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Cardiorenal disease management in type 2 diabetes: An expert consensus
Viswanathan Mohan1, Awadhesh Kumar Singh2, Abdul Hamid Zargar3
1Madras Diabetes Research Foundation & Dr.Mohan's Diabetes Specialities Centre, Chennai, India. Electronic address: http://www.drmohans.com.
Insights
For type 2 diabetes (T2D), sodium-glucose cotransporter-2 inhibitors (SGLT2i) are recommended for heart failure (HF) and chronic kidney disease (CKD). Glucagon-like peptide 1 (GLP-1) agonists are alternatives when SGLT2i are not tolerated.
Area of Science:
- Endocrinology
- Cardiology
- Nephrology
Background:
- The link between cardiovascular disease (CVD), chronic kidney disease (CKD), and type 2 diabetes (T2D) is well-established.
- Managing T2D requires addressing heart failure (HF) and renal complications.
Purpose of the Study:
- To provide expert opinions on preventing and treating HF and renal complications in T2D patients.
- To offer evidence-based recommendations for managing comorbidities in T2D.
Main Methods:
- Consensus recommendations developed by endocrinology, cardiology, and nephrology experts.
- Statements required ≥80% agreement from specialized clinicians.
- Opinions based on scientific evidence and clinical judgment.
Main Results:
- Metformin plus lifestyle modification is the first-line T2D therapy.
- Sodium-glucose cotransporter-2 inhibitors (SGLT2i) are preferred for T2D with HF and CKD.
- Glucagon-like peptide 1 (GLP-1) agonists are options for T2D with atherosclerotic cardiovascular disease (ASCVD) or high-risk indicators, or if SGLT2i are not tolerated.
Conclusions:
- SGLT2i are preferred for T2D patients with HF or ASCVD.
- SGLT2i and GLP-1 receptor agonists (GLP-1RA) reduce cardiovascular outcomes in T2D with ASCVD.
- Treatment selection depends on individual patient profiles.
Background And Aim:
The interplay between cardiovascular disease (CVD), chronic kidney disease (CKD) and type 2 diabetes (T2D) is well established. We aim at providing an evidence-based expert opinion regarding the prevention and treatment of both heart failure (HF) and renal complications in people with T2D.
Method:
ology: The consensus recommendations were developed by subject experts in endocrinology, cardiology, and nephrology. The criteria for consensus were set to statements with ≥80% of agreement among clinicians specialized in endocrinology, cardiology, and nephrology. Key expert opinions were formulated based on scientific evidence and clinical judgment.
Results:
Assessing the risk factors of CVD or CKD in people with diabetes and taking measures to prevent HF or kidney disease are essential. Known CVD or CKD among people with diabetes confers a very high risk for recurrent CVD. Metformin plus lifestyle modification should be the first-line therapy (unless contraindicated) for the management of T2D. Glucagon-like peptide 1 (GLP-1) agonists can be preferred in people with atherosclerotic cardiovascular disease (ASCVD) or with high-risk indicators, along with sodium-glucose cotransporter-2 inhibitors (SGLT2i), whereas SGLT2i are the first choice in HF and CKD. The GLP-1 agonists can be used in people with CKD if SGLT2i are not tolerated.
Conclusion:
Current evidence suggests SGLT2i as preferred agents among people with T2D and HF, and for those with T2D and ASCVD. SGLT2i and GLP-1RA also lower CV outcomes in those with diabetes and ASCVD, and the treatment choice should depend on the patient profile.
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