Hyperproinsulinemia

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Hyperproinsulinemia
Autosomal dominant - en.svg
This condition is inherited in an autosomal dominant manner.

Hyperproinsulinemia is a disease where insulin is not sufficiently processed before secretion [1] and immature forms of insulin make up the majority of circulating insulin immunoreactivity in both fasting and glucose-stimulated conditions (insulin immunoreactivity refers to all molecules detectable by an insulin antibody, i.e. insulin, proinsulin, and proinsulin-like material). The term is composed of hyper - high, proinsulin - immature insulin molecule, and -emia - blood condition.[ citation needed ]

Hyperproinsulinemia is more frequent in type 2 diabetes. It has been attributed to either a direct β-cells defect or an indirect effect of cell dysregulation under sustained elevated blood glucose (hyperglycemia).[ citation needed ]

Some alleles of insulin can cause hyperproinsulinemia (see table 2: monogenic forms of type 1 diabetes, INS (insulin). For a more detailed descriptions of the insulin gene variations leading to hyperproinsulinemia see NCBI's OMIM 176730

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<span class="mw-page-title-main">C-peptide</span> Chemical compound

The connecting peptide, or C-peptide, is a short 31-amino-acid polypeptide that connects insulin's A-chain to its B-chain in the proinsulin molecule. In the context of diabetes or hypoglycemia, a measurement of C-peptide blood serum levels can be used to distinguish between different conditions with similar clinical features.

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References

  1. Dhanvantari S, Shen FS, Adams T, et al. (September 2003). "Disruption of a receptor-mediated mechanism for intracellular sorting of proinsulin in familial hyperproinsulinemia". Mol. Endocrinol. 17 (9): 1856–67. doi: 10.1210/me.2002-0380 . PMID   12829804.