Background: Tenofovir (TDF) has been associated with renal tubular injury. Biomarkers that signal early tubular dysfunction are needed because creatinine rise lags behind TDF-associated kidney dysfunction. We examined several urinary biomarkers to determine if rises accompanying TDF initiation preceded creatinine changes.
Methods: Three urinary biomarkers of tubular impairment—neutrophil gelatinase–associated lipocalin (NGAL), N-acetyl-β-D-glucosaminidase (NAG), and β-2-microglobulin (β2MG)—were measured across 3 time points (one pre-TDF visit and 2 post-TDF visits) in 132 HIV-positive women from the Women's Interagency HIV Study. Women initiating highly active antiretroviral therapy (HAART) containing TDF were propensity score matched to women initiating HAART without TDF and women not on HAART.
Results: There were no differences between groups for NGAL or NAG, but β2MG was 19 times more likely to be elevated among TDF users at the second post-TDF visit compared with non-TDF users at the pre-TDF visit (P < 0.01). History of proteinuria was associated with elevated NGAL (P < 0.01). Factors associated with elevated NAG were glomerular filtration rate <60 mL/minute, history of proteinuria, hepatitis C (P < 0.01 for all), and diabetes mellitus (P = 0.05). Factors associated with increased odds of elevated β2MG were HIV RNA >100,000 copies/mL, hepatitis C, boosted protease inhibitor use, and glomerular filtration rate <60 mL/minute (P ≤ 0.01 for all).
Conclusions: β2MG levels are elevated in women on TDF, indicating probable early renal dysfunction. Biomarker elevation is additionally associated with baseline chronic kidney disease, uncontrolled viremia, and boosted protease inhibitor use. Future studies are needed to explore urinary biomarker thresholds in identifying treated HIV-infected individuals at risk for renal dysfunction.
*Department of Medicine, Division of Infectious Diseases, Johns Hopkins University School of Medicine, Baltimore, MD
†Department of Epidemiology, The Johns Hopkins University, Bloomberg School of Public Health, Baltimore, MD
‡Departments of Medicine, Epidemiology and Population Health, Montefiore Medical Center, Bronx, NY
§Department of Medicine, State University of New York Health Science Center, Brooklyn, NY
‖Department of Medicine, Georgetown University Medical Center, Washington, DC
¶Department of Medicine, Division of Hematology, University of Southern California, Los Angeles, CA
#Department of Medicine, University of California—San Francisco, San Francisco, CA
**Department of Medicine, Cook County Hospital, Chicago, IL
††Department of Pharmacovigilance, Pharmaceutical Product Development, Morrisville, NC.
Correspondence to: Ikwo Oboho, MD, Department of Medicine, Johns Hopkins University School of Medicine, 1830 E Monument Street, Suite 450B, Baltimore, MD 21287 (e-mail: firstname.lastname@example.org).
Supplemental digital content is available for this article. Direct URL citations appear in the printed text and are provided in the HTML and PDF versions of this article on the journal's Web site (www.jaids.com).
Supported by the National Institute of Allergy and Infectious Diseases (UO1-AI-35004, UO1-AI-31834, UO1-AI-34994, UO1-AI-34989, UO1-AI-34993, and UO1-AI-42590) and by the Eunice Kennedy Shriver National Institute of Child Health and Human Development (UO1-HD-32632). The study is co-funded by the National Cancer Institute, the National Institute on Drug Abuse, and the National Institute on Deafness and Other Communication Disorders. Funding is also provided by the National Center for Research Resources (UCSF-CTSI grant number UL1 RR024131).
The authors have no conflicts of interest to disclose.
The contents of this publication are solely the responsibility of the authors and do not necessarily represent the official views of the National Institutes of Health.
