TY - JOUR
T1 - The FimAsartaN proTeinuriA SusTaIned reduCtion in comparison with losartan in diabetic chronic kidney disease (FANTASTIC) trial
AU - Yoo, Tae Hyun
AU - Hong, Soon Jun
AU - Kim, Sunggyun
AU - Shin, Seokjoon
AU - Kim, Dong Ki
AU - Lee, Jung Pyo
AU - Han, Sang Youb
AU - Lee, Sangho
AU - Won, Jong Chul
AU - Kang, Young Sun
AU - Park, Jongha
AU - Han, Byoung Geun
AU - Na, Ki Ryang
AU - Hur, Kyu Yeon
AU - Kim, Yong Jin
AU - Park, Sungha
N1 - Publisher Copyright:
© 2022, The Author(s), under exclusive licence to The Japanese Society of Hypertension.
PY - 2022/12
Y1 - 2022/12
N2 - As angiotensin II type 1 receptor blockers (ARBs) may have different antiproteinuric effects in diabetic kidney disease (DKD), we ascertained the albuminuria-reducing effect of fimasartan and losartan in patients with DKD. This was a randomized, multicenter, double-blind, 4-parallel-group, dose-titration, phase III study designed to compare the efficacy of fimasartan and losartan in reducing albuminuria in patients with DKD (NCT02620306). The primary endpoint was the rate of change in albuminuria from baseline to week 24. A total of 341 patients were randomized to different groups. The urinary albumin-to-creatinine ratio (ACR), systolic blood pressure (SBP), and diastolic blood pressure (DBP) were not different between the fimasartan and losartan groups at baseline (ACR: 1376.84 vs. 1521.07 mg/gCr, SBP: 154.69 vs. 154.47 mmHg, DBP: 83.96 vs. 83.83 mmHg). However, ACR reduction was significantly larger in the fimasartan group than in the losartan group during the entire study period (% changes in the ACR at 4, 8, 12, and 24 weeks were –23.58, –33.06, –35.00, and –38.13 in the fimasartan group vs. –8.74, –10.17, –14.91, and –19.71 in the losartan group, p < 0.01, respectively). The superior antiproteinuric effect of fimasartan compared to losartan was still significant after adjustment for SBP levels. There were no significant differences in adverse events, including the incidences of estimated glomerular filtration decline and hyperkalemia. This study demonstrates that compared to losartan, fimasartan significantly reduces albuminuria in patients with DKD, even after adjustment for SBP and DBP.
AB - As angiotensin II type 1 receptor blockers (ARBs) may have different antiproteinuric effects in diabetic kidney disease (DKD), we ascertained the albuminuria-reducing effect of fimasartan and losartan in patients with DKD. This was a randomized, multicenter, double-blind, 4-parallel-group, dose-titration, phase III study designed to compare the efficacy of fimasartan and losartan in reducing albuminuria in patients with DKD (NCT02620306). The primary endpoint was the rate of change in albuminuria from baseline to week 24. A total of 341 patients were randomized to different groups. The urinary albumin-to-creatinine ratio (ACR), systolic blood pressure (SBP), and diastolic blood pressure (DBP) were not different between the fimasartan and losartan groups at baseline (ACR: 1376.84 vs. 1521.07 mg/gCr, SBP: 154.69 vs. 154.47 mmHg, DBP: 83.96 vs. 83.83 mmHg). However, ACR reduction was significantly larger in the fimasartan group than in the losartan group during the entire study period (% changes in the ACR at 4, 8, 12, and 24 weeks were –23.58, –33.06, –35.00, and –38.13 in the fimasartan group vs. –8.74, –10.17, –14.91, and –19.71 in the losartan group, p < 0.01, respectively). The superior antiproteinuric effect of fimasartan compared to losartan was still significant after adjustment for SBP levels. There were no significant differences in adverse events, including the incidences of estimated glomerular filtration decline and hyperkalemia. This study demonstrates that compared to losartan, fimasartan significantly reduces albuminuria in patients with DKD, even after adjustment for SBP and DBP.
KW - Blood pressure
KW - Diabetic nephropathy
KW - Mortality
KW - Proteinuria
KW - Renal endpoint
UR - http://www.scopus.com/inward/record.url?scp=85138133839&partnerID=8YFLogxK
U2 - 10.1038/s41440-022-01028-6
DO - 10.1038/s41440-022-01028-6
M3 - Article
C2 - 36123398
AN - SCOPUS:85138133839
VL - 45
SP - 2008
EP - 2017
JO - Hypertension Research
JF - Hypertension Research
SN - 0916-9636
IS - 12
ER -