Sodium-glucose Cotransporter-2 Inhibitors in Primary and Secondary Prevention of Cardiovascular and Renal Outcomes in Patients with Type 2 Diabetes Mellitus: A Meta-analysis.


Journal

The Journal of the Association of Physicians of India
ISSN: 0004-5772
Titre abrégé: J Assoc Physicians India
Pays: India
ID NLM: 7505585

Informations de publication

Date de publication:
Aug 2022
Historique:
entrez: 9 9 2022
pubmed: 10 9 2022
medline: 14 9 2022
Statut: ppublish

Résumé

The available evidence was systematically reviewed to evaluate the effects of sodium-glucose cotransporter 2 (SGLT2) inhibitors (SGLT2i) on cardiovascular (CV) and renal outcomes in people with type 2 diabetes mellitus (T2DM) and atherosclerotic cardiovascular disease (ASCVD) or multiple risk factors (MRF), with or without heart failure (HF), and per estimated glomerular filtration rate (eGFR) rate at baseline. We comprehensively searched three electronic databases to retrieve publications up to 30th November 2019, which were screened for inclusion. The data extracted for the outcomes according to baseline ASCVD, HF, and eGFR levels were meta-analyzed using fixed effects model. Of the 735 screened citations, 15 primary and secondary publications from five CV or renal outcome trials were included. SGLT2is reduced the risk of CV death or hospitalization for HF (HHF), HHF alone, and composite renal-specific outcome, irrespective of ASCVD and HF at baseline. The three-point major adverse cardiovascular events (3P-MACE) risk was reduced by 14% (p<0.001) in patients with ASCVD and by 10% (p = 0.018) in those without baseline HF compared with their counterparts. SGLT2is significantly reduced the risk of MACE (18%) in patients with mild kidney dysfunction (eGFR within the range of 60-<90 mL/min/1.73 m2 and <60 mL/min/1.73 m2 ). SGLT2is are effective for both secondary and primary prevention of composite CV outcomes, and secondary prevention of MACE. The upcoming evidence may strengthen the primary prevention benefits of SGLT2is.

Sections du résumé

BACKGROUND BACKGROUND
The available evidence was systematically reviewed to evaluate the effects of sodium-glucose cotransporter 2 (SGLT2) inhibitors (SGLT2i) on cardiovascular (CV) and renal outcomes in people with type 2 diabetes mellitus (T2DM) and atherosclerotic cardiovascular disease (ASCVD) or multiple risk factors (MRF), with or without heart failure (HF), and per estimated glomerular filtration rate (eGFR) rate at baseline.
METHODS METHODS
We comprehensively searched three electronic databases to retrieve publications up to 30th November 2019, which were screened for inclusion. The data extracted for the outcomes according to baseline ASCVD, HF, and eGFR levels were meta-analyzed using fixed effects model.
RESULTS RESULTS
Of the 735 screened citations, 15 primary and secondary publications from five CV or renal outcome trials were included. SGLT2is reduced the risk of CV death or hospitalization for HF (HHF), HHF alone, and composite renal-specific outcome, irrespective of ASCVD and HF at baseline. The three-point major adverse cardiovascular events (3P-MACE) risk was reduced by 14% (p<0.001) in patients with ASCVD and by 10% (p = 0.018) in those without baseline HF compared with their counterparts. SGLT2is significantly reduced the risk of MACE (18%) in patients with mild kidney dysfunction (eGFR within the range of 60-<90 mL/min/1.73 m2 and <60 mL/min/1.73 m2 ).
CONCLUSION CONCLUSIONS
SGLT2is are effective for both secondary and primary prevention of composite CV outcomes, and secondary prevention of MACE. The upcoming evidence may strengthen the primary prevention benefits of SGLT2is.

Identifiants

pubmed: 36082726
doi: 10.5005/japi-11001-0076
doi:

Substances chimiques

Sodium-Glucose Transporter 2 Inhibitors 0
Sodium 9NEZ333N27
Glucose IY9XDZ35W2

Types de publication

Journal Article Meta-Analysis

Langues

eng

Sous-ensembles de citation

IM

Pagination

11-12

Informations de copyright

© Journal of the Association of Physicians of India 2011.

Auteurs

Rajiv Kovil (R)

Diabetologist, Dr. Kovil's Diabetes Care Centre; Corresponding Author.

Manoj Chawla (M)

Diabetologist, Lina Diabetes Care and Mumbai Diabetes Research Centre.

Tejas Shah (T)

Consultant of Diabetology, iVA Speciality Clinic, Mumbai, Maharashtra.

Abhay Sahoo (A)

Endocrinologist, IMS and SUM Hospital, Bhubaneshwar, Odisha.

Brij Makkar (B)

Senior Diabetologist and Obesity Specialist, Dr. Makkar's Diabetes and Obesity Centre, New Delhi, Delhi.

Jothydev Kesavadev (J)

Diabetologist, Jothydev's Diabetes Research Center, Trivandrum, Kerala.

Krishna Seshadri (K)

Senior Consultant-American Board Certified Endocrinology, Diabetes and Metabolism, Chennai Diabetes and Endocrinology Clinic, Chennai, Tamil Nadu.

Mangesh Tiwaskar (M)

Diabetologist, Shilpa Medical Centre, Mumbai, Maharashtra.

Rajesh Rajput (R)

Senior Professor and Head, Department of Medicine VII and Endocrinology, Pt. B.D. Sharma Post Graduate Institute of Medical Sciences, Rohtak, Haryan.

Sanjeev Phatak (S)

Diabetologist and Metabolic Physician, Vijayratna Diabetes Diagnosis and Treatment Centre, Ahmedabad, Gujarat.

Sujoy Majumdar (S)

Endocrinologist, Department of Diabetes, GD Hospital and Diabetes Institute, Kolkata, West Bengal.

Sunil Gupta (S)

Diabetologist, Sunil's Diabetes Care n' Research Centre, Nagpur, Maharashtra, India.

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Classifications MeSH