A. Mweemba, P. Kelly, D. Heimburger, W. Mutale, S. Nzala, W. Wester, Justor Banda, L. Mulenga, M. Siwingwa, J. Todd
{"title":"抗逆转录病毒治疗方案对赞比亚感染艾滋病毒的青少年和年轻人近端肾小管功能的影响:一项横断面研究","authors":"A. Mweemba, P. Kelly, D. Heimburger, W. Mutale, S. Nzala, W. Wester, Justor Banda, L. Mulenga, M. Siwingwa, J. Todd","doi":"10.12688/gatesopenres.14458.1","DOIUrl":null,"url":null,"abstract":"Background: Tenofovir regimens remain the preferred formulations in the HIV guidelines for adolescents and young adults in Zambia and globally. However, some adolescents and young adults are maintained on abacavir by clinicians because of anxiety about possible proximal tubular dysfunction from tenofovir. We assessed the effect of two regimens on proximal tubular function in adolescents and young adults living with HIV. Methods: This was a cross-sectional study involving 180 participants with HIV receiving either tenofovir or abacavir for ≥12 months at the largest tertiary teaching hospital. Two first-morning urine and blood specimens were collected and analyzed for proximal tubular markers, glomerular function, electrolytes, and routine monitoring tests. Proximal tubular function was determined by measuring the fractional excretion of phosphate (FePO4). Proximal tubular dysfunction was defined by FePO4 ≥20% regardless of serum phosphate and FePO4 ≥10-20% when serum phosphate was below 0.81mmol/L. Results: The prevalence of proximal tubular dysfunction was 6% and was higher in the tenofovir group than the abacavir (10% vs. 2%, p<0.058). However, after adjusting for potential confounders, tenofovir was not associated with worse proximal tubular function. Age, urine b2-microglobulin: creatinine ratio, C-reactive protein, and urine protein: creatinine ratio was all associated with worsening proximal tubular dysfunction. Reduced estimated glomelurar filtration rate (eGFR) was found in four (2.2%) participants; three of which were on tenofovir. Conclusions: Proximal tubular dysfunction defined by FePO4 was more prevalent in the tenofovir group than the abacavir group, but not after adjusting for age. Our findings should be interpreted with caution as age differences between the two groups confounded the results.","PeriodicalId":12593,"journal":{"name":"Gates Open Research","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-03-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Effect of anti-retroviral regimen on proximal tubular function in Zambian adolescents and young adults living with HIV: A cross sectional study\",\"authors\":\"A. Mweemba, P. Kelly, D. Heimburger, W. Mutale, S. Nzala, W. Wester, Justor Banda, L. Mulenga, M. Siwingwa, J. Todd\",\"doi\":\"10.12688/gatesopenres.14458.1\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Background: Tenofovir regimens remain the preferred formulations in the HIV guidelines for adolescents and young adults in Zambia and globally. However, some adolescents and young adults are maintained on abacavir by clinicians because of anxiety about possible proximal tubular dysfunction from tenofovir. We assessed the effect of two regimens on proximal tubular function in adolescents and young adults living with HIV. Methods: This was a cross-sectional study involving 180 participants with HIV receiving either tenofovir or abacavir for ≥12 months at the largest tertiary teaching hospital. Two first-morning urine and blood specimens were collected and analyzed for proximal tubular markers, glomerular function, electrolytes, and routine monitoring tests. Proximal tubular function was determined by measuring the fractional excretion of phosphate (FePO4). Proximal tubular dysfunction was defined by FePO4 ≥20% regardless of serum phosphate and FePO4 ≥10-20% when serum phosphate was below 0.81mmol/L. Results: The prevalence of proximal tubular dysfunction was 6% and was higher in the tenofovir group than the abacavir (10% vs. 2%, p<0.058). However, after adjusting for potential confounders, tenofovir was not associated with worse proximal tubular function. Age, urine b2-microglobulin: creatinine ratio, C-reactive protein, and urine protein: creatinine ratio was all associated with worsening proximal tubular dysfunction. Reduced estimated glomelurar filtration rate (eGFR) was found in four (2.2%) participants; three of which were on tenofovir. Conclusions: Proximal tubular dysfunction defined by FePO4 was more prevalent in the tenofovir group than the abacavir group, but not after adjusting for age. 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引用次数: 1
摘要
背景:替诺福韦方案仍然是赞比亚和全球青少年和年轻人艾滋病毒指南的首选配方。然而,由于担心替诺福韦可能导致近端小管功能障碍,一些青少年和年轻人被临床医生坚持服用阿巴卡韦。我们评估了两种方案对感染艾滋病毒的青少年和年轻人近端肾小管功能的影响。方法:这是一项横断面研究,涉及180名在最大的三级教学医院接受替诺福韦或阿巴卡韦治疗≥12个月的HIV感染者。收集两份晨尿和血标本,分析近端小管标志物、肾小球功能、电解质和常规监测试验。通过测量磷酸(FePO4)的分数排泄来确定近端小管功能。无论血清磷酸水平如何,FePO4≥20%为近端肾小管功能障碍;当血清磷酸水平低于0.81mmol/L时,FePO4≥10-20%为近端肾小管功能障碍。结果:替诺福韦组近端肾小管功能障碍发生率为6%,高于阿巴卡韦组(10% vs. 2%, p<0.058)。然而,在调整了潜在的混杂因素后,替诺福韦与近端肾小管功能恶化无关。年龄、尿b2-微球蛋白:肌酐比、c反应蛋白、尿蛋白:肌酐比均与近端小管功能障碍加重有关。4名参与者(2.2%)发现肾小球滤过率(eGFR)降低;其中三人服用替诺福韦。结论:由FePO4定义的近端肾小管功能障碍在替诺福韦组比阿巴卡韦组更普遍,但在调整年龄后情况并非如此。我们的发现应该谨慎解释,因为两组之间的年龄差异混淆了结果。
Effect of anti-retroviral regimen on proximal tubular function in Zambian adolescents and young adults living with HIV: A cross sectional study
Background: Tenofovir regimens remain the preferred formulations in the HIV guidelines for adolescents and young adults in Zambia and globally. However, some adolescents and young adults are maintained on abacavir by clinicians because of anxiety about possible proximal tubular dysfunction from tenofovir. We assessed the effect of two regimens on proximal tubular function in adolescents and young adults living with HIV. Methods: This was a cross-sectional study involving 180 participants with HIV receiving either tenofovir or abacavir for ≥12 months at the largest tertiary teaching hospital. Two first-morning urine and blood specimens were collected and analyzed for proximal tubular markers, glomerular function, electrolytes, and routine monitoring tests. Proximal tubular function was determined by measuring the fractional excretion of phosphate (FePO4). Proximal tubular dysfunction was defined by FePO4 ≥20% regardless of serum phosphate and FePO4 ≥10-20% when serum phosphate was below 0.81mmol/L. Results: The prevalence of proximal tubular dysfunction was 6% and was higher in the tenofovir group than the abacavir (10% vs. 2%, p<0.058). However, after adjusting for potential confounders, tenofovir was not associated with worse proximal tubular function. Age, urine b2-microglobulin: creatinine ratio, C-reactive protein, and urine protein: creatinine ratio was all associated with worsening proximal tubular dysfunction. Reduced estimated glomelurar filtration rate (eGFR) was found in four (2.2%) participants; three of which were on tenofovir. Conclusions: Proximal tubular dysfunction defined by FePO4 was more prevalent in the tenofovir group than the abacavir group, but not after adjusting for age. Our findings should be interpreted with caution as age differences between the two groups confounded the results.