation of tenofovir (adjusted incidence rate ratio [aIRR], 1.72 [95% CI, 1.38-2.14]) but not other ARVs compared with a current eGFR of ≥90 mL/min. Cumulative tenofovir use (aIRR, 1.18/year [95% CI, 1.12-1.25]) and ritonavir-boosted atazanavir use (aIRR, 1.19/year [95% CI, 1.09-1.32]) were independent predictors of a confirmed eGFR of ≤70 but were not significant predictors of CKD whereas ritonavir-boosted lopinavir use was a significant predictor for both end points (aIRR, 1.11/year [95% CI, 1.05-1.17] and 1.22/year [95% CI, 1.16-1.28], respectively). Associations were unaffected by censoring for concomitant ARV use but diminished after discontinuation of these ARVs.Conclusions. Tenofovir, ritonavir-boosted atazanavir, and ritonavir-boosted lopinavir use were independent predictors of chronic renal impairment in HIV-positive persons without preexisting renal impairment. Increased tenofovir discontinuation rates with decreasing eGFR may have prevented further deteriorations. After discontinuation, the ARV-associated incidence rates decreased. © 2013 The Author.
AB - Background. Several antiretroviral agents (ARVs) are associated with chronic renal impairment, but the extent of such adverse events among human immunodeficiency virus (HIV)-positive persons with initially normal renal function is unknown.Methods. D:A:D study participants with an estimated glomerular filtration rate (eGFR) of ≥90 mL/min after 1 January 2004 were followed until they had a confirmed eGFR of ≤70 mL/min (the threshold below which we hypothesized that renal interventions may begin to occur) or ≤60 mL/min (a value indicative of moderately severe chronic kidney disease [CKD]) or until the last eGFR measurement during follow-up. An eGFR was considered confirmed if it was detected at 2 consecutive measurements ≥3 months apart. Predictors and eGFR-related ARV discontinuations were identified using Poisson regression.Results. Of 22 603 persons, 468 (2.1%) experienced a confirmed eGFR of ≤70 mL/min (incidence rate, 4.78 cases/1000 person-years of follow-up [95% confidence interval "CI", 4.35-5.22]) and 131 (0.6%) experienced CKD (incidence rate, 1.33 cases/1000 person-years of follow-up [95% CI, 1.10-1.56]) during a median follow-up duration of 4.5 years (interquartile range [IQR], 2.7-6.1 years). A current eGFR of 60-70 mL/min caused significantly higher rates of discontinuation of tenofovir (adjusted incidence rate ratio [aIRR], 1.72 [95% CI, 1.38-2.14]) but not other ARVs compared with a current eGFR of ≥90 mL/min. Cumulative tenofovir use (aIRR, 1.18/year [95% CI, 1.12-1.25]) and ritonavir-boosted atazanavir use (aIRR, 1.19/year [95% CI, 1.09-1.32]) were independent predictors of a confirmed eGFR of ≤70 but were not significant predictors of CKD whereas ritonavir-boosted lopinavir use was a significant predictor for both end points (aIRR, 1.11/year [95% CI, 1.05-1.17] and 1.22/year [95% CI, 1.16-1.28], respectively). Associations were unaffected by censoring for concomitant ARV use but diminished after discontinuation of these ARVs.Conclusions. Tenofovir, ritonavir-boosted atazanavir, and ritonavir-boosted lopinavir use were independent predictors of chronic renal impairment in HIV-positive persons without preexisting renal impairment. Increased tenofovir discontinuation rates with decreasing eGFR may have prevented further deteriorations. After discontinuation, the ARV-associated incidence rates decreased. © 2013 The Author.
KW - ART
KW - atazanavir
KW - chronic kidney disease
KW - eGFR
KW - HIV
KW - lopinavir
KW - nephrotoxicity
KW - tenofovir
KW - abacavir
KW - antiretrovirus agent
KW - indinavir
KW - nucleoside
KW - proteinase inhibitor
KW - ritonavir
KW - adult
KW - article
KW - clinical assessment
KW - controlled study
KW - disease course
KW - drug efficacy
KW - drug withdrawal
KW - female
KW - human
KW - Human immunodeficiency virus infected patient
KW - Human immunodeficiency virus infection
KW - incidence
KW - kidney function
KW - major clinical study
KW - male
KW - priority journal
KW - risk factor
KW - treatment duration
KW - treatment response
KW - Adult
KW - Anti-Retroviral Agents
KW - Cohort Studies
KW - Female
KW - Glomerular Filtration Rate
KW - HIV Infections
KW - Humans
KW - Incidence
KW - Male
KW - Middle Aged
KW - Prospective Studies
KW - Renal Insufficiency
KW - Withholding Treatment
UR - http://www.ncbi.nlm.nih.gov/pubmed/23382571
U2 - 10.1093/infdis/jit043
DO - 10.1093/infdis/jit043
M3 - Article
C2 - 23382571
SN - 0022-1899
VL - 207
SP - 1359
EP - 1369
JO - J. Infect. Dis.
JF - J. Infect. Dis.
IS - 9
ER -