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Impact of second-line antiretroviral regimens on lipid profiles in an African setting: the DART trial sub-study

Journal Article
Published: March 10, 2025
Authors
Katabira Elly
GomoZvenyika Ar
Hakim James G.
Walker Sarah A.
Tinago Willard
Mandozana Gibson
Kityo Cissy
Munderi Paula
Reid Andrew
Gibb Diana M.
Gilks Charles F.
Abstract

MEDLINE Abstract: BACKGROUND:<BR>Increasing numbers of HIV-infected patients in sub-Saharan Africa are exposed to antiretroviral therapy (ART), but there are few data on lipid changes on first-line ART, and even fewer on second-line.<BR>METHODS:<BR>DART was a randomized trial comparing monitoring strategies in Ugandan/Zimbabwean adults initiating first-line ART and switching to second-line at clinical/immunological failure. We evaluated fasting lipid profiles at second-line initiation and â¥48 weeks subsequently in stored samples from Zimbabwean patients switching before 18 September 2006.<BR>RESULTS:<BR>Of 91 patients switched to second-line ART, 65(73%) had fasting samples at switch and â¥48 weeks, 14(15%) died or were lost <48 weeks, 10(11%) interrupted ART for >14 days and 2(2%) had no samples available. 56/65(86%) received ZDV/d4Tâ+â3TCâ+âTDF first-line, 6(9%) ZDV/d4Tâ+â3TCâ+âNVP and 3(5%) ZDVâ+â3TC with TDF and NVP. Initial second-line regimens were LPV/râ+âNNRTI in 27(41%), LPV/râ+âNNRTIâ+âddI in 33(50%) and LPV/râ+âTDFâ+âddI/3TC/ZDV in 6(9%). At second-line initiation median (IQR) TC, LDL-C, HDL-C and TG (mmol/L) were 3.3(2.8-4.0), 1.7(1.3-2.2), 0.7(0.6-0.9) and 1.1(0.8-1.9) respectively. Levels were significantly increased 48 weeks later, by mean (SE) +2.0(0.1), +1.1(0.1), +0.5(0.05) and +0.4(0.2) respectively (pâ<â0.001; TG pâ=â0.01). 3% at switch vs 25% 48 weeks later had TC >5.2 mmol/L; 3% vs 25% LDL-C >3.4 mmol/L and 91% vs 41% HDL-C <1.1 mmol/L (pâ<â0.001). Similar proportions had TG >1.8 mmol/L (0 vs 3%) and TC/HDL-C â¥5 (40% vs 33%) (pâ>â0.15).<BR>CONCLUSION:<BR>Modest lipid elevations were observed in African patients on predominantly LPV/râ+âNNRTI-based second-line regimens. Routine lipid monitoring during second-line ART regimens may not be warranted in this setting but individual cardiovascular risk assessment should guide practice.<BR>

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