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Neither Gastric Bypass Surgery Nor Diet-Induced Weight-Loss Affect OATP1B1 Activity as Measured by Rosuvastatin Oral Clearance.

Authors :
Hovd, Markus
Robertsen, Ida
Johnson, Line Kristin
Krogstad, Veronica
Wegler, Christine
Kvitne, Kine Eide
Kringen, Marianne Kristiansen
Skovlund, Eva
Karlsson, Cecilia
Andersson, Shalini
Artursson, Per
Sandbu, Rune
Hjelmesæth, Jøran
Åsberg, Anders
Jansson-Löfmark, Rasmus
Christensen, Hege
Source :
Clinical Pharmacokinetics. May2023, Vol. 62 Issue 5, p725-735. 11p.
Publication Year :
2023

Abstract

Introduction: Rosuvastatin pharmacokinetics is mainly dependent on the activity of hepatic uptake transporter OATP1B1. In this study, we aimed to investigate and disentangle the effect of Roux-en-Y gastric bypass (RYGB) and weight loss on oral clearance (CL/F) of rosuvastatin as a measure of OATP1B1-activity. Methods: Patients with severe obesity preparing for RYGB (n = 40) or diet-induced weight loss (n = 40) were included and followed for 2 years, with four 24-hour pharmacokinetic investigations. Both groups underwent a 3-week low-energy diet (LED; < 1200 kcal/day), followed by RYGB or a 6-week very-low-energy diet (VLED; < 800 kcal/day). Results: A total of 80 patients were included in the RYGB group (40 patients) and diet-group (40 patients). The weight loss was similar between the groups following LED and RYGB. The LED induced a similar (mean [95% CI]) decrease in CL/F in both intervention groups (RYGB: 16% [0, 31], diet: 23% [8, 38]), but neither induced VLED resulted in any further changes in CL/F. At Year 2, CL/F had increased by 21% from baseline in the RYGB group, while it was unaltered in the diet group. Patients expressing the reduced function SLCO1B1 variants (c.521TC/CC) showed similar changes in CL/F over time compared with patients expressing the wild-type variant. Conclusions: Neither body weight, weight loss nor RYGB per se seem to affect OATP1B1 activity to a clinically relevant degree. Overall, the observed changes in rosuvastatin pharmacokinetics were minor, and unlikely to be of clinical relevance. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
03125963
Volume :
62
Issue :
5
Database :
Academic Search Index
Journal :
Clinical Pharmacokinetics
Publication Type :
Academic Journal
Accession number :
163719004
Full Text :
https://doi.org/10.1007/s40262-023-01235-5