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Effect of Evogliptin on the Progression of Aortic Valvular Calcification

Authors
 Jae-Kwan Song  ;  Sahmin Lee  ;  Yong-Jin Kim  ;  Hyung-Kwan Kim  ;  Jong-Won Ha  ;  Eui-Young Choi  ;  Seung-Woo Park  ;  Sung-Ji Park  ;  Yong-Hyun Park  ;  Jae-Hyeong Park  ;  Dong Heon Yang  ;  Kye Hun Kim  ;  Dong Hyun Yang  ;  Sangwon Han  ;  Sun Young Chae  ;  Ji Sung Lee  ;  Jong-Min Song  ;  Goo-Yeong Cho 
Citation
 JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, Vol.84(12) : 1064-1075, 2024-09 
Journal Title
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
ISSN
 0735-1097 
Issue Date
2024-09
MeSH
Aged ; Aortic Valve Stenosis* / diagnostic imaging ; Aortic Valve Stenosis* / drug therapy ; Aortic Valve* / diagnostic imaging ; Aortic Valve* / pathology ; Calcinosis* / diagnostic imaging ; Calcinosis* / drug therapy ; Dipeptidyl-Peptidase IV Inhibitors / therapeutic use ; Disease Progression* ; Double-Blind Method ; Female ; Humans ; Male ; Middle Aged ; Piperazines ; Positron-Emission Tomography / methods ; Tomography, X-Ray Computed ; Treatment Outcome
Keywords
aortic stenosis ; calcium signaling ; computed tomography ; evogliptin ; positron emission tomography
Abstract
Background: Medical therapy for aortic stenosis (AS) remains an elusive goal. Objectives: This study sought to establish whether evogliptin, a dipeptidyl peptidase-4 inhibitor, could reduce AS progression. Methods: A total of 228 patients (age 67 ± 11 years; 33% women) with AS were randomly assigned to receive placebo (n = 75), evogliptin 5 mg (n = 77), or evogliptin 10 mg (n = 76). The primary endpoint was the 96-week change in aortic valve calcium volume (AVCV) on computed tomography. Secondary endpoints included the 48-week change in active calcification volume measured using 18F-sodium fluoride positron emission tomography (18F-NaF PET). Results: There were no significant differences in the 96-week changes in AVCV between evogliptin 5 mg and placebo (−5.27; 95% CI: −55.36 to 44.82; P = 0.84) or evogliptin 10 mg and placebo (−18.83; 95% CI: −32.43 to 70.10; P = 0.47). In the placebo group, the increase in AVCV between 48 weeks and 96 weeks was higher than that between baseline and 48 weeks (136 mm3; 95% CI: 108–163 vs 102 mm3; 95% CI: 75–129; P = 0.0485). This increasing trend in the second half of the study was suppressed in both evogliptin groups. The 48-week change in active calcification volume on 18F-NaF PET was significantly lower in both the evogliptin 5 mg (−1,325.6; 95% CI: −2,285.9 to −365.4; P = 0.008) and 10-mg groups (−1,582.2; 95% CI: −2,610.8 to −553.5; P = 0.0038) compared with the placebo group. Conclusions: This exploratory study did not demonstrate the protective effect of evogliptin on AV calcification. Favorable 18F-NaF PET results and possible suppression of aortic valve calcification with longer medication use in the evogliptin groups suggest the need for larger confirmatory trials. (A Multicenter, Double-blind, Placebo-controlled, Stratified-randomized, Parallel, Therapeutic Exploratory Clinical Study to Evaluate the Efficacy and Safety of DA-1229 in Patients With Calcific Aortic Valve Disease; NCT04055883)
Full Text
https://www.sciencedirect.com/science/article/pii/S0735109724078896
DOI
10.1016/j.jacc.2024.06.037
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
Yonsei Authors
Choi, Eui Young(최의영) ORCID logo https://orcid.org/0000-0003-3732-0190
Ha, Jong Won(하종원) ORCID logo https://orcid.org/0000-0002-8260-2958
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/200475
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