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Target Diabetes

Contents

Introduction

Diabetes has been known for well over 3,500 years. About 2,000 years ago, Arataeus of Cappadocia described this condition as ‘...a melting down of the flesh and limbs into urine...’, reflecting the weight loss and excess urine produced in acute diabetes. Just over 200 years ago, the excess sugar in the urine of people with diabetes was recognised – an observation that led to the addition of the word mellitus (from the Latin word for sweet) to the word diabetes. Just over 100 years ago, it was demonstrated that the pancreas was involved, when experimental removal of this organ from animals was shown to cause diabetes. About this time, Langerhans had discovered the clusters of cells (islets) in the pancreas that now bear his name. In 1893, these various observations were brought together when Láguesse suggested that the Islets of Langerhans made a substance that prevented excess blood glucose.

Despite several attempts, it was a further 28 years before two Canadian scientists isolated insulin, the substance formed in the pancreas that is fundamental to diabetes. This discovery has been described as one of the first spectacular triumphs of science and the greatest since the introduction of antiseptics 50 years earlier. Insulin became available in 1922 and has continued to be a life-saving medicine ever since.

Its availability also led to the division of diabetes into two forms: type 1, an autoimmune disease in which most of the beta cells have been destroyed and the individual is insulin-dependent from the start, and type 2, where the body is producing inadequate amounts of insulin, or the insulin that the body produces does not work properly. This type can often be controlled by diet and tablets. In the past 50 years, several other forms of medication for type 2 have become available and with a combination of diet, life-style changes and medicines, many people with diabetes can now enjoy a much improved quality of life and a near normal life span. However, it is important to recognise that diabetes can cause great inconvenience and considerable suffering and can greatly limit an individual’s activity. As diabetes progresses, many people are increasingly prone to complications and a significant number develop damage to their eyes, kidneys, blood vessels, heart and nerves. Major efforts to develop medicines for these problems are being made.

Economically, diabetes is a considerable burden on society and the NHS. About 1.4 million people over the age of 16 have the condition in the UK and a sharp increase is projected by the year 2010, due to the ageing population and the effects of obesity. It has been suggested that as many as half the people with type 2 diabetes are undiagnosed. If treatment of the basic condition plus all the possible complications are considered, diabetes has been estimated to consume from 5.5 to 9.4 per cent of NHS resources. In financial terms, this means an excess cost of £2.1 to £2.4 billion – excess cost is the cost of treating diabetes over and above the cost of treating other diseases. NHS prescriptions for people with diabetes cost some £123.7 million in 1996 – only a small proportion of the total cost of diabetes care.

Diabetes can be tackled in several ways: by the development of improved medicines, by taking steps to improve diet, taking more exercise and avoiding obesity, and by improving the control of high blood pressure. Many current approaches to new medicines development are described in this booklet, and the importance of diet and exercise, which can help prevent type 2 diabetes in many people, is also highlighted. In the longer term, pancreas transplantation and gene therapy may bring about a cure, but such techniques are unlikely ever to be widely available. Hopefully, this booklet may encourage some to adopt an altered lifestyle and thus greatly reduce their risk of developing diabetes.

 

 

Acknowledgements


The ABPI wishes to thank member companies for the information provided in the preparation of this booklet, which was researched and written by Dr Mike Hall. We are also indebted to the British Diabetic Association for the use of many photographs and for its help in editing the text. Our thanks are also extended to Dr Stephen Wood and Dr Raj Gill, University of Southampton, for slides of the 3-D structure of insulin and insulin hexamers, to Eli Lilly and Company Limited for the photographs of insulin crystals and self-inject pens, to Amylin Pharmaceuticals for the pictures of amylin structure and deficiency data, to SmithKline Beecham for the photographs of islets of Langerhans and to Smith & Nephew for illustrations of bioengineered skin. The remaining pictures are from the Science Photo Library.

February 1999

 
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