echemi logo
Product
  • Product
  • Supplier
  • Inquiry
    Home > Active Ingredient News > Endocrine System > The latest data of "fenerone" announced! The cardiorenal benefit of "type 2 diabetes" is not affected by HbA1c variability and course 2022EASD

    The latest data of "fenerone" announced! The cardiorenal benefit of "type 2 diabetes" is not affected by HbA1c variability and course 2022EASD

    • Last Update: 2023-01-07
    • Source: Internet
    • Author: User
    Search more information of high quality chemicals, good prices and reliable suppliers, visit www.echemi.com

    Translator: Dong Bingzi Affiliated Hospital of Qingdao University

     

    Introduction: From September 19 to 23, 2022, the 2022 European Association for the Study of Diabetes Annual Conference, a major international conference in the field of endocrinology, was held
    in Stockholm, Sweden in the form of "online + offline".
    At the meeting, scholars shared a research report
    entitled "The effect of fenerone on patients with chronic kidney disease and type 2 diabetes is not related to baseline HbA1c level, HbA1c variability and diabetes course".

     

     

     

    Previous studies: Phenirenal ketone confers cardiac and renal benefits in type 2 diabetes

     

    Finerenone is a third-generation mineralocorticoid receptor antagonist, and according to the FIDELIO-DKD and FIGARO-DKD study pooled analysis, finelidone can reduce cardiovascular risk and renal outcomes
    in patients with type 2 diabetes and chronic kidney disease (CKD).
    In this study, the team of investigators assessed the effects of
    fenelidone by baseline HbA1c, HbA1c variability, and diabetes course.

     

    Patients with type 2 diabetes and CKD (urine albumin-to-creatinine ratio [UACR] ≥30-≤5000 mg/g and eGFR≥25 ml/min/1.
    73 m2) were randomized to phenelidone or placebo
    .
    To compare the effects
    of fenelidone with placebo on cardiovascular events (including cardiovascular death, non-fatal myocardial infarction, nonfatal stroke or heart failure hospitalization) and renal (renal failure, sustained decline in eGFR from baseline ≥57%, or death from renal cause) by baseline HbA1c quartile analysis, HbA1c variability and diabetes course quartile analysis 。 Among 13,026 participants, the mean baseline HbA1c was 7.
    7% and the mean duration of diabetes was 15.
    4 years
    .
    Higher baseline HbA1c quartiles have longer diabetes duration and more
    diabetes-related complications.

     

    Recent data: Fenelidone cardiorenal benefit, independent of HbA1c fluctuations and diabetes course

     

    ➤ Compared with placebo, the effect of pheniolidone in reducing cardiovascular risk and renal composite endpoints was consistent
    with HbA1c (p-interaction 0.
    52 and 0.
    09, respectively) and diabetes course quartiles (p-interaction 0.
    12 and 0.
    75, respectively).

    ➤ HbA1c variability in the first year of treatment is associated with
    higher cardiorenal risk.

    ➤ For each 1 increase in mean absolute residual of HbA1c, the risk of cardiovascular events increased by 20% (HR 1.
    20; 95% CI 1.
    07-1.
    35; p=0.
    0016) and by 36% (HR 1.
    36; 95% CI 1.
    21-1.
    52; p<0.
    001
    ).

    ➤ The cardiovascular and renal benefits of phenirenal were not affected by HbA1c variability (p-interaction 0.
    48 and 0.
    09, respectively).

     

    Summary of this article

     

    This study showed that increased HbA1c variability was associated with an increased risk of cardiorenal outcomes, and baseline HbA1c, HbA1c variability, or diabetes course did not alter the cardiorenal benefit
    of finerone in patients with CKD and type 2 diabetes.
    In June 2022, China has approved fenerone, a new generation of non-steroidal selective mineralocorticoid receptor antagonists, to improve the risk of cardiovascular and renal events in type 2 diabetes-related chronic kidney disease, which is a new choice
    to improve cardiovascular and renal outcomes in patients with type 2 diabetes.

     

    Translator's introduction

     

     

    Dong Bingzi

     

    Doctor of Medicine, Postdoctoral Fellow, Deputy Chief Physician, Department of Endocrinology, Affiliated Hospital of
    Qingdao University.
    Graduated from Tokushima University (Japanese Ministry of Education, Culture, Sports, Culture, Sports, Scholarship International Student), engaged in clinical and basic research on bone metabolism
    .
    In recent years, he has published 13 SCI papers as the first/corresponding author, published research results in JBMR, Int J Biol Sci, etc.
    , participated in the editing of 3 monographs, 2 main translators, presided over 1 National Natural Science Foundation of China, 2 provincial and ministerial projects, and participated in 2 provincial and ministerial awards
    .
    He is currently a youth committee member of the Endocrinology Branch of the Chinese Geriatrics Association, a member of the Osteoporosis and Bone Mineral Diseases Specialist Branch of Shandong Medical Association, a member of the Osteoporosis and Bone Mineral Diseases Branch of Shandong Medical Association, and a member and secretary
    of the Osteoporosis and Bone Mineral Diseases Specialty Branch of Qingdao Medical Association.

    This article is an English version of an article which is originally in the Chinese language on echemi.com and is provided for information purposes only. This website makes no representation or warranty of any kind, either expressed or implied, as to the accuracy, completeness ownership or reliability of the article or any translations thereof. If you have any concerns or complaints relating to the article, please send an email, providing a detailed description of the concern or complaint, to service@echemi.com. A staff member will contact you within 5 working days. Once verified, infringing content will be removed immediately.

    Contact Us

    The source of this page with content of products and services is from Internet, which doesn't represent ECHEMI's opinion. If you have any queries, please write to service@echemi.com. It will be replied within 5 days.

    Moreover, if you find any instances of plagiarism from the page, please send email to service@echemi.com with relevant evidence.