Type 1 diabetes (T1D)


Diabetes (or diabetes mellitus) is a chronic metabolic disorder caused by an absolute or relative insulin deficiency that leads to abnormally elevated blood sugar (glucose) levels termed as hyperglycaemia. Insulin is the hormone produced by a special type of cells known as β-cells in the pancreas that enables blood sugar to enter cells and be converted into energy.

T1D (formerly known as juvenile-onset diabetes) is an absolute insulin deficiency caused by autoimmune destruction of insulin-producing β cells in the pancreas. Around 5-10% of diabetic cases are T1D, usually affecting children (0-14 years) and young adults (15-19 years), causing severe blood sugar fluctuations that require lifelong insulin treatment to survive.

Risk factors for T1D are still being investigated but include environmental factors, genetic predisposition and viral infections that trigger insulitis and β cell injury from both cellular (T cell) autoimmunity and humoral auto-antibodies responses that lead to a loss of insulin response initially in the pre-diabetic phase and then glucose intolerance in the diabetic phase with a severe loss in beta cell mass. There is an estimated 8 million adults diagnosed with T1D and over 78,000 children develop T1D globally every year, with incidence rising 3.0% per year in children aged 0-14 years.[1],4

Currently T1D cannot be prevented, but research is ongoing to control the environmental factors that trigger the body’s autoimmune destruction of insulin-producing cells.

T1D is acute with the primary clinical signs being ketoacidosis and hypergylcaemia, with symptoms including frequent urination, increased thirst, increased appetite, fatigue, weight loss, lack of concentration, slow-healing wounds and recurrent infections. Other symptoms may include tingling or numbness in hands of feet, blurred vision, and vomiting and stomach pain if ketoacidotic.

Current Treatment


The current treatment (standard of care) for T1D is constant blood sugar monitoring and multiple daily insulin therapy (delivered via injection, infusion pump or transdermal patches) to stabilise blood sugar levels. The goal is to optimise sugar control and minimise complications. There is currently no cure for T1D, treatment is palliative only with limited efficacy providing imperfect sugar control and undesirable side effects that lead to patient compliance issues, diabetes complications and a high patient and public healthcare burden.

Testing methods have improved and better forms of insulin have contributed to improved sugar control and higher life expectancy, but adverse consequences are a major risk for manT1D patients. Many diabetic patients on standard insulin therapy find it difficult to maintain tight sugar levels within the normal range. Side effects of insulin therapy include pain, weight gain and importantly hypoglycaemia that can result in seizures, unconsciousness, brain damage and death.

Reduced Life Expectancy


Chronic hyperglycaemia damages capillaries and small blood vessels in multiple tissues and organs, leading to severe secondary diabetes complications including cardiovascular disease, neuropathy, retinopathy (kidney failure) and strokes that are irreversible, leading to increased morbidity and mortality. Importantly, in addition to quality of life significantly decreased, T1D people’s life expectancy is reduced on average by 20 years.

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