Almost a century ago, in 1901, Eugene L. Opie described "hyalinedegeneration of the islands of Langerhans" in the pancreas ofpatients with hyperglycemia (Figure 1).1 A relation with diabetesmellitus was suggested, although at that time insulin had notyet been identified as an islet protein. The chief componentof the proteinaceous deposits described by Opie laterreferred to as islet amyloid was identified in 1986as a protein of beta-cell origin named islet amyloid polypeptide.2Islet amyloid is a characteristic pathological finding in patientswith type 2 diabetes mellitus, being present in more than . . . [Full Text of this Article]
Amyloid
Islet Amyloid and Type 2 Diabetes Mellitus
Islet Amyloid and Islet Amyloid Polypeptide
The Expression of Human Islet Amyloid Polypeptide in Transgenic Mice
Cytotoxicity of Human Islet Amyloid Polypeptide and Islet Amyloid
Islet Amyloid as a Target for Therapy in Type 2 Diabetes
Inhibition of the Production of Islet Amyloid Polypeptide
Direct Inhibition
Indirect Inhibition
Inhibition of the Formation of Amyloid Fibrils
Conclusions
Source Information
From the Departments of Internal Medicine (J.W.M.H., C.J.M.L.) and Pathology (J.W.M.H.), University Medical Center, Utrecht, the Netherlands; and the Department of Medicine, Lund University and Malmö University Hospital, Malmö, Sweden (B.A.).
Address reprint requests to Dr. Höppener at University Hospital Utrecht, H 04.312, P.O. Box 85500, 3508 GA Utrecht, the Netherlands, or at j.w.m.hoeppener@lab.azu.nl.
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