PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
September 29, 2021Frontiers in Cardiovascular Medicine71 citationsOpen Access

Left Ventricular Hypertrophy in Diabetic Cardiomyopathy: A Target for Intervention

MMMohapradeep MohanADAdel DihoumIMIfy Mordi

Key Result

Pharmacological therapies including allopurinol, metformin, and SGLT2 inhibitors show potential in regressing left ventricular hypertrophy in patients with diabetic cardiomyopathy.

Structured PICO

Do allopurinol, SGLT2 inhibitors, and metformin regress left ventricular hypertrophy in patients with and without T2DM?

P
Population
Patients with and without type 2 diabetes mellitus (T2DM), focusing on those with left ventricular hypertrophy (LVH)
I
Intervention
Allopurinol, SGLT2 inhibitors, and metformin
O
Outcome
Regression of left ventricular hypertrophy (LVH)surrogate

This review highlights the potential of targeting asymptomatic left ventricular hypertrophy with allopurinol, SGLT2 inhibitors, or metformin to prevent heart failure in patients with diabetic cardiomyopathy.

Limitations

  • Clinical studies discussed were proof-of-concept studies with small sample sizes
  • Short follow-up periods and treatment durations
  • Small magnitude of LVH regression observed in the trials

Abstract

Heart failure is an important manifestation of diabetic heart disease. Before the development of symptomatic heart failure, as much as 50% of patients with type 2 diabetes mellitus (T2DM) develop asymptomatic left ventricular dysfunction including left ventricular hypertrophy (LVH). Left ventricular hypertrophy (LVH) is highly prevalent in patients with T2DM and is a strong predictor of adverse cardiovascular outcomes including heart failure. Importantly regression of LVH with antihypertensive treatment especially renin angiotensin system blockers reduces cardiovascular morbidity and mortality. However, this approach is only partially effective since LVH persists in 20% of patients with hypertension who attain target blood pressure, implicating the role of other potential mechanisms in the development of LVH. Moreover, the pathophysiology of LVH in T2DM remains unclear and is not fully explained by the hyperglycemia-associated cellular alterations. There is a growing body of evidence that supports the role of inflammation, oxidative stress, AMP-activated kinase (AMPK) and insulin resistance in mediating the development of LVH. The recognition of asymptomatic LVH may offer an opportune target for intervention with cardio-protective therapy in these at-risk patients. In this article, we provide a review of some of the key clinical studies that evaluated the effects of allopurinol, SGLT2 inhibitor and metformin in regressing LVH in patients with and without T2DM.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Mohan et al. (2021) conducted a review in Diabetic Cardiomyopathy and Left Ventricular Hypertrophy. Allopurinol, Metformin, and SGLT2 inhibitors was evaluated. Pharmacological therapies including allopurinol, metformin, and SGLT2 inhibitors show potential in regressing left ventricular hypertrophy in patients with diabetic cardiomyopathy.

synapsesocial.com/papers/6a0f408404e2b0ba896cbe72https://doi.org/10.3389/fcvm.2021.746382
Ask AI
Helpful
Bookmark
Share
View Full Paper

Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Role of AMP-activated protein kinase in healthy and diseased hearts2006 · 130 citations
  2. 2Prevalence and predictors of cardiac hypertrophy and dysfunction in patients with Type 2 diabetes2008 · 61 citations
  3. 3Screening for left ventricular hypertrophy in patients with type 2 diabetes mellitus in the community2011 · 81 citations
  4. 4Type 2 diabetes mellitus-related changes in left ventricular structure and function in patients with chronic kidney disease2018 · 13 citations
  5. 5Changes in cardiovascular risk by reduction of left ventricular mass in hypertension: a meta-analysis2003 · 310 citations