Are two Gliflozins different: A Prospective Multicenter Randomized Study to Assess Effect of Remogliflozin compared to Empagliflozin on Biomarkers of Heart Failure in Indian Patients of Type 2 diabetes mellitus with Chronic Heart Failure (REMIT-HF study).

Biomarker Gliflozin Heart failure

Journal

Journal of cardiac failure
ISSN: 1532-8414
Titre abrégé: J Card Fail
Pays: United States
ID NLM: 9442138

Informations de publication

Date de publication:
14 Aug 2024
Historique:
received: 19 06 2024
accepted: 09 07 2024
medline: 17 8 2024
pubmed: 17 8 2024
entrez: 16 8 2024
Statut: aheadofprint

Résumé

There is limited data comparing two gliflozins on their effect on biomarkers in diabetic patients with chronic heart failure. A prospective, multicenter, active controlled, double-arm, investigator-initiated, interventional study enrolled 250 adults with T2DM and comorbid CHF (LVEF<40%; NT-proBNP >600pg/ml). 125 patients were allocated each to Remogliflozin (R) and Empagliflozin (E) group and followed up for 24 weeks. The primary endpoint was the mean percentage change from baseline in NT-proBNP level after 24 weeks. There was significant improvement from baseline in mean NT-proBNP level in both groups after 24 weeks however there was no significant difference between the two groups (p= 0.214). The mean NT-proBNP level improved from 2078.15±1764.70 pg/ml at baseline to 1185.06±1164.21 pg/ml at 6 months in R-group (p≤0.001) and from 2283.98±1759.15 pg/ml at baseline to 1395.33±1304.18 pg/ml at 6 months in E-group (p= <0.001). Left ventricular ejection fraction (LVEF) and LV volumes improved in both the groups. The glycemic parameters (HbA1c, FPG and PPG) demonstrated a significant reduction from baseline to week 24 in both groups. Similar improvement was seen in heart rate, blood pressure and weight reduction over 6 months in both groups. There was no drug related serious adverse event in any group. Remogliflozin and Empagliflozin significantly improves glycemic parameters and NT-proBNP levels as the index of the therapeutic effects in T2DM patients with CHF. The positive effects are comparable in both groups.

Sections du résumé

BACKGROUND BACKGROUND
There is limited data comparing two gliflozins on their effect on biomarkers in diabetic patients with chronic heart failure.
METHODS METHODS
A prospective, multicenter, active controlled, double-arm, investigator-initiated, interventional study enrolled 250 adults with T2DM and comorbid CHF (LVEF<40%; NT-proBNP >600pg/ml). 125 patients were allocated each to Remogliflozin (R) and Empagliflozin (E) group and followed up for 24 weeks. The primary endpoint was the mean percentage change from baseline in NT-proBNP level after 24 weeks.
RESULTS RESULTS
There was significant improvement from baseline in mean NT-proBNP level in both groups after 24 weeks however there was no significant difference between the two groups (p= 0.214). The mean NT-proBNP level improved from 2078.15±1764.70 pg/ml at baseline to 1185.06±1164.21 pg/ml at 6 months in R-group (p≤0.001) and from 2283.98±1759.15 pg/ml at baseline to 1395.33±1304.18 pg/ml at 6 months in E-group (p= <0.001). Left ventricular ejection fraction (LVEF) and LV volumes improved in both the groups. The glycemic parameters (HbA1c, FPG and PPG) demonstrated a significant reduction from baseline to week 24 in both groups. Similar improvement was seen in heart rate, blood pressure and weight reduction over 6 months in both groups. There was no drug related serious adverse event in any group.
CONCLUSION CONCLUSIONS
Remogliflozin and Empagliflozin significantly improves glycemic parameters and NT-proBNP levels as the index of the therapeutic effects in T2DM patients with CHF. The positive effects are comparable in both groups.

Identifiants

pubmed: 39151723
pii: S1071-9164(24)00315-4
doi: 10.1016/j.cardfail.2024.07.020
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024. Published by Elsevier Inc.

Déclaration de conflit d'intérêts

Disclosures None

Auteurs

Shantanu Sengupta (S)

Sengupta Hospital and Research Institute, Nagpur, India. Electronic address: senguptasp@gmail.com.

Jayagopal Pb (J)

Lakshmi Hospital, Palakkad, India.

Ashwani Mehta (A)

Sir Gangaram Hospital, Delhi, India.

Jps Sawhney (J)

Sir Gangaram Hospital, Delhi, India.

Satish Suryavanshi (S)

SMC Heart Institute, Raipur, India.

Naveen Jamwal (N)

RML Institute, Lucknow, India.

Dilip Kadam (D)

Care Hospital, Pune, India.

Ambanna Gowda (A)

Citizen Hospital, Bangalore, India.

Ramesh Dargad (R)

Stress test clinic, Mumbai, India.

Amit Bhate (A)

Jeevan Rekha Hospital, Belagavi, India.

Vinod Kapoor (V)

New Leelamani Hospital, Kanpur, India.

Sumit Bhushan (S)

Glenmark Pharmaceuticals, India.

Abhishek Mane (A)

Glenmark Pharmaceuticals, India.

Rujuta Gadkari (R)

Glenmark Pharmaceuticals, India.

Saiprasad Patil (S)

Glenmark Pharmaceuticals, India.

Hanmant Barkate (H)

Glenmark Pharmaceuticals, India.

Classifications MeSH