Received July 07, 2012
Accepted December 04, 2012
Persons with HIV are at high risk for the onset and progression of chronic kidney disease (CKD). In addition to HIV-related kidney disease (HIV-associated nephropathy), the population of people living with HIV/AIDS is aging and developing comorbidities that predispose them to CKD such as diabetes mellitus, hypertension, and cardiovascular disease. Renal toxicity from antiretroviral and other medications also contributes to kidney dysfunction in HIV-infected persons. One such antiretroviral drug, tenofovir (TDF), undergoes renal clearance by a combination of glomerular filtration and active proximal tubular secretion. It has also been implicated as a source of impaired kidney function in HIV-infected individuals.1–3
Although serum creatinine level is a well-accepted marker of kidney function, its disadvantages include its contemporaneous relationship with cellular damage. In addition, it is affected by a number of other factors, including muscle mass, protein intake, proteinuria, race, and age.4,5 Therefore, identifying biomarkers that reflect renal injury in real time and before the rise in creatinine could impact the delivery of care to patients with HIV. Given the multiple processes (direct HIV effects, antiretroviral effects, and increased prevalence of CKD risk factors) that may affect kidney function in persons with HIV, markers that could predict kidney function decline would be of paramount interest to clinicians involved in HIV care.
Over the past decade, novel urine biomarkers specific for tubular injury have been found, which provide an earlier indicator of impairment. Urine neutrophil gelatinase–associated lipocalin (NGAL) is a member of the lipocalin family of proteins that is secreted into the urine by the thick ascending limb of Henle and the collecting ducts of the kidney. Although normally expressed in low levels, increasing concentrations in urine are seen in the presence of epithelial injury and inflammation.6 N-acetyl-β-D-glucosaminidase (NAG) is a proximal tubule lysosomal enzyme whose presence in the urine suggests proximal tubular damage.7 β-2-Microglobulin (β2MG) is a low molecular weight protein, found in all nucleated cells, freely filtered by glomeruli, and catabolized by the proximal tubules.8
These 3 biomarkers have been associated with acute kidney injury (formerly acute renal failure) in people without HIV9,10 and have been found to be elevated in patients with conditions associated with CKD such as diabetes.11 However, it is unclear whether these biomarkers could be clinically useful to monitor nephrotoxicity from antiretroviral therapy. This study sought to explore the relationships between TDF initiation and changes in levels of urinary biomarkers using longitudinal data from a stable outpatient population of women with HIV.
Study Design and Measurements
Women's Interagency HIV Study
The rationale and methods of the Women's Interagency HIV Study (WIHS) have been previously described.12,13 Briefly, the WIHS is a multicenter, prospective cohort study of the natural history of HIV infection among women, conducted in Chicago, Los Angeles, New York City, the San Francisco Bay Area, and Washington, DC. From October 1994 through November 1995, 2623 (2054 HIV+ and 569 HIV−) study participants were enrolled. From October 2001 through September 2002, an additional 1143 (737 HIV+ and 406 HIV−) participants were enrolled for a total of 3766 (2791 HIV+ and 975 HIV−) women. Participants were recruited from HIV primary care clinics, hospital-based outpatient infectious disease clinics, research programs, community outreach sites, women's support groups, drug rehabilitation programs, HIV testing sites, and referrals from previously enrolled participants. HIV infection was determined with enzyme-linked immunosorbent assay and confirmed via Western blot. A standardized interview-based survey was used at enrollment to collect demographic data and prior medical, sexual, and drug use history. Women are evaluated semiannually to obtain weight, CD4 lymphocyte count, HIV RNA level, albumin, creatinine, and other testing. Urine is collected annually and stored in the central repository. Proteinuria was qualitatively assessed during the first 7 study visits. Women were described as having proteinuria if at least 2 urine analyses demonstrated the qualitative presence of greater than or equal to +1 protein. Race, hepatitis C antibody status, and history of proteinuria were determined before study baseline. All other factors were time varying and were determined at each visit biomarkers were measured. The study was approved by the institutional review boards at WIHS Institutions, and informed consent was obtained from every participant.
