The Effect of Malnutrition on the Pharmacokinetics and Virologic Outcomes of Lopinavir, Efavirenz and Nevirapine in Food Insecure HIV-infected Children in Tororo, Uganda

被引:26
作者
Bartelink, Imke H. [1 ,2 ]
Savic, Rada M. [2 ]
Dorsey, Grant [3 ]
Ruel, Theodore [4 ]
Gingrich, David [1 ]
Scherpbier, Henriette J. [6 ]
Capparelli, Edmund [7 ]
Jullien, Vincent [8 ]
Young, Sera L. [9 ]
Achan, Jane [10 ]
Plenty, Albert [5 ]
Charlebois, Edwin [5 ]
Kamya, Moses [11 ]
Havlir, Diane [3 ]
Aweeka, Francesca [1 ]
机构
[1] Univ Calif San Francisco, Dept Clin Pharm, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Bioengn & Therapeut Sci, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Dept Med, San Francisco, CA 94143 USA
[4] Univ Calif San Francisco, Dept Pediat, San Francisco, CA 94143 USA
[5] Univ Calif San Francisco, Ctr AIDS Prevent Studies, San Francisco, CA 94143 USA
[6] Emma Childrens Hosp AMC, Dept Pediat Immunol & Infect Dis, Amsterdam, Netherlands
[7] Univ Calif San Diego, La Jolla, CA 92093 USA
[8] Hop Europeen Georges Pompidou, Dept Pharmacol, Paris Descartes, France
[9] Cornell Univ, Div Nutr Sci, Ithaca, NY 14853 USA
[10] Makerere Univ, Dept Pediat & Child Hlth, Kampala, Uganda
[11] Makerere Univ, Dept Med, Kampala, Uganda
关键词
malnutrition; pharmacokinetics; HIV; virologic failure; protease inhibitors; non-nucleoside reverse transcriptase inhibitor; PLASMA-CONCENTRATIONS; DRUG DISPOSITION; RITONAVIR; LOPINAVIR/RITONAVIR; COMBINATION; THERAPY; BIOAVAILABILITY; UNDERNUTRITION; PHARMACOLOGY; INDIVIDUALS;
D O I
10.1097/INF.0000000000000603
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: Malnutrition may impact the pharmacokinetics (PKs) of antiretroviral medications and virologic responses in HIV-infected children. The authors therefore evaluated the PK of nevirapine (NVP), efavirenz (EFV) and lopinavir (LPV) in associations with nutritional status in a cohort of HIV-infected Ugandan children. Methods: Sparse dried blood spot samples from Ugandan children were used to estimate plasma concentrations. Historical PK data from children from 3 resource-rich countries (RRC) were utilized to develop the PK models. Results: Concentrations in 330 dried blood spot from 163 Ugandan children aged 0.7-7 years were analyzed in reference to plasma PK data (1189 samples) from 204 children from RRC aged 0.5-12 years. Among Ugandan children, 48% was malnourished (underweight, thin or stunted). Compared to RRC, Ugandan children exhibited reduced bioavailability of EFV and LPV; 11% (P = 0.045) and 18% (P = 0.008), respectively. In contrast, NVP bioavailability was 46% higher in Ugandan children (P < 0.001) with a trend toward greater bioavailability when malnourished. Children receiving LPV, EFV or NVP had comparable risk of virologic failure. Among children on NVP, low height and weight for age Z scores were associated with reduced risk of virologic failure (P = 0.034, P = 0.068, respectively). Conclusions: Ugandan children demonstrated lower EFV and LPV and higher NVP exposure compared to children in RRC, perhaps reflecting the consequence of malnutrition on bioavailability. In children receiving NVP, the relation between exposure, malnutrition and outcome turned out to be marginally significant. Further investigations are warranted using more intensive PK measurements and adequate adherence assessments, to further assess causes of virologic failure in Ugandan children.
引用
收藏
页码:E63 / E70
页数:8
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