[Metabolic and cardiovascular adverse events of systemic glucocorticoid therapy]

L Fardet1

  • 1Inserm UMR-S 938, service de médecine interne, faculté de médecine, université Pierre-et-Marie-Curie (UPMC) Paris 6, hôpital Saint-Antoine, AP-HP, 184, rue du Faubourg-Saint-Antoine, 75012 Paris, France. laurence.fardet@sat.aphp.fr

La Revue De Medecine Interne
|January 15, 2013
PubMed

Insights

Systemic glucocorticoid therapy can cause serious adverse events like diabetes and hypertension. More research is needed to understand their incidence, risk factors, and optimal management strategies for better patient outcomes.

Area of Science:

  • Endocrinology
  • Pharmacology

Context:

  • Systemic glucocorticoid therapy is associated with numerous adverse events, including metabolic and cardiovascular complications.
  • Existing data on the incidence and risk factors for glucocorticoid-induced dyslipidemia, weight gain, and lipodystrophy are limited and sometimes conflicting.
  • There is a lack of consensus on the optimal management and screening strategies for these adverse events, leading to variability in clinical practice.

Purpose:

  • To review and synthesize available data on the adverse events associated with systemic glucocorticoid therapy.
  • To identify gaps in knowledge regarding the incidence, risk factors, and management of glucocorticoid-induced metabolic and cardiovascular complications.
  • To explore the potential utility of data from patients with endogenous hypercorticism to inform understanding of glucocorticoid-induced adverse events.

Summary:

  • Glucocorticoid therapy frequently leads to adverse events such as diabetes, dyslipidemia, hypertension, weight gain, lipodystrophy, and cardiovascular events.
  • Key aspects like the precise incidence and risk factors for dyslipidemia, weight gain, and lipodystrophy remain incompletely understood.
  • Uncertainty surrounds the optimal pharmacological treatment for glucocorticoid-induced diabetes and hypertension, and screening/prevention strategies lack standardized consensus.

Impact:

  • Highlights the significant clinical burden and knowledge gaps associated with systemic glucocorticoid therapy's adverse effects.
  • Underscores the need for further research to establish evidence-based guidelines for managing and preventing these complications.
  • Suggests leveraging data from endogenous hypercorticism to potentially address current uncertainties in glucocorticoid-induced adverse event management.

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