Among WIHS participants, we included in the current study HIV-infected women initiating a highly active antiretroviral therapy (HAART) regimen containing TDF who had available stored urine specimens and serum creatinine measurements. For each included participant, 3 visits were selected for urine testing: the visit 1 year before the initial report of TDF (study baseline), the initial visit that TDF was reported (matching visit, second measure), and 1 year after the initial report of TDF (third measure). Participant visits contributed by HIV-infected women using HAART without TDF (non-TDF HAART users) were matched to the visit that TDF was initially reported for each TDF HAART user via propensity score matching with a tolerance of 0.02.14 Propensity scores were estimated from a logistic multivariate regression model containing the following predictors: glomerular filtration rate (GFR) calculated using the CKD Epidemiology Collaboration equation,15 CD4 cell count (CD4), calendar year, HAART duration, HAART interruptions, body mass index (BMI), HIV RNA level, and use of a ritonavir-boosted protease inhibitor (PI). The study design and matching structure are shown in Figure 1. A total of 45 person visits contributed by 45 individual non-TDF HAART users were matched to the visit of the first report of TDF for 45 individual TDF HAART users.
As an additional comparison group, participant visits contributed by HIV-infected women who had not used HAART (but who may have used HAART in the past) within the past 3–9 months (non-HAART users) were matched to the visit that TDF was initially reported for each TDF HAART user via propensity score matching as described above. For this matched analysis, the propensity scores were estimated from a logistic multivariate model containing the following predictors: race, history of proteinuria, GFR, CD4, calendar year, BMI, HIV RNA, hepatitis C virus (HCV) antibody status, and smoking history. A total of 45 person visits contributed by 42 individual non-HAART users were matched to the visit of first reported TDF use for the same 45 individual TDF HAART users described above.
Stored urine specimens were measured for NGAL, NAG, and β2MG for each woman at each of the 3 time points. Urine NGAL level was assessed with the ARCHITECT assay (Abbott Diagnostics, Abbott Park, IL) that specifically detected human NGAL. Urine NAG activity was assessed using an NAG kit (Roche Diagnostics, Indianapolis, IN), and β2MG was assayed using enzyme immunoassay kit from ALPCO Ltd, Salem, NH; the intra-assay and inter-assay variation coefficients were less than 5%. Serum creatinine was measured locally at each WIHS site.
All biomarker values were log transformed, and the unadjusted geometric means were examined graphically. For multivariable analyses, NGAL and NAG were treated as log normally distributed, whereas β2MG was treated as a dichotomous outcome (>0.5 vs. ≤0.5 µg/mL) as a result of a large percentage of undetectable values (limit of detection = 0.06 μg/mL). This dichotomized outcome for β2MG is consistent with previous reports,16 but there is no established cutoff value for either NGAL or NAG in previous studies. The transformed biomarker values were fit using generalized linear models, with generalized estimating equations used to adjust standard errors to account for the repeated measures over time and matched exposure groups.17 Time trends over the 3 biomarker visits were modeled piecewise linearly with a spline at the matching visit (second measure). Models were simplified to linear if the estimated change from the second to the third measure was nonsignificant, indicating no departure from linearity over time across the 3 visits. Final models using the non-TDF HAART group as the comparator were adjusted for age as continuous, race (White, Black, and Latina), proteinuria, diabetes history, and WIHS baseline HCV antibody status as binary indicators, estimated GFR (eGFR) <60 mL/minute per 1.73 m2, hypertension (systolic > 140 mm Hg or diastolic > 90 mm Hg), current smoking status, categorized BMI (BMI: <18.5, 18.5–25, 25–30, >30 kg/m2), CD4 <200 cells/mm3, HIV RNA >100,000 copies/mL, years since HAART initiation, proportion of visits no HAART use was reported since initiation, and boosted PI use. For the additional analysis using a non-HAART comparison group, final models used the same covariates with the exception of the HAART use–related variables. All covariates except race, history of proteinuria, and baseline HCV antibody status were time varying.
