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. 2021 Apr 10;24(4):e25702. doi: 10.1002/jia2.25702

Table 2.

Estimated rates of change in weight a before and after switch from TDF to TAF

On TDF

60 to 0 months

On TAF

0 to 9 months

On TAF

9+ months

kg/year (95% CI) kg/year (95% CI) kg/year (95% CI)
Maintained all other ARVs
Overall 0.48 (0.37, 0.59) 2.43 (2.15, 2.71) 0.24 (0.07, 0.41)
NNRTI 0.66 (0.51, 0.81) 2.25 (1.78, 2.71) 0.20 (−0.14, 0.54)
Boosted PI 0.31 (−0.02, 0.64) 1.98 (1.13, 2.83) −0.11 (−0.57, 0.35)
InSTI 0.42 (0.26, 0.59) 2.64 (2.26, 3.01) 0.29 (0.08, 0.51)
Maintained an InSTI
Elvitegravir/cobicistat 0.71 (0.53, 0.90) 2.51 (2.05, 2.96) 0.36 (0.12, 0.61)
Dolutegravir 0.73 (0.34, 1.11) 2.38 (1.64, 3.13) −0.18 (−0.64, 0.28)
Raltegravir −0.44 (−0.79, −0.08) 1.80 (0.57, 3.03) 0.63 (−0.20, 1.46)
Switched from non‐InSTI to InSTI
Elvitegravir/cobicistat 0.24 (0.04, 0.43) 2.55 (1.86, 3.24) 0.26 (−0.10, 0.61)
Dolutegravir 0.22 (−0.08, 0.52) 3.09 (1.26, 4.93) −0.23 (−1.62, 1.16)
Bictegravir b 0.01 (−0.38, 0.39) 4.47 (0.81, 8.13) −9.97 (−23.79, 3.85)

ARV, antiretroviral; BMI, body mass index; CI, confidence interval; PI, boosted protease inhibitor; InSTI, integrase strand transfer inhibitor; NNRTI, non‐nucleoside reverse transcriptase inhibitor; TAF, tenofovir alafenamide; TDF, tenofovir disoproxil fumarate.

a

Estimated with linear mixed model with linear splines on time, adjusted for age, race, sex (interaction term between age‐sex and race‐sex), BMI, CD4 cell count, endocrine disorders and medications associated with weight gain/loss

b

limited follow‐up beyond nine months.