Calza L, Colangeli V, Magistrelli E, Bussini L, Conti M, Ramazzotti E, Mancini R, Viale P
Department of Medical and Surgical Sciences, Clinics of Infectious Diseases, Bologna, Italy.
Central Laboratory, S. Orsola-Malpighi Hospital, "Alma Mater Studiorum", University of Bologna, Bologna, Italy.
HIV Med. 2017 Aug;18(7):474-481. doi: 10.1111/hiv.12478. Epub 2017 Jan 24.
The aim of the study was to assess plasma concentrations of darunavir/ritonavir and raltegravir in older patients compared with younger patients with HIV-1 infection.
In this observational, open-label study, adult HIV-infected out-patients aged ≤ 40 years (younger patients) or ≥ 60 years (older patients) and treated with tenofovir/emtricitabine plus darunavir/ritonavir (800/100 mg daily) or raltegravir (400 mg twice daily) were asked to participate. The trough concentrations (C ) of darunavir/ritonavir and raltegravir were assessed at steady state using a validated high-performance liquid chromatography (HPLC)-tandem mass spectrometry method.
A total of 88 HIV-positive patients were enrolled in the study. Forty-six patients were treated with darunavir/ritonavir, and 42 with raltegravir. The geometric mean plasma C (coefficient of variation) of raltegravir was comparable between the 19 older and 23 younger subjects: 106 ng/mL (151%) and 94 ng/mL (129%), respectively [geometric mean ratio (GMR) 0.85; 95% confidence interval (CI) 0.71-1.57; P = 0.087]. In contrast, the geometric mean plasma C of darunavir was significantly higher among the 21 older patients [2209 ng/mL (139%)] than among the 25 younger patients [1876 ng/mL (162%); GMR 1.56; 95% CI: 1.22-1.88; P = 0.004]. Similarly, the geometric mean C of ritonavir was significantly higher among older than among younger individuals.
The mean plasma C of darunavir and ritonavir was significantly higher in older patients than in younger patients with HIV-1 infection, while the mean plasma level of raltegravir was comparable in the two groups. However, both regimens showed good tolerability in both younger and older subjects.
本研究旨在评估与年轻的HIV-1感染患者相比,老年患者体内达芦那韦/利托那韦和拉替拉韦的血浆浓度。
在这项观察性、开放标签研究中,邀请年龄≤40岁(年轻患者)或≥60岁(老年患者)且接受替诺福韦/恩曲他滨联合达芦那韦/利托那韦(每日800/100毫克)或拉替拉韦(每日两次,每次400毫克)治疗的成年HIV感染门诊患者参与。使用经过验证的高效液相色谱(HPLC)-串联质谱法在稳态下评估达芦那韦/利托那韦和拉替拉韦的谷浓度(C)。
共有88例HIV阳性患者纳入研究。46例患者接受达芦那韦/利托那韦治疗,42例接受拉替拉韦治疗。在19例老年受试者和23例年轻受试者中,拉替拉韦的几何平均血浆C(变异系数)相当:分别为106纳克/毫升(151%)和94纳克/毫升(129%)[几何平均比(GMR)0.85;95%置信区间(CI)0.71-1.57;P = 0.087]。相比之下,21例老年患者中达芦那韦的几何平均血浆C[2209纳克/毫升(139%)]显著高于25例年轻患者[1876纳克/毫升(162%);GMR 1.56;95% CI:1.22-1.88;P = 0.004]。同样,利托那韦的几何平均C在老年个体中显著高于年轻个体。
与年轻的HIV-1感染患者相比,老年患者体内达芦那韦和利托那韦的平均血浆C显著更高,而两组中拉替拉韦的平均血浆水平相当。然而,两种治疗方案在年轻和老年受试者中均显示出良好的耐受性。