Missing data were imputed according to whether the factor was fixed (history of proteinuria was missing for 8 women and diabetes history for 4 women) or time dependent (9 BMIs, 7 systolic and diastolic blood pressures, 6 eGFR measures, 5 CD4 cell counts, and 3 HIV RNA measures). For fixed covariates, the proportion of cases among individuals with complete data was used to randomly assign case status to individuals with missing data. For time-dependent covariates, missing values were interpolated from neighboring values in time using the average between the last nonmissing value before and the first nonmissing value after the missing value.
Urinary biomarkers were measured at 3 time points for 3 groups of women based on subsequent exposure to antiretroviral therapy (Fig. 1). This comprised 135 person visits from 132 individual women. At baseline, the median age of the women initiating HAART with TDF was 42 years and the racial distribution was 27% White/other, 49% Black, and 24% Latina (Table 1). Eighteen percent of women in the group had a history of proteinuria at baseline, and the average eGFR was 98 mL/minute. Only 4 women reported use of stavudine or atazanavir—both of which have been linked to renal tubular dysfunction—in any of the study visits.18,19 After propensity score matching, all factors were similar between the TDF HAART users and the non-TDF HAART users except for the proportion of women with unknown history of proteinuria (0% vs. 18%, P < 0.01), median HIV RNA (3.5 vs. 1.9, P = 0.01), and categorized HIV RNA (P = 0.01).
The geometric means and 95% confidence limits (95% confidence intervals) for NGAL did not change over time and were not different among exposure groups in the unadjusted analysis (see top row, Figure S1, Supplemental Digital Content, http://links.lww.com/QAI/A384). Although NAG levels increased over time, there were no notable differences among exposure groups (see middle row, Figure S1, Supplemental Digital Content http://links.lww.com/QAI/A384). In contrast, β2MG levels increased over time among women initiating HAART with TDF (see bottom row, Figure S1, Supplemental Digital Content, http://links.lww.com/QAI/A384). The proportion of women with elevated β2MG (>0.5 μg/mL) increased from 7% to 40% among TDF HAART users (P < 0.01), from 11% to 16% among non-TDF HAART users (P = 0.29), and 13% to 18% among non-HAART users, from the first to the third measurement. We calculated Spearman correlation coefficients for the log-transformed values of the 3 urinary biomarkers. The correlation between NGAL and NAG was 0.47 (P < 0.0001). Restricted to pairs with positive β2MG, correlation between β2MG and NGAL was 0.29 (P < 0.0001) and between β2MG and NAG was 0.52 (P < 0.01).
NGAL and NAG
In adjusted models, no differences were seen for NGAL between groups in the main comparison (TDF HAART vs. non-TDF HAART) at baseline or over time. However, NAG rose among TDF HAART users by 20% per year on average (P < 0.05) but did not differ between groups over time (Fig. 2). Both NGAL and NAG were elevated among women with renal parameters, suggestive of CKD at baseline (Table 2). Values of both were between 69% and 62% higher, respectively, among women with a history of proteinuria when compared with women without a history of proteinuria (P < 0.01 for both). Similarly, women with eGFR less than 60 mL/minute at study baseline had approximately a 60% greater value of NGAL (P = 0.10) and 80% greater value of NAG (P = 0.01). With respect to medical history, 2 other factors were marginally associated with higher NGAL and NAG levels. These include years since initiation of HAART for NGAL (P = 0.04) and a history of diabetes mellitus (P = 0.05) and hepatitis C (P < 0.01) for NAG. Race was also highly associated with NGAL and NAG levels. Latina women had NGAL and NAG levels 2 times as high as white women (P 0.01 for both).
In the secondary comparison, levels and change over time for NGAL and NAG among HAART users initiating TDF were compared with a group not taking HAART. NGAL and NAG levels were found to be similar, and there was no significant change over time. However, NAG increased among TDF users by 21% per year on average compared with baseline (P < 0.05) (consistent with results from the main analysis) and also rose among non-TDF HAART users by 33% per year on average compared with baseline (P < 0.05) (compared with non-HAART group). Black women and Latina women had higher NAG levels compared with White women (P = 0.01). Levels of NGAL and NAG were not significantly different among women with a history of proteinuria in this analysis but were more than twice as high among women with eGFR <60 mL/minute (P = 0.01).
