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The insulin resistance syndrome.
1University of Pisa, Italy.
Current Opinion in Nephrology and Hypertension
|December 1, 1992
Summary
Insulin resistance, a key factor in metabolic disorders, involves decreased glucose disposal. Primary insulin resistance, found in healthy individuals and linked to conditions like diabetes and hypertension, may be part of a larger syndrome.
Area of Science:
- Endocrinology and Metabolism
- Human Physiology
- Genetics
Background:
- Insulin resistance is a common metabolic abnormality characterized by reduced insulin-mediated glucose disposal.
- It can be primary (unknown origin, irreversible, organ/pathway-specific) or secondary.
- Primary insulin resistance affects approximately 25% of healthy individuals and is linked to non-insulin-dependent diabetes mellitus, hypertension, and dyslipidemia.
Purpose of the Study:
- To define and characterize primary insulin resistance.
- To explore the concept of an insulin resistance syndrome based on the clustering of related clinical conditions.
- To investigate the potential genetic and atherogenic components of this syndrome.
Main Methods:
- Review and synthesis of existing cross-sectional and longitudinal observations.
- Clinical characterization of primary insulin resistance.
- Conceptual framework development for the insulin resistance syndrome.
Main Results:
- Primary insulin resistance is a distinct entity, often linked to skeletal muscle glucose uptake defects.
- A significant overlap exists between primary insulin resistance and conditions such as non-insulin-dependent diabetes mellitus, essential hypertension, and dyslipidemia.
- These conditions tend to cluster, suggesting a common underlying pathophysiology.
Conclusions:
- The insulin resistance syndrome is proposed as a constellation of interrelated metabolic, anthropometric, and hemodynamic variables centered around insulin resistance or hyperinsulinemia.
- A significant genetic component likely contributes to the syndrome.
- The syndrome may predispose individuals to non-insulin-dependent diabetes mellitus, hypertension, dyslipidemia, and potentially, atherosclerosis.