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Severe insulin resistance syndromes

Authors :
Angelidi, Angeliki M.
Filippaios, Andreas
Mantzoros, Christos S.
Source :
Journal of Clinical Investigation. April, 2021, Vol. 131 Issue 4
Publication Year :
2021

Abstract

Severe insulin resistance syndromes are a heterogeneous group of rare disorders characterized by profound insulin resistance, substantial metabolic abnormalities, and a variety of clinical manifestations and complications. The etiology of these syndromes may be hereditary or acquired, due to defects in insulin potency and action, cellular responsiveness to insulin, and/or aberrations in adipose tissue function or development. Over the past decades, advances in medical technology, particularly in genomic technologies and genetic analyses, have provided insights into the underlying pathophysiological pathways and facilitated the more precise identification of several of these conditions. However, the exact cellular and molecular mechanisms of insulin resistance have not yet been fully elucidated for all syndromes. Moreover, in clinical practice, many of the syndromes are often misdiagnosed or underdiagnosed. The majority of these disorders associate with an increased risk of severe complications and mortality; thus, early identification and personalized clinical management are of the essence. This Review aims to categorize severe insulin resistance syndromes by disease process, including insulin receptor defects, signaling defects, and lipodystrophies. We also highlight several complex syndromes and emphasize the need to identify patients, investigate underlying disease mechanisms, and develop specific treatment regimens.<br />Introduction This Review, inspired by the 100th anniversary of insulin's discovery, focuses on severe insulin resistance syndromes, which constitute only the tip of the iceberg of a wide variety of [...]

Details

Language :
English
ISSN :
00219738
Volume :
131
Issue :
4
Database :
Gale General OneFile
Journal :
Journal of Clinical Investigation
Publication Type :
Academic Journal
Accession number :
edsgcl.652687391
Full Text :
https://doi.org/10.1172/JCI142245