In the adjusted model of β2MG, TDF HAART users had 19 times the odds of having an elevated β2MG at the third time point compared with 2.8 for non-TDF HAART users at the third time point (P < 0.01). Furthermore, CKD risk factors were associated with an elevated β2MG. Women with GFR <60 mL/minute [odds ratio (OR) = 5.67, P = 0.01] and HCV (OR = 9.3, P < 0.01) were more likely to have elevated β2MG, whereas smokers (OR = 0.27, P = 0.04) and Black women (OR = 0.2, P = 0.02) were less likely to have elevated β2MG (Table 3). However, controlling for eGFR, proteinuria was not associated with the likelihood of elevated β2MG (P = 0.22). With respect to HIV-specific parameters, women with HIV RNA >100,000 copies/mL (OR = 23.89, P < 0.01) and boosted PI use (OR = 8.97, P < 0.01) were more likely to have elevated β2MG.
In the secondary comparison, a different pattern of predictors of elevated β2MG was noted. The estimated odds of having an elevated β2MG level at the third time point was 3.9 times higher among TDF initiators compared with 1.1 times higher for non-HAART users at the third time point (P = 0.05). The CKD risk factors of an eGFR <60 and HCV were still significant factors. CD4 ≤200 cells/mm3 was also a significant predictor of elevated β2MG (OR = 9.0, P < 0.05), and obesity was associated with a decreased odds of elevated β2MG (OR = 0.22, P < 0.05)
In this cross-sectional analysis of a cohort of HIV-infected women (WIHS), we evaluated the changes in 3 significant urinary biomarkers over time in a group of women who initiate a TDF-containing antiretroviral regimen compared with women not initiating TDF or not on HAART. At study baseline, there were no differences between groups for NGAL, NAG, and β2MG. The increase over time for NGAL and NAG was not significant among TDF users compared with the non-TDF users. β2MG was more likely to be elevated among TDF users at the third time point compared with non-TDF users, indicating that this marker may be an important indicator of TDF-related kidney dysfunction. Even though increases over time for NGAL and NAG were not significant among TDF users compared with the non-TDF users, our results suggest that elevations in NGAL and NAG among TDF users are more generally related to comorbid diseases commonly associated with CKD. In contrast, the factors specific to HIV infection such as antiretroviral regimen (HAART with TDF and regimen including a boosted PI), lower CD4, and higher HIV RNA level were associated with greater urinary β2MG levels.
Advanced immunosuppression (CD4 <50 cells/mm3) has been associated with a decline in creatinine clearance in a prior observational study.20 However, another study did not find an association between CD4 <200 cells/mm3 and higher β2MG excretion in HIV-infected patients on TDF compared with other nucleoside reverse transcriptase inhibitors.21 Therefore, our study uniquely demonstrates that immunosuppression affects β2MG levels, which has not previously been described. Similarly, uncontrolled HIV viremia has been linked to renal dysfunction in a large randomized trial.22 Our findings of the association between uncontrolled HIV viremia and urinary biomarker elevation support the findings from a recent cohort study, which noted an association between detectable HIV RNA (>400 copies/mL) and elevated cystatin C, another biomarker of renal function.23 This suggests that the development of these biomarkers as clinical guides will need to take into account the medical history of the patient and the effectiveness of their HIV-directed care.
Our findings regarding β2MG confirm prior work demonstrating higher levels of urinary β2MG among persons on TDF-containing antiretroviral regimen and the impact of concurrent PI use. In the abacavir/lamivudine versus tenofovir/emtricitabine, administered with efavirenz, in antiretroviral-naive subjects study, subjects receiving TDF/emtricitabine fixed-dose combination had a 72% greater increase at week 24 and a 133% greater increase at week 48 in urinary β2MG than subjects taking abacavir (ABC)/lamivudine (3TC) fixed-dose combination.24 In addition, a greater decline in kidney function has been noted in persons receiving TDF with a boosted PI compared with TDF without a PI.25 Furthermore, an observational cohort of patients receiving TDF demonstrated that subgroups receiving TDF with ritonavir-boosted lopinavir had greater urinary β2MG levels than those receiving TDF without a PI.16
In addition, our findings confirm prior reports that metabolic factors may play a role in modulating biomarker levels. Low body weight (defined by <60 kg) has been associated with renal function decline in persons on TDF compared with abacavir-containing regimen26 and greater urinary β2MG levels.16 Likewise, our study found that obesity was protective against elevated β2MG in the TDF group compared with the non-HAART group. Furthermore, we found an association between current smoking and reduced β2MG levels in the TDF group compared with non-TDF HAART users contradicting prior reports of smoking and elevated β2MG in an environmental cohort.27
Prior studies have been limited in their ability to examine the relationships between CKD risk factors and these biomarkers because of the exclusion of patients with proteinuria or preexisting history of renal disease; our results reveal the importance of preexisting kidney disease in the interpretation of urinary biomarker elevations in patients on TDF. These results thus add to the literature on the clinical utility of these markers for screening for subclinical renal toxicity in HIV-infected patients.
The interpretation of the results of this study may be limited to women because of gender differences in these biomarker levels. In an HIV-negative population with type 1 diabetes, urinary NGAL levels were significantly higher in females compared with males,28 which may reflect an estrogen-mediated difference in protein expression in renal or urinary tract tissues.29 Furthermore, gender and race differences have been noted in NAG levels. In a cross-sectional study of the early natural history of cardiovascular disease, Black women had higher levels of urinary NAG compared with Black men but White men and women had similar levels.30 Studies assessing β2MG levels in HIV-infected persons have mostly been in men and have not assessed for gender differences.16,24,31
Other limitations to our analysis should be noted. Our conclusion regarding the impact of GFR <60 on biomarkers is limited by the small sample of women with GFR <60. Furthermore, the level of urinary biomarkers is influenced by urine concentration. Urine creatinine measurements, typically used to standardize for urine concentration, were unavailable in this study. However, the impact of not accounting for differences in urine concentration would likely be to attenuate effects by introducing additional variability into the analysis, and thus, our results may be conservative.
In summary, this analysis examined the value of the urinary biomarkers NGAL, NAG, and β2MG as indicators of kidney injury resulting from TDF use. Our results demonstrate the potential utility of urinary β2MG levels in predicting patients at risk for loss of kidney function because of TDF use. Further studies are needed to determine when it is appropriate to use this urinary biomarker and how frequently to monitor. If validated, this biomarker may have clinical utility in identifying higher risk individuals allowing appropriate diagnostic and therapeutic interventions to be delivered earlier with a potential positive impact on kidney function.
Data in the manuscript were collected by the WIHS Collaborative Study Group with centers (Principal Investigators) at New York City/Bronx Consortium (K. Anastos); Brooklyn, NY (Howard Minkoff); Washington, DC, Metropolitan Consortium (M. Young); The Connie Wofsy Study Consortium of Northern California (Ruth Greenblatt); Los Angeles County/Southern California Consortium (Alexandra Levine); Chicago Consortium (M. Cohen); and Data Coordinating Center (Stephen Gange). Reagents to perform ARCHITECT Urine NGAL testing were provided by Abbott Diagnostics. Portions of this manuscript were presented at a Poster session at: Complications of HIV and Antiretroviral Therapy, Poster #1382. Infectious Disease Week: A Joint Meeting of IDSA, SHEA, HIVMA, and PIDS; October 17-21, 2012; San Diego, CA.
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Tenofovir; urinary biomarkers; HIV-infected women
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